A Study to Learn About the Effectiveness of the Medicine Called Elranatamab in People With Relapsed Refractory Multiple Myeloma as Compared With Standard of Care Therapies

Part of paid clinical trials in New York, New York.

Sponsor
Pfizer
Study ID
NCT06592222
Status
Completed

Conditions

Eligibility Criteria

Sex
ALL
Age
18 Years - N/A
Healthy Volunteers
Not accepted

Interventions

  • Elranatamab — DRUG
    BCMA-CD3 bispecific antibody
  • Standard of care — DRUG
    Standard of care

Study Details

This study is to understand how well elranatamab (PF-06863135) may be used for relapsed refractory multiple myeloma (RRMM). 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 used in real-world clinical practice. For people receiving elranatamab, the investigators will use data from the phase 2 clinical trial (MagnetisMM-3). The investigators will also use data from a real-world data source, representing the SOC in clinical practice. This study does not seek any participants for enrollment. The investigators will compare the experiences of people receiving elranatamab to people receiving SOC therapies. This way, it will help the investigators to know how well elranatamab can be used for RRMM treatment.

Key Dates

Start date
Aug 26, 2024
Status verified
May 2025
Primary completion
Mar 3, 2025
Completion
Mar 3, 2025

Study Design

Enrollment
4 participants (actual)

Arms

  • Arm: Elranatamab
    Patients treated with elranatamab from the MagnetisMM-3 trial
  • Arm: Standard of care
    Patients treated with standard-of-care therapies from real-world data sources

Primary Outcome Measure

Progression-free survival [ Time Frame: From the index therapy start until progression or death due to any cause, whichever occurs first, assessed up to 6 years ]

Locations (1)

FacilityCityStateZIPSite coordinators
PfizerNew YorkNew York10001-

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