Condition: Sickle Cell Disease · Sponsor: Agios Pharmaceuticals, Inc.
This clinical trial is a Phase 2/3 study that will determine the recommended dose of mitapivat and evaluate the efficacy and safety of mitapivat in sickle cell disease by testing how well mitapivat works compared to placebo to increase the amount of hemoglobin in the blood and to reduce or prevent the occurrence of sickle cell pain crises. In addition, the long-term effect of mitapivat on efficacy and safety will be explored in an open-label extension portion.
This description comes directly from the study's public registry record.
No contact information is available for this study as per the public registry record.
Always discuss trial participation with your own doctor first.
| University of California San Diego | La Jolla, California, United States | — |
| UCLA Health | Los Angeles, California, United States | — |
| Children's Hospital Oakland | Oakland, California, United States | — |
| University of Connecticut Health Center | Farmington, Connecticut, United States | — |
| Children's National Hospital | Washington D.C., District of Columbia, United States | — |
| MedStar Washington Hospital Center | Washington D.C., District of Columbia, United States | — |
| Sylvester Comprehensive Cancer Center-Miami | Miami, Florida, United States | — |
| University of Chicago Medical Center | Chicago, Illinois, United States | — |
| Riley Hospital For Children | Indianapolis, Indiana, United States | — |
| LSU Health Sciences Center - Shreveport | Shreveport, Louisiana, United States | — |
| National Heart Lung and Blood Institute | Bethesda, Maryland, United States | — |
| Kaiser Permanente - Largo Medical Center | Largo, Maryland, United States | — |
+ 79 more locations — full list on the registry record.
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