Vigil Neuroscience hopes to eventually target ALSP
September 1, 2021
Vigil Neuroscience has revealed the first condition that it will target: a rare, genetic neurodegenerative disorder called ALSP, or adult-onset leukoencephalopathy with axonal spheroids and pigmented glia. The Cambridge, Mass.-based company, which bought the rights to all its current drug candidates from Amgen, also announced a $90 million series
B financing round on Wednesday.
Unveiling Vigil’s first clinical candidate now was entirely a strategic decision, said CEO Ivana Magovčević-Liebisch. Vigil expects to start a Phase 1 safety trial by the end of the year as well as a natural history study — which means generating awareness of the company’s work and the condition itself is a top priority.
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Vigil’s Approach to Patient Engagement
Patients and their caregivers are at the center of our work
We are engaging and collaborating with patient communities, caregivers, and advocacy groups to understand their needs, to inform our research, and to raise awareness.
We strive to alleviate the burden and to improve the lives for those struggling with devastating neurodegenerative diseases.
We recognize the urgency and seek to deliver solutions quickly and safely to patients and caregivers impacted by rare microgliopathies for which there are no treatment options available.