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Terminated Phase 1 Interventional Results available

A Study of Modakafusp Alfa in Adult Participants With Multiple Myeloma

ClinicalTrials.gov ID: NCT05556616

Public ClinicalTrials.gov record NCT05556616. 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 Oct 21, 2026, 9:18 AM 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 1b Open-label Study to Evaluate the Safety and Tolerability of Intravenous Modakafusp Alfa as Part of Combination Therapy in Adult Patients With Multiple Myeloma

Brief summary

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

The main aims of this study are to test for any side effects from modakafusp alfa in combination therapy and to determine the recommended dose of combination therapy with modakafusp alfa. 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. Participants will be given modakafusp alfa through a vein.

Study identification

NCT ID
NCT05556616
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 1
Enrollment
15 participants

Conditions and interventions

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
Jan 12, 2023 (Actual)
Primary completion
Jun 4, 2024 (Actual)
Completion
Jun 4, 2024 (Actual)
Last update posted
Jan 29, 2026

2023 – 2024

United States locations

U.S. sites
14
U.S. states
8
U.S. cities
11
Facility City State ZIP Site status
University of California Davis Comprehensive Cancer Center Sacramento California 95817 —
Scripps Health San Diego California 92121 —
The University of Iowa Hospitals & Clinics Iowa City Iowa 52242 —
Cancer Center At Greater Baltimore Medical Center Baltimore Maryland 21153 —
Comprehensive Cancer Centers of Nevada Las Vegas Nevada 89119 —
NYU Langone Hospital - Long Island Mineola New York 11501 —
New York University School of Medicine New York New York 10016 —
Weill Cornell Medicine/New York Presbyterian Hospital New York New York 10021 —
Icahn School of Medicine at Mount Sinai New York New York 10029 —
Memorial Sloan Kettering Cancer Center - Main Campus New York New York 10065 —
Novant Health Cancer Institute Charlotte North Carolina 28204 —
Novant Health Cancer Institute - Forsyth Medical Center Winston-Salem North Carolina 27103 —
Gabrail Cancer Center Research Canton Ohio 44718 —
The University of Texas MD Anderson Cancer Center Houston Texas 77030 —

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 7 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT05556616, 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 29, 2026 · Synced Oct 21, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT05556616 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →