Nogapendekin alfa inbakicept
| Combination of | |
|---|---|
| Nogapendekin alfa | human IL-15N72D variant |
| Inbakicept | interleukin-15 receptor agonist |
| Clinical data | |
| Trade names | Anktiva |
| Other names | ALT-803, N-803, nogapendekin alfa inbakicept-pmln |
| AHFS/Drugs.com | Monograph |
| MedlinePlus | a624034 |
| License data | |
| Routes of administration | Intravesical |
| ATC code | |
| Legal status | |
| Legal status |
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| Identifiers | |
| PubChem SID | |
| KEGG | |
Nogapendekin alfa inbakicept, sold under the brand name Anktiva, is a fixed-dose combination medication used for the treatment of bladder cancer. It is an interleukin-15 receptor agonist. It is given in combination with Bacillus Calmette-Guérin (BCG) via intravesical drug delivery. It contains nogapendekin alfa, a human IL-15(N72D) variant, which is more potent than regular IL-15; and inbakicept, an interleukin 15 receptor subunit alpha agonist.
The most common adverse reactions include increased creatinine, dysuria, hematuria, urinary frequency, micturition urgency, urinary tract infection, increased potassium, musculoskeletal pain, chills, and pyrexia.
Nogapendekin alfa inbakicept was approved for medical use in the United States in April 2024. The US Food and Drug Administration considers it to be a first-in-class medication.