Semaglutide: The Drug that May Lead to a 'New Era' in Anti-Obesity Medication
Historically, most weight-loss drugs can only reduce weight by 5-10%, and there are many hidden safety risks. In clinical trials, smeglutide not only reduced the weight of obese patients by an average of 15%, but also showed good safety.
As scientists have a deeper understanding of the molecular mechanism of signal communication between the intestine and the brain, a variety of new generations of weight loss therapies are emerging. Recently, a review of Nature Reviews Drug Discovery, a sub-published by Nature, counted these innovative therapies.

Both Tirzepatide and smeglutide reduced the weight of obese patients by more than 10% in phase 3 clinical trials, breaking the historical limitation that weight loss drugs can only reduce weight by 5% to 10%. The review authors stated that they set a new benchmark for the development of a new generation of weight-loss drugs.
2026-07-31
Trade Alert
Delivering the latest product trends and industry news straight to your inbox.
(We'll never share your email address with a third-party.)
Related News
-
Egyptian Pharmaceutical Market Research
-
CPHI China 2023 | At the Heart of Pharma
-
A Guide Into What the Pharmaceutical Use of Hexamine Is
-
In line with the 8201, Hengrui Pharmaceutical plans the HER2 ADC in this way
-
$50 billion in products were 'returned' to rationalize those blockbuster BD deals
-
Tronsound long-acting IL-36R antibody obtained FDA clinical IND
-
Dapagliflozin is approved in the EU for the treatment of symptomatic chronic heart failure
-
The FDA accepted Zuranolone's NDA application and granted it priority review rights for the treatment of MDD and PDD
-
Asia Hong Pharma announced that it has co-developed an innovative tumor therapy based on AI+RNA technology route with ReviR
-
Ribo Biologics announced that the world's first FIH application for a siRNA drug targeting FXI has been successfully approved by HREC in Australia
Recommend Reading
-
“No Artificial Colors” Gets Redefined—Why FDA’s Labeling Shift Is Roiling the Food Additive World
-
FDA Revokes Orange B Authorization and Proposes Removing Citrus Red No. 2
-
EFSA’s Updated Food-Additive Application Guidance Takes Effect
-
India Approves ₹30.3 Billion Chemical-Park Scheme to Build Three Mega Industrial Hubs
-
EFSA Reviews Clodinafop Risk
-
Weak and Volatile Methanol Market in China in July
-
Supply and Demand Weak, Minor Fluctuations in the Melamine Market in China
-
This week, ethylene glycol prices in China began to fall
-
This week's acetic acid market trend in China has risen
-
Supply Tightness Leads to Rising Formic Acid Prices in China