–ย ย ย ย ย ย ย ย ย The 12-week U.S. Phase IIa study is evaluating the efficacy, safety and tolerability ofย the once-monthly subcutaneousย (SQ)ย depot formulation (treatment formulation) of small molecule GLP-1ย receptorย (GLP-1R)ย agonist ASC30ย in 65 participants with obesity or overweight.
–ย ย ย ย ย ย ย ย ย The ultra-long-acting SQย depot treatment formulation of small molecule ASC30 demonstrated a 46-day observed half-life in participants with obesity in the Phase Ib study, supporting once-monthly administration.
–ย ย ย ย ย ย ย ย ย Topline data from the 12-week Phase IIa study of ASC30 once-monthly SQ depot treatment formulation are expected in the first quarter of 2026.
–ย ย ย ย ย ย ย ย ย The Company will host aย conference call in Mandarin today at 10:00 a.m. China Standard Time.ย
HONG KONG, Oct. 19, 2025 /PRNewswire/ — Ascletisย Pharma Inc. (HKEX: 1672, “Ascletis”) announcesย the recentย completion of enrollment in the U.S. Phase IIa study for its once-monthly subcutaneousย (SQ)ย depot formulation (treatment formulation) of small molecule GLP-1 receptor (GLP-1R) agonist ASC30 forย theย treatmentย ofย obesityย (NCT06679959). All 65ย participants are obese or overweight with at least one weight-related comorbidity.
The Phase IIaย studyย of ASC30 once-monthly SQ depot treatment formulation is aย 12-week, randomized, double-blind, placebo-controlled and multi-center study conducted in the U.S. to evaluate the safety, tolerabilityย andย efficacyย in participants with obesityย (body mass index (BMI) โฅ 30 kg/m2) or overweight (BMI โฅ 27 kg/m2 but < 30 kg/m2) with at least one weight-related comorbidity. The study consists of three cohorts of different doses, with a totalย of 65 participants. Topline data are expected in the first quarter of 2026.
The ultra-long-acting SQ depot treatment formulation of small molecule ASC30 demonstrated a 46-day observed half-life (as measured by time to 50% Cmax) in participants with obesity in the Phase Ib studyย (NCT06679959), supporting once-monthly administration.ย ASC30 treatment formulation’s terminal half-life was 36 days.
Furthermore, the U.S. Phase Ib single ascending dose (SAD) study demonstrated that compared to the trough concentration of ASC30 at Day 29, the ultra-long-acting SQ depot treatment formulation showed a peak-to-trough ratio of approximately 1.5 toย 1.ย The proprietary SQ depot slow-release treatment formulation of ASC30 was developed fromย Ascletis’ Ultra-Long-Acting Platformย (ULAP). Ascletis’ ULAP technology does not have the limitations of albumin-dependent half-life extension technology, currently being applied to many peptide drugs and candidates, which limits half-life extension to the half-life of albumin (approximately 20 days).
“Completing enrollment in this study is an important milestone, marking significant progress in our development of this innovative therapy,” said Jinzi Jason Wu, Ph.D., Founder, Chairman and CEO of Ascletis, “Ascletis’ proprietary ultra-long-acting SQ depot treatment formulation of ASC30, with its 46-day observed half-life and favorable peak-to-trough ratio of approximately 1.5 to 1, demonstrated the potential to become a once-monthly treatment option for obesity. We are looking forward to topline data from this Phase IIa studyย inย the first quarter of 2026.”
ASC30 was discovered and developed in-house at Ascletis as a first and only investigational small molecule GLP-1R biased agonist designed to be administered once daily orally and once monthly to once quarterly subcutaneously as a treatment therapyย and a maintenance therapy for chronic weight management.
Conference Call
Ascletis will host a conference callย in Mandarin today, October 20, 2025ย at 10:00 a.m.ย Chinaย Standard Time. A live webcast of the call will beย available via Tecent Meeting/ VooV Meeting, with the Meeting ID: 216-282-339, or access links of:
Chinese Mainland [1]: https://meeting.tencent.com/dm/8LbPT9Fs9HoW; or
International: https://voovmeeting.com/dm/8LbPT9Fs9HoW.
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[1]ย Chinese Mainland:ย the People’s Republic of China, excluding, for the purpose of this press release, Hong Kong, Macau Special Administrative Region and Taiwan, China.ย |
About ASC30
ASC30 is an investigational GLP-1R biased small molecule agonist and has unique and differentiated properties that enable the same small molecule for both oral tablet and subcutaneous injection administrations. ASC30 is a new chemical entityย (NCE),ย with U.S. and global compound patentย protectionย until 2044 without patent extensions.ย
About Ascletis Pharma Inc.
Ascletis Pharma Inc. is a fully integrated biotechnology company focused on the development and commercialization of potential best-in-class and first-in-class therapeutics to treat metabolic diseases. Utilizing its proprietary Artificial Intelligence-Assisted Structure-Based Drug Discovery (AISBDD) and Ultra-Long-Acting Platform (ULAP) technologies, Ascletis has developed multiple drug candidates in-house, including its lead program, ASC30, a small molecule GLP-1R agonist designed to be administered once daily orally and once monthly to once quarterly subcutaneously as a treatment therapy and a maintenance therapy for chronic weight management. Ascletis is listed on the Hong Kong Stock Exchange (1672.HK).
For more information, please visit www.ascletis.com.
Contact๏ผ
Peter Vozzo
ICR Healthcare
443-231-0505 (U.S.)
[email protected]
Ascletis Pharma Inc. PR and IR teams
+86-181-0650-9129 (China)
[email protected]
[email protected]
View original content:SOURCE Ascletis Pharma Inc.
