Ireland
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Priya Life Science Sponsor trial record
Sponsor · clinical trials

mAbxience Research clinical trials

Source: ClinicalTrials.gov, U.S. National Library of Medicine and the EU Clinical Trials Information System (CTIS) — current trials in our Spain, Italy, Portugal, Turkey, Brazil, Poland, Japan, South Korea, Taiwan and EU (CTIS) registers with mAbxience Research as lead sponsor. Synced 13 Nov 2026
3Current trials
1Recruiting now
6Drugs in these trials
10Trial registers
At a glance

mAbxience Research is the lead sponsor of 3 current clinical trials in our Spain, Italy, Portugal, Turkey, Brazil, Poland, Japan, South Korea, Taiwan and EU (CTIS) registers. 1 is recruiting patients now. All registered phases are Phase 3. The drugs named most often in its trials are Carboplatin, Cisplatin and EU-sourced Keytruda. The most-studied condition is Advanced (Unresectable or Metastatic) Melanoma.

ClinicalTrials.gov trials by status

  • Recruiting150%
  • Active, closed150%

Trials by phase

  • Phase 32100%
01

Clinical trials sponsored by mAbxience Research

2 on ClinicalTrials.gov
StudyPhaseStatusStartRegisters
Study to Compare Pharmacokinetics, Efficacy, Safety, and Immunogenicity of MB11 Versus EU-/US-Opdivo® in Subjects With Previously Untreated Advanced [Unresectable or Metastatic] Melanoma
NCT07221734 · ClinicalTrials.gov ↗ · Advanced (Unresectable or Metastatic) Melanoma
Phase 3 Recruiting 2025-12 Spain, Italy, Portugal, Turkey, Brazil
A Study to Compare Pharmacokinetics, Efficacy, Safety, and Immunogenicity of MB12 (Proposed Pembrolizumab Biosimilar) to Keytruda® in Non-small Cell Lung Cancer (BENITO Study)
NCT06687369 · ClinicalTrials.gov ↗ · Non Squamous Non Small Cell Lung Cancer
Phase 3 Active, closed 2024-12 Spain, Italy, Poland, Portugal, Turkey, Brazil, Japan, South Korea, Taiwan

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

mAbxience Research in the EU trials register (CTIS)

1 trial

Authorised or ongoing trials in the EU Clinical Trials Information System with mAbxience Research 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
Randomised, Multicentre, Multinational, Double-Blind Integrated Study to Compare the Pharmacokinetics, Efficacy, Safety, and Immunogenicity of MB11 (Proposed Nivolumab Biosimilar) Versus EU-/US-Opdivo in Subjects With Previously Untreated Advanced (Unresectable or Metastatic) Melanoma (LEON Study)
2025-521562-95-00 · CTIS ↗ · Musculoskeletal Diseases
Drug: Nivolumab
Phase 3 Ongoing Italy, Spain, Slovakia + 4 more
03

Drugs in mAbxience Research trials

6 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 mAbxience Research trials

2 conditions
Advanced (Unresectable or Metastatic) Melanoma1Non Squamous Non Small Cell Lung Cancer1
06

Questions about mAbxience Research trials

How many clinical trials does mAbxience Research sponsor?

mAbxience Research is the lead sponsor of 2 current trials on ClinicalTrials.gov in our Spain, Italy, Portugal, Turkey, Brazil, Poland, Japan, South Korea and Taiwan registers, and 1 authorised or ongoing trial in the EU register (CTIS), as of the registry sync on 13 November 2026. Completed and withdrawn studies are not counted.

Are mAbxience Research trials recruiting?

Yes. 1 of its 2 ClinicalTrials.gov trials is 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 mAbxience Research testing?

Its current trials name 6 drugs and biologicals as interventions. The most frequent are Carboplatin (1), Cisplatin (1), EU-sourced Keytruda (1), Nivolumab (1) and Pemetrexed (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 13 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.