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.
Wie stehen die aktuellen Quoten für FDA decision: Ivonescimab by Summit Therapeutics (in 2026)?
Kalshi bewertet Yes mit 93% (Stand: 1. September 2026).
Wann wird FDA decision: Ivonescimab by Summit Therapeutics (in 2026) entschieden?
FDA decision: Ivonescimab by Summit Therapeutics (in 2026) soll am 1. Januar 2027 entschieden werden.
Wie wird FDA decision: Ivonescimab by Summit Therapeutics (in 2026) abgerechnet?
Kalshi rechnet diesen Markt wie folgt ab: 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.