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NCT07331818Possibly a fitNot yet recruiting

Luspatercept for rare inherited anemias

Hereditary Red Blood Cell Disorder (Disorder)

Part of Blood & lymphatic clinical trials.

This study tests a drug called luspatercept to see if it can improve anemia in people with rare inherited red blood cell disorders. It may help reduce the need for blood transfusions or raise hemoglobin levels.

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

Phase
Phase 2
Enrollment
45 people
Ages
18 years to 99 years
Study type
Interventional

Who can take part

  • You must be 18 years or older.
  • You must have a rare inherited anemia (sideroblastic anemia, dyserythropoietic anemia, or Diamond-Blackfan anemia) with a confirmed genetic cause.
  • Depending on your anemia type, you either need regular blood transfusions, or you have low hemoglobin but receive transfusions only occasionally.
  • Your kidneys and liver must be in good working order as shown by blood tests.
  • If you have Diamond-Blackfan anemia, you must not need regular transfusions, and your genetic mutation must be in certain specific genes (RPS19, RPS26, RPL5, or RPL11).

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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