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Equecabtagene Autoleucel

Generic Name
Equecabtagene Autoleucel
Brand Names
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Indication

用于治疗复发或难治性多发性骨髓瘤成人患者,既往经过至少3线治疗后进展(至少使用过一种蛋白酶体抑制剂及免疫调节剂)。

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globenewswire.com
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Relapsed Multiple Myeloma Clinical Trials Review 2024

The "Relapsed Multiple Myeloma - Global Clinical Trials Review, 2024" report offers an overview of clinical trials worldwide, detailing trials by region, country, phase, status, and sponsor type, including prominent drugs and companies involved.
quantisnow.com
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Innovent and Lilly Expand Collaboration Through Agreement on Commercialization Rights

Innovent Biologics and Eli Lilly announce a Distribution and Promotion Agreement for Lilly's non-covalent BTK inhibitor, Jaypirca®, in Mainland China. Innovent will handle importation, marketing, distribution, and promotion, while Lilly will manage R&D and post-market medical affairs. Jaypirca®, approved by the U.S. FDA in January 2023 and China's NMPA in October 2024, is the first non-covalent BTK inhibitor for mantle cell lymphoma patients previously treated with covalent BTK inhibitors.
drugs.com
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JAMA Oncology Publishes Phase 1b/2 Study Data on IASO Bio's Equecabtagene Autoleucel (Fucaso™) in the Treatment of Relapsed/Refractory Multiple Myeloma

IASO Bio's Equecabtagene Autoleucel (Fucaso™) showed high efficacy and safety in treating relapsed/refractory multiple myeloma, with a 96% overall response rate and 74.3% stringent complete response/complete response rate, published in JAMA Oncology.
prnewswire.com
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IASO Bio Presented Comparative Clinical Outcomes on the Optimal Lymphodepletion Prior

IASO Biotherapeutics presented a poster at the 2024 IMS Annual Meeting comparing outcomes of relapsed/refractory multiple myeloma patients treated with Eque-cel under different lymphodepletion regimens. Results showed full lymphodepletion significantly improved remission depth, duration, and progression-free survival without increased toxicity.
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