KP-483
/ Kaken Pharma
- LARVOL DELTA
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April 21, 2026
Preclinical investigations and first-in-human phase I trial of KP-483 in solid tumors: Safety, antitumor activity, and preliminary efficacy.
(ASCO 2026)
- P | "KP-483 is a potent EP4 antagonist that exerts antitumor effects through modulation of the tumor immune microenvironment. Given its favorable safety and pharmacokinetic profiles, KP-483 represents a promising EP4 receptor–targeted therapeutic strategy with potential for combination with immune checkpoint inhibitors."
First-in-human • P1 data • Preclinical • Hematological Disorders • Oncology • Solid Tumor • CD163 • CD8
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