AL Amyloidosis Bispecific Trial: Who Qualifies, Response , Side Effects & Organ Response | IMS 2026
Description
Giada Bianchi, MD, of Dana-Farber Cancer Institute discusses interim results from a phase 1/2 trial of elranatamab in relapsed light chain (AL) amyloidosis at IMS 2026 in Glasgow. Bispecific antibodies are approved for relapsed myeloma but had not been prospectively studied in AL amyloidosis. In the first 11 patients, this BCMA bispecific produced rapid, deep and lasting responses with mostly mild side effects. She also covers early signs of heart and kidney improvement and the six-month fixed-duration design.
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Timestamps:
0:00 Introduction: Dr. Giada Bianchi, Dana-Farber Cancer Institute
0:22 Trial Overview and How Bispecific T-Cell Engagers Work
1:22 Patient Eligibility: Prior Treatment and Exclusion Criteria
2:16 Results: Universal and Deep Responses
3:09 Side Effects: Cytokine Release Syndrome and Infection Risk
4:24 Organ Response and the Fixed Six-Month Design
5:39 Q&A: Can Myeloma Patients Join This Trial?