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Study to Evaluate the Safety, Tolerability & Efficacy of TNG462 in Combination in PDAC & NSCLC Patients
NCT06922591 · View on ClinicalTrials.gov ↗
Study Summary
TNG462-C102 is a Phase 1/2, open-label, multicenter study designed to determine the safety, tolerability, PK, PD, and preliminary antineoplastic activity of oral TNG462 in combination with RMC-6236, RMC-9805, mFOLFIRINOX or gemcitabine/nab-paclitaxel. The study comprises a dose escalation phase and a dose expansion phase.
Conditions Studied
Interventions
- DRUG mFOLFIRINOX
- DRUG RMC-6236
- DRUG TNG462
- DRUG RMC-9805
- DRUG gemcitabine/nab-paclitaxel
Study Locations (12)
New York
- NYU Langone Health — New York
- Memorial Sloan Kettering Cancer Center — New York
Texas
- University of Texas MD Anderson Cancer Center — Houston
- NEXT Dallas — Irving
Arizona
- Mayo Clinic Scottsdale — Scottsdale
Colorado
- Sarah Cannon Research Institute Denver — Denver
Florida
- Mayo Clinic Jacksonville — Jacksonville
Indiana
- University of Indiana — Indianapolis
Massachusetts
- Dana-Farber Cancer Institute — Boston
Minnesota
- Mayo Clinic Cancer Center — Rochester
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 183 participants |
| Start Date | 2025-05-31 |
| Est. Completion | 2027-12 |
| Phase | Phase 1 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT06922591
The ClinicalTrials.gov registry entry for NCT06922591 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 183 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 8 conditions, with Lung Cancer appearing as the primary indexed condition, and to 5 interventions — of which mFOLFIRINOX 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: NCT06922591 reports 12 study locations spanning 10 distinct geographic areas — top geographies include New York, Texas, Arizona. 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 NCT06922591 about?
NCT06922591 is a clinical study titled "Study to Evaluate the Safety, Tolerability & Efficacy of TNG462 in Combination in PDAC & NSCLC Patients". TNG462-C102 is a Phase 1/2, open-label, multicenter study designed to determine the safety, tolerability, PK, PD, and preliminary antineoplastic activity of oral TNG462 in combination with RMC-6236, RMC-9805, mFOLFIRINOX or gemcitabine/nab-paclitaxel. The study comprises a dose escalation phase and ...
What is the current status of trial NCT06922591?
This trial is currently recruiting. It is a Phase 1 study. The enrollment target is 183 participants. The study started on 2025-05-31. Estimated completion is 2027-12.
What conditions does trial NCT06922591 study?
This clinical trial studies the following conditions: Lung Cancer, NSCLC, Thoracic Cancer, PDAC - Pancreatic Ductal Adenocarcinoma, Pancreatic Cancer Metastatic. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT06922591?
The interventions under investigation include: mFOLFIRINOX (DRUG), RMC-6236 (DRUG), TNG462 (DRUG), RMC-9805 (DRUG), gemcitabine/nab-paclitaxel (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT06922591?
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 NCT06922591 being conducted?
This trial has 12 study locations across Arizona, Colorado, Florida, Indiana, Massachusetts. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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