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BioWorld - Wednesday, April 22, 2026
Home » Authors » David Ho

Articles by David Ho

Scientist injecting vaccine into Earth

Comirnaty wins the vaccine approval race in Hong Kong, ahead of leading rivals

Jan. 26, 2021
By David Ho and Gina Lee
HONG KONG – Shortly after Australia’s recent provisional approval for the mRNA-based COVID-19 vaccine Comirnaty (tozinameran), originally developed by Pfizer Inc. and Biontech SE, Hong Kong has approved it, too, for emergency use ahead of rivals developed in mainland China. It is the first vaccine to be approved in the Chinese territory, made possible through a collaboration between Biontech and Shanghai Fosun Pharmaceutical Group Co. Ltd.
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Dollar arrows pointing upward

Terns closes $87M series C financing to advance NASH pipeline

Jan. 12, 2021
By David Ho
HONG KONG - U.S. and China-based Terns Pharmaceuticals Inc. closed an $87 million series C financing round that will pave the way for the company’s pipeline of candidates to treat nonalcoholic steatohepatitis (NASH).
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Terns closes $87M series C financing to advance NASH pipeline

Jan. 8, 2021
By David Ho
HONG KONG - U.S. and China-based Terns Pharmaceuticals Inc. closed an $87 million series C financing round that will pave the way for the company’s pipeline of candidates to treat nonalcoholic steatohepatitis (NASH).
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Chi-Med wins China approval for first in-house oncology drug

Jan. 5, 2021
By David Ho
HONG KONG – Hutchison China Meditech Ltd. (Chi-Med) earned approval from China’s National Medical Products Administration (NMPA) for Sulanda (surufatinib) for the treatment of non-pancreatic neuroendocrine tumors (NETs).
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COVID-19 vaccine vials

India’s speedy approval of domestic COVID-19 vaccine raises concerns

Jan. 5, 2021
By David Ho
HONG KONG – India’s conditional approval on Jan. 3 of a COVID-19 vaccine developed domestically by Bharat Biotech International Ltd. but still in phase III trials has sparked concerns about its safety. The Drugs Controller General of India (DCGI) gave emergency authorization to the product, Covaxin, along with the Astrazeneca plc and Oxford University vaccine Covishield. The DCGI said the conditional approval granting “restricted use in emergency situation” for Covaxin was done in “clinical trial mode” to account for the fact that the shot is still being tested. But the rush to approve it has created controversy and confusion.
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Map, flag of India

Companies team up to tackle peripheral artery disease amongst India’s poorest citizens

Jan. 4, 2021
By David Ho
HONG KONG – Votis Subdermal Imaging Technologies Ltd. is developing a diagnostics solution that could prevent the loss of feet among India’s impoverished due to affects of peripheral artery disease (PAD). The company has entered an agreement with India’s Ii Ventures Pte. Ltd. (iiV) to develop a system to screen the largely rural Indian population for PAD.
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Chi-Med wins China approval for first in-house oncology drug

Jan. 4, 2021
By David Ho
HONG KONG – Hutchison China Meditech Ltd. (Chi-Med) earned approval from China’s National Medical Products Administration (NMPA) for Sulanda (surufatinib) for the treatment of non-pancreatic neuroendocrine tumors (NETs), marking what CEO Christian Hogg called a “major milestone” as the first drug to be discovered and developed by Chi-Med without the support of a development partner.
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Software screenshot

Rsip Vision develops algorithmic module for heart function assessment

Dec. 31, 2020
By David Ho
HONG KONG – A new algorithmic module developed by Rsip Vision Ltd. makes it possible to generate automated expert-level assessment of heart functions, facilitating quick and reliable detection of cardiac illness and heart attacks.
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Clostridium difficile bacteria

CUHK develops rapid microrobotic diagnostic system for multiple pathogens

Dec. 23, 2020
By David Ho
HONG KONG – A research team at the Chinese University of Hong Kong (CUHK) has developed a fully automated, low-cost and rapid microrobotic diagnostic system that can be used with multiple pathogens, including COVID-19. The system works by integrating fluorescent microrobots with an external magnetic actuation system to detect pathogens in patient samples.
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Health professional touching screen, digital/medical icons

Hummingbird taps Tempus’ AI for clinical trial in rare NRG1 fusion patients

Dec. 22, 2020
By David Ho
HONG KONG – Hummingbird Bioscience Pte. Ltd. is collaborating with artificial intelligence (AI) company Tempus Labs Inc. to advance HMBD-001, a differentiated anti-HER3 neutralizing antibody developed using Hummingbird's Rational Antibody Discovery platform, into clinical trials in HER3-driven cancers.
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