Press Releases September 10, 2026 01:00 PM

Cullinan Therapeutics to Host Virtual Analyst and Investor Event to Showcase Zipalertinib Plus Chemotherapy Phase 3 REZILIENT3 Data Presented at the IASLC 2026 World Conference on Lung Cancer

Cullinan Therapeutics to present positive interim Phase 3 data for zipalertinib plus chemotherapy in EGFR exon 20 insertion NSCLC at IASLC 2026, followed by virtual investor event

By Jordan Park
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CGEM

Cullinan Therapeutics announced that its Phase 3 REZILIENT3 trial of zipalertinib plus chemotherapy for first-line treatment of EGFR exon 20 insertion mutation-positive non-small cell lung cancer (NSCLC) met its primary endpoint of progression-free survival at planned interim analysis. The results will be presented in a Presidential Symposium at the IASLC 2026 World Conference on Lung Cancer. A virtual event for analysts and investors will be held to discuss these encouraging data.

Cullinan Therapeutics to Host Virtual Analyst and Investor Event to Showcase Zipalertinib Plus Chemotherapy Phase 3 REZILIENT3 Data Presented at the IASLC 2026 World Conference on Lung Cancer
CGEM
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Key Points

  • Phase 3 REZILIENT3 trial of zipalertinib plus chemotherapy met primary endpoint of progression-free survival in NSCLC with EGFR exon 20 insertion mutation.
  • Results to be presented in a prestigious Presidential Symposium at IASLC 2026 conference.
  • Cullinan is hosting a virtual analyst and investor event to discuss interim data impact and future plans.
  • Advances affect oncology sector, particularly targeted lung cancer therapies and biopharmaceutical development.

Results from the planned interim analysis of the Phase 3 REZILIENT3 trial of zipalertinib plus chemotherapy in first-line EGFR exon 20 insertion mutation NSCLC to be presented in Presidential Symposium 2 on Sunday, September 13, 2026

Company to host a virtual event on Monday, September 14, 2026, at 8:00 a.m. ET

CAMBRIDGE, Mass., Sept. 10, 2026 (GLOBE NEWSWIRE) -- Cullinan Therapeutics, Inc. (Nasdaq: CGEM), a clinical-stage biopharmaceutical company accelerating potential first- or best-in-class, disease-modifying T cell engagers in autoimmune diseases and cancer, today announced that it will host a virtual event for analysts and institutional investors on Monday, September 14, 2026, at 8:00 a.m. ET to discuss the results from the planned interim analysis of the Phase 3 REZILIENT3 trial presented in Presidential Symposium 2 at the International Association for the Study of Lung Cancer’s (IASLC) 2026 World Conference on Lung Cancer (WCLC), being held September 12-15, 2026 in Seoul, South Korea.

As previously announced, the Phase 3 REZILIENT3 trial of zipalertinib plus chemotherapy in the first-line treatment of patients with epidermal growth factor receptor (EGFR) exon 20 insertion mutation-positive non-small cell lung cancer (NSCLC) met its primary endpoint of progression-free survival at a planned interim analysis.

Virtual Event Details

Cullinan Therapeutics will host a virtual event for analysts and institutional investors on Monday, September 14, 2026, at 8:00 a.m. ET, following the Presidential Symposium presentation. Participants from Cullinan Therapeutics include Nadim Ahmed, Chief Executive Officer, Jeffrey Jones, MD, MBA, Chief Medical Officer.

A live webcast will be available via the events page of Cullinan Therapeutics’ investor relations website at https://investors.cullinantherapeutics.com/events. A replay will be archived on the website following the event.

About Cullinan Therapeutics

Cullinan Therapeutics, Inc. (Nasdaq: CGEM) is a biopharmaceutical company developing potential first- or best-in-class, disease-modifying T cell engagers for autoimmune diseases and cancer. Cullinan pursues promising therapeutic targets while leveraging core expertise in T cell engagers, which are established in oncology and are now advancing into autoimmune diseases. With a clinical-stage pipeline built on a rigorous scientific approach and purposeful innovation, Cullinan is advancing its mission to deliver new standards of care for patients. Learn more about Cullinan at https://cullinantherapeutics.com/, and follow Cullinan on LinkedIn and X.

Contacts

Cullinan Therapeutics
Investors
Nick Smith
+1 401.241.3516
[email protected]

Media
Rose Weldon
+1 215.801.7644
[email protected]


Risks

  • Interim analysis results may not guarantee final trial success or regulatory approval, introducing clinical development risk.
  • Market competition from other therapies targeting EGFR exon 20 insertion mutation NSCLC could impact commercial success.
  • Uncertainties in FDA and global regulatory review processes and timelines could delay product availability and market adoption.

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