Clinical Trials - TVTX

NCT IDTitleStatusPhasesStart DateCompletion DatePrimary Completion Date
NCT06431893A Phase 3 Long-term Extension Study to Assess the Long-term Safety and Efficacy of Pegtibatinase Treatment in Participants ≥5 to ≤65 Years of Age With Classical Homocystinuria (HCU) (ENSEMBLE)ENROLLING_BY_INVITATIONPHASE32024-04-302027-012027-01
NCT06247085A Study to Investigate Efficacy and Safety of Pegtibatinase Compared With Placebo in Participants ≥12 to ≤65 Years of Age With Classical Homocystinuria (HCU) Due to Cystathionine Beta Synthase Deficiency Receiving Standard of Care TreatmentACTIVE_NOT_RECRUITINGPHASE32023-12-282026-012025-12
NCT05856760A Study to Investigate Safety and Effect of Sparsentan in Combination With SGLT2 Inhibition in Participants With IgANCOMPLETEDPHASE22023-05-192024-10-252024-10-14
NCT05003986Study of Sparsentan Treatment in Pediatrics With Proteinuric Glomerular DiseasesRECRUITINGPHASE22021-08-122027-04-122027-03-12
NCT05562362Study to Evaluate the Pharmacokinetics of Oral Sparsentan SuspensionCOMPLETEDPHASE12020-06-182020-11-122020-11-12
NCT03406611Pegtibatinase As an Enzyme Therapy for Patients with Homocystinuria Caused by Cystathionine Beta-Synthase Deficiency (COMPOSE)ACTIVE_NOT_RECRUITINGPHASE1, PHASE22019-01-222026-122026-06
NCT03762850A Study of the Effect and Safety of Sparsentan in the Treatment of Patients With IgA NephropathyACTIVE_NOT_RECRUITINGPHASE32018-12-112026-072023-08-07
NCT03493685Study of Sparsentan in Patients With Primary Focal Segmental Glomerulosclerosis (FSGS)ACTIVE_NOT_RECRUITINGPHASE32018-04-172026-022023-03-20
NCT03041116Efficacy and Safety Study of Fosmetpantotenate (RE-024) in PKAN ParticipantsTERMINATEDPHASE32017-07-172019-12-302019-12-30
NCT01613118Randomized, Double-Blind, Safety and Efficacy Study of RE-021 (Sparsentan) in Focal Segmental GlomerulosclerosisCOMPLETEDPHASE22014-032024-03-252016-06