Humate-P

Manufacturer
CSL Behring GmbH
Effective date
2020-08-17
Label type
PLASMA DERIVATIVE
Version
16
Source
full-release
Hydrated at
2026-06-01 02:49:42

Label at a glance#

ProductHumate-P
Active ingredientHUMAN COAGULATION FACTOR VIII/VON WILLEBRAND FACTOR COMPLEX
Label structure18 sections

Indications and uses

HUMATE-P, Antihemophilic Factor/von Willebrand Factor Complex (Human), is indicated for treatment and prevention of bleeding in adults with hemophilia A (classical hemophilia). HUMATE-P is also indicated in adult and pediatric patients with von Willebrand disease (VWD) for: (1) treatment of spontaneous and trauma-induced bleeding episodes, and (2) prevention of excessive bleeding during and after surgery. This app...

Dosage and administration

One International Unit (IU) of Factor VIII (FVIII) activity per kg body weight will increase the circulating FVIII level by approximately 2.0 International Units (IU)/dL. Dosage must be individualized based on the patient's weight, type and severity of hemorrhage, FVIII level, and presence of inhibitors. Judge the adequacy of treatment by clinical effects and, in all cases, adjust doses as needed based on clinical...

Storage and handling

HUMATE-P is supplied in a single-dose vial containing the labeled amount of VWF:RCo and FVIII activity expressed in International Units (IU). Components are not made with natural rubber latex. When stored at temperatures up to 25°C (77°F), HUMATE-P is stable for 36 months up to the expiration date printed on its label. Do not freeze. HUMATE-P does not contain a preservative and should be used within 3 hours after ...

Label contents#

Full prescribing information#

1 INDICATIONS AND USAGE

INDICATIONS & USAGE SECTION

1.1 Hemophilia A

SPL UNCLASSIFIED SECTION

HUMATE-P, Antihemophilic Factor/von Willebrand Factor Complex (Human), is indicated for treatment and prevention of bleeding in adults with hemophilia A (classical hemophilia).

1.2 Von Willebrand Disease (VWD)

SPL UNCLASSIFIED SECTION

HUMATE-P is also indicated in adult and pediatric patients with von Willebrand disease (VWD) for:

  • treatment of spontaneous and trauma-induced bleeding episodes, and
  • prevention of excessive bleeding during and after surgery. This applies to patients with severe VWD as well as patients with mild to moderate VWD where use of desmopressin (DDAVP) is known or suspected to be inadequate.

Controlled clinical trials to evaluate the safety and efficacy of prophylactic dosing with HUMATE-P to prevent spontaneous bleeding have not been conducted in VWD subjects [see Clinical Studies (14)].

2 DOSAGE AND ADMINISTRATION

DOSAGE & ADMINISTRATION SECTION

2.1 Therapy for Hemophilia A

SPL UNCLASSIFIED SECTION

One International Unit (IU) of Factor VIII (FVIII) activity per kg body weight will increase the circulating FVIII level by approximately 2.0 International Units (IU)/dL. Dosage must be individualized based on the patient's weight, type and severity of hemorrhage, FVIII level, and presence of inhibitors. Judge the adequacy of treatment by clinical effects and, in all cases, adjust doses as needed based on clinical judgment and on frequent monitoring of the patient's FVIII level. Table 1 provides dosing recommendations for the treatment of hemophilia A in adults.

Table 1. Dosing Recommendations for the Treatment of Hemophilia A in Adults1
Hemorrhagic EventDosage (IU FVIII:C/kg Body Weight)
IU = International Units.
Minor hemorrhage:
  • Early joint or muscle bleed
  • Severe epistaxis
Loading dose 15 IU FVIII:C/kg to achieve a FVIII:C plasma level of approximately 30% of normal; one infusion may be sufficient. If needed, half of the loading dose may be given once or twice daily for 1-2 days.
Moderate hemorrhage:
  • Advanced joint or muscle bleed
  • Neck, tongue, or pharyngeal hematoma (without airway compromise)
  • Tooth extraction
  • Severe abdominal pain
Loading dose 25 IU FVIII:C/kg to achieve a FVIII:C plasma level of approximately 50% of normal, followed by 15 IU FVIII:C/kg every 8-12 hours for the first 1-2 days to maintain the FVIII:C plasma level at 30% of normal.
Continue the same dose once or twice daily for up to 7 days or until adequate wound healing is achieved.
Life-threatening hemorrhage:
  • Major surgery
  • Gastrointestinal bleeding
  • Neck, tongue, or pharyngeal hematoma (with potential for airway compromise)
  • Intracranial, intraabdominal, or intrathoracic bleeding
  • Fractures
Initially 40-50 IU FVIII:C/kg, followed by 20-25 IU FVIII:C/kg every 8 hours to maintain the FVIII:C plasma level at 80-100% of normal for 7 days.
Continue the same dose once or twice daily for another 7 days to maintain the FVIII:C level at 30-50% of normal.

2.2 Treatment of Bleeding Episodes in VWD

SPL UNCLASSIFIED SECTION

Administer 40 to 80 International Units (IU) VWF:RCo (corresponding to 17 to 33 International Units (IU) FVIII in HUMATE-P) per kg body weight every 8 to 12 hours. Adjust the dosage based on the extent and location of bleeding. Administer repeat doses as long as needed based on monitoring of appropriate clinical and laboratory measures [see Warnings and Precautions (5.2, 5.3)]. Expected levels of VWF:RCo are based on an expected in vivo recovery (IVR) of 2.0 International Units (IU)/dL rise per International Unit (IU)/kg VWF:RCo administered. The administration of 1 International Unit (IU) of FVIII per kg body weight can be expected to lead to a rise in circulating VWF:RCo of approximately 5 International Units (IU)/dL. Table 2 provides dosing recommendations for adult and pediatric patients [see Use in Specific Populations (8.4)].2

Table 2. VWF:RCo Dosing Recommendations for the Treatment of Bleeding Episodes by VWD Type
VWD TypeSeverity of HemorrhageDosage (IU* VWF:RCo/kg Body Weight)
Type 1 VWD – Mild
(baseline VWF:RCo activity typically >30%)
Minor
(e.g., epistaxis, oral bleeding, menorrhagia)
Typically treatable with desmopressin.
Minor
(when desmopressin is known or suspected to be inadequate)
Major†
(e.g., severe or refractory epistaxis, GI bleeding, CNS trauma, traumatic hemorrhage)
Loading dose 40-60 IU/kg.
Then 40-50 IU/kg every 8-12 hours for 3 days to keep the trough level of VWF:RCo >50%.
Then 40-50 IU/kg daily for up to 7 days.
Type 1 VWD – Moderate or severe (baseline VWF:RCo typically <30%)Minor
(e.g., epistaxis, oral bleeding, menorrhagia)
40-50 IU/kg (1 or 2 doses).
Major
(e.g., severe or refractory epistaxis, GI bleeding, CNS trauma, hemarthrosis, traumatic hemorrhage)
Loading dose 50-75 IU/kg.
Then 40-60 IU/kg every 8-12 hours for 3 days to keep the trough level of VWF:RCo >50%.
Then 40-60 IU/kg daily for up to 7 days.
Type 2 VWD (all variants) and Type 3 VWDMinor
(clinical indications above)
40-50 IU/kg (1 or 2 doses).
Major
(clinical indications above)
Loading dose 60-80 IU/kg.
Then 40-60 IU/kg every 8-12 hours for 3 days to keep the trough level of VWF:RCo >50%.
Then 40-60 IU/kg daily for up to 7 days.

* IU = International Units.

† For major bleeds in all types of VWD where repeated dosing is required, monitor and maintain the patient's FVIII level according to the guidelines for hemophilia A therapy.

2.3 Prevention of Excessive Bleeding During and After Surgery in VWD

SPL UNCLASSIFIED SECTION

The following information provides guidelines for calculating loading and maintenance doses of HUMATE-P for patients undergoing surgery. However in the case of emergency surgery, administer a loading dose of 50 to 60 International Units (IU) VWF:RCo/kg body weight and, subsequently, closely monitor the patient's trough coagulation factor levels.

Measure incremental IVR and assess plasma VWF:RCo and FVIII:C levels in all patients prior to surgery when possible.

To determine IVR:

  1. Measure the baseline plasma VWF:RCo level.
  2. Infuse a calculated dose [International Units (IU)/kg] of VWF:RCo product intravenously at "time 0".
  3. At "time+30 minutes", measure the plasma VWF:RCo level.

Use the following formula to calculate IVR:

IVR = (Plasma VWF:RCotime+30 min – Plasma VWF:RCobaseline International Units (IU)/dL)
Calculated dose (International Units (IU)/kg)

For example, assuming a baseline VWF:RCo of 30 International Units (IU)/dL at "time 0", a calculated dose of 60 International Units (IU)/kg, and a VWF:RCo of 120 International Units (IU)/dL at "time+30 minutes", the IVR would be 1.5 International Units (IU)/dL per International Units (IU)/kg of VWF:RCo administered.

