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Oncology

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FDA news and analysis for pharmaceutical BD, investment, and market access · 12 articles on this page

Global oncology market intelligence for pharma BD, investors, and analysts. Track drug approvals, clinical trials, and competitive landscapes.

Showing 229–240 of 246 articles

High impact NewsApr 9, 2026

FDA Approves Opdivo for Advanced Renal Cell Carcinoma

FDA · renal cell carcinoma · 5 min

Dr. Sarah Mitchell
High impact NewsApr 9, 2026

FDA Approves Keytruda for Adjuvant Treatment of Stage III Melanoma

FDA · oncology · 4 min

Dr. Sarah Mitchell
High impact NewsApr 8, 2026

FDA Approves Imfinzi: Breakthrough for Stage III NSCLC Treatment

FDA · Non-Small Cell Lung Cancer · 4 min

Dr. Sarah Mitchell
High impact NewsApr 6, 2026

FDA Approval Tarzenta: Accelerated Approval for Advanced HER2-Negative Breast Cancer

FDA · breast cancer · 7 min

Dr. Sarah Mitchell
High impact NewsApr 5, 2026

FDA Approves Tevimbra: Breakthrough for Esophageal Squamous Cell Carcinoma

FDA · Esophageal Squamous Cell Carcinoma · 5 min

Dr. Sarah Mitchell
High impact NewsApr 5, 2026

FDA Approves Augtyro: Bristol Myers Squibb’s Repotrectinib for ROS1-NSCLC

FDA · Non-Small Cell Lung Cancer · 4 min

Dr. Sarah Mitchell
High impact NewsApr 4, 2026

FDA Grants Priority Review to Sotorasib for KRAS G12C NSCLC

FDA · non-small cell lung cancer · 4 min

Dr. Sarah Mitchell
High impact NewsApr 3, 2026

FDA Approves Bosulif for Pediatric Chronic Myelogenous Leukemia

FDA · chronic myelogenous leukemia · 7 min

Dr. Sarah Mitchell
High impact NewsApr 2, 2026

FDA Approves Opdivo Plus Chemotherapy for Gastric Cancer

FDA · gastric cancer · 4 min

Dr. Sarah Mitchell
High impact NewsApr 2, 2026

FDA Approves Breyanzi: Novel CAR-T Therapy for Mantle Cell Lymphoma

FDA · mantle cell lymphoma · 4 min

Dr. Sarah Mitchell
High impact NewsApr 2, 2026

FDA Approval Mirvetuximab Soravtansine: Accelerated OK for Elahere in Ovarian Cancer

FDA · Ovarian Cancer · 4 min

Dr. Sarah Mitchell
High impact AnalysisApr 1, 2026

CAR-T Cell Therapy Advancements and FDA Regulatory Pathways 2024

FDA · Hematologic Malignancies · 10 min

Dr. Sarah Mitchell