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NASDAQ:CLLS

Cellectis Q1 2025 Earnings Report

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$4.32 +0.50 (+13.09%)
Closing price 03:58 PM Eastern
Extended Trading
$4.28 -0.04 (-1.04%)
As of 04:04 PM Eastern
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Cellectis EPS Results

Actual EPS
-$0.18
Consensus EPS
-$0.15
Beat/Miss
Missed by -$0.03
One Year Ago EPS
N/A

Cellectis Revenue Results

Actual Revenue
$12.03 million
Expected Revenue
$12.71 million
Beat/Miss
Missed by -$683.00 thousand
YoY Revenue Growth
N/A

Cellectis Announcement Details

Quarter
Q1 2025
Time
After Market Closes
Conference Call Date
Monday, May 12, 2025
Conference Call Time
4:00PM 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.

Cellectis Earnings Headlines

Cellectis S.A. Earnings Call: Progress Amid Challenges
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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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