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GO2 for Lung Cancer Awarded AstraZeneca US ACT on Health Equity Grant to Advance Community-Driven Lung Cancer Screening

2026-02-12T10:55:33-06:00February 12th, 2026|News, Press Releases|

Innovative “SDM Circles” program integrates restorative justice practices to address medical mistrust and improve lung cancer screening among Black communities  WASHINGTON, DC – February 12, 2026 – GO2 for Lung Cancer (GO2) has received support from AstraZeneca US through its 2025 [...]

FDA Approves New Administration Method for Rybrevant (amivantamab) 

2025-12-18T16:07:50-06:00December 18th, 2025|Hot Topics, News, Science and Research|

On December 17, 2025, the U.S. Food and Drug Administration (FDA) approved Rybrevant Faspro (amivantamab and hyaluronidase-lpuj) for subcutaneous injection, commonly known as a shot. This approval included all the same uses of Rybrevant (amivantamab) that the FDA previously approved for adults with metastatic non-small cell lung cancer (NSCLC) whose tumors have an [...]

FDA Approves a New Combination Treatment for Extensive-Stage Small Cell Lung Cancer 

2025-10-03T09:50:38-05:00October 3rd, 2025|Hot Topics, News, Science and Research, Small Cell Lung Cancer|

On October 2, 2025, the U.S. Food and Drug Administration (FDA) approved Zepzelca (lurbinectedin) in combination with Tecentriq (atezolizumab) or Tecentriq Hybreza (atezolizumab and hyaluronidase-tqjs) as maintenance therapy for adult patients with extensive-stage small cell lung cancer (ES-SCLC) whose disease [...]

Statement from GO2 for Lung Cancer on the Government Shutdown and Its Impact on Lung Cancer Research Funding 

2025-10-01T09:10:08-05:00October 1st, 2025|Advocacy in Action, Hot Topics, News|

It’s heartbreaking that our elected leaders can’t find common ground on something as important as the health and well-being of the cancer community. A government shutdown once again puts vital lung cancer research and access to care at risk. This [...]

FDA Approves New Administration Method for Keytruda (pembrolizumab)

2025-09-22T11:46:06-05:00September 22nd, 2025|Hot Topics, News, Science and Research|

On September 19, 2025, the U.S. Food and Drug Administration (FDA) approved a new administration method for Keytruda (pembrolizumab). Under the new approval, Keytruda Qlex (pembrolizumab and berahyaluronidase alfa-pmph) can now be given by subcutaneous injection, commonly known as a shot, [...]

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