Founded in 2016, CatalYm's approach neutralizes GDF-15, a critical immunosuppressant used by tumor cells to survive. Visugromab, CatalYm’s lead antibody, has demonstrated durable anti-tumor efficacy with long-lasting objective responses in relapsed and refractory metastatic solid tumor patients in combination with anti-PD-1 treatment. CatalYm is advancing to Phase IIb studies to confirm visugromab as a new class of cancer immunotherapy in a broad range of anti-cancer regimens.
With its broad Phase IIb development plan, the company targets high-need solid tumor indications including NSCLC, UC, HCC and bladder cancer where existing and acquired resistance are a major problem.
As of Q3 2024, the company is in preparations to launch further randomized, controlled studies in several major cancer indications in combination with checkpoint inhibitors and standard-of-care in first- and second-line treatment in the first half of 2025.
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