SPL UNCLASSIFIED SECTION

Loading Dose

Table 3 provides guidelines for calculating the loading dose for adult and pediatric patients based on the target peak plasma VWF:RCo level, the baseline VWF:RCo level, body weight in kilograms, and IVR. When individual recovery values are not available, a standardized loading dose can be used based on an assumed VWF:RCo IVR of 2.0 International Units (IU)/dL per International Unit (IU)/kg of VWF:RCo administered.

Table 3. VWF:RCo and FVIII:C Loading Dose Calculations for the Prevention of Excessive Bleeding During and After Surgery for All Types of VWD
Type of SurgeryVWF:RCo
Target Peak Plasma Level
FVIII:C
Target Peak Plasma Level
Calculation of Loading Dose
(to be administered 1 to 2 hours before surgery)
IU = International Units.
BW = body weight.
Major100 IU/dL80-100 IU/dLΔ* VWF:RCo × BW (kg)
IVR†
= IU VWF:RCo required
If the IVR is not available, assume an IVR of 2.0 IU/dL per IU/kg and calculate the loading dose as follows:
(100 – baseline plasma VWF:RCo) × BW (kg)/2.0
Minor/Oral‡ 50-60 IU/dL40-50 IU/dLΔ* VWF:RCo × BW (kg)
IVR
= IU VWF:RCo required
Emergency100 IU/dL80-100 IU/dLAdminister a dose of 50-60 IU VWF:RCo/kg body weight.

* Δ = Target peak plasma VWF:RCo level – baseline plasma VWF:RCo level.

† IVR = in vivo recovery as measured in the patient.

‡ Oral surgery is defined as extraction of fewer than three teeth, if the teeth are non-molars and have no bony involvement. Extraction of more than one impacted wisdom tooth is considered major surgery due to the expected difficulty of the surgery and the expected blood loss, particularly in subjects with type 2A or type 3 VWD. Extraction of more than two teeth is considered major surgery in all patients.

For example, the loading dose of HUMATE-P required assuming a target VWF:RCo level of 100 International Units (IU)/dL, a baseline VWF:RCo level of 20 International Units (IU)/dL, an IVR of 2.0 International Units (IU)/dL per International Units (IU)/kg, and a body weight of 70 kg would be 2,800 International Units (IU) VWF:RCo, calculated as follows:

IU = International Units.
(100 IU/dL – 20 IU/dL) × 70 kg= 2,800 IU VWF:RCo required
2.0 (IU/dL)/(IU/kg)

Attaining a target peak FVIII:C plasma level of 80 to 100 International Units (IU) FVIII:C/dL for major surgery and 40 to 50 International Units (IU) FVIII:C/dL for minor surgery or oral surgery might require additional dosing with HUMATE-P. Because the ratio of VWF:RCo to FVIII:C activity in HUMATE-P is 2.4:1, any additional dosing will increase VWF:RCo proportionally more than FVIII:C. Assuming an incremental IVR of 2.0 International Units (IU) VWF:RCo/dL per International Units (IU)/kg infused, additional dosing to increase FVIII:C in plasma will also increase plasma VWF:RCo by approximately 5 International Units (IU)/dL for each International Unit (IU)/kg of FVIII administered.

SPL UNCLASSIFIED SECTION

Maintenance Doses

The initial maintenance dose of HUMATE-P for the prevention of excessive bleeding during and after surgery should be half of the loading dose, irrespective of additional dosing required to meet FVIII:C targets. Subsequent maintenance doses should be based on the patient's VWF:RCo and FVIII levels. Table 4 provides recommendations for target trough plasma levels (based on type of surgery and number of days following surgery) and minimum duration of treatment for subsequent maintenance doses. These recommendations apply to both adult and pediatric patients.

Table 4. VWF:RCo and FVIII:C Target Trough Plasma Level and Minimum Duration of Treatment Recommendations for Subsequent Maintenance Doses for the Prevention of Excessive Bleeding During and After Surgery
Type of SurgeryVWF:RCo
Target Trough Plasma Level*
FVIII:C
Target Trough Plasma Level*
Minimum Duration of Treatment
Up to 3 days following surgeryAfter Day 3Up to 3 days following surgeryAfter Day 3
IU = International Units.
Major>50 IU/dL>30 IU/dL>50 IU/dL>30 IU/dL72 hours
Minor≥30 IU/dL––>30 IU/dL48 hours
Oral† ≥30 IU/dL––>30 IU/dL8-12 hours‡

* Trough levels for either coagulation factor should not exceed 100 IU/dL.

† Oral surgery is defined as extraction of fewer than three teeth, if the teeth are non-molars and have no bony involvement. Extraction of more than one impacted wisdom tooth is considered major surgery due to the expected difficulty of the surgery and the expected blood loss, particularly in subjects with type 2A or type 3 VWD. Extraction of more than two teeth is considered major surgery in all patients.

‡ Administer at least one maintenance dose following oral surgery based on individual pharmacokinetic values. Subsequent therapy with an antifibrinolytic agent is usually administered until adequate healing is achieved.

Based on individual pharmacokinetic-derived half-lives, the frequency of maintenance doses is generally every 8 or 12 hours; patients with shorter half-lives may require dosing every 6 hours. In the absence of pharmacokinetic data, it is recommended that HUMATE-P be administered initially every 8 hours with further adjustments determined by monitoring trough coagulation factor levels. When hemostatic levels are judged insufficient or trough levels are outside the recommended range, consider modifying the administration interval and/or the dose.

It is advisable to monitor trough VWF:RCo and FVIII:C levels at least once a day in order to adjust HUMATE-P dosing as needed to avoid excessive accumulation of coagulation factors. The duration of treatment generally depends on the type of surgery performed, but must be assessed for individual patients based on their hemostatic response [see Clinical Studies (14.2)].

2.4 Reconstitution

SPL UNCLASSIFIED SECTION

  • Prepare and administer using aseptic techniques.
  • Use either the Mix2Vial® filter transfer set provided with HUMATE-P [see How Supplied/Storage and Handling (16)] or a commercially available double-ended needle and vented filter spike.
  • Use plastic disposable syringes with HUMATE-P. Protein solutions of this type tend to adhere to the ground glass surface of all-glass syringes.
  • Reconstitute HUMATE-P at room temperature as follows:
  1. Ensure that the HUMATE-P vial and diluent vial are at room temperature.
  2. Place the HUMATE-P vial, diluent vial and Mix2Vial transfer set on a flat surface.
  3. Remove the HUMATE-P and diluent vial flip caps. Wipe the stoppers with an alcohol swab and allow the stoppers to dry prior to opening the Mix2Vial transfer set package.
  4. Open the Mix2Vial transfer set package by peeling away the lid (Fig. 1). Leave the Mix2Vial transfer set in the clear package.
    Figure 1Figure 1
    Fig. 1
  5. Place the diluent vial on a flat surface and hold the vial tightly. Grip the Mix2Vial transfer set together with the clear package and push the plastic spike at the blue end of the Mix2Vial transfer set firmly through the center of the stopper of the diluent vial (Fig. 2).
    Figure 2Figure 2
    Fig. 2
  6. Carefully remove the clear package from the Mix2Vial transfer set. Make sure that you pull up only the clear package, not the Mix2Vial transfer set (Fig. 3).
    Figure 3Figure 3
    Fig. 3
  7. With the HUMATE-P vial placed firmly on a flat surface, invert the diluent vial with the Mix2Vial transfer set attached and push the plastic spike of the transparent adapter firmly through the center of the stopper of the HUMATE-P vial (Fig. 4). The diluent will automatically transfer into the HUMATE-P vial.
    Figure 4Figure 4
    Fig. 4
  8. With the diluent and Humate-P vial still attached to the Mix2Vial transfer set, gently swirl the HUMATE-P vial to ensure that the HUMATE-P is fully dissolved (Fig. 5). Do not shake the vial.
    Figure 5Figure 5
    Fig. 5
  9. With one hand grasp the HUMATE-P side of the Mix2Vial transfer set and with the other hand grasp the blue diluent-side of the Mix2Vial transfer set, and unscrew the set into two pieces (Fig. 6).
    Figure 6Figure 6
    Fig. 6
  10. Draw air into an empty, sterile syringe. While the HUMATE-P vial is upright, screw the syringe to the Mix2Vial transfer set. Inject air into the HUMATE-P vial. While keeping the syringe plunger pressed, invert the system upside down and draw the concentrate into the syringe by pulling the plunger back slowly (Fig. 7).
    Figure 7Figure 7
    Fig. 7
  11. Now that the concentrate has been transferred into the syringe, firmly grasp the barrel of the syringe (keeping the syringe plunger facing down) and unscrew the syringe from the Mix2Vial transfer set (Fig. 8). Attach the syringe to a suitable intravenous administration set.
    Figure 8Figure 8
    Fig. 8
  12. If patient requires more than one vial, pool the contents of multiple vials into one syringe. Use a separate unused Mix2Vial for each product vial.

2.5 Administration

SPL UNCLASSIFIED SECTION

HUMATE-P is for intravenous use only.

