ILLUCCIX - Telix Pharmaceuticals (US) Inc. | Telix Innovations

After reconstitution and radiolabeling of ILLUCCIX, the vial contains Gallium Ga 68 Gozetotide Injection. Handle Gallium Ga 68 Gozetotide Injection with appropriate safety measures to minimize radiation exposure [see Warnings and Precautions ( 5.2 )]. Use waterproof gloves, effective radiation shielding, and other appropriate safety measures when preparing and handling Gallium Ga 68 Gozetotide Injection.

Radiopharmaceuticals should be used by or under the control of physicians who are qualified by specific training and experience in the safe use and handling of radionuclides, and whose experience and training have been approved by the appropriate governmental agency authorized to license the use of radionuclides.

Recommended Dosage

In adults, the recommended amount of radioactivity to be administered for PET is 111 MBq to 259 MBq (3 mCi to 7 mCi) administered as an intravenous bolus injection.

Administration

• Use aseptic technique and radiation shielding when withdrawing and administering Gallium Ga 68 Gozetotide Injection.
• Calculate the necessary volume to administer based on calibration time and required dose.
• Inspect Gallium Ga 68 Gozetotide Injection visually for particulate matter and discoloration before administration. Only use solutions that are clear, colorless to slightly yellow, and without visible particles.
• Gallium Ga 68 Gozetotide Injection may be diluted with sterile 0.9% Sodium Chloride Injection, USP.
• Assay the final dose in a dose calibrator immediately before administration to the patient.
• After injection of Gallium Ga 68 Gozetotide Injection, administer an intravenous flush of sterile 0.9% Sodium Chloride Injection to ensure full delivery of the dose.
• Dispose of any unused drug in a safe manner in compliance with applicable regulations.
• Unless contraindicated, a diuretic expected to act within the uptake time period may be administered at the time of radiotracer injection to potentially decrease artifact from radiotracer accumulation in the urinary bladder and ureters.

Instruct patients to drink a sufficient amount of water to ensure adequate hydration prior to administration of Gallium Ga 68 Gozetotide Injection and to continue to drink and void frequently following administration to reduce radiation exposure, particularly during the first hour after administration [see Warnings and Precautions ( 5.2 )].

Ga 68 Sources and ILLUCCIX Carton Configurations

ILLUCCIX is supplied as a kit in two different configurations, A or B, for preparation of Gallium Ga 68 Gozetotide Injection with eluate from different Ga 68 sources. See Table 1 for ILLUCCIX carton configurations to be used with different Ga 68 sources.

The Ge 68/Ga 68 generators and cyclotron are not supplied with ILLUCCIX. Follow the instructions for use provided by the Ge 68/Ga 68 generator or cyclotron manufacturer.

Components of ILLUCCIX consist of Vial 1 (Gozetotide), Vial 2A or Vial 2B (Acetate Buffer), and Vial 3 (Sterile Vacuumed Reaction Vial) [see How Supplied/Storage and Handling (16)].

General Instructions

1. Before use, remove the ILLUCCIX kit containing all three components from the refrigerator and allow the kit to reach room temperature for 1 hour.
2. Follow aseptic techniques in all drug preparation and handling.
3. Use suitable shielding to reduce radiation exposure.
4. Wear waterproof gloves.
5. Place a "radioactive" label on Vial 3 (Sterile Vacuumed Reaction Vial) with product name, lot number and date.
6. Remove the vial cap from Vial 1 (Gozetotide), Vial 2A or Vial 2B (Acetate Buffer) and Vial 3 (Sterile Vacuumed Reaction Vial).
7. Swab the top of each vial with alcohol to disinfect the surface and allow the top of each vial to dry.
8. Use the shortest possible needle for the transfer of the Gallium Ga 68 Chloride solution to minimize any potential metallic contamination. The needle should be clean and dilute acid resistant.
9. Use only plastic syringes for preparation and administration. Do not use syringes with rubber plungers.
10. Prior to use of any vial, confirm the correct vial by a visual check of the vial label.
11. Follow the specific preparation procedure dependent on Ga 68 source [see Dosage and Administration (2.5, 2.6, 2.7, 2.8)].

Collection of Gallium Ga 68 Chloride Solution

After purification by the FASTlab Liquid Target System, the Gallium Ga 68 Chloride solution is passed through a sterile filter and into the cassette product vial automatically by the FASTlab Liquid Target System.

