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Priya Life Science Sponsor trial record
Sponsor · clinical trials

Oncomatryx Biopharma clinical trials

Source: ClinicalTrials.gov, U.S. National Library of Medicine and the EU Clinical Trials Information System (CTIS) — current trials in our USA, Spain, Israel and EU (CTIS) registers with Oncomatryx Biopharma as lead sponsor. Synced 11 Nov 2026
3Current trials
2Recruiting now
5Drugs in these trials
4Trial registers
At a glance

Oncomatryx Biopharma is the lead sponsor of 3 current clinical trials in our USA, Spain, Israel and EU (CTIS) registers. 2 are recruiting patients now. All registered phases are Phase 1. The drugs named most often in its trials are OMTX705, Tislelizumab and Gemcitabine. The most-studied condition is Advanced Solid Tumor.

ClinicalTrials.gov trials by status

  • Recruiting2100%

Trials by phase

  • Phase 12100%
01

Clinical trials sponsored by Oncomatryx Biopharma

2 on ClinicalTrials.gov
StudyPhaseStatusStartRegisters
Efficacy and Safety Study of OMTX705, Monotherapy and Anti-PD-1-combined, in Subjects With Advanced Solid Tumors.
NCT05547321 · ClinicalTrials.gov ↗ · Advanced Solid Tumor
Phase 1 Recruiting 2022-10 USA, Spain, Israel
Clinical Trial of OMTX705 in Combination With Gemcitabine/Nab-Paclitaxel and Tislelizumab in Patients With Advanced/Metastatic Pancreatic Adenocarcinoma
NCT07377045 · Pancreatic Adenocarcinoma Metastatic
Phase 1 Recruiting 2025-10 USA, Spain, Israel

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

Oncomatryx Biopharma in the EU trials register (CTIS)

1 trial

Authorised or ongoing trials in the EU Clinical Trials Information System with Oncomatryx Biopharma as sponsor. Some are the same study as a ClinicalTrials.gov record above; the two registries share no common ID. Trials with a site in Ireland are listed first.

StudyPhaseStatusCountries
Phase 1b/2 Trial of OMTX705, an Anti-Fibroblast Activation Protein Antibody-Drug Conjugate, in Combination with Carboplatin, Pemetrexed and Tislelizumab in Patients with Advanced/Metastatic Non-squamous Non-Small Cell Lung Cancer
2025-521989-95-00 · CTIS ↗ · Neoplasms
Phase 1 Authorised Spain
03

Drugs in Oncomatryx Biopharma trials

5 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.

04

Conditions in Oncomatryx Biopharma trials

2 conditions
Advanced Solid Tumor1Pancreatic Adenocarcinoma Metastatic1
05

By trial register

RegisterTrialsRecruiting
Clinical trials in USA22
Clinical trials in Spain22
Clinical trials in Israel22
EU register (CTIS)1—

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

06

Other sponsors in Advanced Solid Tumor

SponsorTrials
BeOne Medicines12
Daiichi Sankyo8
OncoC45
LaNova Medicines5
TORL Biotherapeutics4
MediLink Therapeutics (Suzhou)4
Suzhou Zelgen Biopharmaceuticals4
BioNTech3
EMD Serono Research & Development Institute3
GI Innovation3

Sponsors with the most current trials registered for this condition.

07

Questions about Oncomatryx Biopharma trials

How many clinical trials does Oncomatryx Biopharma sponsor?

Oncomatryx Biopharma is the lead sponsor of 2 current trials on ClinicalTrials.gov in our USA, Spain and Israel registers, and 1 authorised or ongoing trial in the EU register (CTIS), as of the registry sync on 11 November 2026. Completed and withdrawn studies are not counted.

Are Oncomatryx Biopharma trials recruiting?

Yes. 2 of its 2 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 Oncomatryx Biopharma testing?

Its current trials name 5 drugs and biologicals as interventions. The most frequent are OMTX705 (3), Tislelizumab (3), Gemcitabine (1), Nab-paclitaxel (1) and Pembrolizumab (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 11 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.