Over the past year, important contributions have been made in sickle cell research. This progress are critical steps towards finding new treatments and a universal cure for sickle cell conditions.

The Hibiscus Study Seeks Volunteers

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Medicaid and CHIP Sickle Cell Disease Report, T-MSIS Analytic Files (TAF) 2017

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CRISPR Therapeutics and Vertex Present New Data for Investigational CRISPR/Cas9 Gene-Editing Therapy, CTX001™ at American Society of Hematology Annual Meeting and Exposition, Together With Publication in the New England Journal of Medicine

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Aruvant conducts MOMENTUM study to examine one-time investigational treatment to increase levels of fetal hemoglobin in patients with severe sickle cell disease.

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Novartis Investigational Therapy Crizanlizumab (SEG101) Receives FDA Breakthrough Therapy Designation for the Prevention of Vaso-occlusive Crises in Sickle Cell Disease.

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CRISPR Therapeutics and Vertex Announce FDA Fast Track Designation for CTX001 for the Treatment of Sickle Cell Disease.

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GBT Announces the FDA Agrees to Submit a New Drug Application for the Approval of Voxelotor.

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FDA Approves Hydroxyurea Tablets for Pediatric Sickle Cell Anemia

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Imara Doses First Patient in Phase 2a Clinical Trial of IMR-687 for Sickle Cell Disease.

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Emmaus Life Sciences Announces Availability of Endari™ (L-glutamine oral powder) for Sickle Cell Disease in the United States.

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U.S. Food and Drug Administration granted regular approval to hydroxyurea to reduce the frequency of painful crises and the need for blood transfusions in pediatric patients from 2 years of age and older with sickle cell anemia with recurrent moderate to severe painful crises.

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