When Ga 68 is cyclotron-produced, test for Ga 66 and Ga 67 (with specification of ≤2% combined total) when a new lot of Zn 68 is introduced for manufacturing.

Radiolabeling Procedure

1. Use ILLUCCIX "Configuration A" with cyclotron-produced Ga 68 via GE FASTlab Liquid Target System.
2. A schematic diagram for the preparation is provided in Figure 1.
3. Pierce Vial 3 (Sterile Vacuumed Reaction Vial) with a sterile needle connected to a 0.2 micron sterile vented filter (not supplied) to maintain atmospheric pressure within the vial during the reconstitution process.
4. Aseptically transfer 5 mL of Gallium Ga 68 Chloride solution made using the GE FASTlab Liquid Target System into Vial 3.
5. Insert a sterile 10 mL syringe with a needle into Vial 2 (Acetate Buffer Vial Configuration A) and draw up the contents of the vial (target 2.5 mL).
6. Inject the contents of the 10 mL syringe into Vial 1 (Gozetotide Vial).
7. Gently swirl Vial 1 to ensure the product is thoroughly dissolved.
8. Insert a sterile 10 mL syringe with a needle into Vial 1 containing the dissolved gozetotide and draw up the entire contents of the vial.
9. Transfer the contents of the 10 mL syringe to Vial 3 (Sterile Vacuumed Reaction Vial) containing the Gallium Ga 68 Chloride.
10. Wait for 5 minutes for radiolabeling to take place at room temperature (25°C (77°F); excursions permitted to 15°C to 30°C (59°F to 86°F)).
11. Assay the whole vial containing the Gallium Ga 68 Gozetotide Injection for total radioactivity using a dose calibrator, calculate the radioactivity concentration, and record the result.
12. Perform the quality control of Gallium Ga 68 Gozetotide Injection according to the recommended methods [see Dosage and Administration (2.9)].
13. Prior to use, visually inspect the solution behind a shielded screen for radioprotection purposes. Only use solutions that are clear without visible particles.
14. Keep the vial containing the Gallium Ga 68 Gozetotide Injection upright in a radioprotective shield container at room temperature until use.
15. The final volume of the Gallium Ga 68 Gozetotide Injection is 7.5 mL.
16. Use within 4 hours.

Figure 1: Drug Preparation with Cyclotron-Produced Ga 68 via GE FASTlab Liquid Target System

Figure 1

Follow the generator manufacturers' instructions for generator preparation, controls, and continuous routine elution.

Radiolabeling Procedure

1. Use ILLUCCIX "Configuration A" with an EZAG GalliaPharm generator.
2. A schematic diagram for the preparation is provided in Figure 2.
3. Prepare a syringe containing 5 mL of sterile ultrapure 0.1 M HCl provided with the GalliaPharm generator for elution.
4. Pierce Vial 3 (Sterile Vacuumed Reaction Vial) with a sterile needle connected to a 0.2 micron sterile vented filter (not supplied) to maintain atmospheric pressure within the vial during the reconstitution process.
5. Connect the male luer of the outlet line of the GalliaPharm generator to a sterile needle.
6. Connect Vial 3 directly to the outlet line of the GalliaPharm generator by pushing the needle through the rubber septum and place the vial in a radiation shielded container.
7. Ensure the vent needle and needle to the generator outlet are pulled up as far as possible to not contact the solution in the vial.
8. Elute the generator directly with the 5 mL 0.1 M HCl from step 3 into Vial 3 according to the instructions for use of the GalliaPharm generator that are supplied by EZAG. Perform the elution manually or by means of a pump. Collect 5 mL of eluate.
9. At the end of the elution, disconnect the generator from Vial 3 by removing the needle from the rubber septum and remove the sterile vent filter.
10. Insert a sterile 10 mL syringe with a needle into Vial 2 (Acetate Buffer Vial Configuration A) and draw up the contents of the vial (target 2.5 mL).
11. Inject the contents of the 10 mL syringe into Vial 1 (Gozetotide Vial).
12. Gently swirl Vial 1 to ensure the product is thoroughly dissolved.
13. Insert a sterile 10 mL syringe with a needle into Vial 1 containing the dissolved gozetotide and draw up the entire contents of the vial.
14. Transfer the contents of the 10 mL syringe to Vial 3 (Sterile Vacuumed Reaction Vial) containing the Gallium Ga 68 Chloride.
15. Wait for 5 minutes for radiolabeling to take place at room temperature (25°C (77°F); excursions permitted to 15°C to 30°C (59°F to 86°F)).
16. Assay the whole vial containing the Gallium Ga 68 Gozetotide Injection for total radioactivity using a dose calibrator, calculate the radioactivity concentration, and record the result.
17. Perform the quality control of Gallium Ga 68 Gozetotide Injection according to the recommended methods [see Dosage and Administration (2.9)].
18. Prior to use, visually inspect the solution behind a shielded screen for radioprotection purposes. Only use solutions that are clear without visible particles.
19. Keep the vial containing the Gallium Ga 68 Gozetotide Injection upright in a radioprotective shield container at room temperature until use.
20. The final volume of the Gallium Ga 68 Gozetotide Injection is 7.5 mL.
21. Use within 4 hours.

