CRISPR Therapeutics logo — Gene-based medicines for patients with serious diseases

CRISPR Therapeutics

Gene-based medicines for patients with serious diseases

Founded 2013 United States Boston, United States 350 employees IPO Total: $1.05B Biopharma, Biotechnology

General Information

Company Name CRISPR Therapeutics
Founded Year 2013
Location United States Boston, United States +4
Founders / Decision Makers
Team member
Employees 350
Industries Biopharma, Biotechnology
Funding Stage IPO
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AI Insight

Bounce Watch AI
2 months ago

CRISPR Therapeutics has recently secured substantial post-IPO convertible funding of over $585M, closely following a pivotal FDA approval for expanded use of their gene-edited treatment, CASGEVY®, in younger pediatric populations. This strategic timing, combined with active hiring efforts for 15 positions, strongly indicates a dynamic shift towards scaling commercial operations and accelerating market penetration for their groundbreaking therapy. The company is actively positioning itself for significant growth and broader patient access.

Signal Types
Funding Regulatory Approval Hiring
Strategic Labels
Market Expansion Commercialization Talent Acquisition
Next Move: Expansion
·
Impact: 9/10
·
Ideal For: Public Market Biotech Investors — Growth Equity

About CRISPR Therapeutics

CRISPR Therapeutics, a leader in biopharma and biotechnology, stands at the forefront of creating gene-based medicines for patients with serious diseases. Since its founding in 2013, the company has not only evolved but thrived by leveraging CRISPR technology, a Nobel Prize-winning innovation that has reshaped biomedical research.

The company's diverse portfolio includes groundbreaking therapies targeting hemoglobinopathies, oncology, regenerative medicine, cardiovascular, autoimmune, and rare diseases. Notably, CRISPR Therapeutics made history with its CRISPR/Cas9 gene-edited therapy for sickle cell disease and beta thalassemia, receiving broad approval for CASGEVY® (exagamglogene autotemcel [exa-cel]) in late 2023.

Headquartered in the United States, the company maintains strong R&D operations in Boston and San Francisco. Strategic partnerships, including those with Vertex Pharmaceuticals, have bolstered its efforts. CRISPR Therapeutics recently secured a $585.20M post-IPO convertible investment, positioning itself for further growth and innovation.

Taxonomy: Gene-based Medicines, CRISPR Technology, Gene Editing, Hematology, Oncology, Regenerative Medicine, Cardiovascular Diseases, Autoimmune Diseases, Rare Diseases, Transfusion-Dependent Beta Thalassemia, Sickle Cell Disease, Biopharmaceuticals, CRISPR/Cas9 Platform, Strategic Partnerships, Nobel Prize-winning Innovations

Services & Products

Development of gene-based medicines
Gene-editing therapies
Clinical and preclinical research
Patient advocacy

Target Customers

Patients with serious diseases Healthcare providers Biotechnology companies Research institutions

Funding Rounds & Investors (7)

View All
Funding Stage Amount Investors Lead Investors Date
Post Ipo Convertible •••••• - 01 Mar 2026
Post Ipo Equity •••••• 2
Investor Investor
01 Feb 2024
Grant •••••• 1
Investor
01 Dec 2020
IPO •••••• - 01 Oct 2016
Series B •••••• 6
Investor Investor Investor Investor Investor
•••• ••••
01 Jun 2016

View All 7 Funding Rounds

CRISPR Therapeutics Alternatives & Competitors

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FAQ About CRISPR Therapeutics

Gene-based medicines for patients with serious diseases
CRISPR Therapeutics was founded in 2013.
CRISPR Therapeutics is headquartered in Boston, United States.
CRISPR Therapeutics operates in the following industries: Biopharma, Biotechnology.
CRISPR Therapeutics has approximately 350 employees.
CRISPR Therapeutics has completed 7 funding rounds, raising a total of $1.05B. The latest funding stage is IPO.
CRISPR Therapeutics offers: Development of gene-based medicines, Gene-editing therapies, Clinical and preclinical research, Patient advocacy.
Top alternatives and competitors to CRISPR Therapeutics include Casebia Therapeutics, Ligandal, ASC Therapeutics, SNIPR Biome - A CRISPR Company, HuidaGene Therapeutics. These companies operate in related industries and serve comparable markets. You can compare them side by side on Bounce Watch.
CRISPR Therapeutics and Casebia Therapeutics are both companies in similar industries. Compare their funding, team size, growth signals, and market position on Bounce Watch to see which one fits your needs.

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