  • The solution should be clear or slightly opalescent. After filtering/withdrawal, the reconstituted product should be inspected visually for particulate matter and discoloration prior to administration. Even if the directions for use for the reconstitution procedure are precisely followed, it is not uncommon for a few flakes or particles to remain. The filter included in the Mix2Vial device removes those particles completely. Filtration does not influence dosage calculations. Do not use visibly cloudy solutions or solutions still containing flakes or particles after filtration.
  • Do not refrigerate HUMATE-P after reconstitution. Administer within 3 hours after reconstitution.
  • Slowly infuse the solution (maximally 4 mL/minute) with a suitable intravenous administration set.
  • Discard the administration equipment and any unused HUMATE-P after use.

3 DOSAGE FORMS AND STRENGTHS

DOSAGE FORMS & STRENGTHS SECTION

HUMATE-P is available as a sterile, lyophilized powder for intravenous administration following reconstitution. Each single-dose vial of HUMATE-P contains the labeled amount of VWF:RCo and FVIII activity expressed in International Units (IU). The average ratio of VWF:RCo to FVIII is 2.4:1.

Approximate potencies are shown below; check each carton/vial for the actual potency prior to reconstitution:

Table 5. Dosage Forms and Strengths
VWF:RCo/vialFVIII/vialDiluent
IU = International Units.
600 IU250 IU5 mL
1200 IU500 IU10 mL
2400 IU1000 IU15 mL

4 CONTRAINDICATIONS

CONTRAINDICATIONS SECTION

HUMATE-P is contraindicated in individuals who have had an anaphylactic or severe systemic reaction to antihemophilic factor or von Willebrand factor preparations.

5 WARNINGS AND PRECAUTIONS

WARNINGS AND PRECAUTIONS SECTION

5.1 Thromboembolic Events (VWD Patients)

SPL UNCLASSIFIED SECTION

Thromboembolic events have been reported in VWD patients receiving Antihemophilic Factor/von Willebrand Factor Complex replacement therapy, especially in the setting of known risk factors for thrombosis.3,4 Early reports indicate a higher incidence may occur in females. Endogenous high levels of FVIII have also been associated with thrombosis, but no causal relationship has been established. Exercise caution and consider antithrombotic measures in all at-risk VWD patients who are receiving coagulation factor replacement therapy.

5.2 Monitoring for Intravascular Hemolysis

SPL UNCLASSIFIED SECTION

HUMATE-P contains blood group isoagglutinins (anti-A and anti-B). When doses are very large or need to be repeated frequently (for example, when inhibitors are present or when pre- and post-surgical care is involved), monitor patients of blood groups A, B, and AB for signs of intravascular hemolysis and decreasing hematocrit values and treat appropriately.

5.3 Monitoring VWF:RCo and FVIII Levels

SPL UNCLASSIFIED SECTION

Monitor the VWF:RCo and FVIII levels of VWD patients receiving HUMATE-P using standard coagulation tests, especially in cases of surgery. It is advisable to monitor trough VWF:RCo and FVIII:C levels at least once a day in order to adjust the dosage of HUMATE-P as needed to avoid excessive accumulation of coagulation factors [see Dosage and Administration (2.2, 2.3)].

5.4 Transmission of Infectious Agents

SPL UNCLASSIFIED SECTION

Because HUMATE-P is made from human blood, it may carry a risk of transmitting infectious agents, e.g., viruses, the variant Creutzfeldt-Jakob disease (vCJD) agent and, theoretically, the Creutzfeldt-Jakob disease (CJD) agent [see Description (11) and Patient Counseling Information (17)]. The risk that such products will transmit an infectious agent has been reduced by screening plasma donors for prior exposure to certain viruses, by testing for the presence of certain current virus infections, and by inactivating and/or removing certain viruses during manufacturing [see Description (11)].

Despite these measures, such products can still potentially transmit disease. There is also the possibility that unknown infectious agents may be present in such products. Thus the risk of transmission of infectious agents cannot be eliminated completely. Report all infections thought by a physician possibly to have been transmitted by this product to CSL Behring Pharmacovigilance at 1-866-915-6958 or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch.

Some viruses, such as Parvovirus B19 virus (B19V) or hepatitis A (HAV), are particularly difficult to remove or inactivate. B19V may most seriously affect pregnant women and immune-compromised individuals.

Although the overwhelming number of B19V and HAV cases are community acquired, reports of these infections have been associated with the use of some plasma-derived products. Therefore, physicians should be alert to the potential symptoms of B19V and HAV infections [see Patient Counseling Information (17)].

Symptoms of B19V may include low-grade fever, rash, arthralgia, and transient symmetric, nondestructive arthritis. Diagnosis is often established by measuring B19V-specific IgM and IgG antibodies. Symptoms of HAV include low-grade fever, anorexia, nausea, vomiting, fatigue, and jaundice. A diagnosis may be established by measuring specific IgM antibodies.

Physicians should strongly consider administration of hepatitis A and hepatitis B vaccines to individuals receiving plasma derivatives. Potential risks and benefits of vaccination should be weighed by the physician and discussed with the patient.

6 ADVERSE REACTIONS

ADVERSE REACTIONS SECTION

The most serious adverse reaction observed in patients receiving HUMATE-P is anaphylaxis. Thromboembolic events have also been observed in patients receiving HUMATE-P for the treatment of VWD [see Warnings and Precautions (5.1)]. Reports of thromboembolic events in VWD patients with other thrombotic risk factors receiving coagulation factor replacement therapy have been obtained from spontaneous reports, published literature, and a European clinical study. In some cases, inhibitors to coagulation factors may occur. However, no inhibitor formation was observed in any of the clinical studies.

In patients receiving HUMATE-P in clinical studies for treatment of VWD, the most commonly reported adverse reactions observed by >5% of subjects are allergic-anaphylactic reactions (including urticaria, chest tightness, rash, pruritus, and edema). For patients undergoing surgery, the most common adverse reactions are postoperative wound and injection-site bleeding, and epistaxis.

6.1 Clinical Trials Experience

CLINICAL TRIALS EXPERIENCE SECTION

Because clinical trials are conducted under widely varying conditions, the adverse reaction rates observed cannot be directly compared to rates in other clinical trials and may not reflect the rates observed in practice.

SPL UNCLASSIFIED SECTION

Treatment of Bleeding Episodes in VWD

Allergic symptoms, including allergic reaction, urticaria, chest tightness, rash, pruritus, and edema, were reported in 6 of 97 (6%) subjects in a Canadian retrospective study [see Clinical Studies (14.1)]. Four of 97 (4%) subjects experienced seven adverse events that were considered to have a possible or probable relationship to HUMATE-P. These included chills, phlebitis, vasodilation, paresthesia, pruritus, rash, and urticaria. All were mild in intensity with the exception of a moderate case of pruritus.

In a prospective, open-label safety and efficacy study of HUMATE-P in VWD subjects with serious life- or limb-threatening bleeding or undergoing emergency surgery, seven of 71 (10%) subjects experienced nine adverse reactions. These were one occurrence each of mild vasodilation and mild pruritis; two occurrences of mild paresthesia; and one occurrence each of moderate peripheral edema and extremity pain and severe pseudothrombocytopenia (platelet clumping with a false low reading). HUMATE-P was discontinued in the subject who experienced the peripheral edema and extremity pain.

SPL UNCLASSIFIED SECTION

Prevention of Excessive Bleeding During and After Surgery in VWD

Among the 63 VWD subjects who received HUMATE-P for prevention of excessive bleeding during and after surgery, including one subject who underwent colonoscopy without the planned polypectomy, the most common adverse events were postoperative hemorrhage (35 events in 19 subjects with five subjects experiencing bleeding at up to three different sites), postoperative nausea (15 subjects), and postoperative pain (11 subjects). Table 6 presents the postoperative hemorrhagic adverse events.

Table 6. Hemorrhagic Adverse Events in 63 Surgical Subjects
Adverse EventSurgical Procedure CategoryNumber of Subjects/EventsOnset*
(Number of Events)
Severity
(Number of Events)
OnPostMildModSevere
Wound/injection site bleedingMajor8/11749–2
Minor2/22–11–
Oral2/6–633–
EpistaxisMajor4/42231–
Minor1/11–1––
Cerebral hemorrhage/subdural hematomaMajor1/22† ––2–
Gastrointestinal bleedingMajor1/33‡ ––21
MenorrhagiaMajor1/11§ ––1–
Groin bleedOral1/1–11––
Ear bleedMajor1/11–1––
HemoptysisMajor1/11–1––
HematuriaMajor1/11–1––
Shoulder bleedMajor1/11–1––

* On = on-therapy; onset while receiving HUMATE-P or within 1 day of completing HUMATE-P administration. Post = post-therapy; onset at least one day after completing HUMATE-P administration.

† Reported as serious adverse events following intracranial surgery.

‡ Two of these events were reported as serious adverse events following gastrojejunal bypass.

§ Reported as a serious adverse event requiring hysterectomy following hysteroscopy and dilation and curettage.

