RecruitingPhase 1NCT07315113

Study of NXP900 With Osimertinib in Subjects With Advanced, EGFR-Mutated Non-Small Cell Lung Cancer

A Phase 1b Clinical Study of NXP900 in Combination With Osimertinib in Subjects With Advanced, EGFRMut+ Non-Small Cell Lung Cancer


Sponsor

Nuvectis Pharma, Inc.

Enrollment

18 participants

Start Date

Dec 18, 2025

Study Type

INTERVENTIONAL

Conditions

Summary

This is a multi-center, open label, Phase 1b study of NXP900 in combination with osimertinib in subjects with advanced, progressing, EGFR-mutated non-small cell lung cancer (NSCLC)


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This study is testing a new drug called NXP900 used together with osimertinib (a standard targeted therapy) in people with advanced non-small cell lung cancer that has a specific mutation in the EGFR gene. **You may be eligible if...** - You are 18 or older - You have advanced, locally advanced, or metastatic non-small cell lung cancer with an EGFR mutation - You have previously been treated with osimertinib (alone or combined with chemotherapy) - You are in good physical condition (ECOG score 0 or 1) **You may NOT be eligible if...** - Your cancer has a different main driver mutation (other than EGFR) - You have a known EGFR mutation that causes resistance to osimertinib - You have HER2 overexpression - You have a medical condition that prevents you from safely taking osimertinib Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DRUGNXP900

NXP900 is an orally administered inhibitor of SRC family kinases (SFK)

DRUGOsimertinib

Osimertinib is an orally available, irreversible, mutant-selective, epidermal growth factor receptor (EGFR) inhibitor


Locations(3)

Massachusetts General Hospital

Boston, Massachusetts, United States

NEXT Houston

Houston, Texas, United States

NEXT Virginia

Fairfax, Virginia, United States

View Full Details on ClinicalTrials.gov

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NCT07315113