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BioWorld - Sunday, February 15, 2026
Home » Topics » Clinical, BioWorld Asia

Clinical, BioWorld Asia
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Antibodies attacking cancer cell

Innovent’s PD-I inhibitor meets primary endpoint in phase III NSCLC study

Oct. 26, 2021
By Doris Yu
Innovent Biologics Co. Ltd.’s phase III Orient-31 trial for sintilimab in EGFR-mutated nonsquamous non-small-cell lung cancer (nsqNSCLC) met its primary endpoint. In combination with anti-VEGF antibody Byvasda (bevacizumab biosimilar injection) and chemotherapy, the treatment improved progression-free survival vs. chemotherapy alone. “The detailed results of Orient-31 will be released in 2021, and Innovent will file for the new drug application for that indication around early 2022,” Ronnie Ede, chief financial officer and executive director at Innovent, told BioWorld.
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COVID-19 mRNA vaccine vials, syringe

Baidu algorithm-based mRNA vaccine neutralizing antibody titer levels exceed benchmark sequence by up to 20x

Oct. 19, 2021
By Doris Yu
Baidu Inc.’s preclinical studies showed the mRNA vaccine sequences for COVID-19 designed using its Lineardesign algorithm outperformed the benchmark sequences designed by traditional algorithms in terms of stability, protein expression and immunogenicity. The firm teamed up with Stemirna Therapeutics Co. Ltd., which specializes in the R&D of mRNA vaccines and drugs, to test seven mRNA COVID-19 vaccine sequences designed using Lineardesign.
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Antibody-drug conjugate

Third ADC candidate with Synaffix’s tech enters clinic as Miracogen kicks off phase I

Oct. 12, 2021
By David Ho
It looks like Shanghai Miracogen Inc.’s antibody-drug conjugate (ADC) partnership with Synaffix BV is paying off as MRG-004A, an ADC designed to treat solid tumors, has entered a U.S. phase I/II trial to treat solid tumors.
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Cannabidiol

Medlab reformulates cannabinoid pain drug into synthetic as it progresses to phase III

Oct. 12, 2021
By Tamra Sami
PERTH, Australia – After meeting with the FDA, Medlab Clinical Ltd. is reformulating its cannabinoid pain product into a synthetic formulation because the agency indicated it was more likely to register a synthetic compared to a botanic.
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Lung cancer illustration

Cstone presents positive phase III data of sugemalimab for NSCLC

Sep. 28, 2021
By Doris Yu
Cstone Pharmaceuticals Co. Ltd. released positive data from the phase III trial, Gemstone-302, of sugemalimab plus chemotherapy for the first-line treatment of patients with stage IV squamous and non-squamous non-small cell lung cancer.
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Illustration of cancer cells and immunotherapy treatment

HER2/neu space bustling, Greenwich duet shows promise

Sep. 28, 2021
By Randy Osborne
Imugene Ltd.’s recent win with a patent granted in Japan with its HER-Vaxx immunotherapy, in development for HER2-positive gastric cancer, represented a smallish but significant win in the HER2/neu space, where plenty of other players are busy, with Greenwich Life Sciences Inc. a strong emerging name.
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Beyondspring NSCLC phase III hits primary endpoint but stock sags anyway

Sep. 21, 2021
By Lee Landenberger
Despite Beyondspring Pharmaceuticals Inc.’s phase III study meeting its primary and key secondary endpoints of a plinabulin/docetaxel combination in treating non-small-cell lung cancer (NSCLC), the company stock (NADAQ:BYSI) took a pounding. Shares sunk 32.9% on Sept. 20 to close at $15.36 each.
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Jennifer MacDiarmid and Himanshu Brahmbhatt, co-founders and co-CEOs, Engeneic Ltd.

Australia’s Engeneic enters clinic with nanocellular COVID-19 vaccine

Sep. 14, 2021
By Tamra Sami
PERTH, Australia – Engeneic Ltd. has begun a phase I trial of its nanocellular COVID-19 vaccine, which in preclinical animal studies stimulated a broad antiviral response against mutant strains of the virus, including the virulent Delta strain sweeping across Australia.
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Coronavac product packaging

Chinese vaccines show promise as booster shots as more study results shared

Sep. 14, 2021
By Doris Yu
Chinese companies are finding that their COVID-19 vaccines are effective as booster shots and against variants of the virus, as data from more studies emerge. Those who have received the third dose of Sinovac Biotech Ltd.’s COVID-19 vaccine, Coronavac, showed 2.5-fold higher neutralizing potency against the Delta variant, compared to COVID-19 convalescents and two-dose vaccinees.
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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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