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BioWorld - Tuesday, June 30, 2026
Breaking News: Science fiction realized: BCI tech is hereBreaking News: Science fiction realized: BCI tech is here
Home » Topics » BioWorld Asia, Regulatory

BioWorld Asia, Regulatory
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Coin inserted into Australian map

TGA: More feedback needed on repurposing drugs

March 15, 2022
By Mari Serebrov
Given the challenges in repurposing medicines, Australia’s TGA opened a second consultation on the subject March 10.
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Three China firms named to US SEC list under HFCAA

March 15, 2022
Three U.S.-listed China-based biopharmas were among five companies named this week by the U.S. SEC for reportedly failing to submit necessary accounting reports under the Holding Foreign Companies Accountable Act (HFCAA).
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WHO headquarters, Geneva

WHO warns of counterfeit COVID-19 drugs

March 15, 2022
By Mari Serebrov
With the pandemic lingering across the world and more COVID-19 therapies becoming available and in demand, the opportunity for counterfeits is growing.
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Eye and DNA

Hansoh wins China’s first approval for an anti-CD19 antibody to treat NMOSD

March 15, 2022
By Doris Yu

Hansoh Pharmaceutical Group Co. Ltd. has won a green light for inebilizumab, approved by China’s NMPA for the treatment of adults with neuromyelitis optica spectrum disorders (NMOSD) who are anti-aquaporin-4 immunoglobulin G (AQP4-IgG) seropositive. The decision marked Hansoh’s first biologic approval.


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SEC identifies firms for tougher audits, including three biopharmas

March 15, 2022
By Gina Lee
The U.S. Securities and Exchange Commission (SEC) recently issued a provisional list of five U.S.-listed Chinese companies that reportedly failed to submit necessary accounting reports required under Holding Foreign Companies Accountable Act. The list included three biopharmas: Beigene Ltd., Hutchmed Ltd., and Zai Lab Ltd.
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Map of China

Junshi and Mabwell’s adalimumab biosimilar wins NMPA approval

March 8, 2022
By Doris Yu
Shanghai Junshi Biosciences Co. Ltd. and Mabwell Bioscience Co. Ltd. have won marketing approval for the adalimumab biosimilar Junmaikang from China’s NMPA for the treatment of patients with rheumatoid arthritis, ankylosing spondylitis and psoriasis.
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Flag of Australia, sky background

Australia introduces patent box legislation for med-tech and biotech innovations

March 8, 2022
By Tamra Sami
New legislation providing a tax incentive for Australian medical innovations was introduced in Australia’s House of Representatives, and industry stakeholders are lauding the move.
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Shionogi aims for Japan’s first conditional approval for COVID-19 treatment

March 8, 2022
By Gina Lee

Shionogi and Co. Ltd. is looking to become the first company to get approval for a COVID-19 treatment under Japan’s conditional approval system as it prepares a phase III trial for S-217622 (ensitrelvir), its oral antiviral drug for COVID-19. 


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Janssen-Legend BCMA-targeting CAR T therapy crosses the line with US FDA approval

March 1, 2022
By Michael Fitzhugh and Richard Staines

Janssen Pharmaceutical Cos. Inc. has become the second company to get a BCMA-targeting CAR T therapy to market with the approval of ciltacabtagene autoleucel for adults with relapsed or refractory multiple myeloma (MM) after four or more prior lines of therapy, including a proteasome inhibitor, an immunomodulatory agent and an anti-CD38 monoclonal antibody.


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U.S.-China capsule

China-US licensing trending up in China’s quest for innovation

March 1, 2022
By Mari Serebrov
Chinese investment in U.S. companies is dropping, but Chinese biopharma firms are increasingly eyeing licensing deals on early stage inventions patented by U.S. universities, Lin Sun-Hoffman, founding partner at Liu, Chen & Hoffman LLP, said during a Feb. 24 U.S. Patent and Trademark Office webinar on biopharma patents in China.
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