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NCT01245179Possibly a fitRecruiting

Panobinostat for adults with severe sickle cell

Sickle Cell Disease

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

This early-phase study tests panobinostat, a medicine aimed at reducing sickle-cell problems, in adults with severe disease. It’s mainly looking at safety and whether it can improve blood-related issues that drive pain and complications.

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

Phase
Phase 1
Enrollment
18 people
Ages
18 years and older
Study type
Interventional

Who can take part

  • You are 18 years or older and can sign written informed consent
  • You have confirmed sickle cell with either SS disease or S-beta zero thalassemia
  • You cannot tolerate hydroxyurea, do not want it, or it did not work for you
  • You have significant sickle-cell complications in the last time periods (pain crises, hospital stays, ulcers, acute chest syndrome, priapism, or stroke)
  • No recent crisis: your last pain crisis needing injection-type (parenteral) treatment was more than 2 weeks ago
  • Your blood tests and organ function fall in required safe ranges, and your heart rhythm/ECG is acceptable

View the official record on ClinicalTrials.gov

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