Figure 2: Preparation with EZAG GalliaPharm Generator

Figure 2

Collection of Gallium Ga 68 Chloride Solution

After purification by the ARTMS QIS, the Gallium Ga 68 Chloride solution is passed through a sterile filter and into the cassette product vial automatically by the ARTMS QIS.

When Ga 68 is cyclotron-produced, test for Ga 66 and Ga 67 (with specification of ≤2% combined total) when a new lot of Zn 68 is introduced for manufacturing.

Radiolabeling Procedure

1. Use ILLUCCIX "Configuration B" with cyclotron-produced Ga 68 via ARTMS QIS Solid Target System.
2. A schematic diagram for the preparation is provided in Figure 3.
3. Pierce Vial 3 (Sterile Vacuumed Reaction Vial) with a sterile needle connected to a 0.2 micron sterile vented filter (not supplied) to maintain atmospheric pressure within the vial during the reconstitution process.
4. Collect 1.1 mL of Gallium Ga 68 Chloride solution made using the ARTMS QIS Solid Target System into Vial 3.
5. Insert a sterile 10 mL syringe with a needle into Vial 2 (Acetate Buffer Vial Configuration B) and draw up the contents of the vial (target 6.4 mL).
6. Inject the contents of the 10 mL syringe into Vial 1 (Gozetotide Vial).
7. Gently swirl Vial 1 to ensure the product is thoroughly dissolved.
8. Insert a sterile 10 mL syringe with a needle into Vial 1 containing the dissolved gozetotide and draw up the entire contents of the vial.
9. Transfer the contents of the 10 mL syringe to Vial 3 (Sterile Vacuumed Reaction Vial) containing the Gallium Ga 68 Chloride.
10. Wait for 5 minutes for radiolabeling to take place at room temperature (25°C (77°F); excursions permitted to 15°C to 30°C (59°F to 86°F)).
11. Assay the whole vial containing the Gallium Ga 68 Gozetotide Injection for total radioactivity using a dose calibrator, calculate the radioactivity concentration, and record the result.
12. Perform the quality control of Gallium Ga 68 Gozetotide Injection according to the recommended methods [see Dosage and Administration (2.9)].
13. Prior to use, visually inspect the solution behind a shielded screen for radioprotection purposes. Only use solutions that are clear without visible particles.
14. Keep the vial containing the Gallium Ga 68 Gozetotide Injection upright in a radioprotective shield container at room temperature until use.
15. The final volume of the Gallium Ga 68 Gozetotide Injection is 7.5 mL.
16. Use within 4 hours.

Figure 3: Drug Preparation with Cyclotron-Produced Ga 68 via ARTMS QIS Solid Target System

Figure 3

Follow the generator manufacturers' instructions for generator preparation, controls, and continuous routine elution.

