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BioWorld - Friday, June 26, 2026
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Home » Topics » BioWorld Asia

BioWorld Asia
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In the clinic for Sept. 7-13, 2021

Sep. 14, 2021
Clinical updates from Asia, including trial initiations, enrollment status and data readouts and publications: Adlai Nortye, Ascentage, Ascletis, Astrazeneca, Azurrx, Azurx, Cstone, Cytodyn, Edigene, Excalibur Medicines, Gannex, Hutchmed, Innovent Biologics, Kintor, Novavax, Senhwa, Sorrento, Swedish Orphan Biovitrum, Telix.
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Other news to note for Sept. 14, 2021

Sep. 14, 2021
Biopharma happenings in Asia-Pacific, such as deals and partnerships, grants, preclinical data and other news in brief: Agentix, Amolyt, Arctic Vision, Arecor, Astrazeneca, Beroni, Biocentriq, Biodelivery Sciences, Bio-Thera Solutions, Brightgene Biomedical, Citius, Clearside Biomedical, Dr. Reddy’s, Eisai, Exscientia, Eyam Vaccines and Immunotherapeutics, Fujifilm, Fujifilm Diosynth, Genequantum Healthcare, Huadong Medicine, Immunome, Insilico Medicine, Intas, Kintor, Moderna, National Health Research Institutes, National Resilience, Navrogen, Neuexcell, Novartis, Paq, Penao, Peptidream, Radius, Shenzhen Kangtai Biological Products, Spikimm, Telix, Tevogen, TLC, Veristat, Woods Investment.
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Minhai wins approval for 13-valent pneumococcal conjugate vaccine in China

Sep. 14, 2021
By David Ho
Minhai Biotechnology Co. Ltd. has won approval from the NMPA for its 13-valent pneumococcal conjugate vaccine, which makes it the third company with such a vaccine to be greenlighted in China.
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Financings for Sept. 14, 2021

Sep. 14, 2021
Biopharmas in Asia-Pacific raising money in public or private financings: Asahi Kasei, Brii, Cytovia, Haemalogix, ILC, KB Investment, Prism Biolab, RM Global Partners, Xenikos.
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KRAS protein

Innovent acquires KRAS G12C candidate from Genfleet in $312M deal

Sep. 7, 2021
By Doris Yu
Innovent Biologics Inc. has inked a $312 million licensing deal for the development and commercialization of Genfleet Therapeutics Inc.’s KRAS G12C inhibitor, GFH-925, in mainland China, Hong Kong, Macau and Taiwan. Innovent also has additional option-in rights for global development and commercialization.
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Astellas stops dosing gene therapy for rare neuromuscular disease after trial's fourth SAE

Sep. 7, 2021
By Michael Fitzhugh
Astellas Pharma Inc. has halted further dosing of the experimental X-linked myotubular myopathy (XLMTM) gene therapy AT-132 (resamirigene bilparvovec) after one participant in the ongoing Aspiro study experienced a serious adverse event (SAE) of abnormal liver function.
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BMS’ Opdivo greenlighted as first immunotherapy for first-line advanced gastric cancer in China

Sep. 7, 2021
By Doris Yu
Bristol Myers Squibb Co.’s Opdivo (nivolumab) is now the first and only immunotherapy for the first-line treatment of advanced gastric cancer in China.
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Coronavirus variants

COVID-19 vaccine booster debate continues as Delta variant surges

Sep. 7, 2021
By Nuala Moran
LONDON – Conflicting data from around the world on the extent to which the Delta variant of SARS-CoV-2 is reducing the effectiveness of vaccines is generating uncertainty over the need, or not, for booster programs.
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NMPA grants JW approval for China’s first independently developed CAR T therapy

Sep. 7, 2021
By Doris Yu
China’s NMPA has approved JW Therapeutics Co. Ltd.’s relmacabtagene autoleucel, an autologous chimeric antigen receptor T (CAR T) therapy for the treatment of adults with relapsed or refractory large B-cell lymphoma (r/r LBCL) after two or more lines of systemic therapy. It marks the first CAR T product to be independently developed in China and approved as a category I biologic product there, as well as the sixth approved CAR T product globally. The anti-CD19 therapy, sometimes called relma-cel, will be marketed as Carteyva.
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Pill bottle with flag of India

India begins approving long list of banned FDC drugs

Sep. 7, 2021
By T.V. Padma
India’s drug regulator has approved 31 fixed-dose combination (FDC) drugs out of more than 300 banned products, after an assessment by its drugs technical advisory board. It has also asked for more phase IV postmarketing data for 19 others.
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