Rimonabant (also known asSR141716; trade namesAcomplia,Zimulti)[3] is ananorecticantiobesity drug approved in Europe in 2006 but was withdrawn worldwide in 2008 due to serious psychiatric side effects; it was never approved in the United States.[1][2] Rimonabant is aninverse agonist for the cannabinoid receptor CB1 and was first-in-class for clinical development.[4][5]
On 21 June 2006, theEuropean Commission approved the sale of rimonabant in the then-25-member European Union as a prescription drug for use in conjunction with diet and exercise for patients with abody mass index (BMI) greater than 30 kg/m2, or patients with a BMI greater than 27 kg/m2 with associated risk factors, such as type 2diabetes ordyslipidaemia.[7] It was first in its class to be approved anywhere in the world.[5]
Rimonabant was submitted to theFood and Drug Administration (FDA) for approval in the United States in 2005; in 2007, the FDA's Endocrine and Metabolic Drugs Advisory Committee (EMDAC) concluded that Sanofi-Aventis failed to demonstrate the safety of rimonabant and voted against recommending the anti-obesity treatment for approval.[8] The application was deemednot-approvable by FDA, and the company cancelled plans for a re-submission.[9]
In October 2008, theEuropean Medicines Agency recommended the suspension of Acomplia after theCommittee for Medicinal Products for Human Use (CHMP) had determined that the risks of Acompliaoutweighed its benefits due to the risk of serious psychiatric problems, including suicide.[10] In November 2008 an advisory committee in Brazil recommended suspension as well, and that month Sanofi-Aventis suspended sale of the drug worldwide.[2] The EMA approval was withdrawn in January 2009.[11][12] In 2009 India prohibited the manufacture and sale of the drug.[13]
Data from clinical trials submitted to regulatory authorities showed that rimonabant caused depressive disorders or mood alterations in up to 10% of subjects and suicidal ideation in around 1%, and in Europe it was contraindicated for people with any psychiatric disorder, including depressed or suicidal individuals.[7] Data from a large, randomized, clinical trial (CRESCENDO) with > 9,000 patients receiving rimonabant treatment demonstrated a rate of psychiatric adverse events (anxiety, depression, depressed mood, or insomnia) of greater than 30%.[14]
Additionally, nausea and upper respiratory tract infections were very common adverse effects (occurring in more than 10% of people); common adverse effects (occurring in between 1% and 10% of people) includedgastroenteritis, anxiety, irritability, insomnia and other sleep disorders, hot flushes, diarrhea, vomiting, dry or itchy skin, tendonitis, muscle cramps and spasms, fatigue, flu-like symptoms, and increased risk of falling.
The FDA's advisory committee concurred with concerns raised by the review divisions. Based on human and on animal data, it appeared that thetherapeutic window with regard to CNS toxicity, and specifically seizures was narrow.[2][15][16]
EMApostmarketing surveillance data suggested that the risk of psychiatric disorders in people taking rimonabant was doubled.[2]
Along with the clinical trials in obesity that generated the data submitted to regulatory authorities,[19] rimonabant was also studied in clinical trials[2] for diabetes, atherosclerosis, and smoking cessation.[20][21]
^"Drugs banned in India". Central Drugs Standard Control Organization, Dte.GHS, Ministry of Health and Family Welfare, Government of India. Archived fromthe original on 2017-02-22. Retrieved2013-09-17.
^Topol EJ, Bousser MG, Fox KA, Creager MA, Despres JP, Easton JD, et al. (August 2010). "Rimonabant for prevention of cardiovascular events (CRESCENDO): a randomised, multicentre, placebo-controlled trial".Lancet.376 (9740):517–523.doi:10.1016/S0140-6736(10)60935-X.PMID20709233.S2CID36404292.
^Yoshioka T, Fujita T, Kanai T, Aizawa Y, Kurumada T, Hasegawa K, Horikoshi H (February 1989). "Studies on hindered phenols and analogues. 1. Hypolipidemic and hypoglycemic agents with ability to inhibit lipid peroxidation".Journal of Medicinal Chemistry.32 (2):421–428.doi:10.1021/jm00122a022.PMID2913302.
