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Odense University Hospital clinical trials

Source: the EU Clinical Trials Information System (CTIS) — current trials in our EU (CTIS) register with Odense University Hospital as lead sponsor. Synced 26 Sep 2026
7Current trials
0Recruiting now
6Drugs 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

Odense University Hospital is the lead sponsor of 7 current clinical trials in our EU (CTIS) register. The drugs named most often in its trials are Capecitabine, Celecoxib and Ipilimumab.

01

Odense University Hospital in the EU trials register (CTIS)

7 trials

Authorised or ongoing trials in the EU Clinical Trials Information System with Odense University Hospital 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
[⁶⁸Ga]Ga-HKG301 PET/CT for staging and restaging patients with primary breast cancer: a phase II study (FAPILOUS)
2025-521324-29-00 · Neoplasms
Phase 2 Authorised Denmark
The RELEASE Trial: Reconsidering Long-Term Aspirin in the Elderly in Secondary Prevention of Cardiovascular Disease
2026-525442-30-00 · CTIS ↗ · Cardiovascular Diseases
Phase 3 Authorised Denmark
BEAT Fatigue – Benefit of Elevated Administration of Thiamine for Fatigue in Rheumatoid Arthritis: A randomized, double-blind, placebo-controlled trial
2024-519268-41-00 · CTIS ↗ · Musculoskeletal Diseases
Phase 4 Authorised Denmark
COPE-CP: The effect of Celecoxib on pain, quality of life, use of opioids, and inflammation in patients suffering from chronic pancreatitis: a multicenter randomized placebo-controlled, double-blinded clinical trial
2025-522956-25-00 · CTIS ↗ · Digestive System Diseases
Drug: Celecoxib
Phase 3 Authorised Denmark
SCARFREE-001: A Phase 2 Dose-Finding and Proof-of-Concept Study of Intradermal Verteporfin for Scar Prevention in Open and Closed Surgical Wounds
2025-525083-14-00 · CTIS ↗ · Therapeutics
Phase 2 Authorised Denmark
SGL-TX-PTDM: SGLT2i effect on PTDM development and kidney allograft function in kidney transplant recipients: A randomized, double-blind, placebo controlled, national multicenter trial
2024-518774-14-00 · CTIS ↗ · Not possible to specify
Phase 2 Authorised Denmark
Ipilimumab and nivolumab plus temozolomide and capecitabine for patients with chemo-refractory pMMR, MGMT silenced metastatic colorectal cancer: The MAYA2 trial
2025-521941-25-00 · CTIS ↗ · Neoplasms
Phase 2 Authorised Denmark
02

Drugs in Odense University Hospital 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.

03

By trial register

RegisterTrialsRecruiting
EU register (CTIS)7—

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

04

Questions about Odense University Hospital trials

How many clinical trials does Odense University Hospital sponsor?

Odense University Hospital is the lead sponsor of 7 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 Odense University Hospital testing?

Its current trials name 6 drugs and biologicals as interventions. The most frequent are Capecitabine (1), Celecoxib (1), Ipilimumab (1), Nivolumab (1) and Temozolomide (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.