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A Multiple Dose, Dose Escalation Trial of AEB1102 in Patients With AML or MDS
Sponsor: Immedica Pharma AB
Summary
This is the first study of the safety of increasing dose levels of AEB1102 in patients with Relapsed or Refractory Acute Myeloid Leukemia or Myelodysplastic Syndrome. The study will also evaluate the amounts of AEB1102 in blood, the effects of AEB1102 on blood amino acid levels and the antitumor effects of AEB1102.
Official title: A Phase 1 Dose-Escalation Study of AEB1102 (Co-ArgI-PEG) in Patients With Relapsed or Refractory Acute Myeloid Leukemia or Myelodysplastic Syndrome Refractory to Hypomethylating Agents
Key Details
Gender
All
Age Range
18 Years - Any
Study Type
INTERVENTIONAL
Enrollment
21
Start Date
2016-08-15
Completion Date
2017-11-01
Last Updated
2026-08-13
Healthy Volunteers
No
Interventions
Co-ArgI-PEG modified human arginase I
Locations (10)
Comprehensive Cancer Center at University of Michigan
Ann Arbor, Michigan, United States
Washington University Medical School
St Louis, Missouri, United States
University Hospitals Case Medical Center
Cleveland, Ohio, United States
The Cleveland Clinic
Cleveland, Ohio, United States
Vanderbilt-Ingram Cancer Center
Nashville, Tennessee, United States
Baylor Scott & White
Dallas, Texas, United States
University of Texas Southwestern Medical Center
Dallas, Texas, United States
University of Alberta
Edmonton, Alberta, Canada
Princess Margaret Cancer Centre
Toronto, Ontario, Canada
Jewish General Hospital
Montreal, Quebec, Canada