Biopharma Transcript

Travere Therapeutics, Inc. TVTX

Nasdaq · Phase 3 · cardio-renal-metabolic · small molecule · EDGAR · Updated Oct 24, 2026

Travere Therapeutics, Inc. (Nasdaq: TVTX) is a cardio-renal-metabolic drug developer. Its lead program, FILSPARI (sparsentan), is in Phase 3 for Primary IgA nephropathy (IgAN); also FSGS. Its next catalyst on record is sparsentan (Japan): Chugai regulatory filing in Japan (2026).

Upcoming catalysts

No catalyst is dated to the next 30 days or to an FDA action date.

Next further out: sparsentan (Japan) — Chugai regulatory filing in Japan (2026). 2 catalysts on record beyond the next 30 days; subscribers see each with its filing sentence.

Pipeline

ProgramIndicationModalityStage
FILSPARI (sparsentan)IgAN (full approval Sept 2024) and FSGS without nephrotic syndrome (full approval 2026-04-13)small moleculeApproved
Thiola / Thiola EC (tiopronin)Cystinuriasmall moleculeApproved
pegtibatinaseClassical homocystinuria (Phase 3 HARMONY, enrollment restarted)enzyme_replacementPhase 3
civorebrutinibPrimary membranous nephropathy (Phase 1/2 proof of concept); FSGS, MCD plannedsmall moleculePhase 2

Recent results and decisions

  1. May 4, 2026
    started First new patient dosed in April 2026 in the restarted pivotal Phase 3 HARMONY study (about 70 patients, primary endpoint change in plasma tHcy weeks 6-12).In April 2026, the Company dosed the first new patient following the study restart, with topline data anticipated in 2H 2027. Filing
  2. Apr 13, 2026
    approval FDA approved FILSPARI to reduce proteinuria in patients aged 8+ with FSGS without nephrotic syndrome, the first approved FSGS medicine; DUPLEX showed 48% vs 27% proteinuria reduction at Week 108 vs irbesartan in this subgroup (nominal p=0.0075).FILSPARI is the first and only medicine approved by the FDA for the treatment of FSGS, marking its expansion beyond IgA nephropathy (“IgAN”) into a second rare kidney disease. Filing

For subscribers

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