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Onco-Summaries: Daily Oncology Updates at a Glance
23/03/2026 AstraZeneca & Daiichi Sankyo's ENHERTU received approval in Japan for HER2+ solid cancers AstraZeneca & Daiichi Sankyo's ENHERTU received approval in Japan for HER2+ solid cancers ( Ref ) Japan’s Ministry of Health, Labour and Welfare (MHLW) granted approval to AstraZeneca & Daiichi Sankyo's ENHERTU® (trastuzumab deruxtecan) for the treatment of adult patients with HER2+, advanced or recurrent solid cancers refractory or intolerant to standard treatments. The appro
Oncofocus Team
Mar 241 min read


Onco-Summaries: Daily Oncology Updates at a Glance
15/12/2025 Daiichi Sankyo and AstraZeneca's trastuzumab deruxtecan + pertuzumab has been approved for first-line HER2+ve breast cancer FibroGen's roxadustat received the FDA Orphan Drug Designation for myelodysplastic syndromes Eli Lilly's TECVAYLI plus DARZALEX FASPRO combo has been selected for the FDA's CNPV Pilot program Daiichi Sankyo and AstraZeneca's trastuzumab deruxtecan + pertuzumab has been approved for first-line HER2+ve breast cancer ( Ref ) The US FDA granted ap
Oncofocus Team
Dec 16, 20252 min read


Onco-Summaries: Daily Oncology Updates at a Glance
01/10/2025 The US FDA accepted the sBLA for Enhertu® followed by THP for HER2+ve early-stage Breast Cancer ( Ref ) Daiichi Sankyo and...
Oncofocus Team
Oct 3, 20251 min read


Onco-Summaries: Daily Oncology Updates at a Glance
29/09/2025 In an ~$8B deal, Genmab will acquire Merus in an all-cash transaction ( Ref ) Genmab and Merus announced a transaction...
Oncofocus Team
Sep 29, 20251 min read


Onco-Summaries: Daily Oncology Updates at a Glance
11/09/2025 Daiichi Sankyo and AstraZeneca’s trastuzumab deruxtecan has been accepted for review in the EU for HER2 +ve solid tumors ( Ref...
Oncofocus Team
Sep 12, 20251 min read


Onco-Summaries: Daily Oncology Updates at a Glance
17/07/2025 Johnson & Johnson received Priority Review for TAR-200 from the US FDA in high-risk non-muscle invasive bladder cancer ( Ref )...
Oncofocus Team
Jul 18, 20251 min read
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