Bimagrumab: an investigational human monoclonal antibody against activin type II receptors for treating obesity.

activin type II receptors (ActRII) bimagrumab myostatin obesity

Journal

Journal of basic and clinical physiology and pharmacology
ISSN: 2191-0286
Titre abrégé: J Basic Clin Physiol Pharmacol
Pays: Germany
ID NLM: 9101750

Informations de publication

Date de publication:
10 Oct 2024
Historique:
received: 27 04 2024
accepted: 19 09 2024
medline: 10 10 2024
pubmed: 10 10 2024
entrez: 10 10 2024
Statut: aheadofprint

Résumé

Bimagrumab is a human monoclonal antibody that prevents activin type II receptors (ActRII) from functioning. This antibody has a higher affinity for muscle activin-2 receptors than natural ligands such as activin and myostatin, which act as negative muscle growth regulators. Blocking the activin receptor with bimagrumab could be a new pharmaceutical approach for managing patients with obesity and type 2 diabetes mellitus (T2DM). Bimagrumab has anabolic effects on skeletal muscle mass by preventing myostatin binding and other negative muscle growth regulators. Preclinical animal models have also shown that ActRII blockade promotes actions beyond skeletal muscle, including effects on brown adipose tissue (BAT) differentiation and activity. In a phase 2 randomized clinical trial, ActRII blockade with bimagrumab led to significant loss of total body fat mass (FM), lean mass (LM) gain, and metabolic improvements over 48 weeks in overweight or obese patients with type 2 diabetes. The trial involved [number of participants], and the results showed [specific findings]. Currently, Bimagrumab is being evaluated for its potential to treat muscle wasting, functional loss in hip fractures and sarcopenia, as well as obesity. However, it is essential to note that Bimagrumab also blocks the effects of other ActRII ligands, which play a role in the neurohormonal axes, pituitary, gonads, and adrenal glands. These observations suggest that bimagrumab might represent a new approach for treating patients with obesity and related metabolic disturbances.

Identifiants

pubmed: 39385353
pii: jbcpp-2024-0065
doi: 10.1515/jbcpp-2024-0065
doi:

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

© 2024 Walter de Gruyter GmbH, Berlin/Boston.

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Safety, pharmacokinetics and efficacy of bimagrumab in overweight and obese patients with type 2 diabetes. NCT03005288 . U.S. National Library of Medicine; 2024. Available from: https://clinicaltrials.gov/study/NCT03005288?intr=Bimagrumab&page=1&rank=6
Effect of bimagrumab on body composition, insulin sensitivity, and bone in adults with obesity. NCT05933499 . U.S. National Library of Medicine; 2024. Available from: https://clinicaltrials.gov/study/NCT05933499?intr=Bimagrumab&page=2&rank=14
An extension study of the efficacy, safety and tolerability of BYM338 (Bimagrumab) in patients with sporadic inclusion body myositis who previously participated in the core study CBYM338B2203. NCT02573467 . U.S. National Library of Medicine; 2024. Available from: https://clinicaltrials.gov/study/NCT02573467?intr=Bimagrumab&page=1&rank=2
Study of efficacy and safety of bimagrumab in patients after hip fracture surgery. NCT02152761 . U.S. National Library of Medicine; 2024. Available from: https://clinicaltrials.gov/study/NCT02152761?intr=Bimagrumab&page=1&rank=3
Effect of bimagrumab on body composition, insulin sensitivity, and bone in adults with obesity. NCT05933499 . U.S. National Library of Medicine; 2024 Available from: https://clinicaltrials.gov/study/NCT05933499?intr=Bimagrumab&page=2&rank=14
Clinical study of BYM338 for the treatment of unintentional weight loss in patients with cancer of the lung or the pancreas NCT01433263 . U.S. National Library of Medicine; 2024. Available from: https://clinicaltrials.gov/study/NCT01433263?intr=Bimagrumab&page=2&rank=13
BYM338 in chronic obstructive pulmonary disease (COPD) patients with cachexia NCT01669174 . U.S. National Library of Medicine; 2024. Available from: https://clinicaltrials.gov/study/NCT01669174?intr=Bimagrumab&page=2&rank=11

Auteurs

Manmeet Kaur (M)

Department of Pharmacology, Kalpana Chawla Government Medical College, Karnal, India.

Saurav Misra (S)

Department of Pharmacology, Kalpana Chawla Government Medical College, Karnal, India.

Classifications MeSH