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tti-101

·Code: TTI-101

tti-101: developed by 1 company · 5 clinical trials tracked.

tti-101 evidence translation

What we can confirm

What it means

Source-backed records connect tti-101 to TVRD; that link alone does not prove the drug works.

What to watch

Watch trial status, endpoints, and the next source-backed update.
BioSniper AIPage evidence connected

Prepared research question

How could tti-101 → TVRD affect its developer, and what evidence supports the link?

Run cited research

Traceable citations · Unknowns marked

See linked entities and source evidence5 indications · 0 study sponsors

Related indications

Study sponsors

No additional listed-company sponsor is linked.

Development Pipeline (1)
CompanyPhase
Tvardi Therapeutics, Inc. (TVRD)
Hepatocellular Carcinoma; Idiopathic Pulmonary Fibrosis
Phase 1/Phase 2
Clinical Trials (5)

Phase I/II Open Label Study Evaluating the Safety and Efficacy of Combining STAT3 Inhibition (TTI-101) With Anti-PD-1 Therapy (Pembrolizumab) in Patients With Recurrent or Metastatic (RM) Head and Neck Squamous Cell Carcinoma (HNSCC)

NCT05668949·Phase 1/Phase 2
Withdrawn

Primary endpoint: Overall Response Rate (ORR)

InterventionalRandomizedopen0 targetStarted 2025-09Completion 2025-09M.D. Anderson Cancer Center

Randomized Pre-surgical Window-of-Opportunity Trial of TTI-101 in Patients With Stage II-IV Resectable HPV-negative Squamous Cell Carcinoma of the Head and Neck

NCT05845307·Early Phase 1
Withdrawn

Primary endpoint: Incidence of Adverse Events, Graded According to National Cancer Institute Common Terminology Criteria for Adverse Events (NCI CTCAE) Version (v) 5.0

Interventionalopen0 targetStarted 2025-06Completion 2025-11M.D. Anderson Cancer Center

Phase I/IB Trial of Radiotherapy in Combination With TTI-101 in Borderline Resectable and Locally Advanced Pancreatic Ductal Adenocarcinoma

NCT06141031·Phase 1
Recruiting

Primary endpoint: Maximum tolerated dose (MTD) and/or recommended phase II dose (RP2D) of TTI-101 and SBRT

Interventionalopen24 targetStarted 2024-01Completion 2029-062 sites · United StatesWashington University School of Medicine

REVERT-IPF: A Phase 2 Multicenter, Randomized, Double-blind, Placebo-controlled Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Efficacy of TTI-101 in Participants With Idiopathic Pulmonary Fibrosis

NCT05671835·Phase 2·TVRD
Completed

Primary endpoint: Number of Participants with an Adverse Event (AE)

InterventionalRandomizedquadruple100 enrolledStarted 2023-05Completion 2025-0828 sites · United StatesTvardi Therapeutics, Incorporated

REVERT- Liver Cancer: A Phase 1b/2 Multicenter, Open-label Study to Evaluate the Safety and Efficacy of TTI-101 as Monotherapy and in Combination in Participants With Locally Advanced or Metastatic, and Unresectable Hepatocellular Carcinoma

NCT05440708·Phase 1/Phase 2·TVRD
Recruiting

Primary endpoint: Incidence of Adverse Events (AE)

Interventionalopen193 targetStarted 2023-03Completion 2027-0621 sites · United StatesTvardi Therapeutics, Incorporated

Frequently asked questions

Who is developing tti-101?

tti-101 is being developed by Tvardi Therapeutics, Inc..

How many clinical trials involve tti-101?

BioSniper tracks 5 clinical trials involving tti-101.