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CRISPR Therapeutics
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Latest analysis
Updated Nov 2, 2026
CASGEVY hits $99M quarterly revenue (30% QoQ) as CTX310 RMAT designations and imminent Phase 1b readout mark CRISPR Therapeutics' pipeline inflection point.
CASGEVY delivered $99 million in Q3 2026 revenue — nearly six times the prior-year quarter — driven by patient volume doubling in the first nine months versus all of 2025 and new approvals for children as young as 2. The FDA's dual RMAT designations for CTX310 in severe hypertriglyceridemia and elevated LDL-C, combined with an AHA Phase 1b data readout on November 9, represent the most significant near-term clinical catalyst for CRISPR Therapeutics beyond CASGEVY. Zugo-cel data in systemic sclerosis and completed enrollment in the CTX611 Phase 2 trial add further pipeline optionality at a moment when the company holds $2.3 billion in cash.
Tone: bullishRevenue
$3.5M
CRSP 10-K · FY 2025
Revenue FY2024
$37.3M
Headquarters
Zug, Switzerland
Profile
CRSP 10-K Item 1 · Feb 12, 2026CRISPR Therapeutics AG is a Swiss-incorporated biopharmaceutical company focused on developing CRISPR/Cas9-based gene-editing therapeutics for serious diseases. Its most advanced product, CASGEVY, is the world's first approved CRISPR therapy, co-developed and co-commercialized with Vertex Pharmaceuticals for sickle cell disease and transfusion-dependent beta thalassemia. The company is advancing a pipeline spanning in vivo liver editing, allogeneic CAR T cell therapy, siRNA programs, and regenerative medicine.
Read filing description ↓ Collapse description ↑
Our mission is to create transformative gene-based medicines for serious human diseases. We are a leading biopharmaceutical company focused on the development of CRISPR-based therapeutics, including by using CRISPR/Cas9 technology. CRISPR/Cas9 is a revolutionary technology for gene editing, the process of precisely altering specific sequences of genomic DNA. We have advanced this technology from discovery to an approved medicine with unparalleled speed, culminating in the landmark first approval of a CRISPR-based therapy, CASGEVY (exagamglogene autotemcel [exa-cel]), in 2023 with our collaborators at Vertex Pharmaceuticals Incorporated, or Vertex. We have established a portfolio of therapeutic programs spanning four core franchises: hemoglobinopathies, in vivo, CAR T approaches and regenerative medicine. Depending on the program, we take either an ex vivo approach, in which we edit cells outside of the human body before administering them to the patient, or an in vivo editing approach, where we deliver the CRISPR-based therapeutic directly to target cells within the human body. We continue to innovate on our platform to develop next-generation technologies that can enable new therapies. We are developing other technologies, including delivery technologies and other gene editing technologies, like SyNTase. Through our efforts, we aim to unlock the full potential of gene-based therapeutics to create medicines that can transform people's lives. We believe that our innovative research, translational expertise, and clinical development experience, position us as a leader in the development of CRISPR-based therapeutics and may enable us to create an entirely new class of highly effective and potentially curative therapies for patients with both common and rare diseases for whom current biopharmaceutical approaches have had limited success.
Primary products
- CASGEVY (exagamglogene autotemcel [exa-cel])
- zugocabtagene geleucel (zugo-cel; formerly CTX112)
- CTX310
- CTX611 (formerly SRSD107)
- CTX340
- CTX321
Business segments
End markets
Geographies
Named customers
Named competitors
“We believe that our technology, development experience and scientific knowledge provide us with competitive advantages, we currently face, and will continue to face, substantial competition from many different sources, including large pharmaceutical, specialty pharmaceutical and biotechnology companies; academic institutions and governmental agencies; and public and private research institutions, some or all of which may have greater access to capital or resources than we do.” Competitive position, as stated in the filing
Revenue commentary · FY 2025
Total revenue fell sharply in 2025 to $3.5 million from $37.3 million in 2024, driven by the absence of any collaboration revenue in 2025 versus $35.0 million in collaboration revenue in 2024, with only grant revenue of $3.5 million recognized in 2025.
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