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Clinical Trials in the EU / 2024-519010-31-00
Authorised Phase I

A Multicentre, Randomised Phase Ib Trial to evaluate Neoadjuvant Immunotherapy Combination of Nivolumab alone or plus Ipilimumab with the IL-2 Superkine MDNA11 alone or with Tocilizumab in Patients with High-Risk, Surgically Resectable Melanoma – NEO-CYT

2024-519010-31-00 · tracked via the Priya Life Science EU tracker
Sponsor
Fondazione Melanoma Onlus
Sponsor type
Laboratory/Research/Testing facility
Therapeutic area
Neoplasms
Decision date
15/09/2025
Enrollment target
80
Sites
Italy

Condition studied

High-Risk, Surgically Resectable Melanoma

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 2024-519010-31-00 on CTIS ↗ ← All trials in the EU