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
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.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
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
Trial Officials
Pfizer CT.gov Call Center
Study Director
Pfizer
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported