Innovent Announces Mazdutide, First Dual GCG/GLP-1 Receptor Agonist, Received Approval from China's NMPA for Chronic Weight Management
Innovent Biologics (IVBIY) has received approval from China's NMPA for mazdutide, the world's first dual GCG/GLP-1 receptor agonist for chronic weight management in Chinese adults with overweight or obesity.
The approval is based on the GLORY-1 Phase 3 study, which demonstrated significant results at week 48: 14.8% mean body weight reduction with 6mg dose, 82.8% of participants achieving ≥5% weight loss, and 50.6% achieving ≥15% weight loss. The drug also showed impressive liver fat content reduction of up to 80.24% in the 6mg group.
This approval addresses a critical healthcare need in China, where over 500 million adults live with overweight or obesity, costing the country approximately $283.3 billion in GDP loss in 2020.
Innovent Biologics (IVBIY) ha ottenuto l'approvazione dalla NMPA cinese per mazdutide, il primo agonista duale GCG/GLP-1 al mondo per la gestione cronica del peso negli adulti cinesi con sovrappeso o obesità.
L'approvazione si basa sullo studio GLORY-1 di Fase 3, che ha mostrato risultati significativi alla settimana 48: una riduzione media del peso corporeo del 14,8% con la dose da 6 mg, l'82,8% dei partecipanti ha raggiunto una perdita di peso ≥5% e il 50,6% ha ottenuto una perdita ≥15%. Il farmaco ha inoltre evidenziato una notevole riduzione del contenuto di grasso epatico fino all'80,24% nel gruppo da 6 mg.
Questa approvazione risponde a un bisogno sanitario critico in Cina, dove oltre 500 milioni di adulti convivono con sovrappeso o obesità, con un costo per il paese di circa 283,3 miliardi di dollari in perdita di PIL nel 2020.
Innovent Biologics (IVBIY) ha recibido la aprobación de la NMPA de China para mazdutide, el primer agonista dual GCG/GLP-1 del mundo para el manejo crónico del peso en adultos chinos con sobrepeso u obesidad.
La aprobación se basa en el estudio GLORY-1 de Fase 3, que demostró resultados significativos en la semana 48: una reducción media del peso corporal del 14,8% con la dosis de 6 mg, el 82,8% de los participantes lograron una pérdida de peso ≥5%, y el 50,6% alcanzó una pérdida ≥15%. El medicamento también mostró una impresionante reducción del contenido de grasa hepática de hasta un 80,24% en el grupo de 6 mg.
Esta aprobación responde a una necesidad crítica de salud en China, donde más de 500 millones de adultos viven con sobrepeso u obesidad, lo que costó al país aproximadamente 283,3 mil millones de dólares en pérdidas de PIB en 2020.
Innovent Biologics (IVBIY)가 중국 NMPA로부터 mazdutide의 승인을 받았습니다. 이 약물은 과체중 또는 비만인 중국 성인을 위한 세계 최초의 이중 GCG/GLP-1 수용체 작용제입니다.
승인은 GLORY-1 3상 연구를 기반으로 하며, 48주차에 6mg 투여군에서 평균 체중 14.8% 감소, 82.8%의 참가자가 5% 이상의 체중 감량을 달성했고, 50.6%는 15% 이상의 체중 감량을 기록했습니다. 또한 이 약물은 6mg 그룹에서 최대 80.24%의 간 지방 함량 감소도 보여주었습니다.
이번 승인은 중국 내 과체중 또는 비만인 5억 명 이상의 성인이라는 심각한 의료 문제를 해결하며, 2020년 기준 약 2833억 달러의 GDP 손실을 초래했습니다.
Innovent Biologics (IVBIY) a reçu l'approbation de la NMPA chinoise pour mazdutide, le premier agoniste double GCG/GLP-1 au monde pour la gestion chronique du poids chez les adultes chinois en surpoids ou obèses.
Cette approbation repose sur l'étude GLORY-1 de phase 3, qui a démontré des résultats significatifs à la semaine 48 : une réduction moyenne du poids corporel de 14,8% avec une dose de 6 mg, 82,8% des participants ayant atteint une perte de poids ≥5%, et 50,6% une perte ≥15%. Le médicament a également montré une réduction impressionnante du taux de graisse hépatique allant jusqu'à 80,24% dans le groupe à 6 mg.
