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ARI-6000 is an experimental fibroblast activation protein (FAP)–activated prodrug designed to remain largely inert in circulation and become pharmacologically active only within the tumor microenvironment, where FAP is overexpressed on cancer-associated fibroblasts. By exploiting proteolytic cleavage by FAP to release a cytotoxic payload locally, ARI-6000 aims to enhance antitumor efficacy while reducing systemic toxicity compared with conventional chemotherapy. It is being developed within Arisaph Pharmaceuticals’ tumor-activated prodrug oncology program as a targeted cancer therapeutic.
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