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ACTIVE NOT RECRUITING
NCT04184050
PHASE1

Study of HPN217 in Participants With Relapsed/Refractory Multiple Myeloma MK-4002 (MK-4002-001)

Sponsor: Harpoon Therapeutics, Inc., a subsidiary of Merck & Co., Inc. (Rahway, New Jersey USA)

View on ClinicalTrials.gov

Summary

Researchers want to learn if MK-4002 (also known as HPN217) can treat relapsed or refractory multiple myeloma (RRMM). The goals of this study are to learn about the safety of different doses of MK-4002 and how well people tolerate them. Researchers also want to learn what happens to different doses of MK-4002 in a person's body over time.

Official title: A Phase 1 Open-label, Multicenter, Dose Escalation Study of the Safety, Tolerability, and Pharmacokinetics of HPN217 in Patients With Relapsed/Refractory Multiple Myeloma

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

INTERVENTIONAL

Enrollment

100

Start Date

2020-04-13

Completion Date

2026-12-31

Last Updated

2025-12-05

Healthy Volunteers

No

Interventions

DRUG

MK-4002

IV infusion

Locations (12)

Banner MD Anderson Cancer Center

Gilbert, Arizona, United States

Mayo Clinic Arizona

Phoenix, Arizona, United States

UC San Diego Moores Cancer Center

La Jolla, California, United States

The University of Kansas Cancer Center

Fairway, Kansas, United States

Roswell Park Comprehensive Cancer Center

Buffalo, New York, United States

University of Rochester James P Wilmot Cancer Institute

Rochester, New York, United States

OHSU

Portland, Oregon, United States

University of Washington - Seattle Cancer Center Alliance

Seattle, Washington, United States

Centre Hospitalier Universitaire De Nantes

Nantes, France

Centre Hospitalier Universitaire de Poitiers

Poitiers, France

Josep Carreras Leukaemia Research Institute

Barcelona, Spain

Hospital Universitario Fundacion Jimenez Diaz (UAM-FJD)

Madrid, Spain