CRISPR Therapeutics (NASDAQ: CRSP) is a leading gene-editing company focused on developing transformative medicines using CRISPR/Cas9 gene-editing technology. Founded in 2013, the company is headquartered in Boston, Massachusetts, with operations in the US, UK, and Switzerland.
CRISPR Therapeutics (NASDAQ: CRSP) is a leading gene-editing company focused on developing transformative medicines using CRISPR/Cas9 gene-editing technology. Founded in 2013, the company is headquartered in Boston, Massachusetts, with operations in the US, UK, and Switzerland.
Target: Amyloid precursor protein (APP) gene editing
Approach: Reduce Aβ production through gene knockout
Status: Discovery stage
Parkinson's Disease
Target: Alpha-synuclein (SNCA) gene silencing
Approach: Reduce toxic protein aggregation
Status: Discovery stage
Huntington's Disease
Target: Mutant huntingtin (HTT) gene
Approach: Allele-selective editing
Status: Discovery stage
Clinical Progress
| Year | Milestone | |------|-----------| | 2013 | Company founded by Emmanuelle Charpentier | | 2016 | IPO on NASDAQ | | 2018 | First IND submission (CTX001 with Vertex) | | 2020 | Positive Phase 1 data for CTX001 (sickle cell) | | 2023 | FDA approval of Casgevy for sickle cell disease | | 2024 | Multiple CAR-T programs in clinical trials |
Partnerships
Vertex Pharmaceuticals
Focus: Hematopoietic stem cell therapies
Programs: CTX001 for sickle cell and beta-thalassemia
Deal: Up to $2.6B in milestone payments
ViaCyte
Focus: Cell replacement therapy for diabetes
Programs: Encapsulated cell devices with gene editing
Competitive Landscape
| Company | Technology | Focus | |---------|------------|-------| | Editas Medicine | CRISPR/Cas9 | In vivo editing | | Intellia Therapeutics | CRISPR/Cas9 | LNP delivery | | Caribou Biosciences | CRISPR/Cas9 | Off-the-shelf CAR-T | | Beam Therapeutics | Base editing | Precise editing |
FDA Approval
Casgevy (exa-cel)
In December 2023, the FDA approved Casgevy (exagamglogene autotemcel), the first CRISPR-based therapy for sickle cell disease:
Indication: Sickle cell disease
Efficacy: 94% of patients achieved sustained VOC-free outcomes
Manufacturer: CRISPR Therapeutics (partnered with Vertex)
Price: $2.2M per treatment
NeuroWiki Cross-References
CRISPR Gene Editing
[Gene Therapy](/therapeutics/gene-therapy-neurodegeneration) Gene Therapy for Neurological Diseases