2026-526119-12-00Not yet recruitingPhase 1
A Phase I dose escalation study of intrapleural administration of Oncofid-P-M in patients with unresectable recurrent/progressive pleural mesothelioma after first-line treatment
Source: EU CTIS (euclinicaltrials.eu) · Last updated 16 Sept 2026
- Status (registry)
- Not yet recruiting
- Phase (registry)
- Phase 1
- Study type
- Interventional
- Enrollment
- 30 (estimated)
- First submitted
- 4 Jun 2026
- Start date
- 1 Sept 2026
- Lead sponsor
- Fidia Farmaceutici S.p.A.
- Diseases
- Mesothelioma
- EU CT number
- 2026-526119-12-00
What you commit to
- Study type: Interventional · Phase 1
- Planned participants: 30
- 1 site in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of EU CTIS (euclinicaltrials.eu). It describes the study design.
AI-kivonat: who the study is looking for
Machine-read from the registry text on this page, so it can be wrong. The registry text below and the trial team decide who can take part.
The trial is looking for adults with pleural mesothelioma that cannot be removed by surgery and has come back or is getting worse after first-line treatment.
- Age
- 18 years or older
- Sex
- Women and men can join.
- Disease stage
- Pleural mesothelioma that cannot be removed by surgery and has come back or is progressing.
- Earlier treatment
- Must have had first-line treatment already.
Read by machine on 9 Nov 2026.
Sites (1)
Sites in registry order. Save your city in your profile to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Istituto Oncologico Veneto | Padova | Italy | Not yet recruiting |
This page is information, not medical advice. Discuss any trial with your doctor.