CervoMed's neflamapimod gains inclusion in UK's accelerated ALS clinical trial platform

GlobeNewswire Inc.GlobeNewswire Inc.
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Key Takeaway

CervoMed's neflamapimod selected for UK's accelerated EXPERTS-ALS trial platform. The drug will be evaluated in 35-80 ALS patients over 18-24 weeks.

CervoMed's neflamapimod gains inclusion in UK's accelerated ALS clinical trial platform

CervoMed Inc. has secured a position in the EXPERTS-ALS platform, a government-backed clinical trial initiative designed to expedite the evaluation of potential treatments for amyotrophic lateral sclerosis. The selection marks a significant milestone for the company's investigational drug neflamapimod, which demonstrated promising results in previous trials for dementia with Lewy bodies.

The EXPERTS-ALS trial will initially enroll approximately 35 ALS patients for an evaluation period spanning 18 to 24 weeks, with provisions for potential expansion to 80 participants pending interim results. The trial structure reflects the platform's goal of rapidly identifying effective therapies for the progressive neurodegenerative disease. CervoMed's nomination was based on neflamapimod's mechanism of action and its clinical performance data from earlier-stage development.

The inclusion represents an opportunity for neflamapimod to advance through a streamlined development pathway while contributing to the broader landscape of ALS therapeutic options. The EXPERTS-ALS platform continues to serve as a vehicle for bringing promising candidates to clinical evaluation more efficiently than traditional trial structures.

Source: GlobeNewswire Inc.

Back to newsPublished Feb 18

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