Table 7 lists the non-hemorrhagic adverse events reported in at least two subjects, regardless of causality, and the adverse events that were possibly related to HUMATE-P. Pulmonary embolus considered possibly related to HUMATE-P occurred in one elderly subject who underwent bilateral knee replacement.

Table 7. Non-Hemorrhagic and Possibly Related Adverse Events in 63 Surgical Subjects
Body SystemAdverse Event (AE)Number of Subjects with an AE Possibly Related to HUMATE-PNumber of Subjects with an AE Regardless of Causality*
Body as a wholePain–11
Fever–4
Abdominal pain–3
Infection–3
Surgery–3
Back pain–2
Facial edema–2
CardiovascularChest pain–3
Pulmonary embolus† 11
Thrombophlebitis† 11
DigestiveNausea115
Constipation–7
Vomiting13
Sore throat–2
Hemic and lymphatic systemAnemia/decreased hemoglobin–2
Metabolic/nutritionalIncreased SGPT11
NervousDizziness15
Headache14
Increased sweating–3
Insomnia–2
Skin and appendagesPruritus–3
Rash11
UrogenitalUrinary retention–4
Urinary tract infection–2

* Events occurring in two or more subjects.

† Events occurring in separate subjects.

Eight subjects experienced 10 postoperative serious adverse events: one with subdural hematoma and intracerebral bleeding following intracranial surgery related to an underlying cerebrovascular abnormality; one with two occurrences of gastrointestinal bleeding following gastrojejunal bypass; and one each with sepsis, facial edema, infection, menorrhagia requiring hysterectomy following hysteroscopy and dilation and curettage, pyelonephritis, and pulmonary embolus.

6.2 Postmarketing Experience

POSTMARKETING EXPERIENCE SECTION

The following adverse reactions have been identified during postapproval use of HUMATE-P. Because these reactions are reported voluntarily from a population of uncertain size, it is not always possible to reliably estimate their frequency or establish a causal relationship to HUMATE-P exposure.

Adverse reactions reported in patients receiving HUMATE-P for treatment of VWD or hemophilia A are allergic-anaphylactic reactions (including urticaria, chest tightness, rash, pruritus, edema, and shock), development of inhibitors to FVIII, and hemolysis. Additional adverse reactions reported for VWD are thromboembolic complications, chills and fever, and hypervolemia.

7 DRUG INTERACTIONS

DRUG INTERACTIONS SECTION

None reported.

8 USE IN SPECIFIC POPULATIONS

USE IN SPECIFIC POPULATIONS SECTION

8.1 Pregnancy

PREGNANCY SECTION

Animal reproduction studies have not been conducted with HUMATE-P. It is also not known whether HUMATE-P can cause fetal harm when administered to a pregnant woman or can affect reproduction capacity. HUMATE-P should be given to a pregnant woman only if clearly needed.

8.2 Labor and Delivery

LABOR & DELIVERY SECTION

It is not known whether HUMATE-P can cause harm to the mother or the fetus when administered during labor and delivery. HUMATE-P should be given during labor and delivery only if clearly needed.

8.3 Nursing Mothers

NURSING MOTHERS SECTION

It is not known whether this drug is excreted in human milk. Because many drugs are excreted in human milk, caution should be exercised when HUMATE-P is administered to a nursing woman.

8.4 Pediatric Use

PEDIATRIC USE SECTION

SPL UNCLASSIFIED SECTION

Hemophilia A

Adequate and well-controlled studies with long-term evaluation of joint damage have not been done in pediatric subjects. Joint damage may result from suboptimal treatment of hemarthroses.

SPL UNCLASSIFIED SECTION

VWD

The safety and effectiveness of HUMATE-P for the treatment of VWD was demonstrated in 26 pediatric subjects, including infants, children, and adolescents, but have not been evaluated in neonates. The safety of HUMATE-P for the prevention of excessive bleeding during and after surgery was demonstrated in eight pediatric subjects (ages 3 to 15) with VWD. Of the 34 pediatric subjects studied for either treatment of bleeding episodes in VWD or prevention of excessive bleeding during and after surgery, four were infants (1 month to under 2 years of age), 23 were children (2 through 12 years), and seven were adolescents (13 through 15 years).

As in adults, pediatric patients should be dosed based on body weight (kg) [see Dosage and Administration (2.2, 2.3)].

8.5 Geriatric Use

GERIATRIC USE SECTION

Clinical studies of HUMATE-P did not include sufficient numbers of subjects 65 years of age and older to determine whether they respond differently from younger subjects. As for all patients, dosing for geriatric patients should be appropriate to their overall situation.

11 DESCRIPTION

DESCRIPTION SECTION

HUMATE-P, Antihemophilic Factor/von Willebrand Factor Complex (Human), is a purified, sterile, lyophilized concentrate of Factor VIII (FVIII) and von Willebrand Factor (VWF) (Human) for intravenous administration in the treatment of patients with classical hemophilia (hemophilia A) and VWD [see Clinical Pharmacology (12)].

HUMATE-P is purified from the cold insoluble fraction of pooled human plasma. The pooled human plasma used to produce HUMATE-P is collected from licensed facilities in the United States (US). All source plasma used in the manufacture of HUMATE-P is tested by FDA-licensed Nucleic Acid Tests (NAT) for hepatitis C virus (HCV), human immunodeficiency virus-1 (HIV-1), hepatitis A virus (HAV), and hepatitis B virus (HBV) and found to be nonreactive (negative).

Each vial of HUMATE-P contains the labeled amount of von Willebrand Factor:Ristocetin Cofactor (VWF:RCo) and FVIII activity expressed in International Units (IU) [see Dosage Forms and Strengths (3)], as defined by the current international standard established by the World Health Organization. One International Unit (IU) of VWF:RCo or FVIII is approximately equal to the amount of VWF:RCo or FVIII in 1.0 mL of fresh-pooled human plasma. The average ratio of VWF:RCo to FVIII is 2.4:1. Fibrinogen content in HUMATE-P is less than or equal to 0.2 mg/mL. HUMATE-P contains anti-A and anti-B blood group isoagglutinins [see Warnings and Precautions (5.2)].

When reconstituted with the volume of Sterile Water for Injection, USP provided, each mL of HUMATE-P contains 72 to 224 International Units (IU) VWF:RCo activity15, 40 to 80 International Units (IU) FVIII activity, 15 to 33 mg of glycine, 3.5 to 9.3 mg of sodium citrate, 2 to 5.3 mg of sodium chloride, 8 to 16 mg of Albumin (Human), 2 to 4 mg of other proteins, and 10 to 20 mg of total proteins. HUMATE-P contains no preservative.

The manufacturing procedure for HUMATE-P includes multiple processing steps that reduce the risk of virus transmission. The virus inactivation/removal capacity consists of four steps:

  • Cryoprecipitation
  • Al(OH)3 adsorption, glycine precipitation, and NaCl precipitation, studied in combination
  • Heat treatment at 60°C for 10 hours in aqueous solution
  • Lyophilization

The total cumulative virus reductions range from 6.0 to ≥11.7 log10 as shown in Table 8.

Table 8. Cumulative Virus Reduction Factors for HUMATE-P
Manufacturing StepVirus Reduction Factor (log10)
Enveloped VirusesNon-Enveloped Viruses
HIV-1BVDVPRVWNVHAVCPVB19V
HIV-1, human immunodeficiency virus type 1, model for HIV-1 and HIV-2
BVDV, bovine viral diarrhea virus, model for HCV
PRV, pseudorabies virus, model for large enveloped DNA viruses
WNV, West Nile virus
HAV, hepatitis A virus
CPV, canine parvovirus, model for B19V
B19V, human parvovirus B19
ND, not determined
NA, not applicable
CryoprecipitationNDND1.6NDND1.9ND
Al(OH)3 Adsorption/Glycine Precipitation/NaCl Precipitation3.82.83.9ND2.33.0ND
Heat Treatment* ≥6.4≥8.94.7≥7.84.21.1≥3.9†
LyophilizationNDNDNDND1.3NDND
Cumulative Virus Reduction [log10]≥10.2≥11.710.2NA7.86.0NA

* At 60°C for 10 hours in aqueous solution.

† The virus evaluation studies for B19V employed a novel experimental infectivity assay using a clone of the cell line UT7 that contains erythropoietic progenitor cells; (residual) virus titer was determined using an immunofluorescence-based detection method.

15 This correlates to a VWF:RCo to FVIII activity average ratio of 2.4:1, which is used to calculate the nominal values of VWF:RCo activity and is the average VWF:RCo activity.

12 CLINICAL PHARMACOLOGY

CLINICAL PHARMACOLOGY SECTION

12.1 Mechanism of Action

MECHANISM OF ACTION SECTION

The active components of HUMATE-P consist of two different noncovalently bound proteins (FVIII and VWF). FVIII is an essential cofactor in activation of factor X, leading ultimately to the formation of thrombin and, subsequently, fibrin. VWF promotes platelet aggregation and platelet adhesion on damaged vascular endothelium; activated platelets interact with clotting proteins to form a clot. VWF also serves as a stabilizing carrier protein for the procoagulant protein FVIII.5,6 The activity of VWF is measured as VWF:RCo.

