drugset / Trial / NCT04456634

Assess Safety, Tolerability, Pharmacokinetic and Pharmacodynamic Profile of Ruxolitinib With Artemether-lumefantrine

NCT04456634

RandomizedSequentialSingle-blindTreatment

Summary

Phase 1, single -center study in 2 parts. The study designs for each part are well established for first-in-human studies and are appropriate to assess safety, tolerability and preliminary pharmacokinetics\& pharmacodynamics.

Timeline

Start
2020-09-10
Primary completion
2020-11-17
Completion
2020-11-17

Drugs

EvaluationDrugModalityDoseRoute
Subject Artemether-lumefantrine Unknown 20 mg Oral
Subject Artemether-lumefantrine Unknown 120 mg Oral
Subject Ruxolitinib Small molecule 20 mg Oral

Indications