mocravimod
DrugS1PR modulator
NCT Number: NCT05429632
This is a multi-center, randomized, double-blinded, placebo controlled trial.
Interested in participating?
Request Info18 year–75 year
All sexes
Interventional
Phase 3
Centro de Educacion Medica E Investigacines Clinicas Norberto Quirno CEMIC, Buenos Aires, Argentina
The purpose of this study is to evaluate the efficacy and safety of mocravimod as an adjunctive and maintenance treatment in adult acute myeloid leukemia (AML) patients undergoing allogeneic hematopoietic cell transplantation (HCT).
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
S1PR modulator
Time frame: 12 months
To compare the efficacy of mocravimod to that of placebo
Time frame: 24 months
To compare mocravimod's effect on overall survival (OS) to that of placebo
Contact information is provided by the study sponsor or research team.
Jens Hasskarl, MD
CONTACT
Malika Souquieres, MSc
CONTACT
Priothera SAS
Industry
Randomized, Double-blind, Placebo-controlled, Multi-center Phase III Study to Evaluate the Efficacy and Safety of Mocravimod as Adjunctive and Maintenance Treatment in Adult AML Patients Undergoing Allogeneic HCT
Acronym: MO-TRANS
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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