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Clinical Trials in the EU / 2026-526119-12-00
Authorised, not yet recruiting Phase I

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

2026-526119-12-00 · tracked via the Priya Life Science EU tracker
Sponsor
Fidia Farmaceutici S.p.A
Sponsor type
Pharmaceutical company
Therapeutic area
Neoplasms
Decision date
03/09/2026
Enrollment target
30
Sites
Italy

Condition studied

unresectable recurrent/progressive pleural mesothelioma

Eligibility

Age group
18-64 years, 65+ years
Sex
Female, Male
Official registry record

This page summarises publicly available CTIS data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View 2026-526119-12-00 on CTIS ↗ ← All trials in the EU