Clin2
NCT07347249Possibly a fitRecruiting

New drug for congenital Factor VII deficiency

Congenital Factor VII Deficiency

Part of Blood & lymphatic, Genetic & congenital clinical trials.

This study tests a new drug called Sutacimig for people with congenital Factor VII deficiency, a rare bleeding disorder. The drug is designed to help prevent or control bleeding episodes.

Summary written for real people, not researchers, by Clin2.

Phase
Phase 2
Enrollment
18 people
Ages
18 years to 60 years
Study type
Interventional

Who can take part

  • You are between 18 and 60 years old.
  • You have confirmed Factor VII deficiency with an activity level below 10% (measured at least twice).
  • You have a history of severe bleeding or have needed treatment with Factor VII or fresh frozen plasma for a bleed.
  • You do not have inhibitors (antibodies) to Factor VII.
  • You have not had a blood clot (such as a deep vein thrombosis or pulmonary embolism).
  • You are not pregnant or breastfeeding.

View the official record on ClinicalTrials.gov

Quick eligibility check

Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.

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