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Linkedin

Imfinzi approved in the US for patients with BCG-naïve, high-risk NMIBC

June 2, 2026

European Commission Authorizes Expanded Label for VENCLYXTO® (venetoclax) to Include Additional Combinations in 1L CLL

June 2, 2026

DARZALEX® (daratumumab) injectable approved for administration by patients or caregivers for treatment of multiple myeloma

June 2, 2026

Opdivo in Combination with AVD Receives Expanded EU Label with Approval in Frontline Advanced Classical Hodgkin Lymphoma

June 2, 2026

Datroway approved in the US in 1L metastatic TNBC patients not PD-1/PD-L1 inhibitor candidates

May 26, 2026

US FDA Approves INQOVI® in Combination with Venetoclax in AML Patients Ineligible for Intensive Induction Chemo

May 21, 2026

Enhertu approved for use before surgery based on DESTINY-Breast11 Ph 3 trial and following surgery based on DESTINY-Breast05 Ph 3 trial in HER2-positive early breast cancer

May 21, 2026

BEQALZI™ (sonrotoclax) Approved by US FDA for R/R Mantle Cell Lymphoma

May 21, 2026

FDA Approves BIZENGRI® (Zenocutuzumab-zbco) for NRG1 Fusion-Positive Cholangiocarcinoma Following Receipt of FDA Commissioner’s National Priority Voucher

May 12, 2026

FDA Approves VEPPANU (vepdegestrant) for the Treatment of ESR1m, ER+/HER2- Advanced Breast Cancer

May 6, 2026

FDA Approves Jakafi XR™ (ruxolitinib) Extended-Release Tablets for the Treatment of Myelofibrosis

May 6, 2026

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
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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.