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https://www.businesswire.com/news/home/20260130221586/en/Exelixis-Announces-U.S.-FDA-Accepted-the-New-Drug-Application-for-Zanzalintinib-in-Combination-with-an-Immune-Checkpoint-Inhibitor-for-Patients-with-Metastatic-Colorectal-Cancer

BUSINESSWIRE
02 Feb 2026
Natera Submits Signatera CDx PMA to FDA
Natera Submits Signatera CDx PMA to FDA

02 Feb 2026

// BUSINESSWIRE

https://www.businesswire.com/news/home/20260129560151/en/Natera-Submits-Signatera-CDx-PMA-to-FDA

BUSINESSWIRE
02 Feb 2026

https://www.globenewswire.com/news-release/2026/01/12/3216966/0/en/Oncolytics-Biotech-Announces-Updated-Clinical-Data-from-GOBLET-Cohort-4-Demonstrating-Activity-of-Pelareorep-Plus-Atezolizumab-in-Third-Line-Anal-Cancer.html

GLOBENEWSWIRE
12 Jan 2026

https://www.indianpharmapost.com/drug-approval/chugais-tecentriq-gets-green-light-in-japan-for-hard-to-treat-thymic-carcinoma-18691

INDPHARMAPOST
27 Dec 2025

https://www.businesswire.com/news/home/20251119270996/en/KaliVir-Immunotherapeutics-Announces-Clinical-Trial-Collaboration-and-Supply-Agreement-with-Roche-to-Evaluate-VET3-TGI-in-Combination-with-Atezolizumab-Tecentriq-in-Advanced-Solid-Tumors

BUSINESSWIRE
19 Nov 2025

https://www.globenewswire.com/news-release/2025/11/07/3183723/0/en/Xilio-Therapeutics-Announces-Late-Breaking-Phase-2-Data-for-Vilastobart-in-Patients-with-MSS-mCRC-and-High-Plasma-Tumor-Mutational-Burden-at-Society-for-Immunotherapy-of-Cancer-SIT.html

GLOBENEWSWIRE
07 Nov 2025