12.3 Pharmacokinetics

PHARMACOKINETICS SECTION

SPL UNCLASSIFIED SECTION

Hemophilia A

After infusion of HUMATE-P, a rapid increase of plasma FVIII:C is followed by a rapid decrease in activity and, subsequently, a slower rate of decrease in activity. Studies with HUMATE-P in subjects with hemophilia A have demonstrated a mean half-life of 12.2 (range: 8.4 to 17.4) hours.

SPL UNCLASSIFIED SECTION

VWD

The pharmacokinetics of HUMATE-P were studied in 41 subjects in a US study and in 28 subjects in a European study [see Clinical Studies (14.2)]. In both studies, subjects were evaluated in the nonbleeding state prior to a surgical procedure. Table 9 summarizes the pharmacokinetics of HUMATE-P based on these studies. Wide inter-subject variability was observed in pharmacokinetic values obtained from these studies.

Table 9. Pharmacokinetics of HUMATE-P in Two Studies of Subjects in the Non-Bleeding State Prior to Surgery
US StudyEuropean Study
IU = International Units.
BW = body weight.
Number of subjects4128
  Type 1 VWD1610
  Type 2A VWD210
  Type 2B VWD4--
  Type 2M VWD61
  Type 3 VWD137
Dosage of HUMATE-P60 IU VWF:RCo/kg BW80 IU VWF:RCo/kg BW
Median terminal half-life of VWF:RCo (range)11 hours*
(3.5-33.6)
10 hours†
(2.8-28.3)
Median clearance (range)3.1 mL/hr/kg
(1-16.6)
4.8 mL/hr/kg
(2.1-53)
Volume of distribution at steady state (range)53 mL/kg
(29-141)
59 mL/kg
(32-290)
Median IVR for VWF:RCo activity (range)2.4 IU/dL per IU/kg
(1.1-4.2)
1.9 IU/dL per IU/kg
(0.6-4.5)

* Excluding 5 subjects with a half-life exceeding the blood sampling time of 24 or 48 hours.

† Excluding 1 subject with a half-life exceeding the blood sampling time of 48 hours.

HUMATE-P has been demonstrated in several studies to contain the high molecular weight multimers of VWF. The presence of a multimeric composition of VWF in HUMATE-P is similar to that found in normal plasma and this component is considered to be important for correcting the coagulation defect in patients with VWD.7,8

The multimeric patterns of HUMATE-P in the US study were measured in 13 subjects with type 3 VWD; 11 had absent or barely detectable multimers at baseline. Of those 11 subjects, all had some high molecular weight multimers present 24 hours after infusion of HUMATE-P. In the European study, infusion of HUMATE-P corrected the defect of the multimer pattern in subjects with types 2A and 3 VWD. High molecular weight multimers were detectable until at least 8 hours after infusion.

Based on the small sample size evaluation, it appears that age, sex, and type of VWD have no impact on the pharmacokinetics of VWF:RCo.

14 CLINICAL STUDIES

CLINICAL STUDIES SECTION

Controlled clinical studies to evaluate the safety and efficacy of prophylactic dosing with HUMATE-P to prevent spontaneous bleeding have not been conducted in VWD subjects. Adequate data are not presently available on which to evaluate or to base dosing recommendations in this setting.

14.1 Treatment of Bleeding Episodes in VWD

SPL UNCLASSIFIED SECTION

Clinical efficacy of HUMATE-P in the control of bleeding in subjects with VWD was determined by a retrospective review of clinical safety and efficacy data obtained from 97 Canadian VWD subjects who received product under an Emergency Drug Release Program. The dosage schedule and duration of therapy were determined by the medical practitioner.

There were 514 requests for product use for surgery, bleeding, or prophylaxis in the 97 subjects. Of these, HUMATE-P was not used in 151 cases, and follow-up safety and/or efficacy information was available for 303 (83%) of the remaining 363 requests. In many cases, HUMATE-P from a single request was used for several treatment courses in one subject. Therefore, there are more reported treatment courses than requests.

HUMATE-P was administered to 97 subjects in 530 treatment courses: 73 for surgery, 344 for treatment of bleeding, and 20 for prophylaxis of bleeding. The majority of the 93 "other" uses involved dental procedures, diagnostic procedures, prophylaxis prior to a procedure, or test doses.

Table 10 summarizes the dosing information (all subjects) for bleeding episodes.

Table 10. Dosing Information for Bleeding Episodes in VWD
Type/Location of Bleeding Episode
Digestive SystemNose+Mouth
+Pharynx
Integument SystemFemale
Genital System
Musculo-skeletal
SD, standard deviation.
No. of Subjects142911422
Loading DoseMean Dose (SD)* 62.1 (31.1)66.9 (24.3)73.4 (37.7)88.5 (28.3)50.2 (24.9)
No. of Infusions† 37127227107
Maintenance DoseMean Dose (SD)* 61.5 (38.0)67.5 (22.4)56.5 (63.3)74.5 (17.7)63.8 (28.8)
No. of Infusions† 25055415121
No. of Treatment Days per Bleeding EpisodeMean (SD)
No. of Events
4.6 (3.6)
49
1.4 (1.2)
130
1.1 (0.4)
22
2.8 (2.9)
9
2.0 (1.9)
108
No. of Infusions by Treatment Day
No. of Subjects142911422
Day 1‡ Mean (SD)
No. of Events
1.2 (0.4)
49
1.1 (0.2)
130
1.0 (0.2)
22
1.0 (0.0)
9
1.0 (0.1)
108
No. of Subjects1393115
Day 2Mean (SD)
No. of Events
1.2 (0.6)
41
1.3 (0.5)
12
1.0 (0.0)
3
1.0 (-)
1
1.2 (0.5)
26
No. of Subjects126-210
Day 3Mean (SD)
No. of Events
1.5 (0.8)
25
1.4 (0.7)
9
-
-
1.0 (0.0)
3
1.2 (0.4)
18

* IU VWF:RCo/kg.

† Number of infusions where the dose per kg body weight was available.

‡ Day 1, first treatment day.

14.2 Prevention of Excessive Bleeding During and After Surgery in VWD

SPL UNCLASSIFIED SECTION

Two prospective, open-label, non-controlled, multicenter clinical studies, one in the US and one in Europe, investigated the safety and hemostatic efficacy of HUMATE-P in subjects with VWD undergoing surgery.

SPL UNCLASSIFIED SECTION

• US clinical study – The primary objective of this study was to demonstrate the safety and hemostatic efficacy of HUMATE-P in preventing excessive bleeding in adult and pediatric subjects with VWD undergoing surgery. The 35 subjects (21 female and 14 male) ranged in age from 3 to 75 years (mean 32.9); seven were age 15 or younger and two were age 65 or older. Twelve subjects had type 1 VWD, two had type 2A, three had type 2B, five had type 2M, and 13 had type 3. Twenty-eight of the surgical procedures were classified as major (e.g., orthopedic joint replacement, intracranial surgery, multiple tooth extractions, laparoscopic cholecystectomy), four as minor (e.g., placement of intravenous access device), and three subjects had oral surgery23. Seven of the 13 subjects with type 3 VWD had major surgery.

The first 15 subjects received a loading dose of HUMATE-P corresponding to 1.5 times the "full dose" (defined as the dose predicted to achieve a peak VWF:RCo level of 100 International Units (IU)/dL as determined by each subject's calculated IVR and baseline VWF:RCo level); the loading dose did not vary with the type of surgery performed (i.e., major, minor, or oral). The remaining 20 subjects were dosed based on individual pharmacokinetic assessments and target peak VWF:RCo levels of 80 to 100 International Units (IU)/dL for major surgery and 50 to 60 International Units (IU)/dL for minor or oral surgery, respectively. All 35 subjects received initial maintenance doses corresponding to 0.5 times the full dose at intervals of 6, 8, or 12 hours after surgery as determined by their individual half-lives for VWF:RCo; subsequent maintenance doses were adjusted based on regular measurements of trough VWF:RCo and FVIII:C levels. The median duration of treatment was 1 day (range: 1 to 2 days) for oral surgery, 5 days (range: 3 to 7 days) for minor surgery, and 5.5 days (range: 2 to 26 days) for major surgery.

23 Oral surgery is defined as extraction of fewer than three teeth, if the teeth are non-molars and have no bony involvement. Extraction of more than one impacted wisdom tooth is considered major surgery due to the expected difficulty of the surgery and the expected blood loss, particularly in subjects with type 2A or type 3 VWD. Extraction of more than two teeth is considered major surgery in all patients.