Radiolabeling Procedure

1. Use ILLUCCIX "Configuration B" with an IRE ELiT Galli Eo generator.
2. A schematic diagram for the preparation is provided in Figure 4.
3. Pierce Vial 3 (Sterile Vacuumed Reaction Vial) with a sterile needle connected to a 0.2 micron sterile vented filter (not supplied) to maintain atmospheric pressure within the vial during the reconstitution process.
4. Connect the male luer of the outlet line of the Galli Eo generator to a sterile needle.
5. Connect Vial 3 directly to the outlet line of the Galli Eo generator by pushing the needle through the rubber septum and place the vial in a radiation shielded container.
6. Ensure the needle to the generator outlet is pulled up as far as possible to not contact the solution in the vial.
7. Elute 1.1 mL from the generator directly into Vial 3 (Sterile Vacuumed Reaction Vial) according to the instructions for use of the Galli Eo generator that are supplied by IRE. Collect 1.1 mL of eluate.
8. At the end of the elution, disconnect the generator from Vial 3 by removing the needle from the rubber septum and remove the sterile vent filter.
9. Insert a sterile 10 mL syringe with a needle into Vial 2 (Acetate Buffer Vial Configuration B) and draw up the contents of the vial (target 6.4 mL).
10. Inject the contents of the 10 mL syringe into Vial 1 (Gozetotide Vial).
11. Gently swirl Vial 1 to ensure the product is thoroughly dissolved.
12. Insert a sterile 10 mL syringe with a needle into Vial 1 containing the dissolved gozetotide and draw up the entire contents of the vial.
13. Transfer the contents of the 10 mL syringe to Vial 3 (Sterile Vacuumed Reaction Vial) containing the Gallium Ga 68 Chloride.
14. Wait for 5 minutes for radiolabeling to take place at room temperature (25°C (77°F); excursions permitted to 15°C to 30°C (59°F to 86°F)).
15. Assay the whole vial containing the Gallium Ga 68 Gozetotide Injection for total radioactivity using a dose calibrator, calculate the radioactivity concentration, and record the result.
16. Perform the quality control of Gallium Ga 68 Gozetotide Injection according to the recommended methods [see Dosage and Administration (2.9)].
17. Prior to use, visually inspect the solution behind a shielded screen for radioprotection purposes. Only use solutions that are clear without visible particles.
18. Keep the vial containing the Gallium Ga 68 Gozetotide Injection upright in a radioprotective shield container at room temperature until use.
19. The final volume of the Gallium Ga 68 Gozetotide Injection is 7.5 mL.
20. Use within 4 hours.

Figure 4: Preparation with IRE ELiT Galli Eo Generator

Figure 4

Perform the quality controls in Table 2 behind a lead glass shield for radioprotection purposes.

Table 2: Specifications for Gallium Ga 68 Gozetotide Injection

Procedure for instant Thin Layer Chromatography (iTLC)

1. Pour ammonium acetate 1 M/methanol (1/1 v/v) solution to a depth of 3 mm to 4 mm in the developing chamber, cover the chamber and allow it to equilibrate.
2. Using a pencil and ruler, carefully draw a solid pencil line at 1 cm from the bottom of the iTLC strip, and a dotted line 5 cm from the pencil line. See Figure 5 for an example of how to mark the iTLC strip.
3. Apply a drop of gallium Ga 68 gozetotide solution into the center of the solid line at 1 cm from the bottom of the TLC plate.
4. Place the iTLC strip into the development chamber, with the bottom of the iTLC strip containing drop of gallium Ga 68 gozetotide into the solution at the bottom of the developing chamber. Ensure that the bottom of the iTLC strip sits in the liquid in the chamber, but that the liquid does not touch the drop of gallium Ga 68 gozetotide.
5. Allow the iTLC strip to develop in the covered chamber over a distance of 10 cm from the point of application.
6. Remove the iTLC strip. Allow the plate to dry before proceeding with analysis using one of the methods described below.

Perform one of the following:

Radiochemical Purity Analysis Using Cutting Technique

1. Cut the iTLC strip into 2 parts by cutting horizontally at the dotted line 5 cm above the solid line at the bottom of the iTLC strip. See Figure 5 for where to cut the iTLC strip.
2. This cutting will result in the following 2 portions:
   1. A bottom portion with a solid pencil line containing the Origin and free/colloidal Ga 68 species (Bottom Portion)
   2. A top portion containing the solvent front and gallium Ga 68 gozetotide (Top Portion)
3. Using a dose calibrator, measure and record the radioactivity in the bottom portion of the cut TLC plate that contains the Origin and free/colloidal Ga 68 species (Bottom Portion).
4. Using a dose calibrator, measure and record the radioactivity in the top portion containing the solvent front and gallium Ga 68 gozetotide (Top Portion).
5. Calculate the quantity (in percent) of gallium Ga 68 gozetotide in the solution using the formula:

   Radiochemical Purity (%)
   	=	Counts Top Portion	× 100
   		Counts from Top Portion + Counts from Bottom Portion

Figure 5: iTLC Strip Preparation and Cutting Point for the Cutting Technique

Figure 5

Radiochemical Purity Analysis Using Scanning Technique

1. Scan the iTLC with a radiometric iTLC scanner.
2. Calculate the quantity (in percent) of gallium Ga 68 gozetotide in the solution by integration of the peaks on the chromatogram.
3. The retention factor (Rf) specifications are:
   • Free and colloidal Ga 68 species, Rf = 0 to 0.1,
   • Gallium Ga 68 gozetotide, Rf = 0.6 to 1.

