COMPANY
Travere Therapeutics
FDA-approved therapeutic company Clinical Phase 3
Since the raise (Nov 12, 2024): 44 of 44 open jobs were first seen after it.
Hiring
| Title | Location (from posting) | Employer posted | First seen |
|---|---|---|---|
| Executive Director, Clinical Development | 2 locations (listed on the posting) | Oct 20, 2026 | Oct 21, 2026 |
| Executive Director, Health Economics & Outcomes Research (HEOR) | 2 locations (listed on the posting) | Oct 20, 2026 | Oct 21, 2026 |
| Executive Director, Field Operations Strategy & Excellence | 2 locations (listed on the posting) | Oct 20, 2026 | Oct 21, 2026 |
| Director, Enterprise Infrastructure Engineering & Operations | 2 locations (listed on the posting) | Oct 16, 2026 | Oct 5, 2026 |
| Senior Director, Marketing & Launch Lead, Pegtibatinase | 2 locations (listed on the posting) | Oct 16, 2026 | Oct 5, 2026 |
Timeline
- Board tracked Radar started tracking this company’s job board (44 open jobs at last check). source ↗
- Debt Debt: $475M (not counted as a raise), announced May 11, 2026. Source: SEC filing. source ↗
- FDA FDA New indication / efficacy supplement: FILSPARI (sparsentan) — NDA216403/6, Apr 13, 2026. Applicant at approval: Travere Therapeutics, Inc. source ↗
- Trial start Phase 4: Sparsentan in Posttransplant Immunoglobulin A Nephropathy or Focal Segmental Glomerulosclerosis source ↗
- FDA FDA New indication / efficacy supplement: FILSPARI (sparsentan) — NDA216403/5, Aug 27, 2025. Applicant at approval: Travere Therapeutics, Inc. source ↗
- Raise Follow-on offering: $143.8M (total, as published), announced Nov 12, 2024. Source: company release on GlobeNewswire. source ↗
- Trial start Phase 3: 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) source ↗
- Trial start Phase 3: Pegtibatinase as a Treatment for Participants With Classical Homocystinuria (HCU) Receiving Standard of Care Treatment source ↗
- Trial start Phase 2: A Study to Investigate Safety and Effect of Sparsentan in Combination With SGLT2 Inhibition in Participants With IgAN source ↗
- Trial start —: Humanistic Burden of (FSGS) Focal Segmental Glomerulosclerosis and IgAN (Immunoglobulin A Nephropathy) source ↗
- Trial start Phase 2: Study of Sparsentan Treatment in Pediatrics With Proteinuric Glomerular Diseases source ↗
- Trial start Phase 1: Study to Evaluate the Pharmacokinetics of Oral Sparsentan Suspension source ↗
- Trial start Phase 1/Phase 2: Pegtibatinase as a Treatment for Patients With Classical Homocystinuria (HCU) (Also Known as the COMPOSE Study) source ↗
- Trial start Phase 3: A Study of the Effect and Safety of Sparsentan in the Treatment of Patients With IgA Nephropathy source ↗
- Trial start Phase 3: Study of Sparsentan in Patients With Primary Focal Segmental Glomerulosclerosis (FSGS) source ↗
- Trial start Phase 3: Efficacy and Safety Study of Fosmetpantotenate (RE-024) in PKAN Participants source ↗
- Trial start —: Natural History Study of Homocystinuria Caused by Cystathionine Beta-Synthase Deficiency (ACAPPELLA) source ↗
- Trial start —: Cerebrotendinous Xanthomatosis (CTX) Prevalence Study source ↗
- Trial start Phase 2: Randomized, Double-Blind, Safety and Efficacy Study of RE-021 (Sparsentan) in Focal Segmental Glomerulosclerosis source ↗
Upcoming milestones
- 2027-03 (ESTIMATED) · Phase 4 · Sparsentan in Posttransplant Immunoglobulin A Nephropathy or Focal Segmental Glomerulosclerosis · NCT07219121
- Mar 12, 2027 (ESTIMATED) · Phase 2 · Study of Sparsentan Treatment in Pediatrics With Proteinuric Glomerular Diseases · NCT05003986
- 2027-07 (ESTIMATED) · Phase 1/Phase 2 · Pegtibatinase as a Treatment for Patients With Classical Homocystinuria (HCU) (Also Known as the COMPOSE Study) · NCT03406611
- 2027-08 (ESTIMATED) · Phase 3 · Pegtibatinase as a Treatment for Participants With Classical Homocystinuria (HCU) Receiving Standard of Care Treatment · NCT06247085
- 2030-08 (ESTIMATED) · Phase 3 · 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) · NCT06431893
Open jobs 44
| Title | Location (from posting, not HQ) | Employer posted | First seen | Level |
|---|---|---|---|---|
