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Intellectia

CGEM News

Cullinan Therapeutics Q4 Earnings Miss Expectations

19h agoseekingalpha

Growth Prospects for the EGFR-NSCLC Market Analyzed

Feb 11 2026Newsfilter

Major Stocks on the Rise Monday: Paramount Skydance, Wave Life Sciences, Ocular Therapeutix, Carvana, and More

Dec 08 2025Benzinga

Cullinan Therapeutics' CLN-049 Shows 31% Complete Response Rate in R/R AML Patients

Dec 08 2025Globenewswire

Cullinan Therapeutics' CLN-049 Shows 31% Complete Response Rate in R/R AML Patients

Dec 08 2025Newsfilter

Cullinan Secures FDA Fast Track Designation for CLN-049 in Relapsed/Refractory AML

Dec 01 2025NASDAQ.COM

Cullinan Receives FDA Fast Track Designation for CLN-049 in AML Treatment

Dec 01 2025Newsfilter

Cullinan Therapeutics Receives Fast Track Designation for CLN-049

Dec 01 2025NASDAQ.COM

CGEM Events

03/10 07:10
Cullinan Expects Cash Resources to Last Until 2029
Cash, cash equivalents, short- and long-term investments, and interest receivable were $439.0 million as of December 31, 2025. Cullinan expects its cash resources to provide runway into 2029 under its current operating plan.
03/10 07:10
Cullinan Therapeutics Set to Deliver Multiple Value-Driving Catalysts by 2026
"Cullinan Therapeutics is poised to deliver multiple value-driving catalysts across our programs throughout 2026. Strong enrollment momentum for CLN-978 positions us to deliver the first company-sponsored data for a potential best-in-class CD19 T cell engager in autoimmune diseases in the second quarter, followed by important additional data updates throughout the year. CLN-978 is the ideal therapy for immune reset, with the optimal combination of target, CD19, and modality, T cell engager, together with the convenience of subcutaneous administration. This program has the potential to transform the treatment landscape in autoimmune diseases and deliver a compelling commercial opportunity," said Nadim Ahmed, President and CEO of Cullinan Therapeutics. "We are also pleased to begin the year with strong momentum in our oncology portfolio. With our partner, Taiho, we have completed the second line rolling NDA submission for zipalertinib and have fully enrolled the frontline study, REZILIENT3, both important milestones as zipalertinib moves closer to being available for patients. Finally, after sharing compelling clinical data at ASH 2025 and with U.S. FDA Fast Track Designation, we expect to rapidly advance CLN-049 to registrational development in AML."

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