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Nuvectis Pharma clinical trials

Source: ClinicalTrials.gov, U.S. National Library of Medicine — current trials in our USA and UK registers with Nuvectis Pharma as lead sponsor. Synced 26 Sep 2026
3Current trials
3Recruiting now
3Drugs in these trials
2Trial registers
Maintained by Sreepriya Prasannan
MSc Digital Transformation of Life Sciences (Innopharma Education / Griffith College); MSc & BSc Botany HSE Spark Ignite 2026 — Top 14 finalist
Compiled from ClinicalTrials.gov and CTIS registry records · Last verified · Editorial standards
At a glance

Nuvectis Pharma is the lead sponsor of 3 current clinical trials in our USA and UK registers. 3 are recruiting patients now. All registered phases are Phase 1. The drugs named most often in its trials are NXP900, Lorlatinib and Osimertinib. The most-studied condition is Advanced Solid Tumor.

ClinicalTrials.gov trials by status

  • Recruiting3100%

Trials by phase

  • Phase 13100%
01

Clinical trials sponsored by Nuvectis Pharma

3 on ClinicalTrials.gov
StudyPhaseStatusStartRegisters
A Phase 1 Clinical Study of NXP900 in Subjects With Advanced Cancers
NCT05873686 · Advanced Solid Tumor, NSCLC (Non-small Cell Lung Cancer), Renal Cancer
Drug: NXP900
Phase 1 Recruiting 2023-10 UK, USA
Study of NXP900 With Lorlatinib in ALK+ Lung Cancer
NCT07784959 · ALK Positive, ALK Positive Non-small Cell Lung Cancer, NSCLC
Phase 1 Recruiting 2026-08 USA
Study of NXP900 With Osimertinib in Subjects With Advanced, EGFR-Mutated Non-Small Cell Lung Cancer
NCT07315113 · ClinicalTrials.gov ↗ · EGFR Mutation Positive Non-small Cell Lung Cancer, EGFR Mutated Non-small Cell Lung Cancer Patients
Phase 1 Recruiting 2025-12 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. Titles and statuses are copied from the registry as published.

02

Drugs in Nuvectis Pharma trials

3 compounds

Drugs and biologicals named as interventions in these trials, with the number of this sponsor's trials that name each one. Placebos and generic comparators are excluded.

03

Conditions in Nuvectis Pharma trials

10 conditions
Advanced Solid Tumor1NSCLC (Non-small Cell Lung Cancer)1Renal Cancer1Mesothelioma1ALK Positive1ALK Positive Non-small Cell Lung Cancer1NSCLC1ALK+ Non-Small-Cell Lung Carcinoma1EGFR Mutation Positive Non-small Cell Lung Cancer1EGFR Mutated Non-small Cell Lung Cancer Patients1
04

By trial register

RegisterTrialsRecruiting
Clinical trials in USA33
Clinical trials in UK11

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

05

Other sponsors in Advanced Solid Tumor

SponsorTrials
BeOne Medicines11
Daiichi Sankyo7
TORL Biotherapeutics5
OncoC45
LaNova Medicines5
MediLink Therapeutics (Suzhou)4
Suzhou Zelgen Biopharmaceuticals4
BioNTech3
EMD Serono Research & Development Institute3
Hansoh BioMedical R&D Company3

Sponsors with the most current trials registered for this condition.

06

Questions about Nuvectis Pharma trials

How many clinical trials does Nuvectis Pharma sponsor?

Nuvectis Pharma is the lead sponsor of 3 current trials on ClinicalTrials.gov in our USA and UK registers, as of the registry sync on 26 September 2026. Completed and withdrawn studies are not counted.

Are Nuvectis Pharma trials recruiting?

Yes. 3 of its 3 ClinicalTrials.gov trials are recruiting. Eligibility and site contacts are on each trial's record. Only the study team can confirm whether a patient is eligible.

Which drugs is Nuvectis Pharma testing?

Its current trials name 3 drugs and biologicals as interventions. The most frequent are NXP900 (3), Lorlatinib (1) and Osimertinib (1). The number in brackets is how many of its trials name each drug.

Where does this information come from?

Every trial, status, phase and condition on this page is copied from public ClinicalTrials.gov and EU CTIS records by a daily sync, grouped by the sponsor name each registry records. It says nothing about the organisation beyond its registered trials, and it is not medical advice.

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How this page is built

Everything on this page is copied from public registry records — it is not written from memory, and nothing here describes the organisation beyond its registered trials. 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 trial registers and groups every current trial by its lead sponsor name, ignoring legal-form suffixes such as Inc. or Ltd. A small, hand-checked list joins the same organisation's different registry names (for example its EU legal entity). There is no AI drafting and no per-sponsor editorial pass. 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 the registries data on this page was last retrieved on 26 Sep 2026.

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.