| Executive Director, Clinical Development | 2 locations (listed on the posting) | Oct 20, 2026 | Oct 21, 2026 | Not stated |
| Executive Director, Health Economics & Outcomes Research (HEOR) | 2 locations (listed on the posting) | Oct 20, 2026 | Oct 21, 2026 | Not stated |
| Executive Director, Field Operations Strategy & Excellence | 2 locations (listed on the posting) | Oct 20, 2026 | Oct 21, 2026 | Not stated |
| Director, Enterprise Infrastructure Engineering & Operations | 2 locations (listed on the posting) | Oct 16, 2026 | Oct 5, 2026 | Senior |
| Senior Director, Marketing & Launch Lead, Pegtibatinase | 2 locations (listed on the posting) | Oct 16, 2026 | Oct 5, 2026 | Senior |
| Associate Director, Search and Evaluation | 2 locations (listed on the posting) | Oct 15, 2026 | Oct 5, 2026 | Senior |
| Executive Director, Translational Medicine & Pediatric Planning | 2 locations (listed on the posting) | Oct 15, 2026 | Oct 16, 2026 | Not stated |
| Senior Manager, Statistical Programming | 2 locations (listed on the posting) | Oct 15, 2026 | Oct 16, 2026 | Not stated |
| Associate Director, Data Management | 2 locations (listed on the posting) | Oct 15, 2026 | Oct 16, 2026 | Not stated |
| Senior Manager, Drug Safety & Pharmacovigilance | 2 locations (listed on the posting) | Oct 15, 2026 | Oct 16, 2026 | Not stated |
| Senior Thought Leader Liaison (Southwest) | 4 locations, including Remote, California | Oct 13, 2026 | Oct 13, 2026 | Senior |
| Director, Medical Science Liaison - Metabolic | USA- Remote | Oct 12, 2026 | Oct 12, 2026 | Senior |
| Associate Director, Clinical Scientist | 2 locations (listed on the posting) | Oct 12, 2026 | Oct 12, 2026 | Senior |
| Associate Director, Quality Assurance - Technical | 2 locations (listed on the posting) | Oct 12, 2026 | Oct 13, 2026 | Senior |
| Director, Scientific Communications - Medical Content (Sparsentan) | 2 locations (listed on the posting) | Oct 8, 2026 | Oct 8, 2026 | Senior |
| Director, Specialty Pharmacy, Trade, & Distribution | 2 locations (listed on the posting) | Oct 7, 2026 | Oct 8, 2026 | Senior |
| Director, Clinical Science | 2 locations (listed on the posting) | Oct 2, 2026 | Oct 5, 2026 | Senior |
| Director, Biologics CMC Technical Writing | 2 locations (listed on the posting) | Sep 30, 2026 | Oct 5, 2026 | Senior |
| Associate Director, Commercial Manufacturing & Packaging | 2 locations (listed on the posting) | Sep 29, 2026 | Oct 5, 2026 | Senior |
| Associate Director, Technical Operations | 2 locations (listed on the posting) | Sep 29, 2026 | Oct 5, 2026 | Senior |
| Associate Director, Customer Engagement Platforms & Data | 2 locations (listed on the posting) | Sep 25, 2026 | Oct 5, 2026 | Senior |
| Vice President, US Patient Access | 2 locations (listed on the posting) | Sep 25, 2026 | Oct 5, 2026 | Executive |
| Senior Director, Enterprise Technology & Solutions | 2 locations (listed on the posting) | Sep 24, 2026 | Oct 5, 2026 | Senior |
| Thought Leader Liaison (South Central) | 3 locations, including Remote, Texas | Sep 23, 2026 | Oct 5, 2026 | Senior |
| Access & Reimbursement Manager (Southern California) | California - Remote | Sep 23, 2026 | Oct 5, 2026 | Mid |
| Director, Product & Pipeline Communications | 2 locations (listed on the posting) | Sep 23, 2026 | Oct 5, 2026 | Senior |
| Associate Director, Regulatory Labeling Strategy | 2 locations (listed on the posting) | Sep 23, 2026 | Oct 5, 2026 | Senior |
| Executive Director, Corporate Development | 2 locations (listed on the posting) | Sep 23, 2026 | Oct 5, 2026 | Executive |
| Director, New Product Planning & Commercial Diligence | San Diego | Sep 23, 2026 | Oct 5, 2026 | Senior |
| Senior Quality Assurance Associate - GMP/GDP Auditing | 2 locations (listed on the posting) | Sep 23, 2026 | Oct 5, 2026 | Senior |
| Associate Director, Clinical Pharmacology | 2 locations (listed on the posting) | Sep 23, 2026 | Oct 7, 2026 | Senior |
| Principal Data Manager | 2 locations (listed on the posting) | Sep 23, 2026 | Oct 7, 2026 | Senior |
| Executive Director, R&D Strategy & Operations | 2 locations (listed on the posting) | Sep 23, 2026 | Oct 7, 2026 | Executive |
