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Study of VIP943 in Subjects With Advanced CD123+ Hematologic Malignancies
Sponsor: Vincerx Pharma, Inc.
Summary
Dose Escalation - Determine the maximum tolerated dose (MTD), if possible, or minimum optimal biologic dose (OBD), and evaluate the safety and tolerability of VIP943 in subjects with advanced CD123+ hematologic malignancies
Official title: An Open-label, Multicenter Phase 1 Study to Characterize Safety, Tolerability, Preliminary Antitumor Activity, Pharmacokinetics, and Pharmacodynamics of VIP943 Monotherapy in Subjects With Advanced CD123+ Hematologic Malignancies
Key Details
Gender
All
Age Range
18 Years - Any
Study Type
INTERVENTIONAL
Enrollment
36
Start Date
2023-09-13
Completion Date
2025-12-31
Last Updated
2024-11-15
Healthy Volunteers
No
Conditions
Interventions
VIP943 (QW)
VIP943 will be administered by IV Infusion weekly
VIP943 (BIW)
VIP943 will be administered by IV Infusion bi-weekly
Locations (5)
University of Alabama at Birmingham
Birmingham, Alabama, United States
University of Cincinnati
Cincinnati, Ohio, United States
TriStar Bone Marrow Transplant
Nashville, Tennessee, United States
MD Anderson Cancer Center
Houston, Texas, United States
Fred Hutchinson Cancer Center
Seattle, Washington, United States