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A Prospective, Non-interventional, Multinational, Observational Study With Isatuximab in Patients With Relapsed and/or Refractory Multiple Myeloma (RRMM)

Completed · NCT04458831

Conditions: Plasma Cell Myeloma

At a glance

Research payments reported, 2025
$111,477
U.S. investigators named
11
Sites paid
11
Planned or actual enrollment
583

About the trial

Sponsor
Sanofi
Tested
isatuximab SAR650984 (drug), Pomalidomide (drug), Dexamethasone (drug), Carfilzomib (drug)
Dates
Started 2020-08-13; completion 2026-02-23
Results posted
Not yet

Primary Objective: To assess the effectiveness, in terms of overall response rate (ORR) of isatuximab patients with RRMM in routine clinical practice, within 12 months To assess other effectiveness parameters such as progression free survival (PFS), PFS rate (PFSR), duration of response (DoR), time to response, time and intent to first subsequent therapy, rate of very good partial response or better, rate of complete response (CR) or better of isatuximab patients with RRMM in routine clinical practice To assess the profile of patients (demographic, disease characteristics, comorbidities and prior MM treatment history) who are treated with isatuximab in routine clinical practice To describ…

From ClinicalTrials.gov, last updated 2026-07-29. Full record, eligibility and contacts (opens in a new tab)

Industry funding

Sanofi US Services Inc. reported $111,477 in research payments for this study in 2025 (52 payments).

Products named: Sarclisa

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.