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Priya Life Science Compound trial record
Compound · clinical trials

NXP900 clinical trials

Source: ClinicalTrials.gov, U.S. National Library of Medicine — the 3 trials in our USA and UK registers that name NXP900 as an intervention. Synced 9 Nov 2026
3Current trials
2Recruiting now
1Lead sponsor
2Country registers
At a glance

NXP900 is named as an intervention in 3 current clinical trials in our USA and UK registers. 2 are recruiting patients now. All registered phases are Phase 1. The lead sponsor is Nuvectis Pharma, Inc. The most-studied condition is Advanced Solid Tumor.

How NXP900 works

All drug targets →
Diseases it has been tested for in clinical trials, by furthest phase
  • Non-small cell lung carcinomaPhase 1

Mechanisms and diseases from ChEMBL via the Open Targets Platform (release 26.09), ChEMBL record CHEMBL3824089, CC BY-SA 3.0. The Guide to Pharmacology has no record of this medicine, so its targets rest on ChEMBL alone. Trial phases are not approvals: approved uses are shown from the regulators' own records where we hold them.

Patient leaflets for NXP900

The package leaflet is the official guide for patients that comes with every medicine. These links go to the regulators that publish it.

  • UK
    United Kingdom: Search MHRA Products
    Patient information leaflets and SmPCs for UK-licensed products.
  • US
    United States: Search DailyMed
    FDA-approved labels, including patient and medication guides.

Leaflets differ between brands and countries; always read the one that comes with your own medicine. This is regulatory information, not medical advice.

Trials by status

  • Recruiting267%
  • Active, closed133%

Trials by phase

  • Phase 13100%
01

Clinical trials of NXP900

3 trials
StudyPhaseStatusLead sponsorRegisters
Study of NXP900 With Osimertinib in Subjects With Advanced, EGFR-Mutated Non-Small Cell Lung Cancer
NCT07315113 · EGFR Mutation Positive Non-small Cell Lung Cancer, EGFR Mutated Non-small Cell Lung Cancer Patients
Phase 1 Recruiting Nuvectis Pharma, Inc USA
Study of NXP900 With Lorlatinib in ALK+ Lung Cancer
NCT07784959 · ALK Positive, ALK Positive Non-small Cell Lung Cancer, NSCLC
Phase 1 Recruiting Nuvectis Pharma, Inc USA
A Phase 1 Clinical Study of NXP900 in Subjects With Advanced Cancers
NCT05873686 · Advanced Solid Tumor, NSCLC (Non-small Cell Lung Cancer), Renal Cancer
Phase 1 Active, closed Nuvectis Pharma, Inc UK, USA

Registers list studies that are recruiting, about to open, active but closed to enrolment, or enrolling by invitation. The UK and USA registers cover industry-sponsored studies only. Trial titles and statuses are copied from the registry as published.

02

Conditions studied with NXP900

10 conditions
Advanced Solid Tumor1NSCLC (Non-small Cell Lung Cancer)1Renal Cancer1Mesothelioma1EGFR Mutation Positive Non-small Cell Lung Cancer1EGFR Mutated Non-small Cell Lung Cancer Patients1ALK Positive1ALK Positive Non-small Cell Lung Cancer1NSCLC1ALK+ Non-Small-Cell Lung Carcinoma1
03

Sponsors

lead sponsor per trial
Lead sponsorTrials
Nuvectis Pharma, Inc3
04

By country register

RegisterTrialsRecruiting
Clinical trials in USA32
Clinical trials in UK10

A trial with sites in more than one country appears in each of those registers.

05

Related compounds

06

Questions about NXP900 trials

How many clinical trials are testing NXP900?

3 current trials in our USA and UK registers name NXP900 as a drug or biological intervention, as of the registry sync on 9 November 2026. Completed and withdrawn studies are not counted.

Are NXP900 trials recruiting patients?

Yes. 2 of the 3 trials are recruiting: 2 with sites in USA. Eligibility and site contacts are on each trial's record. Only the study team can confirm whether a patient is eligible.

Who sponsors NXP900 clinical trials?

The lead sponsor is Nuvectis Pharma, Inc. The number in brackets is how many trials each organisation leads.

Where does this information come from?

Every trial, status, phase and sponsor on this page is copied from public ClinicalTrials.gov records by a daily sync. Nothing here describes how NXP900 works or whether it is effective, and it is not medical advice.

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How this page is built

Everything on this page is copied from public ClinicalTrials.gov registry records — it is not written from memory, and nothing here describes how NXP900 works or whether it is effective. Each trial links to its own record so you can check it yourself.

This page is built automatically: a daily sync job reads the registry records behind our country trial registers, collects every trial that lists NXP900 (or a registered synonym) as a drug or biological intervention, and tabulates the registry fields directly. Placebos and generic comparators are excluded. There is no AI drafting and no per-compound editorial pass, and the page has not been clinically reviewed. The “last verified” date above is the timestamp of that sync, not a review date. Our general editorial approach is described in our editorial standards and corrections policy. The ClinicalTrials.gov data on this page was last retrieved on 9 Nov 2026. How every register is built: methodology · fixes we have made: corrections log.

Please verify before you rely on this. This page is general information for life-science and pharmaceutical professionals. It is not medical advice, and it has not been reviewed by a clinician — our editorial team holds life-science qualifications, not clinical ones. It is not exhaustive and may not reflect the most recent label change. Always check the official prescribing information (US Prescribing Information or EU SmPC) and speak to your doctor or pharmacist before acting on anything here. Drugs in the same class are not automatically interchangeable, and approvals, brand names and indications differ between the US, the EU/Ireland (EMA/HPRA) and other regions. Spotted an error? Tell us — we correct promptly and log it.