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

RecruitingPhase 1

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

Who can join

Ages 18 and older · All sexes

Full eligibility criteria
Inclusion Criteria:

1. Provide written informed consent.
2. 18 years old or older.
3. Eastern Cooperative Oncology Group (ECOG) performance status of 0-1.
4. Unresectable, metastatic or locally advanced EGFR-mutated NSCLC.
5. Prior treatment with osimertinib as first or second line, as single agent or in combination with chemotherapy, in the metastatic or locally advanced setting.

Exclusion Criteria:

1. Subject's cancer has a known oncogenic driver alteration other than EGFR.
2. Known EGFR mutations that cause resistance to osimertinib
3. Known human epidermal growth factor receptor 2 (HER2) overexpression
4. Any contraindications to treatment with osimertinib

About the study

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)

What is being tested

Sponsor: Nuvectis Pharma, Inc. · Participants: 18 · Started: Dec 18, 2025

Contact the study team

Official record on ClinicalTrials.gov — NCT07315113

Locations in the U.S.

MarylandMaryland Oncology Hematology, Calverton
MassachusettsMassachusetts General Hospital, Boston (Not yet recruiting)
OregonWillamette Valley Cancer Institute and Research Center, Eugene
PennsylvaniaUPMC Hillman Cancer Center, Pittsburgh
TexasNEXT Houston, Houston
VirginiaNEXT Virginia, Fairfax

Conditions

From ClinicalTrials.gov, data retrieved Sep 29, 2026. Each study sets its own eligibility; the study team decides who can join.