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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
A Gene Therapy Study of SPK-8011QQ in Adults With Severe or Moderately Severe Hemophilia ACongenital, Hereditary, and Neonatal Diseases and Abnormalities, Hemic and Lymphatic Diseases, blood coagulation disease, coagulation protein disease, hematologic disorder, hemophilia A, hemorrhagic disease, hereditary disease, inherited blood coagulation disorderRecruitingPhase 1 / Phase 22026-09-11NCT07226206