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Synchronisé depuis ClinicalTrials.gov — NCT06392386

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Essais cliniques associés

9
MoléculeIndication / populationPhaseNCTTitreStatut
Inavolisib Cancer Phase 3 NCT06790693 INAVO123 — A Study Evaluating the Efficacy and Safety of Inavolisib Plus CDK4/6 Inhibitor and Letrozole vs Placebo + CDK4/6i and Letrozole in Participants With Endocrine-Sensitive PIK3CA-Mutated, Hormone Receptor-Positive, HER2-Negative Advanced Breast Cancer RECRUITING
Efgartigimod PH20 SC Myasthénie Phase 2/3 NCT06392386 ADAPT Jr SC — A Study of Efgartigimod PH20 SC in Children Between 2 and Less Than 18 Years of Age With Generalized Myasthenia Gravis RECRUITING
PF-06939926 Myopathies Phase 3 NCT04281485 Study to Evaluate the Safety and Efficacy of PF-06939926 for the Treatment of Duchenne Muscular Dystrophy ACTIVE_NOT_RECRUITING
delandistrogene moxeparvovec Myopathies Phase 2 NCT06128564 ENVOL — A Gene Delivery Study to Evaluate the Safety and Expression of Delandistrogene Moxeparvovec in Participants Under the Age of Four With Duchenne Muscular Dystrophy (DMD) ACTIVE_NOT_RECRUITING
Efgartigimod IV or Efgartigimod PH20 SC Myasthénie Phase 2/3 NCT05374590 ADAPT Jr + — Evaluating Long-term Safety of Efgartigimod Administered Intravenously and Efgartigimod PH20 Administered Subcutaneously in Children With Generalized Myasthenia Gravis ENROLLING_BY_INVITATION
MEDI0618 Migraine Phase 2 NCT06602479 AURORA — A Study to Investigate the Safety and Efficacy of MEDI0618 Compared to Placebo in Adult Participants With Episodic Migraine RECRUITING
Relief — Peripheral Nerve Stimulation Registry for Intractable Migraine Headache Migraine À vérifier NCT02227758 Relief — Peripheral Nerve Stimulation Registry for Intractable Migraine Headache COMPLETED
Efgartigimod IV Myasthénie Phase 2 NCT04833894 ADAPT Jr — Evaluating the Pharmacokinetics, Pharmacodynamics, and Safety of Efgartigimod Administered Intravenously in Children With Generalized Myasthenia Gravis RECRUITING
Casimersen Myopathies Phase 3 NCT03532542 An Extension Study to Evaluate Casimersen or Golodirsen in Patients With Duchenne Muscular Dystrophy TERMINATED