Promising New Research Offers Hope for Opioid Use Disorder Treatment
Synopsis
Key Takeaways
- New research into GLP-1 receptor agonists shows promise for opioid use disorder.
- Phase I trial reported a 40% reduction in cravings.
- GLP-1RAs initially developed for diabetes management.
- Potential to address other neurological conditions as well.
- Current treatment landscape for OUD lacks innovation.
New Delhi, Feb 25 (NationPress) Recent investigations into the GLP-1 receptor unveil exciting new therapeutic options for addressing opioid use disorder (OUD), according to a report released on Tuesday.
A three-week Phase I trial conducted at the Caron Treatment Centers in Pennsylvania, USA, involved 20 participants in residential treatment for OUD, examining the efficacy of Novo Nordisk’s Saxenda (liraglutide), a GLP-1 receptor agonist (GLP-1RA), as a standalone treatment for OUD.
The findings indicated its potential to compete with existing therapies, revealing a 40 percent decrease in opioid cravings among participants administered Saxenda, as reported by GlobalData, a prominent data and analytics firm.
Initially designed for diabetes management, GLP-1RAs function by enhancing insulin secretion and inhibiting glucagon release, thus aiding blood sugar regulation.
“Nevertheless, GLP-1 receptors are present in the brain's mesolimbic system, closely associated with motivation and reward. This has attracted the attention of pharmaceutical developers eager to broaden their product labels to address the opioid epidemic,” stated Jos Opdenakker, a pharma analyst at GlobalData.
Preliminary clinical studies suggest that GLP-1RAs represent a promising new direction in the management of OUD, given that the current treatment landscape is hindered by a shortage of innovation and a heavy dependence on opioid agonist therapies, he emphasized.
According to GlobalData’s Drug Database, six out of seven agents currently in late-stage development (Phase IIb–III) are non-opioid alternatives.
At present, there is a significant lack of efficacy data for many upcoming agents. Thus, despite the presence of non-opioids, a high-efficacy non-opioid treatment for OUD remains a valuable opportunity.
In addition to OUD, GLP-1RAs are being explored for other neurological conditions, including Alzheimer’s disease and related cognitive impairments, Parkinson’s disease, alcohol dependence, peripheral neuropathy, and intracranial hypertension.
Developers are increasingly recognizing the potential of GLP-1RAs, leading to the emergence of a new class of neurological treatments.