Travere Therapeutics, Inc. (TVTX)
Travere Therapeutics, Inc. is a biopharmaceutical company developing therapies for rare kidney and metabolic diseases. Its lead product, FILSPARI (sparsentan), is an oral, once-daily, non-immunosuppressive medication targeting two pathways of disease progression (endothelin-1 and angiotensin-II). Sparsentan received accelerated FDA approval in February 2023 and full approval in September 2024 to slow kidney function decline in adults with primary IgA nephropathy (IgAN) at risk of progression. In April 2026, the FDA approved FILSPARI to reduce proteinuria in adult and pediatric patients aged 8 and older with focal segmental glomerulosclerosis (FSGS) without nephrotic syndrome, making it the first and only FDA-approved medicine for FSGS. The company also markets Thiola and Thiola EC (tiopronin tablets) for cystinuria, a rare genetic disorder causing recurring kidney stones. Its pipeline includes pegtibatinase, an investigational enzyme replacement therapy for classical homocystinuria (HCU). Formerly Retrophin, Inc. (renamed November 2020), Travere is headquartered in San Diego, California, and incorporated in Delaware.
Sector: Pharmaceutical Preparations
Industry: Biotechnology
Travere Therapeutics, Inc.
Trials need funding. See this company's dilution risk and cash position.
- Phase 4Active, not recruiting
Sparsentan in Posttransplant Immunoglobulin A Nephropathy or Focal Segmental Glomerulosclerosis
Sparsentan
Proteinuria, Immunoglobulin A (IgA) Nephropathy +2
NCT07219121Enrollment20StartOct 2025Primary CompletionMar 2027est.CompletionMay 2027est. - Phase 3Terminated
Efficacy and Safety Study of Fosmetpantotenate (RE-024) in PKAN Participants
Fosmetpantotenate, Placebo
Pantothenate Kinase-Associated Neurodegeneration
NCT03041116Enrollment84StartJul 2017Primary CompletionDec 2019CompletionDec 2019 - Phase 3Completed
Study of Sparsentan in Patients With Primary Focal Segmental Glomerulosclerosis (FSGS)
sparsentan, Irbesartan
Focal Segmental Glomerulosclerosis
NCT03493685Enrollment371StartApr 2018Primary CompletionMar 2023CompletionMar 2026 - Phase 3Completed
A Study of the Effect and Safety of Sparsentan in the Treatment of Patients With IgA Nephropathy
sparsentan, irbesartan
Immunoglobulin A Nephropathy
NCT03762850Enrollment406StartDec 2018Primary CompletionAug 2023CompletionAug 2026 - Phase 3Recruiting
Pegtibatinase as a Treatment for Participants With Classical Homocystinuria (HCU) Receiving Standard of Care Treatment
Pegtibatinase
Homocystinuria
NCT06247085Enrollment70StartDec 2023Primary CompletionAug 2027est.CompletionSep 2027est. - Phase 3Enrolling by invitation
A 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)
Pegtibatinase
Homocystinuria
NCT06431893Enrollment100StartApr 2024Primary CompletionAug 2030est.CompletionAug 2030est. - Phase 2Completed
Randomized, Double-Blind, Safety and Efficacy Study of RE-021 (Sparsentan) in Focal Segmental Glomerulosclerosis
RE-021 (Sparsentan), Irbesartan
Focal Segmental Glomerulosclerosis
NCT01613118Enrollment109StartMar 2014Primary CompletionJun 2016CompletionMar 2024 - Phase 2Recruiting
Study of Sparsentan Treatment in Pediatrics With Proteinuric Glomerular Diseases
Sparsentan, Sparsentan
Focal Segmental Glomerulosclerosis, Minimal Change Disease +3
NCT05003986Enrollment67StartAug 2021Primary CompletionMar 2027est.CompletionApr 2027est. - Phase 2Completed
A Study to Investigate Safety and Effect of Sparsentan in Combination With SGLT2 Inhibition in Participants With IgAN
Sparsentan
Immunoglobulin A Nephropathy
NCT05856760Enrollment48StartMay 2023Primary CompletionOct 2024CompletionOct 2024 - Phase 1/2Recruiting
Pegtibatinase as a Treatment for Patients With Classical Homocystinuria (HCU) (Also Known as the COMPOSE Study)
Pegtibatinase, Placebo
Homocystinuria
NCT03406611Enrollment39StartJan 2019Primary CompletionJul 2027est.CompletionJul 2027est. - Phase 1Completed
Study to Evaluate the Pharmacokinetics of Oral Sparsentan Suspension
RE-021, sparsentan
Healthy Subjects
NCT05562362Enrollment47StartJun 2020Primary CompletionNov 2020CompletionNov 2020 - ObservationalCompleted
Cerebrotendinous Xanthomatosis (CTX) Prevalence Study
-
Cerebrotendinous Xanthomatosis (CTX)
NCT02638220Enrollment442StartSep 2015Primary CompletionFeb 2021CompletionFeb 2021 - ObservationalCompleted
Natural History Study of Homocystinuria Caused by Cystathionine Beta-Synthase Deficiency (ACAPPELLA)
-
Homocystinuria Due to CBS Deficiency
NCT02998710Enrollment110StartJan 2017Primary CompletionJul 2026CompletionJul 2026 - ObservationalCompleted
Humanistic Burden of (FSGS) Focal Segmental Glomerulosclerosis and IgAN (Immunoglobulin A Nephropathy)
-
Focal Segmental Glomerulosclerosis, Immunoglobulin A Nephropathy
NCT05200871Enrollment487StartFeb 2022Primary CompletionOct 2023CompletionOct 2023
| Drug / Therapy | Link | ||
|---|---|---|---|
| Phase 4 | Active, not recruiting | Sparsentan | NCT07219121 |
| Phase 3 | Terminated | Fosmetpantotenate, Placebo | NCT03041116 |
| Phase 3 | Completed | sparsentan, Irbesartan | NCT03493685 |
| Phase 3 | Completed | sparsentan, irbesartan | NCT03762850 |
| Phase 3 | Recruiting | Pegtibatinase | NCT06247085 |
| Phase 3 | Enrolling by invitation | Pegtibatinase | NCT06431893 |
| Phase 2 | Completed | RE-021 (Sparsentan), Irbesartan | NCT01613118 |
| Phase 2 | Recruiting | Sparsentan, Sparsentan | NCT05003986 |
| Phase 2 | Completed | Sparsentan | NCT05856760 |
| Phase 1/2 | Recruiting | Pegtibatinase, Placebo | NCT03406611 |
| Phase 1 | Completed | RE-021, sparsentan | NCT05562362 |
| Observational | Completed | - | NCT02638220 |
| Observational | Completed | - | NCT02998710 |
| Observational | Completed | - | NCT05200871 |