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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

Next steps

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.

SiteCityCountrySite status
Istituto Oncologico VenetoPadovaItalyNot yet recruiting

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This page is information, not medical advice. Discuss any trial with your doctor.