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NASDAQ:CLLS

Cellectis Q2 2024 Earnings Report

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$4.24 +0.43 (+11.13%)
As of 02:15 PM Eastern
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Cellectis EPS Results

Actual EPS
-$0.28
Consensus EPS
-$0.33
Beat/Miss
Beat by +$0.05
One Year Ago EPS
N/A

Cellectis Revenue Results

Actual Revenue
$9.50 million
Expected Revenue
$6.00 million
Beat/Miss
Beat by +$3.50 million
YoY Revenue Growth
N/A

Cellectis Announcement Details

Quarter
Q2 2024
Time
N/A
Conference Call Date
Tuesday, August 6, 2024
Conference Call Time
10:30AM ET

Upcoming Earnings

Cellectis' Q3 2025 earnings is scheduled for Monday, November 3, 2025, with a conference call scheduled on Tuesday, November 4, 2025 at 8:00 AM ET. Check back for transcripts, audio, and key financial metrics as they become available.

Earnings Documents

Cellectis Earnings Headlines

Cellectis S.A. Earnings Call: Progress Amid Challenges
Trump’s national nightmare is here
Porter Stansberry and Jeff Brown say a new U.S. national emergency is already underway — and it could trigger the biggest forced rotation of capital since World War II. They reveal why Trump is mobilizing America’s tech giants… and name the two stocks most likely to soar as trillions shift behind the scenes.tc pixel
Cellectis S.A. (CLLS) Q2 2025 Earnings Call Transcript
See More Cellectis Headlines
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About Cellectis

Cellectis (NASDAQ:CLLS) is a clinical‐stage biopharmaceutical company specializing in the development of gene‐edited cell therapies for oncology. Founded in 1999 and headquartered in Paris, France, the company also maintains operations in New York City and Raleigh, North Carolina. Cellectis applies its proprietary TALEN genome editing platform to engineer allogeneic chimeric antigen receptor T‐cell (CAR‐T) candidates designed to target blood cancers and solid tumors.

The company’s core business activities encompass the discovery, development and manufacturing of off‐the‐shelf immunotherapies. Its pipeline includes multiple CAR‐T candidates, such as those targeting CD19 and CD22 antigens for B‐cell malignancies and other programs addressing acute myeloid leukemia. Cellectis advances these investigational therapies through preclinical research and early‐ to mid‐stage clinical trials, often in partnership with leading pharmaceutical firms to enhance development and commercialization capabilities.

Cellectis operates research and process development laboratories as well as GMP manufacturing facilities across Europe and North America. Clinical trials are conducted in premier cancer centers in the United States and Europe, reflecting the company’s global reach. Strategic collaborations and licensing agreements support the expansion of its gene‐edited therapies into new indications and geographic markets, with an emphasis on scalable production and regulatory readiness.

Under the leadership of founder and Chief Executive Officer Dr. André Choulika, Cellectis has established itself as a pioneer in TALEN‐based genome editing. The management team combines scientific and commercial expertise to drive innovation, with a focus on delivering next‐generation allogeneic CAR‐T therapies to patients worldwide.

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