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OncoMatch/Clinical Trials/NCT06922591

Study to Evaluate the Safety, Tolerability & Efficacy of TNG462 in Combination in PDAC & NSCLC Patients

Is NCT06922591 recruiting? Yes, currently enrolling (Jun 2026). This Phase 1/2 trial studies multiple treatments for pdac.

Phase 1/2RecruitingTango Therapeutics, Inc.NCT06922591Data as of Jun 2026

Treatment: TNG462 · RMC-9805 · RMC-6236 · mFOLFIRINOX · gemcitabine/nab-paclitaxelTNG462-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.

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Extracted eligibility criteria

Treatments studied

Chemotherapy

gemcitabine/nab-paclitaxel

Other

TNG462RMC-9805RMC-6236mFOLFIRINOX

Cancer type

Pancreatic Cancer

Non-Small Cell Lung Carcinoma

Biomarker criteria

Required: MTAP loss of protein

Has a tumor with loss of MTAP protein

Required: MTAP bi-allelic deletion

bi-allelic deletion of the MTAP gene

Required: KRAS mutation

Arms A and B only: Has a tumor with a RAS mutation

Required: NRAS mutation

Arms A and B only: Has a tumor with a RAS mutation

Required: HRAS mutation

Arms A and B only: Has a tumor with a RAS mutation

Disease stage

Required: Stage IV, III

metastatic PDAC or locally advanced, recurrent or metastatic NSCLC

Performance status

ECOG 0–1(Restricted strenuous activity)

Prior therapy

Min 1 prior line

Must have received: standard therapy

Has received prior standard therapy

Cannot have received: RAS-targeted therapy

Exception: Arms A and B only

Arms A and B only: Must not have received prior RAS-targeted therapy

Cannot have received: PRMT5 inhibitor

Has received prior treatment with a PRMT5 inhibitor

Cannot have received: MAT2A inhibitor

Has received prior treatment with a MAT2A inhibitor

Lab requirements

Blood counts

Kidney function

Liver function

Adequate organ function

Structured fields extracted by AI. May contain errors — verify against the official protocol.

US trial sites

  • Mayo Clinic Scottsdale · Scottsdale, Arizona
  • Sarah Cannon Research Institute Denver · Denver, Colorado
  • Mayo Clinic Jacksonville · Jacksonville, Florida
  • University of Indiana · Indianapolis, Indiana
  • Dana-Farber Cancer Institute · Boston, Massachusetts

Showing up to 5 US sites.

See all sites on ClinicalTrials.gov →

Frequently asked questions

Is NCT06922591 currently recruiting?

Yes, this trial is currently recruiting patients.

Are there prior therapy exclusions?

Yes. Prior RAS-targeted therapy, PRMT5 inhibitor, MAT2A inhibitor disqualifies patients from enrollment.

Does this trial require MTAP?

Yes, MTAP loss of protein is a required biomarker for enrollment.

Does this trial require MTAP?

Yes, MTAP bi-allelic deletion is a required biomarker for enrollment.

Does this trial require KRAS?

Yes, KRAS mutation is a required biomarker for enrollment.

What disease stage is eligible?

Stage IV or III is required.

Could you qualify for this trial?

Enter your biomarker results to see how this trial's eligibility criteria match your specific cancer profile.

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