| Associate Director, FILSPARI HCP Marketing | 2 locations (listed on the posting) | Sep 23, 2026 | Oct 7, 2026 | Senior |
| Flex Medical Science Liaison - West | 9 locations, including Remote, California | Sep 23, 2026 | Oct 7, 2026 | Mid |
| Flex Medical Science Liaison - East | 8 locations, including Remote, New York | Sep 23, 2026 | Oct 7, 2026 | Mid |
| Senior Specialist, Regulatory Affairs | Rapperswil-Jona (SG), Switzerland | Sep 23, 2026 | Oct 7, 2026 | Senior |
| Associate Director, Technical Operations (Small Molecule CMC) | 2 locations (listed on the posting) | Sep 23, 2026 | Oct 7, 2026 | Senior |
| Chief Scientific Officer | 2 locations (listed on the posting) | Sep 23, 2026 | Oct 7, 2026 | Executive |
| Associate Director, Legal Contracts | San Diego | Sep 23, 2026 | Oct 7, 2026 | Senior |
| Vice President, Financial Planning & Analysis | 2 locations (listed on the posting) | Sep 23, 2026 | Oct 7, 2026 | Executive |
| Associate Director, Technical Operations - Drug Product | 2 locations (listed on the posting) | Sep 23, 2026 | Oct 7, 2026 | Senior |
| Senior Total Rewards Analyst | San Diego | Sep 23, 2026 | Oct 7, 2026 | Senior |
| Manager, Regulatory Affairs Strategy | 2 locations (listed on the posting) | Sep 23, 2026 | Oct 7, 2026 | Mid |
Funding
Clinical trials (lead sponsor) 14
| Record | Title | Phase | Status | Start | Primary completion |
|---|---|---|---|---|---|
| NCT06247085 | Pegtibatinase as a Treatment for Participants With Classical Homocystinuria (HCU) Receiving Standard of Care Treatment | Phase 3 | Recruiting | Dec 28, 2023 | 2027-08 (estimated) |
| NCT02998710 | Natural History Study of Homocystinuria Caused by Cystathionine Beta-Synthase Deficiency (ACAPPELLA) | Not listed | Completed | 2017-01 | Jul 31, 2026 (actual) |
| NCT03406611 | Pegtibatinase as a Treatment for Patients With Classical Homocystinuria (HCU) (Also Known as the COMPOSE Study) | Phase 1/Phase 2 | Recruiting | Jan 22, 2019 | 2027-07 (estimated) |
| NCT07219121 | Sparsentan in Posttransplant Immunoglobulin A Nephropathy or Focal Segmental Glomerulosclerosis | Phase 4 | Active, not recruiting | Oct 7, 2025 | 2027-03 (estimated) |
| NCT06431893 | 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) | Phase 3 | Enrolling by invitation | Apr 30, 2024 | 2030-08 (estimated) |
| NCT05003986 | Study of Sparsentan Treatment in Pediatrics With Proteinuric Glomerular Diseases | Phase 2 | Recruiting | Aug 12, 2021 | Mar 12, 2027 (estimated) |
| NCT03762850 | A Study of the Effect and Safety of Sparsentan in the Treatment of Patients With IgA Nephropathy | Phase 3 | Active, not recruiting | Dec 11, 2018 | Aug 7, 2023 (actual) |
| NCT03493685 | Study of Sparsentan in Patients With Primary Focal Segmental Glomerulosclerosis (FSGS) | Phase 3 | Completed | Apr 17, 2018 | Mar 20, 2023 (actual) |
| NCT05856760 | A Study to Investigate Safety and Effect of Sparsentan in Combination With SGLT2 Inhibition in Participants With IgAN | Phase 2 | Completed | May 19, 2023 | Oct 14, 2024 (actual) |
| NCT01613118 | Randomized, Double-Blind, Safety and Efficacy Study of RE-021 (Sparsentan) in Focal Segmental Glomerulosclerosis | Phase 2 | Completed | 2014-03 | 2016-06 (actual) |
| NCT02638220 | Cerebrotendinous Xanthomatosis (CTX) Prevalence Study | Not listed | Completed | 2015-09 | Feb 19, 2021 (actual) |
| NCT05200871 | Humanistic Burden of (FSGS) Focal Segmental Glomerulosclerosis and IgAN (Immunoglobulin A Nephropathy) | Not listed | Completed | Feb 5, 2022 | Oct 31, 2023 (actual) |
| NCT05562362 | Study to Evaluate the Pharmacokinetics of Oral Sparsentan Suspension | Phase 1 | Completed | Jun 18, 2020 | Nov 12, 2020 (actual) |
| NCT03041116 | Efficacy and Safety Study of Fosmetpantotenate (RE-024) in PKAN Participants | Phase 3 | Terminated | Jul 17, 2017 | Dec 30, 2019 (actual) |
FDA records (last 2 years)
- FDA New indication / efficacy supplement: FILSPARI (sparsentan) — NDA216403/6, Apr 13, 2026. Applicant at approval: Travere Therapeutics, Inc. source ↗
- FDA New indication / efficacy supplement: FILSPARI (sparsentan) — NDA216403/5, Aug 27, 2025. Applicant at approval: Travere Therapeutics, Inc. source ↗
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