Position the patient supine with arms above the head. Begin PET scanning 50 minutes to 100 minutes after the intravenous administration of Gallium Ga 68 Gozetotide Injection. Patients should void immediately prior to image acquisition and image acquisition should begin at the proximal thighs and proceed cranially to the skull base or skull vertex. Adapt imaging technique according to the equipment used and patient characteristics in order to obtain the best image quality possible.

Gallium Ga 68 gozetotide binds to PSMA. Based on the intensity of the signals, PET images obtained using gallium Ga 68 gozetotide indicate the presence of PSMA in tissues.

Imaging Prior to Initial Definitive Therapy or for Biochemical Recurrence

Lesions should be considered suspicious if uptake is greater than physiologic uptake in that tissue or greater than adjacent background if no physiologic uptake is expected. Tumors that do not express PSMA will not be visualized. Increased uptake in tumors is not specific for prostate cancer [see Warnings and Precautions (5.1)].

Imaging to Select Patients for PSMA-Directed Therapy

For instructions on patient selection, refer to the prescribing information of the PSMA-directed therapeutic product.

Estimated radiation absorbed doses per injected activity for organs and tissues of adult male patients following an intravenous bolus of Gallium Ga 68 Gozetotide Injection are shown in Table 3.

The effective radiation dose resulting from the administration of 259 MBq (7 mCi) is about 4.4 mSv. The radiation doses for this administered dose to the critical organs, which are the kidneys, urinary bladder, and spleen, are 96.2 mGy, 25.4 mGy, and 16.8 mGy, respectively.

These radiation doses are for Gallium Ga 68 Gozetotide Injection alone. If CT or a transmission source are used for attenuation correction, the radiation dose will increase by an amount that varies by technique.

Table 3: Estimated Radiation Absorbed Dose per Injected Activity in Selected Organs and Tissues of Adults after Intravenous Administration of Gallium Ga 68 Gozetotide Injection

Image interpretation errors can occur with ILLUCCIX PET. A negative image does not rule out the presence of prostate cancer and a positive image does not confirm the presence of prostate cancer. Gallium Ga 68 gozetotide uptake is not specific for prostate cancer and may occur with other types of cancer as well as non-malignant processes such as Paget's disease, fibrous dysplasia, and osteophytosis. Clinical correlation, which may include histopathological evaluation of the suspected prostate cancer site, is recommended.

The performance of ILLUCCIX for imaging of biochemically recurrent prostate cancer seems to be affected by serum PSA levels and by site of disease. The performance of ILLUCCIX for imaging of metastatic pelvic lymph nodes prior to initial definitive therapy seems to be affected by Gleason score [see Clinical Studies (14.1, 14.2)].

Gallium Ga 68 gozetotide contributes to a patient's overall long-term cumulative radiation exposure. Long-term cumulative radiation exposure is associated with an increased risk for cancer. Ensure safe handling to minimize radiation exposure to the patient and health care providers. Advise patients to hydrate before and after administration and to void frequently after administration [see Dosage and Administration ( 2.1 , 2.3 )].

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

The safety of ILLUCCIX has been established based on three prospective studies of gallium Ga 68 gozetotide in patients with prostate cancer (i.e., Studies 1, 2, and 3). Adverse reactions from these studies are reported below.

In Studies 1 and 2 using another formulation of gallium Ga 68 gozetotide injection, 960 patients received one dose of gallium Ga 68 gozetotide intravenously with the amount (mean ± SD) of radioactivity 188.7 ± 40.7 MBq (5.1 ± 1.1 mCi) [see Clinical Studies (14.1, 14.2)]. The most commonly reported adverse reactions were nausea, diarrhea, and dizziness, occurring at a rate of <1%.

