Pharmacoscopy-guided Clinical Standard-of-care in r/r AML

Recruiting Phase 2 Interventional Study
AML, Adult
No Placebo Group Every participant receives an active treatment — no one gets a placebo. Prior Safety Data This treatment has already been tested in at least one earlier human trial.
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At a Glance
Age
18 – 70
Sex
Any
Trial phase
Phase 2
Study type
Interventional
Purpose
Diagnostic
Participants needed
88 (estimated)
Sponsor
ETH Zurich · Other
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About This Trial
With an overall survival of below 12 months, the outcome of relapsed/refractory AML (RR AML) is poor, making it a critical challenge to identify effective therapies at this stage. The RAPID-01 trial aims to show for the first time in a randomized and controlled clinical trial that Pharmacoscopy (PCY), a functional precision medicine platform, helps improve clinical standard-of-care treatment selec…
Trial Locations
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Eligibility Criteria
Inclusion criteria * Patient with refractory or relapsed AML according to ELN2022 criteria. * Age 18-70 years. * Considered to be eligible for intensive chemotherapy. * Written informed consent. Exclusion criteria * Acute promyelocytic leukemia (APL) with PML-RARA or one of the other pathognomoni…
Contacts

Berend Snijder, PhD

+41 44 633 71 49

bsnijder@ethz.ch

CONTACT