Cette approbation répond à un besoin critique de santé publique en Chine, où plus de 500 millions d'adultes vivent avec un surpoids ou une obésité, coûtant au pays environ 283,3 milliards de dollars de perte de PIB en 2020.
Innovent Biologics (IVBIY) hat von der chinesischen NMPA die Zulassung für mazdutide erhalten, den weltweit ersten dualen GCG/GLP-1-Rezeptoragonisten zur chronischen Gewichtskontrolle bei chinesischen Erwachsenen mit Übergewicht oder Adipositas.
Die Zulassung basiert auf der GLORY-1 Phase-3-Studie, die nach 48 Wochen signifikante Ergebnisse zeigte: 14,8% durchschnittliche Gewichtsreduktion bei 6 mg Dosierung, 82,8% der Teilnehmer erreichten ≥5% Gewichtsverlust und 50,6% erreichten ≥15% Gewichtsverlust. Das Medikament zeigte zudem eine beeindruckende Reduktion des Leberfettgehalts um bis zu 80,24% in der 6-mg-Gruppe.
Diese Zulassung adressiert einen kritischen Gesundheitsbedarf in China, wo über 500 Millionen Erwachsene mit Übergewicht oder Adipositas leben, was dem Land im Jahr 2020 etwa 283,3 Milliarden US-Dollar an BIP-Verlusten verursachte.
- First-in-class dual GCG/GLP-1 receptor agonist approved globally for weight loss
- Impressive efficacy with 14.8% mean body weight reduction in 6mg dose group
- Strong market potential with 500 million adults in China living with overweight/obesity
- Significant liver fat content reduction of 80.24% in 6mg group
- Recognition in multiple clinical guidelines and expert consensus
- Publication in high-impact journals including Nature and New England Journal of Medicine
- Will face competition in growing obesity treatment market
- Requires ongoing treatment for chronic weight management
- Limited to Chinese market approval currently
SAN FRANCISCO and SUZHOU, China, June 27, 2025 /PRNewswire/ -- Innovent Biologics, Inc. ("Innovent") (HKEX: 01801), a world-class biopharmaceutical company that develops, manufactures and commercializes high-quality medicines for the treatment of oncologic, autoimmune, cardiovascular and metabolic, ophthalmologic and other major diseases, announces that
The increasing prevalence of overweight and obesity in
Scientific and effective treatment options for weight loss are urgently needed in
Overweight and obesity are chronic metabolic diseases characterized by excessive fat accumulation in the body. The pathogenesis of overweight and obesity includes genetic, metabolic, environmental, and behavioral factors. Obesity can significantly increase the risk of various diseases, such as cardiovascular and cerebrovascular, endocrine, specific tumors, respiratory, reproductive, and skeletal diseases, and can seriously affect quality of life[1]. In
In response to the escalating obesity problem, several national policies and clinical guidelines have underscored the need for structured outpatient weight management and earlier pharmacological intervention. The National Health Commission's "Notice on Effective Outpatient Settings and Management of Weight Management" encourages the development of optimized outpatient care models. Additionally, "Guidelines for the Diagnosis and Treatment of Obesity (2024 Edition)" recommended pharmacotherapy when lifestyle interventions fail to meet weight loss goals. The "Guidelines for Long-term Weight Management and Clinical Application of Drugs for Obese Patients (2024 Edition)" issued by the Chinese Society of Endocrinology further advocates for initiating drug treatment early in patients with obesity-related comorbidities.
Mazdutide is supported by robust clinical data published in multiple high-impact journals, including Nature, the Lancet sub-journals, and the New England Journal of Medicine. As the first marketed dual GCG/GLP-1 receptor agonist , mazdutide has been recommended by multiple clinical guidelines in
Multiple metabolic benefits of mazdutide in supporting weight management
GCG receptors are mainly expressed in the liver, and GCG receptor agonism can inhibit hepatic fat synthesis and promote hepatic lipolysis. As a dual GCG/GLP-1 receptor agonist weight loss drug, mazdutide can deliver significant weight loss efficacy and metabolic benefits such as waist circumstance and liver fat content reductions to adults with overweight or obesity.