SPL UNCLASSIFIED SECTION

• European clinical study – The primary objective of this study was to assess the ability of HUMATE-P to effectively correct the coagulation defect in subjects with VWD undergoing elective surgery, as demonstrated by an increase in VWF:RCo and FVIII, a shortening of the prolonged bleeding time, and the prevention and/or cessation of excessive bleeding. This study did not have a pre-stated hypothesis to evaluate hemostatic efficacy. The 27 subjects (18 females and nine males) ranged in age from 5 to 81 years (median age: 46 years); one was age 5, and five were older than 65. Ten subjects had type 1 VWD, nine had type 2A, one had type 2M, and seven had type 3. Sixteen of the surgical procedures were classified as major (orthopedic joint replacement, hysterectomy, multiple tooth extractions, laparoscopic adnexectomy, laparoscopic cholecystectomy, and basal cell carcinoma excision). Six of the seven subjects with type 3 VWD had major surgery.

Dosing was individualized based on a pharmacokinetic assessment performed before surgery. The median duration of treatment was 3.5 days (range: 1 to 17 days) for minor surgery and 9 days (range: 1 to 17 days) for major surgery.

In both studies, assessments of the hemostatic efficacy of HUMATE-P in preventing excessive bleeding were performed at the end of surgery, 24 hours after the last infusion of HUMATE-P, and at the end of the study (14 days following surgery).

Table 11 summarizes the end-of-surgery hemostatic efficacy assessments in subjects participating in either the US or European study.

Table 11. Investigator's End-of-Surgery Hemostatic Efficacy Assessments for the US and European Surgical Studies
Number of SubjectsEnd-of-Surgery Hemostatic Efficacy Assessments
Effective
(Excellent / Good)*
95% Confidence Interval (CI) for Effective Proportion†
US study3532 (91.4%)78.5-97.6%
European study26‡ 25 (96%)82-99.8%

* Excellent: Hemostasis clinically not significantly different from normal.
Good: Mildly abnormal hemostasis in terms of quantity and/or quality (e.g., slight oozing).

† 95% CIs according to Blyth-Still-Casella.

‡ One subject with missing information.

Table 12 summarizes the overall hemostatic efficacy assessments in subjects participating in either the US or European study. HUMATE-P was effective in preventing excessive bleeding during and after surgery.

Table 12. Investigator's Overall Hemostatic Efficacy Assessments for the US and European Surgical Studies
Number of SubjectsOverall Hemostatic Assessments
Effective
(Excellent / Good)*
95% CI for Effective Proportion†
US study‡ 3535 (100%)91.3-100%
European study§ 2726 (96.3%)82.5-99.8%

* Excellent: Hemostasis clinically not significantly different from normal.
Good: Mildly abnormal hemostasis in terms of quantity and/or quality (e.g., slight oozing).

† 95% CIs according to Blyth-Still-Casella.

‡ Overall hemostatic efficacy was assessed 24 hours after the last HUMATE-P infusion or 14 days after surgery, whichever came earlier.

§ Overall hemostatic efficacy was not prospectively defined for the European study; the efficacy result displayed is the least efficacious ranking assigned by an investigator between surgery and Day 14.

In the US study, all efficacy assessments were reviewed by an independent Data Safety Monitoring Board (DSMB). The DSMB agreed with the investigators' assessments of the overall hemostatic efficacy for all but two subjects (neither of whom had type 3 VWD). Based on this, the DSMB judged hemostatic efficacy as "effective" in 33 (94.3%) (95% CI: 81.1% to 99.0%) of the 35 subjects.

In the US study, the median actual estimated blood loss did not exceed the median expected blood loss, regardless of the type of surgery. Table 13 shows the median expected and actual estimated blood loss during surgery in the US study.

Table 13. Expected and Actual Estimated Blood Loss During Surgery in the US Study
Estimated Blood LossOral Surgery
(n=3)
Minor Surgery
(n=4)
Major Surgery
(n=28)
Total
(n=35)
Expected – Median (range) mL10 (5-50)8 (0-15)50 (0-300)* 20 (0-300)*
Actual – Median (range) mL3 (0-15)3 (0-10)26 (0-300)† 18 (0-300)†

* One subject with missing information

† Five subjects with missing information

In the US study, four subjects received transfusions, three due to adverse events and one due to pre-existing anemia. In the European study, one subject received transfusions to treat pre-existing anemia.

14.3 Virus Transmission Studies

SPL UNCLASSIFIED SECTION

Clinical evidence of the absence of virus transmission in HUMATE-P was obtained in additional studies.

In one study, none of the evaluable subjects (31 of 67) who received HUMATE-P developed HBV infection or showed clinical signs of non-A, non-B (NANB) hepatitis infection.

In another study, 32 lots of HUMATE-P were administered to 26 subjects with hemophilia or VWD who had not previously received any blood products. No subject developed any signs of an infectious disease, and the 10 subjects not previously vaccinated remained seronegative for markers of infection with HBV, HAV, cytomegalovirus (CMV), Epstein-Barr virus, and HIV.

In a retrospective study, 155 subjects evaluated remained negative for the presence of HIV-1 antibodies for time periods ranging from 4 months to 9 years from the initial administration of HUMATE-P. All 67 of the subjects tested for HIV-2 antibodies remained seronegative.

15 REFERENCES

REFERENCES SECTION

  1. Levine PH, Brettler DB. Clinical aspects and therapy for hemophilia A. In: Hoffman R, Benz JB, Shattil SJ, Furie B, Cohen HJ, eds. Hematology: Basic Principles and Practice. New York: Churchill Livingstone Inc.; 1991:1296-1297.
  2. Scott JP, Montgomery RT. Therapy of von Willebrand disease. Semin Thromb Hemost. 1993;19:37-47.
  3. Mannucci, PM. Venous Thromboembolism in Von Willebrand Disease. Thromb Haemostas. 2002;88:378-379.
  4. Markis M, Colvin B, Gupta V, Shields ML, Smith MP. Venous thrombosis following the use of intermediate purity FVIII concentrate to treat patients with von Willebrand's disease. Thromb Haemostas. 2002;88:387-388.
  5. Hoyer LW. The factor VIII complex: structure and function. Blood. 1981;58:1-13.
  6. Meyer D, Girma J-P. von Willebrand factor: structure and function. Thromb Haemostas. 1993;70:99-104.
  7. Berntorp E, Nilsson IM. Biochemical and in vivo properties of commercial virus-inactivated factor VIII concentrates. Eur J Haematol. 1988;40:205-214.
  8. Berntorp E. Plasma product treatment in various types of von Willebrand's disease. Haemostasis. 1994;24:289-297.

16 HOW SUPPLIED/STORAGE AND HANDLING

HOW SUPPLIED SECTION

  • HUMATE-P is supplied in a single-dose vial containing the labeled amount of VWF:RCo and FVIII activity expressed in International Units (IU).
  • Components are not made with natural rubber latex.
  • When stored at temperatures up to 25°C (77°F), HUMATE-P is stable for 36 months up to the expiration date printed on its label. Do not freeze.
  • HUMATE-P does not contain a preservative and should be used within 3 hours after reconstitution.

STORAGE AND HANDLING SECTION

Table 14. How Supplied

Each product presentation includes a package insert and the following components:

PresentationCarton NDC NumberComponents
600 IU VWF:RCo and 250 IU FVIII63833-615-02
  • HUMATE-P in a single-dose vial [NDC 63833-625-01]
  • 5 mL vial of Sterile Water for Injection, USP [NDC 63833-765-53]
  • Mix2Vial transfer set
1200 IU VWF:RCo and 500 IU FVIII63833-616-02
  • HUMATE-P in a single-dose vial [NDC 63833-626-01]
  • 10 mL vial of Sterile Water for Injection, USP [NDC 63833-765-54]
  • Mix2Vial transfer set
2400 IU VWF:RCo and 1000 IU FVIII63833-617-02
  • HUMATE-P in a single-dose vial [NDC 63833-627-01]
  • 15 mL vial of Sterile Water for Injection, USP [NDC 63833-765-55]
  • Mix2Vial transfer set

17 PATIENT COUNSELING INFORMATION

INFORMATION FOR PATIENTS SECTION

Inform patients that HUMATE-P is made from human plasma (part of the blood) and may contain infectious agents that can cause disease (e.g., viruses, the variant Creutzfeldt-Jakob disease (vCJD) agent and, theoretically, the Creutzfeldt-Jakob (CJD) agent). Explain that the risk that HUMATE-P may transmit an infectious agent has been reduced by screening plasma donors, by testing the donated plasma for certain virus infections, and by inactivating and/or removing certain viruses during manufacturing [see Warnings and Precautions (5.4)].

Inform patients that some viruses, such as B19V and HAV, may be particularly difficult to remove or inactivate. Advise patients, especially pregnant women and immune-compromised individuals, to report low-grade fever, rash, joint pain, anorexia, nausea, vomiting, fatigue, and jaundice [see Warnings and Precautions (5.4)].

SPL UNCLASSIFIED SECTION

Manufactured by:
CSL Behring GmbH
35041 Marburg, Germany
US License No. 1765

Distributed by:
CSL Behring LLC
Kankakee, IL 60901 USA

Mix2Vial® is a registered trademark of West Pharma. Services IL, Ltd., a subsidiary of West Pharmaceutical Services, Inc.

