Research programme: in vivo gene editing therapies - Capsida Biotherapeutics/CRISPR Therapeutics
Latest Information Update: 24 Mar 2022
At a glance
- Originator Capsida Biotherapeutics; CRISPR Therapeutics
- Class Gene therapies
- Mechanism of Action Gene modulators
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Orphan Drug Status
Orphan designation is assigned by a regulatory body to encourage companies to develop drugs for rare diseases.
- New Molecular Entity No
Highest Development Phases
- Research Amyotrophic lateral sclerosis; Friedreich's ataxia
Most Recent Events
- 24 Mar 2022 Capsida Biotherapeutics has patent protection for Adeno-associated virus compositions for targeted gene therapy in the US
- 15 Jun 2021 CRISPR Therapeutics and Capsida Biotherapeutics agree to co-promote and co-develop in vivo gene editing therapies for Amyotrophic lateral sclerosis and Friedreich’s ataxia
- 15 Jun 2021 Early research in Amyotrophic lateral sclerosis in USA (Parenteral)