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Linkedin

EC Approves ADCETRIS + AVD combo for Adult Patients with 1L CD30+ Stage III Hodgkin Lymphoma

October 25, 2023

FDA Approves Opdivo® (nivolumab) as Adjuvant Treatment for Eligible Patients with Completely Resected Stage IIB or Stage IIC Melanoma

October 25, 2023

FDA Approves Pfizer’s BRAFTOVI + MEKTOVI for BRAF V600E-Mutant mNSCLC

October 16, 2023

European Commission Approves Enrylaze for the Treatment of Acute Lymphoblastic Leukemia and Lymphoblastic Lymphoma

October 3, 2023

European Commission Approves TEPKINLY (epcoritamab) for Adults with R/R DLBCL

October 3, 2023

MHLW approves Phesgo, the Fixed-Dose Subcutaneous Combination of Perjeta and Herceptin for HER2-Positive Breast and Colorectal Cancer

October 3, 2023

European Commission approved INAQOVI® (oral decitabine and cedazuridine) for the treatment of adults with newly diagnosed acute myeloid leukaemia

September 26, 2023

European Commission Approves ORSERDU in Patients with ER+, HER2- Locally Advanced or Metastatic Breast Cancer with an Activating ESR1 Mutation

September 26, 2023

Calquence approved in China for chronic lymphocytic leukaemia

September 14, 2023

Tecentriq subcutaneous (SC) is approved in Great Britain for all indications of IV Tecentriq, offering a faster, more convenient option to receive treatment

September 6, 2023

European Commission Approves KEYTRUDA + Trastuzumab and Chemo as 1L Treatment for HER2-Positive Advanced GEJ Adenocarcinoma Expressing PD-L1

September 6, 2023

Calquence approved in China for chronic lymphocytic leukaemia

September 6, 2023

Lynparza + abiraterone approved in Japan for the treatment of BRCA-mutated mCRPC

September 1, 2023

LREXFIO™ Receives U.S. FDA Accelerated Approval for R/R Multiple Myeloma

August 23, 2023

European Commission Approves Reduced Dosing Frequency for TECVAYLI (teclistamab)

August 23, 2023

FDA Approves TALVEY™ (talquetamab-tgvs) for the Treatment of Patients with Heavily Pretreated Multiple Myeloma

August 16, 2023

FDA Approves AKEEGA™ (Niraparib and Abiraterone Acetate) for the Treatment of Patients with BRCA-Positive mCRPC

August 16, 2023

European Commission Approves LONSURF® (Trifluridine/tipiracil) in Combination With Bevacizumab in 3rd Line Refractory mCRC

August 9, 2023

Jemperli (dostarlimab) + chemo approved in the US as 1L treatment for dMMR/MSI-H primary advanced or recurrent endometrial cancer

August 9, 2023

European Commission Approves Trodelvy For Pre-Treated HR+/HER2- Metastatic Breast Cancer

August 2, 2023

VANFLYTA First FLT3 Inhibitor Approved in the U.S. Specifically for Patients with Newly Diagnosed FLT3-ITD Positive AML

July 27, 2023

European Commission approves fixed-duration Columvi (glofitamab) for people with R/R DLBCL

July 19, 2023

Enhertu approved in China as the first HER2-directed therapy for patients with HER2-low metastatic breast cancer

July 19, 2023

European Commission Grants Conditional Marketing Authorization for Taiho’s LYTGOBI Tablets for the Treatment of Adults With Cholangiocarcinoma

July 19, 2023

NMPA Approves FUCASO for the Treatment of R/R Multiple Myeloma in China

July 11, 2023
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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.