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NCT07816237Possibly a fitNot yet recruiting

Study of VSA012 for paroxysmal nocturnal hemoglobinuria

Paroxysmal Nocturnal Hemoglobinuria, PNH

Treatments studied

Part of Blood & lymphatic clinical trials.

This study tests a new medicine called VSA012 for people with paroxysmal nocturnal hemoglobinuria (PNH), a rare blood disease. The goal is to see if VSA012 can help manage symptoms like fatigue and low blood counts better than the current standard treatment.

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

Phase
Phase 3
Enrollment
70 people
Ages
18 years to 75 years
Study type
Interventional

Who can take part

  • You are 18 years or older
  • You have been diagnosed with PNH and have a large enough clone of affected blood cells
  • Your hemoglobin (a protein in red blood cells that carries oxygen) is below normal
  • You have not received complement inhibitor therapy before (a type of treatment for PNH)
  • You are willing to receive vaccinations against certain bacterial infections before starting the study

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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