New drug combo aims to outsmart resistant lung cancer
NCT ID NCT07315113
First seen Jun 27, 2026 · Last updated Jul 10, 2026 · Updated 2 times
Summary
This early-phase trial tests a new oral drug called NXP900 combined with the standard drug osimertinib in 18 adults with advanced EGFR-mutated non-small cell lung cancer that has progressed on prior osimertinib. The main goals are to check safety and see if the combination can shrink tumors or control the disease. Because it is a Phase 1 study, the focus is on finding the right dose and watching for side effects.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- NXP900 combined with osimertinib
- What this could lead to
- If it works, this could point toward a new combination treatment for advanced EGFR-mutated lung cancer that has stopped responding to osimertinib alone.
- What could go wrong
- This is a very early Phase 1b trial with only 18 participants, so it is primarily testing safety and dosing. The combination may not shrink tumors or may cause unexpected side effects.
Why investors are watching
Nuvectis Pharma is testing its experimental drug NXP900 together with the standard lung cancer medicine osimertinib in 18 patients whose EGFR-mutated non-small cell lung cancer has stopped responding to treatment. For a micro-cap company with few assets, this early-stage readout on safety and disease control is a major value driver, because a favorable result could validate the combination and support further development.
If it works: A positive result could show that NXP900 adds benefit in patients who have progressed on osimertinib, which would strengthen Nuvectis's case for advancing the drug into later trials and could attract partnership interest.
If it fails: The trial could fail to show adequate safety or disease control, or the small sample size could produce unclear results. Early-stage cancer trials often fail, and a negative outcome would leave Nuvectis with limited options and could delay or end the program.
AI-written from the trial record. Speculative, and not investment advice.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
-
Phase 1
The first testing in people. Mainly checks safety and dose, usually in a small group.
- Participants
-
About 18 people
The number the study aims to enrol. It can still change while the study runs.
- Started
-
Dec 2025
- Expected to finish
-
Jun 2027
An estimate. End dates often move.
- Lead sponsor
-
A company
The lead sponsor is a pharmaceutical, biotech, or medical-device company.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
-
18 years and older
- Sex
-
Anyone
- Healthy volunteers
-
Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
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
Get updates
Get notified about this study
Sign up to get updates when this study changes or when new studies for EGFR mutated non-small cell lung cancer patients are added.
Genom att skicka in godkänner du våra Användarvillkor
Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
-
The places running it
6 sites. The list below names each one and where it is.
-
The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
-
A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
-
Maryland Oncology Hematology
RECRUITINGCalverton, Maryland, 20705, United States
-
Massachusetts General Hospital
NOT_YET_RECRUITINGBoston, Massachusetts, 02114, United States
-
NEXT Houston
RECRUITINGHouston, Texas, 77054, United States
-
NEXT Virginia
RECRUITINGFairfax, Virginia, 22031, United States
-
UPMC Hillman Cancer Center
RECRUITINGPittsburgh, Pennsylvania, 15232, United States
-
Willamette Valley Cancer Institute and Research Center
RECRUITINGEugene, Oregon, 97401, United States