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aBLA Filing Intelligence & Biosimilar Opportunity

Anktiva

Nogapendekin Alfa Inbakicept-Pmln
Anticancer
Intravesical Injection

Anktiva is the first FDA-approved immunotherapy that activates the immune system to treat BCG-unresponsive non-muscle invasive bladder cancer (CIS), offering some patients a lasting complete response.

Approval Date
22-Apr-24
Data Exclusivity Expiry
22-Apr-28
Market Exclusivity Expiry
22-Apr-36
Commercial snapshot

Market performance & projections

Revenue ($M)
113
CAGR (%)
84.45%
Projected sales, 2026–2032 ($M)
Analyst projection, $M per year
2026
155
2027
360
2028
734
2029
1,308
2030
2,078
2031
3,156
2032
4,098
Molecule profile

Details & specifications

Molecule
Nogapendekin Alfa Inbakicept-Pmln
Innovator
IMMUNITYBIO, INC.
Dosage Form
Intravesical Injection
Strength
400 mcg/0.4 mL
Therapeutic Category
Anticancer
Usage
To treat bladder cancer
Good to know

Frequently asked questions

Ready to act on this opportunity?

Talk to Spring Bio Solution about sourcing, licensing, and filing support for this molecule.

Why Spring Bio Solution

Supported 1000+ clinical trials globally

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Global sourcing capability across US, EU, South Africa, Canada, Japan, Australia, New Zealand, Southeast Asia, and other key markets

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