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BioWorld - Sunday, March 29, 2026
Home » Topics » Disease categories and therapies » Cancer

Cancer
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Encouraging phase II results seen with bomedemstat in essential thrombocythemia, myelofibrosis

June 30, 2021

Antitumor activity of novel prodrug TRN-000546

June 30, 2021

Henan Zhiwei Biomedicine, Henan Normal University patent Bruton tyrosine kinase inhibitors

June 30, 2021

Medshine Discovery identifies new ERK-2 inhibitors

June 30, 2021

Shanghai Yingli Pharmaceutical describes new GTPase KRAS inhibitors

June 30, 2021

Wigen Biomedicine Technology presents new Aurora kinase inhibitors

June 30, 2021
Green approved stamp

China grants first CAR T approval to Fosun Kite

June 29, 2021
By Elise Mak
China’s drug regulator granted a first CAR T therapy approval to Fosun Kite Biotechnology Co. Ltd.’s FKC-876. Marketed as Yescarta (axicabtagene ciloleucel) in the U.S. and EU, the approval by the National Medical Production Administration for the CD19-directed CAR T therapy came 3.5 years after the FDA nod.
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Green approved stamp

Hutchmed earns NMPA approval for savolitinib amid IPO plan

June 29, 2021
By Elise Mak
Hutchmed Ltd.’s savolitinib became the first selective MET inhibitor approved in China to treat patients with non-small-cell lung cancer with MET exon 14 skipping alterations who have progressed following prior systemic therapy or are unable to receive chemotherapy.
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Currus-Biologics-team-6-29
Newco news

Currus Biologics launches with AU$10M series A to tackle CAR T combo in solid tumors

June 29, 2021
By Tamra Sami
PERTH, Australia – Startup Currus Biologics Pty Ltd. has launched with a AU$10 million (US$7.5 million) series A round with the mission of improving the success of CAR T-cell therapies against solid tumors such as breast, ovarian and pancreatic cancers.
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Back to the dojo

Underwhelmed by lead cancer vaccine, Sensei moves to reprioritize, refocus

June 29, 2021
By Michael Fitzhugh
Shares of Sensei Biotherapeutics Inc. (NASADQ:SNSE) fell 16% to $9.10 on June 29 after an announcement by President and CEO John Celebi that the antigen display technology used in its prior lead candidate, SNS-301, "is suboptimal for use in an active cancer vaccine." A phase I/II trial evaluating it will be discontinued, he said. Now, work on a next-generation vaccine, SNS-401-NG, and the monoclonal antibody SNS-VISTA will take precedence in a portfolio reprioritization at the company, with IND-enabling studies for the anti-VISTA program planned to start by the end of 2021 and for the next-gen vaccine in second half of 2022.
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