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ABP 102 refers to two distinct therapeutic candidates in development by different companies. The first is a bispecific T-cell engager (BiTE) developed by Abpro and licensed to Celltrion for the treatment of HER2-positive cancers, including breast, gastric, and pancreatic cancers. Developed using the MultiMab platform, it is designed to simultaneously bind HER2 on tumor cells and CD3 on T-cells, thereby facilitating the targeted destruction of malignant cells. The second is an AAV-based gene therapy originally developed by Apic Bio and licensed to uniQure (renamed AMT-162) for the treatment of superoxide dismutase 1 (SOD1) amyotrophic lateral sclerosis (ALS). This therapy utilizes an adeno-associated virus (AAV) vector to deliver a microRNA payload designed to silence the expression of mutant SOD1, which is a key driver of disease progression in this subset of ALS patients.
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