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Clinical Trials in the EU / 2025-524725-41-00
Completed Phase I

Single-centre Phase I/II study with dose escalation of tocilizumab in combination with venetoclax and azacitidine chemotherapy in patients with Acute Myeloid Leukaemia (AML): TOCIVENA

2025-524725-41-00 · tracked via the Priya Life Science EU tracker
Sponsor
Centre Hospitalier Universitaire De Nantes
Sponsor type
Hospital/Clinic/Other health care facility
Therapeutic area
Not possible to specify
Decision date
10/04/2026
Enrollment target
12
Sites
France

Condition studied

Acute Myeloblastic Leukemia

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 2025-524725-41-00 on CTIS ↗ ← All trials in the EU