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CRISPR Therapeutics Q4 Earnings and Revenues Surpass Estimates

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CRISPR Therapeutics CRSP reported fourth-quarter 2024 loss of 44 cents per share, narrower than the Zacks Consensus Estimate of a loss of $1.15. In the year-ago period, the company recorded earnings of $1.10 per share on account of higher collaboration revenues.

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Total revenues, comprising grant and collaboration revenues, amounted to $35.7 million in the quarter, which surpassed the Zacks Consensus Estimate of $10 million. In the year-ago period, the company recorded total revenues of $201.2 million, primarily comprising collaboration revenues received from Vertex Pharmaceuticals VRTX in connection with the approval of Casgevy for two blood disorder indications.

More on CRSP’s Q4 Earnings

Research and development expenses fell 14% year over year to $82.2 million. This was due to reduced variable external research and manufacturing costs.

General and administrative expenses increased 10% year over year to $18.1 million in the quarter.

CRISPR Therapeutics did not record any collaboration expense for the fourth quarter of 2024, as it had reached the cost deferral limit for the Casgevy program in the previous quarter.

As of Dec. 31, 2024, the company had cash, cash equivalents and marketable securities worth $1.90 billion compared with $1.94 billion as of Sept. 30, 2024.

Shares of CRISPR Therapeutics have lost 20.4% in the past three months compared with the industry’s decline of 7.9%.

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CRSP’s Full-Year 2024 Results

For 2024, CRISPR Therapeutics generated total revenues of $37.3 million, reflecting a substantial decrease over the previous year’s revenues of $371.2 million, fueled by high collaboration revenues from Vertex.  

For the same period, the company reported a loss of $4.34 per share, wider than the year-ago loss of $1.94.

CRSP/VRTX’s Strong Global Launch Efforts for Casgevy

CRISPR Therapeutics and partner Vertex’s one-shot ex-vivo gene therapy, Casgevy, was approved in late 2023/early 2024 for two blood disorders — sickle cell disease and transfusion-dependent beta thalassemia — in the United States, Europe and several other countries. VRTX leads the global development and commercialization of Casgevy under the terms of the 2021 agreement with support from CRSP.

Per management, more than 50 authorized treatment centers (ATCs) have been activated globally as of the end of 2024 and more than 50 patients have already had at least one cell collection across all regions. New patient starts are expected to grow significantly throughout 2025. During its fourth-quarter earnings release on Monday, Vertex recorded $8 million in product revenues from Casgevy sales.