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Ascletis Selects a Best-in-Class Once-Monthly Subcutaneously Administered Amylin Receptor Agonist, ASC36, for Clinical Development

ASC36 shows 91% greater weight loss efficacy than petrelintide in preclinical studies and aims for FDA IND submission in Q2 2026 as a once-monthly obesity treatment.

  • Ascletis Pharma Inc. selected ASC36 as a clinical candidate and plans to submit an IND to the U.S. Food and Drug Administration in Q2 2026.
  • Using its AISBDD and ULAP platforms, Ascletis designed ASC36 in-house to support once-monthly subcutaneous dosing with injection volume under one milliliter and scalable manufacturing.
  • Study results indicate ASC36's half-life in NHP studies was approximately 15 days, three-fold longer than petrelintide, and caused-10.01% weight loss versus-5.25% in DIO rats.
  • Ascletis Pharma Inc. will host a conference call in Mandarin at 10:00 a.m. China Standard Time on October 30, 2025 and plans to combine ASC36 with ASC35.
  • Company rationale: Ascletis aims to make ASC36 a cornerstone therapy and basis for ASC36-based combination therapies for cardio-metabolic diseases, reflecting Jinzi Jason Wu, Ph.D.'s commitment to novel obesity treatments.
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Ascletis Selects a Best-in-Class Once-Monthly Subcutaneously Administered Amylin Receptor Agonist, ASC36, for Clinical Development

In head-to-head non-human primate (NHP) studies, average observed half-life of ASC36 was approximately 15 days, 3-fold longer than petrelintide, which supports once-monthly subcutaneous (SQ) dosing in humans.

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Charleston Gazette-Mail broke the news in Charleston, United States on Thursday, October 30, 2025.
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