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Radboud universitair medisch centrum Stichting clinical trials

Source: the EU Clinical Trials Information System (CTIS) — current trials in our EU (CTIS) register with Radboud universitair medisch centrum Stichting as lead sponsor. Synced 26 Sep 2026
10Current trials
0Recruiting now
4Drugs in these trials
1Trial register
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

Radboud universitair medisch centrum Stichting is the lead sponsor of 10 current clinical trials in our EU (CTIS) register. The drugs named most often in its trials are Amphotericin B, Liraglutide and Obinutuzumab.

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Radboud universitair medisch centrum Stichting in the EU trials register (CTIS)

10 trials

Authorised or ongoing trials in the EU Clinical Trials Information System with Radboud universitair medisch centrum Stichting 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
Attenuating Calciprotein particles Transformation and Inhibiting Vascular calcification Evolution by Sodium ThioSulphate trial
2026-525680-41-00 · Therapeutics
Phase 2 Authorised Netherlands
Propranolol Dosefinding Assessment in Reactive Aggression Treatment (PRO-DART)
2026-526545-95-00 · Behavior and Behavior Mechanisms
Phase 2 Authorised Netherlands
Preventive Dendritic Cell vaccination for Lynch Syndrome (PREVENT-Lynch)
2025-524046-10-00 · Digestive System Diseases
Phase 1 Authorised Netherlands
Do GLP-1 based therapies improve the immunological response to vaccination in diabetes?
2026-525909-13-00 · Immune System Diseases
Phase 4 Authorised Netherlands
PET imaging For eaRly predictiOn of respoNse to neoadjuvanT tReatment in lUNg caNcER
2025-524791-30-00 · CTIS ↗ · Respiratory Tract Diseases
Phase 1 Authorised Netherlands, Germany
REpurposed drug evaluation for DEceleration of immunE aging & Mitigation of chronic inflammation (REDEEM)
2026-526084-38-00 · CTIS ↗ · Immune System Diseases
Phase 2 Authorised Netherlands
T cell imaging in kidney transplantation (TIK)
2025-522490-11-00 · CTIS ↗ · Immune system processes
Phase 1 Authorised Netherlands
Modafinil for debilitating fatigue in quiescent inflammatory bowel disease: a multicentre, randomised, double-blind, placebo-controlled, clinical trial (MODIFI-IBD trial)
2026-525163-41-00 · CTIS ↗ · Digestive System Diseases
Phase 3 Ongoing Netherlands
Ultimate dePletion of autoReactive b cells using Obinutuzumab from sjÖgren's syndrome affected Tissues study- UPROOT study
2024-519884-16-00 · CTIS ↗ · Immune System Diseases
Phase 2 Authorised Netherlands
Nebulised lIposomal aMphotericin B in chronic pUlmonary aSpergillosis: a deposition study
2025-521770-34-00 · CTIS ↗ · Bacterial Infections and Mycoses
Phase 1 Authorised Netherlands
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Drugs in Radboud universitair medisch centrum Stichting trials

4 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

By trial register

RegisterTrialsRecruiting
EU register (CTIS)10—

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

04

Questions about Radboud universitair medisch centrum Stichting trials

How many clinical trials does Radboud universitair medisch centrum Stichting sponsor?

Radboud universitair medisch centrum Stichting is the lead sponsor of 10 authorised or ongoing trials in the EU register (CTIS), as of the registry sync on 26 September 2026. Completed and withdrawn studies are not counted.

Which drugs is Radboud universitair medisch centrum Stichting testing?

Its current trials name 4 drugs and biologicals as interventions. The most frequent are Amphotericin B (1), Liraglutide (1), Obinutuzumab (1) and Propranolol (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.