PRINCIPAL DISPLAY PANEL - Kit Carton - NDC 63833-615-02

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC 63833-615-02
One Single-dose Vial and Sterile Water for Injection, USP

Antihemophilic Factor/
von Willebrand Factor Complex (Human)

HUMATE-P®

Powder for Reconstitution

For intravenous use only.

CSL Behring

PRINCIPAL DISPLAY PANEL - Kit Carton - NDC 63833-615-02
PRINCIPAL DISPLAY PANEL - Kit Carton - NDC 63833-615-02

PRINCIPAL DISPLAY PANEL - Kit Carton - NDC 63833-616-02

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC 63833-616-02
One Single-dose Vial and Sterile Water for Injection, USP

Antihemophilic Factor/
von Willebrand Factor Complex (Human)

HUMATE-P®

Powder for Reconstitution

For intravenous use only.

CSL Behring

PRINCIPAL DISPLAY PANEL - Kit Carton - NDC 63833-616-02
PRINCIPAL DISPLAY PANEL - Kit Carton - NDC 63833-616-02

PRINCIPAL DISPLAY PANEL - Kit Carton - NDC 63833-617-02

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC 63833-617-02
One Single-dose Vial and Sterile Water for Injection, USP

Antihemophilic Factor/
von Willebrand Factor Complex (Human)

HUMATE-P®

Powder for Reconstitution

For intravenous use only.

CSL Behring

PRINCIPAL DISPLAY PANEL - Kit Carton - NDC 63833-617-02
PRINCIPAL DISPLAY PANEL - Kit Carton - NDC 63833-617-02

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1661332antihemophilic factor / von Willebrand factor complex, human 1 UNT InjectionPSN16
1661352Humate-P (expressed as von Willebrand factor) 1 UNT InjectionPSN16
1661352factor VIII, human 1 UNT / von Willebrand factor, human 1 UNT Injection [Humate-P]SBD16
1661332factor VIII, human 1 UNT / von Willebrand factor, human 1 UNT InjectionSCD16
1661332factor VIII / von Willebrand Factor complex, human 1 UNT InjectionSY16
1661352Humate-P (expressed as von Willebrand factor) 1 UNT InjectionSY16

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
0ca1d589-929b-4b33-bc5b-1d84abdafa6aProduct name120150324
fc363c46-397b-4476-ac0f-70e43e8e4592Product name120150324

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
63833-615-02Humate-P1 in 1 CARTONKIT116
63833-625-01Humate-P5 mL in 1 VIALINJECTION, POWDER, LYOPHILIZED,5 mL80 [iU] in 1mL16
63833-616-02Humate-P1 in 1 CARTONKIT116
63833-626-01Humate-P10 mL in 1 VIALINJECTION, POWDER, LYOPHILIZED,10 mL80 [iU] in 1mL16
63833-617-02Humate-P1 in 1 CARTONKIT116
63833-627-01Humate-P15 mL in 1 VIALINJECTION, POWDER, LYOPHILIZED,15 mL80 [iU] in 1mL16

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
63833-615HUMATE-P (ANTIHEMOPHILIC FACTOR/VON WILLEBRAND FACTOR COMPLEX (HUMAN)) KIT [CSL BEHRING GMBH]16Current NDC, Legacy NDC, 2 package rows20200826_c5f4b63b-8d8b-45b3-b530-2f1c32a1b852.zip
63833-616HUMATE-P (ANTIHEMOPHILIC FACTOR/VON WILLEBRAND FACTOR COMPLEX (HUMAN)) KIT [CSL BEHRING GMBH]16Current NDC, Legacy NDC, 2 package rows20200826_c5f4b63b-8d8b-45b3-b530-2f1c32a1b852.zip
63833-617HUMATE-P (ANTIHEMOPHILIC FACTOR/VON WILLEBRAND FACTOR COMPLEX (HUMAN)) KIT [CSL BEHRING GMBH]16Current NDC, Legacy NDC, 2 package rows20200826_c5f4b63b-8d8b-45b3-b530-2f1c32a1b852.zip
63833-625HUMATE-P (ANTIHEMOPHILIC FACTOR/VON WILLEBRAND FACTOR COMPLEX (HUMAN)) KIT [CSL BEHRING GMBH]16Unmatched20200826_c5f4b63b-8d8b-45b3-b530-2f1c32a1b852.zip
63833-626HUMATE-P (ANTIHEMOPHILIC FACTOR/VON WILLEBRAND FACTOR COMPLEX (HUMAN)) KIT [CSL BEHRING GMBH]16Unmatched20200826_c5f4b63b-8d8b-45b3-b530-2f1c32a1b852.zip
63833-627HUMATE-P (ANTIHEMOPHILIC FACTOR/VON WILLEBRAND FACTOR COMPLEX (HUMAN)) KIT [CSL BEHRING GMBH]16Unmatched20200826_c5f4b63b-8d8b-45b3-b530-2f1c32a1b852.zip
63833-765HUMATE-P (ANTIHEMOPHILIC FACTOR/VON WILLEBRAND FACTOR COMPLEX (HUMAN)) KIT [CSL BEHRING GMBH]16Unmatched20200826_c5f4b63b-8d8b-45b3-b530-2f1c32a1b852.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
63833-615-02EA - Each63833-615b4a89be6-792c-4c94-a610-d8cfa30e6b2212012-07-24
63833-616-02EA - Each63833-6166f66d773-6edb-459e-9d68-57c6a03cfbd012012-07-24
63833-617-02EA - Each63833-617a0d9a13a-1b7f-4154-8a1f-9a5bad6f4da312012-07-24

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
HUMAN COAGULATION FACTOR VIII/VON WILLEBRAND FACTOR COMPLEXACTIVE INGREDIENT5T6B772R4Q8
HUMAN COAGULATION FACTOR VIII/VON WILLEBRAND FACTOR COMPLEXACTIVE MOIETY5T6B772R4Q8
albumin (human)INACTIVE INGREDIENTZIF514RVZR8
GlycineINACTIVE INGREDIENTTE7660XO1C8
Sodium ChlorideINACTIVE INGREDIENT451W47IQ8X8
Sodium CitrateINACTIVE INGREDIENT1Q73Q2JULR8
WaterINACTIVE INGREDIENT059QF0KO0R8

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Purple Book Biologic Products#

BLA, Proprietary name, Proper name table
BLAProprietary nameProper nameLicense typeStatusLatest source
103960Humate-PAntihemophilic Factor/von Willebrand Factor Complex (Human)351(a)Rx2026-09-01

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 18 matching rows.

Source Document#

Source XML

Inactive ingredient matches#

Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.

