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

Terminated · Phase 1, Phase 2 · NCT03215030

Conditions: Multiple Myeloma

At a glance

Research payments reported, 2025
$903,767
U.S. investigators named
17
Sites paid
17
Planned or actual enrollment
272

About the trial

Sponsor
Teva Branded Pharmaceutical Products R&D LLC
Tested
Modakafusp alfa (drug), Dexamethasone (drug)
Dates
Started 2017-10-04; completion 2024-11-07
Results posted
Yes

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 rec…

From ClinicalTrials.gov, last updated 2026-01-29. Full record, eligibility and contacts (opens in a new tab)

Industry funding

Takeda Pharmaceuticals U.S.A., Inc. reported $903,767 in research payments for this study in 2025 (39 payments).

Research payments usually go to hospitals, universities and research sites to run a study, not to the investigators personally. A payment is not evidence of wrongdoing.

U.S. investigators named on this study

Clinicians the company named as principal investigators in its Open Payments reports.

Sites paid to run it

Sources: CMS Open Payments research payments (program year 2025) and ClinicalTrials.gov, U.S. National Library of Medicine.