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Search / Trial NCT06057402

Elranatamab Post Trial Access Study for Participants With Multiple Myeloma (MM)

Launched by PFIZER · Sep 21, 2023

Trial Information

Current as of October 02, 2025

Recruiting

Keywords

Multiple Myeloma Elranatamab Post Trial Access Roll Over Study Extension Study Mm 15 Magnetis Mm15 Bcma Bcma Antibody Magnetism Bispecific Antibody Elrexfio

ClinConnect Summary

This clinical trial is designed for individuals with Multiple Myeloma, a type of blood cancer, who have previously participated in a related study and found benefit from a treatment called elranatamab. The main goal of this study is to continue providing access to elranatamab for those who are still experiencing positive effects from it after their original participation has ended. The trial is currently recruiting participants aged 65 and older, and it welcomes individuals of any gender.

To qualify for this study, participants must have completed a previous study involving elranatamab and must still be benefiting from the treatment at the time their original study ends. However, individuals with certain medical or mental health conditions that could pose risks or who have not previously participated in a qualifying study will not be eligible. Those who join the study can expect to continue receiving elranatamab and will be monitored by healthcare professionals to ensure their safety and well-being throughout the process.

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:
  • Participants must agree to follow the reproductive criteria as outlined in the protocol
  • Participants have completed a qualifying Parent Study, were still receiving elranatamab when the Parent Study terminated or completed, and are deriving clinical benefit from elranatamab (as determined by the investigator).
  • Exclusion Criteria:
  • Any medical or psychiatric condition including recent (within the past year) or active suicidal ideation/behavior or laboratory abnormality that may increase the risk of study participation or, in the investigator's judgment, make the participant inappropriate for the study.
  • Participants not previously enrolled or who have discontinued study treatment in a Parent Study are ineligible for participation in this study.

About Pfizer

Pfizer Inc. is a global leader in biopharmaceutical innovation, dedicated to discovering, developing, and delivering advanced therapies that enhance patient outcomes across a wide range of medical conditions. With a rich history of scientific research and a commitment to quality, Pfizer focuses on areas such as oncology, immunology, cardiology, and rare diseases. The company leverages cutting-edge technology and collaborates with healthcare professionals, regulatory bodies, and academic institutions to conduct rigorous clinical trials that ensure the safety and efficacy of its products. Pfizer's mission is to bring breakthroughs that change patients' lives, exemplifying its commitment to health and wellness worldwide.

Locations

Edmonton, Alberta, Canada

Taipei, Taiwan

Calgary, Alberta, Canada

Taipei, Taiwan

Paris, France

Richmond, Victoria, Australia

Jinan, Shandong, China

Nagoya, Aichi, Japan

Beijing, Beijing, China

Kobe, Hyogo, Japan

Kyoto, Japan

Orange, California, United States

Guangzhou, Guangdong, China

Sendai Shi, Miyagi, Japan

Montréal, Quebec, Canada

Shibuya Ku, Tokyo, Japan

Indianapolis, Indiana, United States

Pierre Bénite, Rhône, France

Melbourne, Victoria, Australia

Hangzhou, Zhejiang, China

Fort Collins, Colorado, United States

Greeley, Colorado, United States

Guangzhou, Guangdong, China

Loveland, Colorado, United States

Richmond, Victoria, Australia

Fort Collins, Colorado, United States

Longmont, Colorado, United States

Calgary, Alberta, Canada

Longmont, Colorado, United States

Patients applied

0 patients applied

Trial Officials

Pfizer CT.gov Call Center

Study Director

Pfizer

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported