Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

RECRUITING Phase 1

Study of TNG260 and an Anti-PD Antibody in STK11 Mutated Solid Tumors

NCT05887492 · View on ClinicalTrials.gov ↗

Study Summary

The goal of this interventional clinical trial is to learn about TNG260, a CoREST inhibitor, in combination with pembrolizumab in patients with advanced solid tumors with a known STK11 mutation. The main question\[s\] it aims to answer are: * the recommended dose for Phase 2 * to evaluate the safety and tolerability of the combination therapy * to determine the pharmacokinetics of TNG260 * to evaluate the initial antineoplastic activity Participants will receive study treatment until they experience an undesirable side effect, their disease progresses or until they withdraw consent.

Interventions

  • DRUG Pembrolizumab
  • DRUG TNG260

Study Locations (13)

Michigan

  • Henry Ford Health System — Detroit
  • START MidWest — Grand Rapids

New York

  • NYU Langone Hematology Oncology Associates-Mineola — Mineola
  • New York University Langone Health — New York

Texas

  • US Oncology Investigational Products Center — Dallas
  • The University of Texas MD Anderson Cancer Center — Houston

Virginia

  • NEXT Oncology Virginia — Fairfax
  • US Oncology Investigational Products Center — Norfolk

California

  • UCLA Hematology/Oncology — Santa Monica

Colorado

  • SCRI at HealthOne — Denver

Florida

  • Florida Cancer Specialists — Sarasota

Massachusetts

  • Dana Farber Cancer Institute — Boston

Trial Details

FieldValue
Enrollment Target 126 participants
Start Date 2023-06-12
Est. Completion 2026-06
Phase Phase 1

Sponsor

Tango Therapeutics

36 total trials

Interested in This Trial?

Always speak with your doctor before enrolling in a clinical trial.

Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT05887492

The ClinicalTrials.gov registry entry for NCT05887492 describes a study currently listed as recruiting. It is categorized as Phase 1, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 126 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Tango Therapeutics, which has 36 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 4 conditions, with Lung Cancer appearing as the primary indexed condition, and to 2 interventions — of which Pembrolizumab is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT05887492 reports 13 study locations spanning 9 distinct geographic areas — top geographies include Michigan, New York, Texas. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT05887492 about?

NCT05887492 is a clinical study titled "Study of TNG260 and an Anti-PD Antibody in STK11 Mutated Solid Tumors". The goal of this interventional clinical trial is to learn about TNG260, a CoREST inhibitor, in combination with pembrolizumab in patients with advanced solid tumors with a known STK11 mutation. The main question\[s\] it aims to answer are: * the recommended dose for Phase 2 * to evaluate the safe...

What is the current status of trial NCT05887492?

This trial is currently recruiting. It is a Phase 1 study. The enrollment target is 126 participants. The study started on 2023-06-12. Estimated completion is 2026-06.

What conditions does trial NCT05887492 study?

This clinical trial studies the following conditions: Lung Cancer, Non Small Cell Lung Cancer, Lung Adenocarcinoma, Solid Tumors, Adult. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT05887492?

The interventions under investigation include: Pembrolizumab (DRUG), TNG260 (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT05887492?

This trial is sponsored by Tango Therapeutics, which has 36 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT05887492 being conducted?

This trial has 13 study locations across California, Colorado, Florida, Massachusetts, Michigan. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial