Travere Therapeutics
TVTXApprovedTravere Therapeutics is a publicly traded biopharma company singularly focused on rare diseases, particularly in nephrology and metabolism. Its strategic pipeline includes the commercially available therapy for IgA nephropathy and late-stage investigational candidates for FSGS and classical homocystinuria, aiming to set new standards of care. The company operates with a deep sense of urgency, guided by its 'In Rare For Life' ethos and a leadership team that includes rare disease patients and survivors, fostering strong community and advocacy partnerships.
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AI Company Overview
Travere Therapeutics is a publicly traded biopharma company singularly focused on rare diseases, particularly in nephrology and metabolism. Its strategic pipeline includes the commercially available therapy for IgA nephropathy and late-stage investigational candidates for FSGS and classical homocystinuria, aiming to set new standards of care. The company operates with a deep sense of urgency, guided by its 'In Rare For Life' ethos and a leadership team that includes rare disease patients and survivors, fostering strong community and advocacy partnerships.
Technology Platform
Travere's core approach is patient-centric drug development and commercialization in niche rare diseases, focusing on strategic target identification, late-stage clinical development, and integrated advocacy to support diagnosis and care.
Pipeline Snapshot
1414 drugs in pipeline, 5 in Phase 3
| Drug | Indication | Stage | Watch |
|---|---|---|---|
| Sparsentan | Proteinuria | Approved | |
| sparsentan + Irbesartan | Focal Segmental Glomerulosclerosis | Phase 3 | |
| Pegtibatinase | Homocystinuria | Phase 3 | |
| sparsentan + irbesartan + Dapagliflozin | Immunoglobulin A Nephropathy | Phase 3 | |
| Fosmetpantotenate + Placebo | Pantothenate Kinase-Associated Neurodegeneration | Phase 3 |
Funding History
3Total raised: $115M
FDA Approved Drugs
1Opportunities
Risk Factors
Competitive Landscape
In IgAN, Travere competes with other therapies like SGLT2 inhibitors and Novartis's atrasentan. In FSGS, it aims to be first-to-market against generic standards of care. For HCU, it faces little direct pharmacological competition. Differentiation is built on rare disease specialization, patient advocacy, and a comprehensive support ecosystem.
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