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BioWorld - Friday, July 10, 2026
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BioWorld Asia, Regulatory
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Ascletis’ all-oral HCV treatment approved for marketing in China

Aug. 11, 2020
By Bryan Wong
HONG KONG – The recent approval of all-oral hepatitis C virus (HCV) drug RDV/DNV, a combination of Asclevir (ravidasvir) and Ganovo (danoprevir), helped boost shares of Ascletis Pharma Inc. (HK:1672), which ended July with a 10% jump to HK$3.36 (US43 cents), as the Hangzhou, China-based company continues to push its pipeline of treatments forward and improve its outlook.
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Pakistan flag-map

Import bans hit Pakistan’s pharma industry

Aug. 11, 2020
By Khawar Khan
KARACHI, Pakistan – Geopolitics and a fraught relationship with its neighbors are hurting Pakistan’s pharmaceutical industry and the ability of people to access active pharmaceutical ingredients (APIs) and modern drugs.
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Financial chart, downward arrow

Mesoblast sees stock tumble 31% ahead of FDA adcom meeting

Aug. 11, 2020
By Tamra Sami
PERTH, Australia – Australian regenerative medicine company Mesoblast Ltd. saw its stock tumble more than 30% following the release of briefing documents from the FDA ahead of an Aug. 13 advisory committee meeting to review the company’s BLA for Ryoncil (remestemcel-L) for steroid-refractory acute graft versus host disease (SR-aGVHD) in children.
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Architectural pillars

Regulatory front for Aug. 4, 2020

Aug. 4, 2020
The latest global regulatory news, changes and updates affecting biopharma, including: Medicines and Healthcare Products Agency, Presidential Advisory Council on Combating Antibiotic-Resistant Bacteria.
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Covaxin vial

Indian deadline for COVID-19 vaccine raises doubts

Aug. 4, 2020
By T.V. Padma
NEW DELHI – If India’s government has its way, the country could launch a vaccine for COVID-19 in mid-August, an extremely short deadline that has caused controversy and pushed companies to speed up their development and the trials of prospective vaccines.
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Henlius’ Herceptin biosimilar wins EU approval, marks Chinese players entry to Europe

Aug. 4, 2020
By Elise Mak
Chinese biosimilar maker Shanghai Henlius Biotech Inc. won EMA approval for its Zercepac, a biosimilar to Roche Holding AG’s Herceptin (trastuzumab) on July 28. Henlius CEO Scott Liu told BioWorld that Zercepac will be the first Chinese monoclonal antibody biosimilar to enter the EU market, setting a precedent for Chinese drugmakers seeking to join the global race in biosimilars.
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Antibodies fighting coronavirus

Celltrion doubles pace for COVID-19 antibody treatment CT-P59

Aug. 4, 2020
By Gina Lee
HONG KONG – Incheon, South Korea-based Celltrion Inc. is rapidly advancing CT-P59, its antiviral antibody treatment for the COVID-19 virus, after receiving its second green light to begin phase I trials.
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Cybersecurity data lock

Culture of scientific exchange seen as a risk factor for life science cybersecurity

July 28, 2020
By Mark McCarty
The U.S. government has charged two citizens of China with cybercrime in connection with purported hacking of research into vaccines for the SARS-CoV-2 virus, but more than one speaker on a July 22 webinar said scientists involved in basic life science research at universities fail to appreciate the need for cybersecurity, a problem they may take with them to the private sector.
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Architectural pillars

Regulatory front for July 28, 2020

July 28, 2020
The latest global regulatory news, changes and updates affecting biopharma, including: EMA.
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Flag of India

Biocon’s repurposed psoriasis drug gets Indian approval for COVID-19

July 21, 2020
By T.V. Padma
NEW DELHI – Bangalore-based Biocon Ltd. has received the Indian drug regulator's approval for restricted emergency use of its psoriasis biologic, itolizumab, to treat patients with severe cases of COVID-19 in need of ventilator support.
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