Kisunla Purple Book BLA 761248
- BLA number
- 761248
- Proprietary names
- Kisunla
- Proper names
- donanemab-azbt
- Applicant
- Eli Lilly and Company
- Center
- CDER
- First observed release
- 2024-07-01
- Latest observed release
- 2026-06-01
- Newest archive release
- 2026-06-01
- FDA patent list
- No patents listed in the captured FDA patent list; source updated 2025-06-11
- Coverage
- Present in newest release
Latest Known Product Presentations#
Product, Proprietary name, Proper name table| Product | Proprietary name | Proper name | License type | Strength | Dosage form | Route | Presentation | Marketing | Licensure | Approval | Patent list provided |
|---|
| 001 | Kisunla | donanemab-azbt | 351(a) | 350MG/20ML (17.5MG/ML) | Injection | Intravenous | Single-Dose Vial | Rx | Licensed | 2024-07-02 | |
Published Patent List#
No patents for this BLA were listed in the FDA Purple Book patent list captured from the source updated 2025-06-11.
Official Monthly Change Events#
Release, Event, Product table| Release | Event | Product | Name | License type | Status | Applicant |
|---|
| 2024-07-01 | N | 001 | Kisunla | 351(a) | Rx | Eli Lilly and Company |
Observed Product State History#
Release, Product, Name table| Release | Product | Name | License type | Marketing | Licensure | Approval |
|---|
| 2024-07-01 | 001 | Kisunla | 351(a) | Rx | Licensed | 2024-07-02 |