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Linkedin

Ojemda® approved in the EU in R/R pediatric low-grade glioma regardless of BRAF alteration

April 28, 2026

ZEPZELCA + Tecentriq approved for use in Australia and Singapore as 1L maintenance treatment for adult patients with ES-SCLC

April 21, 2026

Blenrep (belantamab mafodotin) approved in China for treatment of 2L+ relapsed/refractory multiple myeloma

April 21, 2026

European Commission Approves KEYTRUDA + Paclitaxel ± Bevacizumab for the Treatment of Adults With PD-L1 (CPS ≥1) Platinum-Resistant Recurrent Ovarian Carcinoma Who Have Received One or Two Prior Systemic Treatment Regimens

April 7, 2026

US FDA Grants Full Approval of Tecartus® for Adult Patients with R/R MCL

April 7, 2026

Japan’s MHLW approves risovalisib (Risovalisib Mesilate Hydrate or Heitzexin) after chemo for ovarian clear cell carcinoma with advanced PIK3CA gene mutations

March 31, 2026

FDA Approves Lifyorli™ (relacorilant) Plus Nab-Paclitaxel for Treatment of Patients with Platinum-Resistant Ovarian Cancer

March 31, 2026

EMA Approves Daratumumab Administration by Patients/Caregivers for Multiple Myeloma

March 31, 2026

ENHERTU Followed by THP Approved in China for the Neoadjuvant Treatment of HER2+ve Breast Cancer

March 31, 2026

Opdivo combination regimens received FDA approval for previously untreated, Stage III or IV cHL and EC approval in R/R cHL after one prior line of therapy

March 24, 2026

Imfinzi approved in the EU in patients with early gastric and gastroesophageal cancers

March 17, 2026

European Commission approves AKEEGA (niraparib & abiraterone dual action tablet) for the treatment of patients with BRCA1/2-mutated metastatic HSPC patients

March 10, 2026

FDA Approves TECVAYLI + DARZALEX FASPRO for R/R 2L Multiple Myeloma

March 10, 2026

SC RYBREVANT approved by European Commission for Q3W and Q4W dosing for patients with advanced EGFR-mutated NSCLC

March 3, 2026

FDA approves HERNEXEOS in 1L HER2-mutant advanced NSCLC

March 3, 2026

FDA tentatively approves AND Application for Lutetium Lu 177 Dotatate (PNT2003) for the treatment of somatostatin receptor-positive GEP-NETs

March 3, 2026

FDA Grants Full Approval to BRAFTOVI Combination Regimen in 1L Metastatic CRC

March 3, 2026

MHRA approves zanidatamab (Ziihera) for the treatment of biliary tract cancer

February 25, 2026

FDA approves monthly RYBREVANT FASPRO™ (amivantamab and hyaluronidase-lpuj) in 1L EGFR+ NSCLC

February 25, 2026

European Commission grants conditional marketing authorization for ANKTIVA + BCG in BCG-unresponsive NMIBC CIS, with or without papillary tumors

February 25, 2026

Calquence + venetoclax approved in the US as oral, fixed-duration combination for 1L CLL patients

February 25, 2026

KEYTRUDA and KEYTRUDA QLEX, Plus Paclitaxel ± Bevacizumab, Approved for 2L/3L PD-L1+ (CPS ≥1) Platinum-Resistant Ovarian Carcinoma 

February 17, 2026

US FDA Approves Novocure’s Optune Pax® for the Treatment of Locally Advanced Pancreatic Cancer

February 17, 2026

FDA Approves Label Update for Yescarta for R/R Primary Central Nervous System Lymphoma

February 9, 2026

FDA Approves Larger Vial Size for Nelarabine IV Administration for the Treatment of T-ALL and T-LBL

February 1, 2026
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Disclaimer: The OTW team takes care to share authentic information. In case of any discrepancies please write to newsletter@onco-this-week.com. Our website is an aggregator for open-source oncology news. The information on our website is provided without any representations or warranties. OTW is part of RLS Consultants, a global consulting and training firm focusing exclusively on the healthcare and life sciences industries. RLS is a leading provider of opportunity assessment services, utilizing its comprehensive expertise in strategic market research, forecasting, and modeling, as well as pricing and market access to facilitate commercial assessments. RLS does not have any influence on any news reported on OTW. The views and opinions expressed in this article are those of the authors and do not necessarily reflect the official policy or position of RLS. The content on our website is intended strictly for news and information purposes only and should not be treated as a substitute for medical advice, diagnosis, or treatment. News shared on OTW should not be utilized in real-world analytic products as they are based only on limited and dated open-source information.