Biopharma Transcript

Protara Therapeutics, Inc. TARA

Nasdaq · Phase 2 · oncology · cell therapy · EDGAR · Updated Oct 24, 2026

Protara Therapeutics, Inc. (Nasdaq: TARA) is an oncology drug developer. Its lead program, TARA-002 (intravesical), ADVANCED-2, is in Phase 2 for BCG-unresponsive / BCG-naive high-grade NMIBC with CIS. Its next catalyst on record is IV Choline Chloride (THRIVE-3): Interim results from dose-confirmation portion (Q4 2026).

Upcoming catalysts

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

Next further out: IV Choline Chloride (THRIVE-3) — Interim results from dose-confirmation portion (Q4 2026). 3 catalysts on record beyond the next 30 days; subscribers see each with its filing sentence.

Pipeline

ProgramIndicationModalityStage
TARA-002 ADVANCED-2 (Cohort B registrational; Cohort A BCG-naive enrolled)Non-muscle invasive bladder cancer (CIS)cell therapyPhase 2
TARA-002 STARBORN-1 (pivotal Phase 2)Macrocystic and mixed-cystic lymphatic malformationscell therapyPhase 2
IV Choline Chloride THRIVE-3 (seamless Phase 2b/3)Choline source for patients on long-term parenteral supportsmall moleculePhase 2
TARA-002 ADVANCED-3 (redesigned exploratory multi-cohort)BCG-naive/exposed CIS and papillary NMIBCcell therapyPhase 2

Recent results and decisions

  1. Feb 23, 2026
    positive BCG-Unresponsive interim: CR 68.2% (15/22) at 6 months, 33.3% (5/15) at 12 months, 65.7% (23/35) at any time; no Grade 3+ treatment-related AEs.The CR rate was 68.2% (15 of 22) at six months and 33.3% (5 of 15) at 12 months Filing
  2. Dec 3, 2025
    positive Updated interim in BCG-Naive NMIBC: CR at any time 72% (21/29), 69% (18/26) at 6 months, 50% (7/14) at 12 months; no Grade 3+ treatment-related AEs.The CR rate at any time was 72% (21/29). Filing
  3. Dec 3, 2025
    n/a FDA provided written feedback supporting a controlled registrational design in BCG-Naive patients, with CR at month 6 as primary endpoint and chemotherapy an acceptable comparator.The FDA has provided written feedback supporting a registrational design for a controlled trial in BCG-Naïve patients Filing

1 more on record.

For subscribers

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