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BioWorld - Wednesday, January 7, 2026
Home » Authors » Shannon Ellis

Articles by Shannon Ellis

Hutchison's fruquintinib meets phase III study endpoints in CRC

March 8, 2017
By Shannon Ellis
SHANGHAI – Hutchison Medipharma Ltd. (Chi-Med) announced its first phase III win with fruquintinib, a targeted VEGFR inhibitor studied as a third-line therapy in 416 Chinese patients with colorectal cancer (CRC). Sharing only top-line results at this time, the FRESCO study met primary and secondary endpoints of improving overall survival and progression-free survival.
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Hutchison's fruquintinib meets phase III study endpoints in CRC

March 7, 2017
By Shannon Ellis
SHANGHAI – Hutchison Medipharma Ltd. (Chi-Med) announced its first phase III win with fruquintinib, a targeted VEGFR inhibitor studied as a third-line therapy in 416 Chinese patients with colorectal cancer (CRC).
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Toolgen’s AAV delivery could move CRISPR/Cas9 beyond genetic disease

March 1, 2017
By Shannon Ellis
SHANGHAI – In the midst of a busy news week for CRISPR/Cas9 – a powerful tool that gives cut-and-paste accuracy to gene editing by using adapted immune bacteria – Toolgen Inc. has made advances of its own. The Seoul, South Korea-based company shared encouraging results in Nature Communications in a study evaluating Campylobacter jejuni Cas9 (CjCas9), the smallest Cas9 orthologue characterized to date, for efficient genome editing in vivo.
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Toolgen's AAV delivery could move CRISPR/Cas9 beyond genetic disease

Feb. 24, 2017
By Shannon Ellis
SHANGHAI – In the midst of a busy news week for CRISPR/Cas9 – a powerful tool that gives cut-and-paste accuracy to gene editing by using adapted immune bacteria – Toolgen Inc. has made advances of its own. The Seoul, South Korea-based company shared encouraging results in Nature Communications in a study evaluating Campylobacter jejuni Cas9 (CjCas9), the smallest Cas9 orthologue characterized to date, for efficient genome editing in vivo.
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Chi-Med's savolitinib hits phase II endpoints in Met-driven PRCC

Feb. 22, 2017
By Shannon Ellis
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. Presented over the weekend at the Genitourinary Cancers Symposium sponsored by the American Society of Clinical Oncology (ASCO) held in Orlando, Fla., the study concluded savolitinib to be generally well-tolerated with antitumor activity in Met-driven PRCC patients.
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Chi-Med's savolitinib hits phase II endpoints in Met-driven PRCC

Feb. 22, 2017
By Shannon Ellis
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.
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Beigene's BGB-3111 goes head to head against Imbruvica in phase III trial for WM

Feb. 1, 2017
By Shannon Ellis
SHANGHAI – Beigene Co. Ltd., of Beijing, is advancing its small-molecule Bruton's tyrosine kinase (BTK) inhibitor candidate, BGB-3111, in a global phase III trial for patients with Waldenström's macroglobulinemia (WM, or lymphoplasmacytic lymphoma), a type of non-Hodgkin lymphoma.
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Beigene’s BGB-3111 goes head to head against Imbruvica in phase III trial for WM

Jan. 27, 2017
By Shannon Ellis
SHANGHAI – Beigene Co. Ltd., of Beijing, is advancing its small-molecule Bruton’s tyrosine kinase (BTK) inhibitor candidate, BGB-3111, in a global phase III trial for patients with Waldenström’s macroglobulinemia (WM, or lymphoplasmacytic lymphoma), a type of non-Hodgkin lymphoma.
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AZ advances creative China strategy as IL-6 antibody green-lighted

Jan. 25, 2017
By Shannon Ellis
SHANGHAI – The Shanghai-based joint venture Wuxi-Medimmune has received the go-ahead to start clinical trials from Chinese regulators for anti-IL-6 antibody WBP216 (MEDI5117) as a therapeutic for autoimmune and inflammatory diseases, in particular rheumatoid arthritis (RA).
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AZ advances creative China strategy as IL-6 antibody green-lighted

Jan. 23, 2017
By Shannon Ellis
SHANGHAI – The Shanghai-based joint venture Wuxi-Medimmune has received the go-ahead to start clinical trials from Chinese regulators for anti-IL-6 antibody WBP216 (MEDI5117) as a therapeutic for autoimmune and inflammatory diseases, in particular rheumatoid arthritis (RA).
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