Development leap in addressing neurological conditions

This first-in-human study aims to assess the safety, tolerability, pharmacokinetics, and pharmacodynamics of NBI-1117567 in healthy adult participants.

The compound, a muscarinic M1 preferring (M1/M4) selective agonist, holds promise for addressing cognitive symptoms in patients with neurological and neuropsychiatric conditions.

Muscarinic receptors, pivotal in various bodily functions including brain activity, have long been targeted for treating cognitive and neuropsychological symptoms associated with diseases like Schizophrenia, Alzheimer’s, and Parkinson’s.

Previous attempts hindered by side effects

However, previous attempts at developing selective agonists have been hindered by side effects linked to the activation of other receptor subtypes. NBI-1117567, with its purported selectivity for M1 and M4 receptors, represents a breakthrough in this regard, potentially offering effective treatment options without the drawbacks of previous compounds.

The collaboration and licensing agreement between Nxera Pharma and Neurocrine Biosciences, established in November 2021, underpin this developmental leap. Neurocrine holds global development and commercialization rights to a range of muscarinic receptor agonists discovered by Nxera, while Nxera retains rights to develop M1 agonists in Japan. Under the terms of the agreement, Nxera stands to receive substantial R&D funding, development milestones, and royalties, contingent upon meeting specified criteria.

This development highlights the collaborative effort between pharmaceutical entities in advancing innovative therapies for addressing unmet medical needs in neurological and neuropsychiatric disorders. As the Phase 1 clinical study progresses, stakeholders anticipate further insights into the therapeutic potential of NBI-1117567 and its role in transforming treatment paradigms for cognitive symptoms associated with neurological conditions.

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