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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
Study of SRP-1003 in Participants With Type 1 Myotonic DystrophyCongenital, Hereditary, and Neonatal Diseases and Abnormalities, Muscular Disorders, Atrophic, hereditary disease, inherited neurodegenerative disorder, muscle tissue disorder, muscular dystrophy, musculoskeletal system disorder, myotonic dystrophy, myotonic syndrome, nervous system disorder, neurodegenerative disease, neuromuscular diseaseEnrolling by invitationPhase 1 / Phase 22026-10-05NCT06138743
European Newborn Study: Early Markers for a Better LifEBrain Damage, Chronic, brain disorder, central nervous system disorder, cerebral palsy, nervous system disorderRecruitingNot stated2025-09-24NCT07189494
Avelumab and Methotrexate in in Low-risk Gestational Trophoblastic Neoplasias as First Line TreatmentGestational Trophoblastic Neoplasias (GTN)RecruitingPhase 1 / Phase 22024-02-29NCT04396223