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Sutacimig

Bispecific antibody · developed by Hemab ApS

Phase 2 Most advanced trial
COAG Developer
1 Registered trials

What is Sutacimig?

Sutacimig is a subcutaneously administered bispecific antibody being developed as a prophylactic treatment for congenital bleeding disorders.

Summary written with AI from the sources listed at the end of this page.

At a glance

Drug type
Bispecific antibody
Therapy area
Hematology
Developer
Hemab ApS (COAG)
FDA status
Investigational, not approved in the US. Most advanced trial: Phase 2
UNII
2QP8468SQP

🧪 Clinical trials

TrialPhaseConditionStatusSponsor
NCT07347249 Phase 2 Congenital Factor VII Deficiency Recruiting COAG

Trials of the companies BioRadar tracks, from ClinicalTrials.gov, most advanced phase first.

Conditions studied

Congenital Factor VII Deficiency

More from Hemab ApS

Sources

Updated Oct 11, 2026. Something wrong or missing? Report it on the COAG page.

Follow COAG, the company behind Sutacimig

See COAG's upcoming FDA decisions, trial readouts, cash runway and dilution risk, updated every day from SEC, FDA and ClinicalTrials.gov filings.

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Data: FDA (Drugs@FDA, Purple Book, DailyMed), NIH (NCI Thesaurus, GSRS, RxNorm), ClinicalTrials.gov • Informational purposes only, not medical or investment advice. • All drugs A–Z

This data is for informational purposes only, not investment advice. BioRadar does not provide buy/sell recommendations. Past performance does not guarantee future results. Always do your own due diligence.