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The purpose of this study is to determine the highest tolerated dose, safety and activity of HCD122 in patients with Multiple Myeloma who are relapsed after receiving prior treatment.
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Lead Sponsor
Novartis Pharmaceuticals
NCT06953960 · Multiple Myeloma
NCT02682667 · Multiple Myeloma, Lymphoma, Non-Hodgkin, and more
NCT01676805 · Hodgkin Disease, Lymphoma, Non-Hodgkin, and more
NCT05892393 · Multiple Myeloma, Plasma Cell Myeloma
NCT05737732 · Multiple Myeloma
Dana Farber Cancer Institute StudyCoordinator:CHCD122A2102
Boston, Massachusetts
St. Vincent's Comprehensive Cancer Center Dept. of St. Vincent's Cancer
New York, New York
Oregon Health Sciences University
Portland, Oregon
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This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
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