RecruitingPHASE1, PHASE2NCT06922591
Study to Evaluate the Safety, Tolerability & Efficacy of TNG462 in Combination in PDAC & NSCLC Patients
Studying NON RARE IN EUROPE: Non-small cell lung cancer
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- Tango Therapeutics, Inc.
- Principal Investigator
- Maxim Pimpkin, MD, PhD, MDTango Therapeutics, Inc.
- Intervention
- TNG462(drug)
- Enrollment
- 183 enrolled
- Eligibility
- 18 years · All sexes
- Timeline
- 2025 – 2027
Study locations (12)
- Mayo Clinic Scottsdale, Scottsdale, Arizona, United States
- Sarah Cannon Research Institute Denver, Denver, Colorado, United States
- Mayo Clinic Jacksonville, Jacksonville, Florida, United States
- University of Indiana, Indianapolis, Indiana, United States
- Dana-Farber Cancer Institute, Boston, Massachusetts, United States
- Mayo Clinic Cancer Center, Rochester, Minnesota, United States
- Nebraska Cancer Specialists, Omaha, Nebraska, United States
- NYU Langone Health, New York, New York, United States
- Memorial Sloan Kettering Cancer Center, New York, New York, United States
- University of Texas MD Anderson Cancer Center, Houston, Texas, United States
- NEXT Dallas, Irving, Texas, United States
- NEXT Oncology, Fairfax, Virginia, United States
Collaborators
Revolution Medicines, Inc.
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
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