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MavriX Bio

Ownership: Private
Development stage: Commercial

Overview

MavriX Bio is advancing MVX-220, an investigational adeno-associated virus (AAV) gene replacement therapy for Angelman syndrome. The FDA has cleared its IND application, enabling the first clinical trial in humans. This represents a significant milestone as there are currently no approved disease-modifying treatments for Angelman syndrome. Clinical trial details and timelines will be announced soon.

Therapeutic areas: Neurology
Modalities: Gene therapyAdeno-associated virus (AAV) gene therapyBiologic (as AAV vectors are biologics)
Industry: Biotech

Drug pipeline

1 asset

MVX-220

Unknown

Partnerships

FAST / AS²Bio acceleratorresearch foundation support from Dr. Jim Wilson’s laboratory at University of Pennsylvania/Gemma Bio

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