The approval of mazdutide was mainly based on data from GLORY-1, a Phase 3 pivotal clinical study conducted in Chinese adults with overweight or obesity. The primary endpoint and all key secondary endpoints of the study were successfully achieved in 2024. Results showed that at weeks 32 and 48, the percentage of body weight reduction from baseline and the proportions of participants with a body weight reduction of ≥
- Based on the efficacy estimand, at week 48, the mean percentage changes in body weight relative to baseline in the mazdutide 4 mg, mazdutide 6 mg, and placebo groups were −
12.0% , −14.8% , and −0.5% , respectively; - The proportion of participants with a body weight reduction ≥
5% relative to baseline were73.5% ,82.8% , and11.5% , respectively; the proportion of participants with a body weight reduction ≥15% relative to baseline were37.0% ,50.6% , and2.1% , respectively; - The mean changes in waist circumference relative to baseline were −9.5 cm, −11.0 cm, and −1.5 cm, respectively.
- In addition, mazdutide reduced liver fat content in adults with overweight or obesity. Among participants with baseline liver fat content ≥
10% , the mean percent change from baseline in liver fat content to week 48 were −65.85% , −80.24% , and −5.27% in the mazdutide 4 mg, 6 mg, and placebo groups, respectively.
The results of GLORY-1 study have been presented at the American Diabetes Association (ADA) Annual Meeting and published in the New England Journal of Medicine, which have received widespread attention from industry experts and scholars.
Mazdutide addresses a critical unmet need in
Professor Linong Ji, the Leading Principal Investigator of GLORY-1, Peking University People's Hospital, stated, "Obesity is a chronic disease that demands a coordinated societal response. With
Dr. Lei Qian from Innovent Biologics, stated, "Mazdutide represents the next-generation dual GCG/GLP-1 receptor agonist. Its clinical development has been made possible by pooling the collective expertise of leading endocrinology experts across
About Obesity/Overweight
Obesity is a chronic metabolic disease with complex causes, and it serves as a major risk factor for a range of diseases including diabetes, fatty liver disease, cardiovascular and cerebrovascular diseases, kidney disease, joint disorders, sleep-disordered breathing, and cancer.
Despite the chronic nature of obesity and its need for long-term management, treatment options remain limited. While lifestyle interventions remain the cornerstone of treatment, many patients struggle to achieve or maintain meaningful weight reduction. This underscores the urgent need for safe, effective, and sustainable pharmacological interventions.
About Mazdutide
Innovent entered into an exclusive license agreement with Eli Lilly and Company (Lilly) for the development and potential commercialization of mazdutide, a dual GCG /GLP-1 receptor agonist, in
Mazdutide is approved by NMPA for chronic weight management in adults with overweight or obesity*; and mazdutide currently has another NDA accepted for review by NMPA, for glycemia control in adults with type 2 diabetes.
Mazdutide has currently conducted seven Phase 3 clinical studies, including:
- GLORY-1: A Phase 3 clinical study conducted in Chinese adults with overweight of obesity;
- GLORY-2: A Phase 3 clinical study conducted in Chinese adults with moderately to severely obesity;
- GLORY-3: A Phase 3 clinical study comparing mazdutide versus semaglutide in Chinese adults with overweight of obesity accompanied metabolic-associated fatty liver disease (MAFLD);
- GLORY-OSA: A Phase 3 trial in Chinese participants with obstructive sleep apnea (OSA) and obesity;
- DREAMS-1: A Phase 3 clinical study conducted in Chinese adults with untreated type 2 diabetes;
- DREAMS-2: A Phase 3 clinical study comparing mazdutide versus dulaglutide in Chinese adults with type 2 diabetes who have poor glycemia control with oral medication;
- DREAMS-3: A Phase 3 clinical study comparing mazdutide versus semaglutide in Chinese adults with type 2 diabetes and obesity;
Among these, GLORY-1, DREAMS-1, and DREAMS-2 have already met their primary endpoints and the other four studies are currently ongoing.
