Skip to main content

anti-mutant calreticulin monoclonal antibody inca033989

Generic: Anti-mutant Calreticulin Monoclonal Antibody INCA033989

anti-mutant calreticulin monoclonal antibody inca033989: 4 clinical trials tracked.

anti-mutant calreticulin monoclonal antibody inca033989 evidence translation

What we can confirm

4 tracked trials

No verified listed company relationship

What it means

AI will separate confirmed drug evidence from unknown company context.

What to watch

Watch trial status, endpoints, and the next source-backed update.
BioSniper AIPage evidence connected

Prepared research question

What is verified about anti-mutant calreticulin monoclonal antibody inca033989, and what remains unknown?

Run cited research

Traceable citations · Unknowns marked

See linked entities and source evidence2 indications · 1 study sponsors
Clinical Trial Registry Records (4)

A Phase 3, Randomized, Open-Label Study of INCA033989 Versus Best Available Therapy in Participants With Essential Thrombocythemia and a CALR Mutation Previously Treated With Cytoreductive Therapy (EXCALIBUR-ET2)

NCT07623200Registry updated 2026-10-08·Phase 3·INCY
Recruiting

Primary endpoint: Durable clinicohematologic response (DCR)

InterventionalRandomizedopen426 targetStarted 2026-09Completion 2030-11178 sites · Australia, Austria, Belgium, Canada…Incyte Corporation

A Phase 1, Single Dose, Open-Label, Parallel Study to Evaluate the Pharmacokinetics, Safety, and Tolerability of INCA033989 Following Subcutaneous or Intravenous Administration in Healthy Adult Participants

NCT07448155Registry updated 2026-07-08·Phase 1·INCY
Recruiting

Primary endpoint: Pharmacokinetics Parameter: Cmax of INCA33989 following a single SC administration compared with a single IV infusion

Interventionalopen126 targetStarted 2026-03Completion 2026-101 site · United StatesIncyte Corporation

A Phase 1, Open-Label, Multicenter Study of INCA033989 Administered as a Monotherapy or in Combination With Ruxolitinib in Participants With Myeloproliferative Neoplasms

NCT06034002Registry updated 2026-04-17·Phase 1·INCY
Recruiting

Primary endpoint: Number of participants with Dose Limiting Toxicities (DLTs)

Interventionalopen290 targetStarted 2023-12Completion 2028-1013 sites · United StatesIncyte Corporation

A Phase 1, Open-Label, Multicenter Study of INCA033989 Administered as a Monotherapy or in Combination With Ruxolitinib in Participants With Myeloproliferative Neoplasms

NCT05936359Registry updated 2026-08-10·Phase 1·INCY
Active, not recruiting

Primary endpoint: Number of participants with Dose Limiting Toxicities (DLTs)

Interventionalopen160 enrolledStarted 2023-09Completion 2028-0228 sites · Australia, Canada, Denmark, France…Incyte Corporation