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Clinical Trials in the EU / 2025-522243-17-00
Authorised Phase I

A Phase I study to evaluate the safety and efficacy of L19IL2 in combination with ruxolitinib in patients with advanced solid tumors.

2025-522243-17-00 · tracked via the Priya Life Science EU tracker
Sponsor
Philogen S.p.A.
Sponsor type
Pharmaceutical company
Therapeutic area
Neoplasms
Decision date
22/12/2025
Enrollment target
96
Sites
Italy

Condition studied

Advanced solid tumors, specifically: • metastatic clear cell renal carcinoma • proficient mismatch repair / microsatellite stable (pMMR/MSS), BRAF-V600E-mutant negative colorectal carcinoma • locally advanced or metastatic pancreatic adenocarcinoma

Eligibility

Age group
65+ years, 18-64 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 2025-522243-17-00 on CTIS ↗ ← All trials in the EU