Chinese Developers Showcase Potentially Differentiated Weight Loss Assets At ADA

Including First-In-Class ActRIIA Antibody

Multiple Chinese firms presented at this year’s ADA meeting, with a focus on weight reduction efficacy for mostly early clinical stage assets. While limited information was given on lean mass preservation, several companies are progressing drugs and combos to address this need.

Scientists (miniature) are gathering at a conference hall for a meeting.
This year’s ADA indicated that muscle-preserving drugs developed by Chinese firms for weight management are mostly in preclinical stage currently. (Shutterstock/AI-generated)

Among Chinese developers of weight management medicines presenting at the June 20–23 American Diabetes Association (ADA) congress, Sciwind Biosciences and Laekna Therapeutics appeared to be the stand-outs in terms of new data on self-developed assets — ecnoglutide in Phase III and the Phase I first-in-class combination therapy LAE102, respectively.

The Chinese-origin, clinical-stage drugs presented at the Chicago meeting were in a notably narrow band in terms of therapeutic targets,...

Read the full article – start your free trial today!

Join thousands of industry professionals who rely on Scrip for daily insights

  • Start your 7-day free trial
  • Explore trusted news, analysis, and insights
  • Access comprehensive global coverage
  • Enjoy instant access – no credit card required

More from R&D

EADV: Leo Makes A Big Leap With Eczema Drug Temtokibart Set For Phase III

 
• By 

CSO Jacob Thyssen tells Scrip that the monoclonal antibody which blocks the IL-22RA1 receptor subunit is a very safe and effective option to treat the chronic inflammatory skin disease.

Incyte’s Povorcitinib Wins Stack Up, Will It Be Enough To Hedge Jakafi Loss?

 
• By 

With patent expiry for its blockbuster blood cancer drug Jakafi on the horizon, Incyte will need to translate these povorcitinib wins from clinic to market.

Publisher’s Spotlight: Shortlist Unveiled For Citeline Japan Awards

 
• By 

Shortlists of potential winners in all categories of the Citeline Japan Awards 2025 have now been released. Join us at the event in Tokyo on October 21, it’s not too late to book your table!

Regeneron’s Garetosmab May Become Second Drug For Rare Bone Disease FOP

 

The company announced positive Phase III data for the drug in fibrodysplasia ossificans progressiva, as well as Phase II combination data among patients with obesity.

More from Therapy Areas

Roivant Sets The Stage For Commercial Return With Brepocitinib Data

 

Positive Phase III data positions Roivant to launch the oral TYK2/JAK1 inhibitor for dermatomyositis, with an NDA filing planned in early 2026.

AstraZeneca’s Fasenra RESOLUTE Failure Highlights The Limits Of Biologics In COPD

 

AstraZeneca’s IL-5 blocker has again missed in COPD, adding to a number of disappointments for biologics in this disease. Complex biology and overlapping inflammatory pathways seem to be at the heart of the problem.

Lilly’s Orforglipron Bests Novo Rival In First Oral Head-To-Head Study

 

The company’s cardiometabolic leader Ken Custer discusses the topline ACHIEVE-3 results in diabetes and just-published full results of ATTAIN-1 in obesity of orforglipron, with a pledge to maximize access to the oral GLP-1 therapy worldwide, once approved.