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Terminated Phase 1Phase 2 Interventional Results available

A Study of Modakafusp Alfa on Adult Participants With Relapsed/Refractory Multiple Myeloma

ClinicalTrials.gov ID: NCT03215030

Public ClinicalTrials.gov record NCT03215030. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Sep 4, 2026, 9:46 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Phase 1/2 Open-label Study to Investigate the Safety and Tolerability, Efficacy, Pharmacokinetics, and Immunogenicity of Modakafusp Alfa (TAK-573) as a Single Agent in Patients With Relapsed Refractory Multiple Myeloma

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The main aims of this 3-part study are as follows: Part 1: To determine any side effects from modakafusp alfa single treatment and how often they occur. The dose of modakafusp alfa will be increased a little at a time until the highest dose that does not cause harmful side effects is found. Part 2: To assess clinical activity of one or more dosing schedules of modakafusp alfa alone in participants with relapsed/refractory multiple myeloma. Dexamethasone standard dose will be administered with one or more selected dose of modakafusp alfa in selected group of participants. Part 3: To find the optimal dose with the more favorable risk-benefit profile of modakafusp alfa. Participants will receive modakafusp alfa at one of two doses which will be given through a vein.

Study identification

NCT ID
NCT03215030
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 1, Phase 2
Enrollment
272 participants

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Oct 3, 2017
Primary completion
Jun 30, 2024
Completion
Nov 6, 2024
Last update posted
Jan 28, 2026

2017 – 2024

United States locations

U.S. sites
27
U.S. states
19
U.S. cities
26
Facility City State ZIP Site status
Highlands Oncology Group Springdale Arkansas 72762
Los Angeles Cancer Network - Glendale Adventist Medical Center Glendale California 91204
University of California Irvine Orange California 92868
Office of James R. Berenson MD West Hollywood California 90069
Smilow Cancer Hospital at Yale New Haven New Haven Connecticut 06520
Winship Cancer Institute of Emory University Atlanta Georgia 30322
Northwestern Medicine - Northwestern Medical Group Chicago Illinois 60611
Loyola University Medical Center Maywood Illinois 60153
Investigative Clinical Research of Indiana, LLC Noblesville Indiana 46062
June E. Nylen Cancer Center Sioux City Iowa 51101
Johns Hopkins Hospital Baltimore Maryland 21287
Boston Medical Center Boston Massachusetts 02118
Dana Farber Cancer Institute Boston Massachusetts 02215
Univeristy of Nebraska Medical Center Omaha Nebraska 68198
USOR - Comprehensive Cancer Centers of Nevada - Central Valley Las Vegas Nevada 89119
John Theurer Cancer Center Hackensack New Jersey 07601
University of Rochester Rochester New York 14627
Montefiore Medical Center The Bronx New York 10467
Levine Cancer Center Charlotte North Carolina 28402
Levine Cancer Institute - Concord Concord North Carolina 28205
Duke University Medical Center Durham North Carolina 27710
Gabrail Cancer Center Canton Ohio 44718-2566
The Ohio State University Columbus Ohio 43210
Oregon Health and Science University Portland Oregon 97239
University of Pennsylvania Philadelphia Pennsylvania 19104
Baptist Cancer Center - Memphis - Walnut Grove Memphis Tennessee 38120
Lumi Research Houston Texas 77002

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 67 non-U.S. sites.

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Other public records listing Multiple Myeloma. Sorted by last update posted; newest first. Not a recommendation.

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About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT03215030, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jan 28, 2026 · Synced Sep 4, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT03215030 live on ClinicalTrials.gov.

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