Biopharma Transcript

Travere Therapeutics, Inc. TVTX

Nasdaq · Phase 3 · rare genetic · protein/peptide · EDGAR · Updated Nov 5, 2026

Travere Therapeutics, Inc. (Nasdaq: TVTX) is a rare genetic drug developer. Its lead program, Pegtibatinase, is in Phase 3 for Classical homocystinuria (HCU). Its next catalyst on record is Pegtibatinase: Topline data from Phase 3 HARMONY Study (H2 2027).

Upcoming catalysts

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

Next further out: Pegtibatinase — Topline data from Phase 3 HARMONY Study (H2 2027). 1 catalyst on record beyond the next 30 days; subscribers see each with its filing sentence.

Pipeline

ProgramIndicationModalityStage
FILSPARI (sparsentan)IgANsmall moleculeApproved
FILSPARI (sparsentan)FSGSsmall moleculeApproved
Thiola / Thiola EC (tiopronin)Cystinuriasmall moleculeApproved
PegtibatinaseClassical homocystinuria (HCU)protein/peptidePhase 3
CivorebrutinibPMN, FSGS, MCDsmall 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

Other phase 3 rare genetic companies