Inactive ingredient links page 1 of 16 · 930 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
GlycineGLYCINETE7660XO1CPASTE, DENTIFRICE / DENTAL0.34 %w/wExact identifier — unii candidate
120 equally ranked IID candidates
Sodium ChlorideSODIUM CHLORIDE451W47IQ8XPOWDER / RESPIRATORY (INHALATION)NAExact identifier — unii candidate
804 equally ranked IID candidates
Sodium ChlorideSODIUM CHLORIDE451W47IQ8XINJECTION, SUSPENSION / INTRAVENOUS0.9 %w/vExact identifier — unii candidate
804 equally ranked IID candidates
GlycineGLYCINETE7660XO1CINJECTION, POWDER, FOR SOLUTION / INTRAVENOUS3.76 mgExact identifier — unii candidate
120 equally ranked IID candidates
Sodium ChlorideSODIUM CHLORIDE451W47IQ8XSOLUTION/ DROPS / AURICULAR (OTIC)18 mgExact identifier — unii candidate
804 equally ranked IID candidates
Sodium ChlorideSODIUM CHLORIDE451W47IQ8XSOLUTION / IONTOPHORESIS0.6 %w/vExact identifier — unii candidate
804 equally ranked IID candidates
Sodium ChlorideSODIUM CHLORIDE451W47IQ8XSUSPENSION/ DROPS / AURICULAR (OTIC)3 mgExact identifier — unii candidate
804 equally ranked IID candidates
Sodium ChlorideSODIUM CHLORIDE451W47IQ8XINJECTION / INTRA-ARTICULAR26 mgExact identifier — unii candidate
804 equally ranked IID candidates
GlycineGLYCINETE7660XO1CTABLET, ORALLY DISINTEGRATING / ORAL60 mgExact identifier — unii candidate
120 equally ranked IID candidates
Sodium ChlorideSODIUM CHLORIDE451W47IQ8XINHALANT / RESPIRATORY (INHALATION)3 mgExact identifier — unii candidate
804 equally ranked IID candidates
Sodium ChlorideSODIUM CHLORIDE451W47IQ8XGEL / OPHTHALMIC0.9 %w/vExact identifier — unii candidate
804 equally ranked IID candidates
Sodium ChlorideSODIUM CHLORIDE451W47IQ8XTABLET, FILM COATED / ORAL100 mgExact identifier — unii candidate
804 equally ranked IID candidates
Sodium ChlorideSODIUM CHLORIDE451W47IQ8XCREAM / TOPICAL0.4 %w/wExact identifier — unii candidate
804 equally ranked IID candidates
Sodium ChlorideSODIUM CHLORIDE451W47IQ8XINJECTION / PARENTERAL584 mgExact identifier — unii candidate
804 equally ranked IID candidates
Sodium ChlorideSODIUM CHLORIDE451W47IQ8XINJECTION / INTRA-ARTERIAL278 mgExact identifier — unii candidate
804 equally ranked IID candidates
Sodium ChlorideSODIUM CHLORIDE451W47IQ8XSOLUTION / RECTALNAExact identifier — unii candidate
804 equally ranked IID candidates
Sodium ChlorideSODIUM CHLORIDE451W47IQ8XSPRAY / NASAL30 mgExact identifier — unii candidate
804 equally ranked IID candidates
Sodium ChlorideSODIUM CHLORIDE451W47IQ8XSOLUTION/ DROPS / OPHTHALMIC55 mgExact identifier — unii candidate
804 equally ranked IID candidates
Sodium ChlorideSODIUM CHLORIDE451W47IQ8XSOLUTION/ DROPS / AURICULAR (OTIC)18 mgExact identifier — unii candidate
804 equally ranked IID candidates
Sodium ChlorideSODIUM CHLORIDE451W47IQ8XINJECTION, SOLUTION / SUBCUTANEOUS1486 mgExact identifier — unii candidate
804 equally ranked IID candidates
Sodium ChlorideSODIUM CHLORIDE451W47IQ8XINJECTION / INFILTRATION648 mgExact identifier — unii candidate
804 equally ranked IID candidates
Sodium ChlorideSODIUM CHLORIDE451W47IQ8XINJECTION / SUBCUTANEOUS1486 mgExact identifier — unii candidate
804 equally ranked IID candidates
Sodium ChlorideSODIUM CHLORIDE451W47IQ8XTABLET, DELAYED RELEASE / ORAL97 mgExact identifier — unii candidate
804 equally ranked IID candidates
Sodium ChlorideSODIUM CHLORIDE451W47IQ8XINJECTION, SUSPENSION / INTRAVITREAL6 mgExact identifier — unii candidate
804 equally ranked IID candidates
Sodium ChlorideSODIUM CHLORIDE451W47IQ8XINJECTION / INTRACAVITARY0.82 %w/vExact identifier — unii candidate
804 equally ranked IID candidates
GlycineGLYCINETE7660XO1CPOWDER, FOR SUSPENSION / ORAL400 mgExact identifier — unii candidate
120 equally ranked IID candidates
Sodium ChlorideSODIUM CHLORIDE451W47IQ8XGEL / TOPICAL0.18 %w/wExact identifier — unii candidate
804 equally ranked IID candidates
GlycineGLYCINETE7660XO1CINJECTION, POWDER, FOR SOLUTION / INTRAMUSCULAR40 mgExact identifier — unii candidate
120 equally ranked IID candidates
Sodium ChlorideSODIUM CHLORIDE451W47IQ8XINJECTION / DENTAL0.4 %w/vExact identifier — unii candidate
804 equally ranked IID candidates
Sodium ChlorideSODIUM CHLORIDE451W47IQ8XINJECTION / INTRALESIONAL0.9 %w/vExact identifier — unii candidate
804 equally ranked IID candidates
Sodium ChlorideSODIUM CHLORIDE451W47IQ8XINJECTION, SOLUTION / INTRATHECAL131 mgExact identifier — unii candidate
804 equally ranked IID candidates
GlycineGLYCINETE7660XO1CINJECTION, POWDER, FOR SOLUTION / INTRAVENOUS3.76 mgExact identifier — unii candidate
120 equally ranked IID candidates
GlycineGLYCINETE7660XO1CINJECTABLE, LIPOSOMAL / INTRAVENOUS0.38 %w/vExact identifier — unii candidate
120 equally ranked IID candidates
GlycineGLYCINETE7660XO1CINJECTION, SOLUTION / INTRAVENOUS0.42 %w/vExact identifier — unii candidate
120 equally ranked IID candidates
GlycineGLYCINETE7660XO1CPOWDER / RESPIRATORY (INHALATION)2 mgExact identifier — unii candidate
120 equally ranked IID candidates
Sodium ChlorideSODIUM CHLORIDE451W47IQ8XTABLET, DELAYED RELEASE / ORAL97 mgExact identifier — unii candidate
804 equally ranked IID candidates
Sodium ChlorideSODIUM CHLORIDE451W47IQ8XINJECTION, SOLUTION / EPIDURAL3535 mgExact identifier — unii candidate
804 equally ranked IID candidates
Sodium ChlorideSODIUM CHLORIDE451W47IQ8XINJECTION, SUSPENSION / INTRASYNOVIAL4 mgExact identifier — unii candidate
804 equally ranked IID candidates
Sodium ChlorideSODIUM CHLORIDE451W47IQ8XSOLUTION / INTRAVENOUS90 mgExact identifier — unii candidate
804 equally ranked IID candidates
GlycineGLYCINETE7660XO1CSOLUTION / ORAL50 mgExact identifier — unii candidate
120 equally ranked IID candidates
Sodium ChlorideSODIUM CHLORIDE451W47IQ8XSOLUTION / INTRAMUSCULAR90 mgExact identifier — unii candidate
804 equally ranked IID candidates
Sodium ChlorideSODIUM CHLORIDE451W47IQ8XSUSPENSION/ DROPS / TOPICAL0.23 %w/vExact identifier — unii candidate
804 equally ranked IID candidates
GlycineGLYCINETE7660XO1CINJECTION, POWDER, FOR SOLUTION / INTRAMUSCULAR40 mgExact identifier — unii candidate
120 equally ranked IID candidates
Sodium ChlorideSODIUM CHLORIDE451W47IQ8XINJECTION / PERIDURAL8.07 mgExact identifier — unii candidate
804 equally ranked IID candidates
Sodium ChlorideSODIUM CHLORIDE451W47IQ8XLOTION / TOPICAL0.3 %w/vExact identifier — unii candidate
804 equally ranked IID candidates
Sodium ChlorideSODIUM CHLORIDE451W47IQ8XSOLUTION / INTRAVASCULARNAExact identifier — unii candidate
804 equally ranked IID candidates
Sodium ChlorideSODIUM CHLORIDE451W47IQ8XELIXIR / ORAL1 mgExact identifier — unii candidate
804 equally ranked IID candidates
Sodium ChlorideSODIUM CHLORIDE451W47IQ8XINJECTION, SOLUTION / PARENTERAL210 mgExact identifier — unii candidate
804 equally ranked IID candidates
Sodium ChlorideSODIUM CHLORIDE451W47IQ8XINJECTION, SUSPENSION / INTRAVENOUS0.9 %w/vExact identifier — unii candidate
804 equally ranked IID candidates
Sodium ChlorideSODIUM CHLORIDE451W47IQ8XINHALANT / RESPIRATORY (INHALATION)3 mgExact identifier — unii candidate
804 equally ranked IID candidates
Sodium ChlorideSODIUM CHLORIDE451W47IQ8XSOLUTION / INTRAVENOUS90 mgExact identifier — unii candidate
804 equally ranked IID candidates
GlycineGLYCINETE7660XO1CCAPSULE / ORAL62 mgExact identifier — unii candidate
120 equally ranked IID candidates
GlycineGLYCINETE7660XO1CTABLET / ORAL163.31 mgExact identifier — unii candidate
120 equally ranked IID candidates
Sodium ChlorideSODIUM CHLORIDE451W47IQ8XLIQUID / INTRAVENOUS6320 mgExact identifier — unii candidate
804 equally ranked IID candidates
Sodium ChlorideSODIUM CHLORIDE451W47IQ8XINJECTION / INTRAVENOUS28773 mgExact identifier — unii candidate
804 equally ranked IID candidates
Sodium ChlorideSODIUM CHLORIDE451W47IQ8XSOLUTION / IONTOPHORESIS0.6 %w/vExact identifier — unii candidate
804 equally ranked IID candidates
Sodium ChlorideSODIUM CHLORIDE451W47IQ8XSOLUTION / ORAL148 mgExact identifier — unii candidate
804 equally ranked IID candidates
Sodium ChlorideSODIUM CHLORIDE451W47IQ8XDROPS / OPHTHALMIC0.08 %w/wExact identifier — unii candidate
804 equally ranked IID candidates
Sodium ChlorideSODIUM CHLORIDE451W47IQ8XINJECTION / INTRA-ARTICULAR26 mgExact identifier — unii candidate
804 equally ranked IID candidates
Sodium ChlorideSODIUM CHLORIDE451W47IQ8XTABLET, DELAYED RELEASE / ORAL97 mgExact identifier — unii candidate
804 equally ranked IID candidates

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
80ddcb9a-9526-4911-b7dc-7833c387a591c5f4b63b-8d8b-45b3-b530-2f1c32a1b8522010-01-14Warnings, Adverse reactionsExact identifier
spl set id: c5f4b63b-8d8b-45b3-b530-2f1c32a1b852

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.