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Brief Title: Elranatamab Post Trial Access Study for Participants With Multiple Myeloma (MM)
Official Title: ELRANATAMAB POST TRIAL ACCESS: AN OPEN-LABEL, SINGLE-ARM STUDY FOR PARTICIPANTS WITH MULTIPLE MYELOMA CONTINUING FROM PFIZER-SPONSORED ELRANATAMAB CLINICAL STUDIES
Study ID: NCT06057402
Brief Summary: This is a post-trial access (PTA) open-label, single-arm study in Multiple Myeloma participants who continue to derive clinical benefit from elranatamab monotherapy in the Pfizer-sponsored elranatamab Parent Studies.
Detailed Description: This is a single-arm elranatamab post-trial access study. Participants will receive elranatamab. All participants will receive elranatamab until disease progression, unacceptable toxicity, withdrawal of consent, study termination or, elranatamab becomes commercially accessible in the participant's country.
Minimum Age: 18 Years
Eligible Ages: ADULT, OLDER_ADULT
Sex: ALL
Healthy Volunteers: No
UC Irvine Health, Orange, California, United States
Franciscan Health, Indianapolis, Indiana, United States
Epworth Freemasons, Melbourne, Victoria, Australia
Epworth Hospital, Richmond, Victoria, Australia
Slade Pharmacy, Richmond, Victoria, Australia
Tom Baker Cancer Center, Calgary, Alberta, Canada
Cross Cancer Institute, Edmonton, Alberta, Canada
McGill University Health Centre, Montréal, Quebec, Canada
Centre Hospitalier Lyon Sud, Pierre-Bénite, Rhône, France
Hôpital Saint-Louis, Paris, , France
Nagoya City University Hospital, Nagoya, Aichi, Japan
Kobe City Medical Center General Hospital, Kobe, Hyogo, Japan
Tohoku University Hospital, Sendai-shi, Miyagi, Japan
Name: Pfizer CT.gov Call Center
Affiliation: Pfizer
Role: STUDY_DIRECTOR