This market will resolve to No if the FDA's decision is a denial (CRL issued), a withdrawal by the sponsor, or a conditional approval — or if no decision is issued.
Ivonescimab (also called AK112 or SMT112) is a bispecific antibody — think of it as a single engineered drug molecule that carries two different "hooks" instead of one, allowing it to grab and block two disease-promoting proteins at the same time.
It was developed by Akeso and is being commercialized outside China by Summit Therapeutics.
By simultaneously neutralizing both targets, ivonescimab is designed to slow cancer growth more effectively than drugs that block only one pathway at a time.
This market and these products have not been endorsed by any aforementioned brands or its affiliates.
Quelles sont les probabilités actuelles pour FDA decision: Ivonescimab by Summit Therapeutics (in 2026) ?
Kalshi cote Yes à 93% au 1 septembre 2026.
Quand FDA decision: Ivonescimab by Summit Therapeutics (in 2026) sera-t-il résolu ?
FDA decision: Ivonescimab by Summit Therapeutics (in 2026) doit être résolu le 1 janvier 2027.
Comment FDA decision: Ivonescimab by Summit Therapeutics (in 2026) est-il réglé ?
Kalshi règle ce marché comme suit : If the FDA's decision on Ivonescimab by Summit Therapeutics in 2026 is a full approval or an accelerated approval, the market resolves to Yes.