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NASDAQ:CLLS

Cellectis Q3 2025 Earnings Report

Cellectis logo
$1.34 -0.06 (-4.29%)
Closing price 04:00 PM Eastern
Extended Trading
$1.34 0.00 (0.00%)
As of 05:55 PM Eastern
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Cellectis EPS Results

Actual EPS
$0.01
Consensus EPS
-$0.10
Beat/Miss
Beat by +$0.11
One Year Ago EPS
N/A

Cellectis Revenue Results

Actual Revenue
$37.16 million
Expected Revenue
$8.22 million
Beat/Miss
Beat by +$28.95 million
YoY Revenue Growth
N/A

Cellectis Announcement Details

Quarter
Q3 2025
Time
After Market Closes
Conference Call Date
Thursday, November 13, 2025
Conference Call Time
4:30PM ET

Upcoming Earnings

Cellectis' Q3 2026 earnings is estimated for Friday, November 13, 2026, based on past reporting schedules

Earnings Documents

Cellectis Earnings Headlines

Monthly information on share capital and company voting rights
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About Cellectis

Cellectis (NASDAQ:CLLS) is a clinical-stage biotechnology company focused on developing gene-edited, allogeneic cell therapies for the treatment of cancer. The company uses its TALEN gene-editing technology to modify immune cells, including T cells, with the goal of creating “off-the-shelf” therapies that can be manufactured in advance and administered to multiple patients.

Cellectis’ development programs include UCART, or Universal Chimeric Antigen Receptor T-cell, therapies designed to target specific cancer antigens. Its research and development activities cover hematologic malignancies and solid tumors, with programs involving engineered T cells and other genetically modified immune-cell products. The company’s approach is intended to improve the scalability and accessibility of cell therapy compared with treatments manufactured individually for each patient.

Founded in France in 1999, Cellectis has operations and research activities in Europe and the United States and conducts clinical development internationally. The company was co-founded by André Choulika and David Sourdive; David Sourdive has served as chief executive officer. Cellectis has also pursued strategic collaborations to advance the development and potential commercialization of its gene-edited cell therapies.

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