In a randomized, multicenter, open-label clinical study (NCT03511664, referred to as Study 3) in which gallium Ga 68 gozetotide was used to identify PSMA-positive patients on PET imaging to determine eligibility for PSMA-directed therapy, 1,003 patients with progressive metastatic castration-resistant prostate cancer (mCRPC) received one dose of gallium Ga 68 gozetotide intravenously with the amount of radioactivity 167.1 ± 23.1 MBq (4.52 ± 0.62 mCi). Patients were males with median age of 70 years (range, 40 to 94 years), were White (87%), Black or African American (7%), or Asian (2.4%), and had median baseline PSA levels of 74 ng/mL (range, 0 to 8,995 ng/mL).

Adverse reactions occurring at ≥ 0.5% in patients with metastatic prostate cancer who received gallium Ga 68 gozetotide injection in Study 3 are presented in Table 4.

Table 4: Adverse Reactions (≥ 0.5%) in Patients with Metastatic Prostate Cancer Who Received Gallium Ga 68 Gozetotide Injection in Study 3

Adverse reactions occurring at a rate of < 0.5% in the study were diarrhea, dry mouth, injection site reactions, including injection site hematoma and injection site warmth and chills.

The following adverse reactions have been identified during postapproval use of ILLUCCIX. 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 drug exposure.

General Disorders and Administration Site Conditions: injection site pain.

Risk Summary

ILLUCCIX is not indicated for use in females. There are no available data with gallium Ga 68 gozetotide injection use in pregnant women to evaluate for a drug-associated risk of major birth defects, miscarriage, or adverse maternal or fetal outcomes. All radiopharmaceuticals, including ILLUCCIX, have the potential to cause fetal harm depending on the fetal stage of development and the magnitude of the radiation dose. Animal reproduction studies have not been conducted with gallium Ga 68 gozetotide.

Risk Summary

ILLUCCIX is not indicated for use in females. There are no data on the presence of gallium Ga 68 gozetotide in human milk, the effect on the breastfed infant, or the effect on milk production.

The safety and effectiveness of gallium Ga 68 gozetotide in pediatric patients have not been established.

The efficacy of gallium Ga 68 gozetotide PET in geriatric patients with prostate cancer is based on data from three prospective studies.

Of the total number of patients in Studies 1 and 2 [see Clinical Studies (14.1, 14.2)], 691 of 960 (72%) patients were 65 years of age and older while 195 (20%) were 75 years of age and older.

Of the total number of patients in Study 3 [see Adverse Reactions (6.1) ], 752 of 1,003 (75%) patients were 65 years of age and older while 284 (28%) were 75 years of age and older.

The efficacy and safety profiles of gallium Ga 68 gozetotide appear similar in younger adult and geriatric patients with prostate cancer and other reported clinical experience has not identified differences in responses between the elderly and younger adult patients.

ILLUCCIX (kit for the preparation of gallium Ga 68 gozetotide injection), after radiolabeling with Ga 68, is a radioactive diagnostic agent for intravenous use. Gozetotide is also known as PSMA-11.

Gallium Ga 68 gozetotide is a radioconjugate composed of a human prostate specific membrane antigen (PSMA)-targeting ligand peptide conjugated via the acyclic radiometal chelator, N,N'-bis [2-hydroxy-5-(carboxyethyl)benzyl] ethylenediamine-N,N'-diacetic acid (HBED-CC) to the radioisotope Ga 68. The amino acid sequence of the gozetotide peptide is Glu-NH-CO-NH-Lys(Ahx), (Ahx = 6-aminohexanoic acid). Gallium Ga 68 gozetotide has a molecular weight of 1011.9 g/mol and its chemical structure is shown in Figure 6.

Figure 6: Chemical Structure of Gallium Ga 68 Gozetotide

Figure 6

Kit Characteristics

ILLUCCIX is supplied as a kit which contains the non-radioactive ingredients needed to produce Gallium Ga 68 Gozetotide Injection. There are two configurations, A or B, available to allow preparation of Gallium Ga 68 Gozetotide Injection using Ga 68 from different generator or cyclotron sources. Each configuration consists of gozetotide (Vial 1), acetate buffer (Vial 2A or Vial 2B), and a sterile vacuumed reaction vial (Vial 3).

