Low start dose of Amgen experimental weight-loss drug limits side effects
June 23 (Reuters) - People started on a low dose of Amgen's long-acting experimental obesity drug MariTide lost as much weight as those given high doses but with milder side effects, according to full results of a mid-stage trial presented at a medical meeting on Monday.
As a result, Amgen (AMGN.O), opens new tab said its recently launched 72-week Phase 3 trial will randomize obese or overweight adults to three different doses, with each group started at a much lower dose that will be increased over an eight-week period.
"MariTide is a long-acting drug, but side effects are short-lived, which is a great learning and gives us confidence to go into Phase 3," Jay Bradner, executive vice president of research and development at Amgen, told Reuters.
The company previously announced top-line results from the year-long Phase 2 trial showing that MariTide, injected monthly or every other month, helped overweight or obese patients shed up to 20% of their body weight.
The full results were presented at the American Diabetes Association meeting in Chicago and published in the New England Journal of Medicine.
The data show that for people with type 2 diabetes, MariTide lowered blood sugar by up to 2.2 percentage points. Amgen said weight loss with MariTide also improved pre-specified cardiometabolic measures, including waist circumference, blood pressure, inflammation markers and blood lipids.
MariTide is an antibody linked to a pair of peptides that activates receptors for the appetite- and blood sugar-reducing hormone GLP-1 while simultaneously blocking a second gut hormone called GIP.
Amgen said no new safety signals were identified in the study and tolerability was consistent with the GLP-1 class, which is associated with gastrointestinal side effects such as nausea.
In late-stage trials, Novo Nordisk's (NOVOb.CO), opens new tab GLP-1 obesity drug Wegovy had a vomiting rate of 24%, while Eli Lilly's (LLY.N), opens new tab Zepbound, which is designed to activate both GLP-1 and GIP, had a rate of 13%. Each of those drugs are given as weekly injections.
In the mid-stage MariTide study, vomiting was reported by nearly 90% of patients started at the highest tested dose, compared with 50% of patients ramped up to a full dose in one step and 22% of those brought to their target dose over eight weeks.
Amgen said trial discontinuation rates due to gastrointestinal issues of up to 7.8% were lower for groups treated with escalating doses.
The company said it plans to start additional Phase 3 studies this year for MariTide in patients with a variety of serious health issues, including cardiovascular disease caused by clogging arteries, heart failure, and obstructive sleep apnea.
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