CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 633 enrolled
Drug / intervention
Elranatamab +1 moredrug
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT06504524
NCT06504524N/ACompleted

Comparative Effectiveness of Elranatamab (PF 06863135) in Clinical Study C1071003 Versus Standard of Care (SOC) in a Real-World (RW) External Control Arm of Patients With Triple-Class Refractory (TCR) Multiple Myeloma (MM) From TherapyMonitor MM Germany

Pfizer·observational·Posted Jul 16, 2024·Updated Jun 27, 2025

In Brief

An observational study evaluating Elranatamab and Standard of Care for Multiple Myeloma. Completed, enrolled 633 participants across 2 sites in 2 countries.

Detailed Summary

The purpose of the study is to understand how well elranatamab (PF-06863135) may be used for relapsed refractory multiple myeloma (RRMM). MM is a type of cancer that begins in plasma cells (white blood cells that produce antibodies). Sometimes MM might improve at first, but then gets resistant to the treatment and starts growing again (known as relapsed refractory). This study medicine will be compared with standard-of-care (SOC) therapies. SOC are treatments that are accepted by medical experts as a proper treatment for a certain type of disease and that are widely used by doctors in real world. For people receiving elranatamab, the study doctors will use data from the other clinical trial (MagnetisMM-3). The study doctors will also use data from multiplemany real-world sources (TherapyMonitor MM Germany and Flatiron Health), for SOC in clinical practice. This study does not seek any participants for enrollment. The study doctors will compare the experiences of people receiving elranatamab to people receiving SOC therapies. This way, it will help the study doctors to know how well elranatamab can be used for RRMM treatment.

Study Details

Study Typeobservational
Allocation--
Masking--
Primary Purpose--
CountriesGermany, United States
Collaborators--

Timeline

N/ACompletedFinished
202420252026
First PostedJul 16, 2024
Enrollment StartSep 1, 2023
Primary CompletionMay 31, 2024
TodayJul 2, 2026
Enrollment to primary: 9 monthsPosted 2.0 years ago

Interventions

Elranatamabdrug

BCMA-CD3 bispecific antibody

Standard of Caredrug

control arm