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BioWorld - Sunday, December 28, 2025
Home » Newsletters » BioWorld Asia

BioWorld Asia

Feb. 22, 2017

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Other news to note

Immuron Ltd., of Sydney, said Emory University has enrolled its first patient in the company's IMM-124E pediatric non-alcoholic fatty liver disease (NAFLD) phase II trial. Read More

Appointments and advancements

Astellas Pharma US Inc., of Northbrook, Ill., part of Astellas Pharma Inc., of Tokyo, named Linda Friedman executive vice president, general counsel, with responsibility for the company's Legal organization worldwide. Read More

Takeda lands Japan rights for cabozantinib in Exelixis agreement

TOKYO – Exelixis Inc. and Takeda Pharmaceutical Co. Ltd. reached an exclusive licensing agreement for the commercialization and further clinical development in Japan of oncology drug cabozantinib. The deal grants Takeda exclusive commercial and further clinical development rights in Japan for cabozantinib. Read More

Taiwan authorities move to expedite drug approval process

HONG KONG – Imminent changes to Taiwan's drug approval process could dramatically improve the country's pharmaceutical sector, potentially shortening approval times and boosting growth. Drug developers operating in the country are paying close attention to upcoming reforms, which should be implemented soon. Read More

Tivantinib misses OS endpoint in phase III liver cancer trial

The oral c-Met inhibitor tivantinib missed its primary endpoint of improving overall survival vs. placebo in a phase III hepatocellular carcinoma (HCC) study, calling into question the future of the program, licensed by Arqule Inc. to Tokyo-based Daiichi Sankyo Group in December 2008, even as another phase III study of the candidate in Japan progresses. Shares in Arqule (NASDAQ:ARQL) fell 18.4 percent, closing at $1.20 on Friday. Read More

Germline gene editing should be allowed – in certain situations

LONDON – Clinical trials involving genome editing in gametes or early embryos could be permitted in the future, but only for serious conditions and under stringent oversight, said experts after a year-long review of the scientific and ethical issues thrown up by CRISPR/Cas9. Read More

Samsung's biosimilars come to fruition despite scandals, company says

HONG KONG – It is a tumultuous year for Korean conglomerate Samsung, whose group chief Jay Y. Lee was arrested Friday in connection to a corruption scandal, and Samsung Biologics Co. Ltd., the company's contract manufacturer arm of biologic drugs, coming under scrutiny with allegations of being involved in unlawful accounting practices. Read More

Chi-Med's savolitinib hits phase II endpoints in Met-driven PRCC

SHANGHAI – Hutchison China Meditech Ltd. (Chi-Med) and its partner, Astrazeneca plc, of London, shared phase II safety and efficacy data for savolitinib in patients with papillary renal cell carcinoma (PRCC), a fatal form of kidney cancer. Read More

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