In addition, several new clinical studies of mazdutide are initiated or planned, including:
- A Phase 3 trial in adolescents with obesity;
- New studies in patients with metabolic dysfunction-associated steatohepatitis (MASH) and heart failure with preserved ejection fraction (HFpEF).
*Mazdutide is indicated as an adjunct to a reduced-calorie diet and increased physical activity for chronic weight management in adult patients with an initial Body Mass Index (BMI) of:
- BMI ≥ 28 kg/m² (obesity); or
- BMI ≥ 24 kg/m² (overweight) in the presence of at least one weight-related comorbid condition (e.g., hyperglycemia, hypertension, dyslipidemia, fatty liver, or obstructive sleep apnea syndrome and etc.).
About Innovent Biologics
Innovent is a leading biopharmaceutical company founded in 2011 with the mission to empower patients worldwide with affordable, high-quality biopharmaceuticals. The company discovers, develops, manufactures and commercializes innovative medicines that target some of the most intractable diseases. Its pioneering therapies treat cancer, cardiovascular and metabolic, autoimmune and eye diseases. Innovent has launched 16 products in the market. It has 2 new drug applications under regulatory review, 4 assets in Phase 3 or pivotal clinical trials and 15 more molecules in early clinical stage. Innovent partners with over 30 global healthcare companies, including Eli Lilly, Sanofi, Incyte, LG Chem and MD Anderson Cancer Center.
Guided by the motto, "Start with Integrity, Succeed through Action" Innovent maintains the highest standard of industry practices and works collaboratively to advance the biopharmaceutical industry so that first-rate pharmaceutical drugs can become widely accessible. For more information, visit www.innoventbio.com, or follow Innovent on Facebook and LinkedIn.
Statement: Innovent does not recommend the use of any unapproved drug (s)/indication (s). |
Forward-looking statement
This news release may contain certain forward-looking statements that are, by their nature, subject to significant risks and uncertainties. The words "anticipate", "believe", "estimate", "expect", "intend" and similar expressions, as they relate to Innovent, are intended to identify certain of such forward-looking statements. Innovent does not intend to update these forward-looking statements regularly.
These forward-looking statements are based on the existing beliefs, assumptions, expectations, estimates, projections and understandings of the management of Innovent with respect to future events at the time these statements are made. These statements are not a guarantee of future developments and are subject to risks, uncertainties and other factors, some of which are beyond Innovent's control and are difficult to predict. Consequently, actual results may differ materially from information contained in the forward-looking statements as a result of future changes or developments in our business, Innovent's competitive environment and political, economic, legal and social conditions.
Innovent, the Directors and the employees of Innovent assume (a) no obligation to correct or update the forward-looking statements contained in this site; and (b) no liability in the event that any of the forward-looking statements does not materialize or turn out to be incorrect.
REFERENCES
[1] Multidisciplinary Clinical Consensus on Diagnosis and Treatment of Obesity (2021 edition), Chinese Journal of Endocrinology and Metabolism. 2021;37(11):959-972. |
[2] Qin X, Pan J. The Medical Cost Attributable to Obesity and Overweight in |
[3] Guideline for Chronic Weight Management and Clinical Practice of Anti-obesity Medications (2024 version). Chinese Journal of Endocrinology and Metabolism. 2024,40(7): 545-564 |
[4] Expert Consensus on Weight Management for Type 2 Diabetes Mellitus. International Journal of Endocrinology and Metabolism.2024,44(5):359-370 |
[5] Expert Consensus on Glucagon-like Peptide-1 Receptor Agonist Analogs Combined with Lifestyle Intervention for Weight Loss (2024 Edition). Chinese Journal of Diabetes, 2024 |
[6] Interpretation of National Health Commission of |
[7] Pan XF, Wang L, Pan A. Epidemiology and determinants of obesity in |
[8] Institute for Health Metrics and Evaluation. Global Health Data Exchange. GBD results tool. http://ghdx.healthdata.org/gbd-resultstool (accessed Jan 10, 2021). |
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