• Vial 1 (Gozetotide): Each vial contains 25 mcg gozetotide and 10 mcg D-mannose.
• Vial 2A (Acetate Buffer): Each vial contains 150 mg anhydrous sodium acetate in 2.5 mL of 0.292 M hydrochloric acid.
• Vial 2B (Acetate Buffer): Each vial contains 150 mg anhydrous sodium acetate in 6.4 mL of 0.175 M hydrochloric acid.
• Vial 3 (Sterile Vacuumed Reaction Vial): a sterile, evacuated vial that serves as the collection vial for Ga 68 chloride and radiolabeling reaction.

The prepared Gallium Ga 68 Gozetotide Injection is a sterile, pyrogen free, clear, colorless to slightly yellow, buffered solution containing up to 1,850 MBq (50 mCi) of gallium Ga 68 gozetotide in 7.5 mL with a pH between 4.0 to 5.0.

Gallium-68 (Ga 68) decays with a half-life of 68 minutes to stable zinc-68. Table 5, Table 6, and Table 7 display the principal radiation emission data, radiation attenuation by lead shielding, and physical decay of Ga 68.

Table 5: Principal Radiation Emission Data (>1%) for Ga 68

Table 6: Radiation Attenuation of 511 keV Photons by Lead (Pb) Shielding

Table 7: Physical Decay Chart for Ga 68

Gallium Ga 68 gozetotide binds to PSMA. It binds to cells that express PSMA, including malignant prostate cancer cells, which usually overexpress PSMA. Gallium 68 (Ga 68) is a β+ emitting radionuclide that allows positron emission tomography.

The relationship between gallium Ga 68 gozetotide plasma concentrations and successful imaging was not explored in clinical trials.

Distribution

Intravenously injected gallium Ga 68 gozetotide is cleared from the blood and is accumulated preferentially in the liver (15%), kidneys (7%), spleen (2%), and salivary glands (0.5%). Gallium Ga 68 gozetotide uptake is also seen in the adrenals and prostate. There is no uptake in the cerebral cortex or in the heart, and usually lung uptake is low.

Elimination

A total of 14% of the injected dose is excreted in urine in the first 2 hours post-injection.

No long-term animal studies were performed to evaluate the carcinogenicity potential of gallium Ga 68 gozetotide.

The efficacy of ILLUCCIX for PET of PSMA-positive lesions in men with prostate cancer with suspected metastasis who are candidates for initial definitive therapy has been established based on a study of another formulation of gallium Ga 68 gozetotide. Below is a display of the results of the prospective, open label study PSMA-PreRP (NCT03368547 and NCT02919111, referred to as Study 1).

This two-center study enrolled 325 patients with biopsy-proven prostate cancer who were considered candidates for prostatectomy and pelvic lymph node dissection. All enrolled patients met at least one of the following criteria: serum prostate-specific antigen (PSA) of at least 10 ng/mL, tumor stage cT2b or greater, or Gleason score greater than 6. Each patient received a single gallium Ga 68 gozetotide PET/CT or PET/MR from mid-thigh to skull base.

A total of 123 patients (38%) proceeded to standard-of-care prostatectomy and template pelvic lymph node dissection and had sufficient histopathology data for evaluation (evaluable patients). Three members of a pool of six central readers independently interpreted each PET scan for the presence of abnormal gallium Ga 68 gozetotide uptake in pelvic lymph nodes located in the common iliac, external iliac, internal iliac, and obturator subregions bilaterally as well as in any other pelvic location. The readers were blinded to all clinical information except for the history of prostate cancer prior to definitive treatment. Extrapelvic sites and the prostate gland itself were not analyzed in this study. For each patient, gallium Ga 68 gozetotide PET results and reference standard histopathology obtained from dissected pelvic lymph nodes were compared by region (left hemipelvis, right hemipelvis, and other).

For the 123 evaluable patients, the mean age was 65 years (range 45 to 76 years), and 89% were White. The median serum PSA was 11.8 ng/mL. The summed Gleason score was 7 for 44%, 8 for 20%, and 9 for 31% of the patients, with the remainder of the patients having Gleason scores of 6 or 10.

Table 8 compares majority PET reads to pelvic lymph node histopathology results at the patient-level with region matching, such that at least one true positive region defines a true positive patient. As shown, approximately 24% of subjects studied were found to have pelvic nodal metastases based on histopathology (95% confidence interval: 17%, 32%).

Among the pool of six readers, sensitivity ranged from 36% to 60%, specificity from 83% to 96%, positive predictive value from 38% to 80%, and negative predictive value from 80% to 88%.

