Overview

RVU120 in Patients With Intermediate or High-risk, Primary or Secondary Myelofibrosis

Status:
RECRUITING
Trial end date:
2027-10-01
Target enrollment:
Participant gender:
Summary
The objective of this clinical trial is to evaluate the efficacy (how well the drug works), safety, pharmacokinetics (PK), and pharmacodynamics (PD) of the study drug, RVU120, in treating adult patients with intermediate or high-risk, primary or secondary myelofibrosis. RVU120 will be given as a single agent or in combination with ruxolitinib.
Phase:
PHASE2
Details
Lead Sponsor:
Ryvu Therapeutics SA
Treatments:
ruxolitinib