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RECRUITING
NCT06034275
PHASE1

Study of VIP943 in Subjects With Advanced CD123+ Hematologic Malignancies

Sponsor: Vincerx Pharma, Inc.

View on ClinicalTrials.gov

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

Interventions

DRUG

VIP943 (QW)

VIP943 will be administered by IV Infusion weekly

DRUG

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