In an exploratory subgroup analysis based on summed Gleason score, there was a numerical trend toward more true positives in patients with Gleason score of 8 or higher compared to those with Gleason score of 7 or lower.

An exploratory analysis was performed to estimate the sensitivity and specificity for pelvic nodal metastasis detection in all scanned patients, including the patients who were lacking histopathology reference standard. An imputation method was used based on patient-specific factors. This exploratory analysis resulted in an imputed sensitivity of 47%, with a 95% confidence interval ranging from 38% to 55%, and an imputed specificity of 74%, with a 95% confidence interval ranging from 68% to 80% for all patients imaged with gallium Ga 68 gozetotide PET.

The efficacy of ILLUCCIX for PET of PSMA-positive lesions in men with prostate cancer with suspected recurrence based on elevated serum PSA level has been established based on a study of another formulation of gallium Ga 68 gozetotide. Below is a display of the results of the prospective, open label study PSMA-BCR (NCT02940262 and NCT02918357, referred to as Study 2).

This two-center study enrolled 635 patients with biochemical evidence of recurrent prostate cancer after definitive therapy, defined by serum PSA of >0.2 ng/mL more than 6 weeks after prostatectomy or by an increase in serum PSA of at least 2 ng/mL above nadir after definitive radiotherapy. All patients received a single gallium Ga 68 gozetotide PET/CT or PET/MR from mid-thigh to skull base. Three members of a pool of nine independent central readers evaluated each scan for the presence and regional location (20 subregions grouped into four regions) of abnormal gallium Ga 68 gozetotide uptake suggestive of recurrent prostate cancer. The readers were blinded to all clinical information other than type of primary therapy and most recent serum PSA level.

A total of 469 patients (74%) had at least one positive region detected by gallium Ga 68 gozetotide PET majority read. The distribution of gallium Ga 68 gozetotide PET positive regions was 34% bone, 25% prostate bed, 25% pelvic lymph node, and 17% extrapelvic soft tissue. Two hundred and ten patients had composite reference standard information collected in a PET positive region (evaluable patients), consisting of at least one of the following: histopathology, imaging (bone scintigraphy, CT, or MRI) acquired at baseline or within 12 months after gallium Ga 68 gozetotide PET, or serial serum PSA. Composite reference standard information for gallium Ga 68 gozetotide PET negative regions was not systematically collected in this study.

In the 210 evaluable patients, the mean age was 70 years (range 49 to 88 years) and 82% were 65 years of age or older. White patients made up 90% of the group. The median serum PSA was 3.6 ng/mL. Prior treatment included radical prostatectomy in 64% and radiotherapy in 73%.

Of the 210 evaluable patients, 192 patients (91%) were found to be true positive in one or more regions against the composite reference standard (95% confidence interval: 88%, 95%). Among the pool of nine readers used in the study, the proportion of patients who were true positive in one or more regions ranged from 82% to 97%. The prostate bed had the lowest proportion of true positive results at the region-level (76% versus 96% for non-prostate regions).

An exploratory analysis was also performed in which gallium Ga 68 gozetotide PET positive patients who lacked reference standard information were imputed using an estimated likelihood that at least one location-matched PET positive lesion was reference standard positive based on patient-specific factors. In this exploratory analysis, 340 of 475 patients (72%) were imputed as true positive in one or more regions (95% confidence interval: 68%, 76%).

In another exploratory analysis using the same imputation approach for PET positive patients who lacked reference standard information, 340 of 635 patients (54%) were correctly detected as true positive (95% confidence interval: 50%, 57%) among all BCR patients who received a PET scan, whether it was read as positive or negative.

The likelihood of identifying a gallium Ga 68 gozetotide PET positive lesion in this study increased with higher serum PSA level. Table 9 shows the patient-level gallium Ga 68 gozetotide PET results stratified by serum PSA level. The mean time between PSA measurement and PET scan was 40 days with a range of 0 to 367 days. Percent PET positivity was calculated as the proportion of patients with a positive gallium Ga 68 gozetotide PET out of all patients scanned. Percent PET positivity includes patients determined to be either true positive or false positive as well as those in whom such determination was not made due to the absence of composite reference standard data.

Refer to the prescribing information of the PSMA-directed therapy for description of the studies in which the efficacy of gallium Ga 68 gozetotide for selecting patients has been established.