Ascletis Pharma's Oral GLP-1 Shows Promise in Obesity Treatment

Ascletis Pharma, a Chinese biotech company, has made significant strides in the competitive field of obesity drug development with its oral GLP-1 receptor agonist, ASC30. The company recently published data from a multiple ascending dose study, demonstrating promising results in weight loss efficacy.
Phase 1 Study Results
The phase 1 study, conducted at a site in Utah, enrolled 20 patients across two cohorts. Sixteen participants received escalating doses of ASC30, while four received placebo. The study showed:
- Cohort two (2 mg to 40 mg dosing) achieved a mean body weight loss of 6.3% after 28 days
- Cohort one (2 mg to 20 mg dosing) showed a mean weight loss of 4.3% after 28 days
- A clear dose response was observed between the two cohorts
The average daily doses were 9.25 mg and 18 mg for cohort one and cohort two, respectively. Ascletis reported that ASC30 was generally well-tolerated, with all gastrointestinal-related adverse events being mild or moderate. Importantly, no clinically significant changes in liver enzymes were observed.
Competitive Landscape
Ascletis' results appear competitive within the burgeoning obesity treatment market:
- Roche's oral GLP-1 candidate CT-996 showed 6.1% weight loss after 28 days
- Eli Lilly's orforglipron achieved 3.9% weight loss
- Novo Nordisk's amycretin resulted in 4% weight loss
- Pfizer's danuglipron demonstrated 5.2% weight loss
However, differences in trial designs and small patient numbers make direct comparisons challenging. Longer trials are expected to yield improved efficacy data, as evidenced by Novo Nordisk's amycretin, which showed 13.1% weight loss after 12 weeks.
Ascletis' Obesity Pipeline
Ascletis is pursuing a multi-pronged approach to obesity treatment:
- ASC30: Oral and weekly injectable formulations of the GLP-1 receptor agonist
- ASC47: A muscle-preserving weight loss drug candidate
The company is also exploring combination therapies, testing ASC47 with established treatments like Eli Lilly's tirzepatide (Zepbound) and Novo Nordisk's semaglutide (Wegovy). This strategy aligns with industry trends, as leading companies are developing similar combination approaches to enhance weight loss while preserving muscle mass.
As Ascletis continues to advance its obesity pipeline, the pharmaceutical industry watches closely. The company's swift progress and competitive data position it as a potential key player in the rapidly evolving obesity treatment landscape.
References
- Ascletis' swift surge into obesity continues with competitive oral GLP-1 data
Ascletis Pharma’s rapid-fire expansion into obesity drug development has passed another milestone. The Chinese biotech ticked the publication of multiple ascending dose data off its to-do list Wednesday, linking its oral GLP-1 prospect to 6.3% mean body weight loss after 28 days.
Explore Further
What were the specific safety outcomes observed for ASC30 in the phase 1 study?
How does Ascletis Pharma plan to differentiate ASC30 from its competitors in the obesity drug market?
What are the potential reasons for the observed dose response in the ASC30 study?
How do Ascletis Pharma's combination therapies compare in terms of efficacy to their standalone treatments?
What future studies are planned for ASC30 to further assess its weight loss efficacy and safety over longer periods?