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BioWorld - Wednesday, February 18, 2026
Home » Topics » Japan, BioWorld Asia

Japan, BioWorld Asia
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Japan mulls ways to boost cell, gene therapy approvals

Oct. 22, 2024
By Marian (YoonJee) Chu
The Japanese government, industry and academia are deliberating health care policies and initiatives to boost Japan’s role in the future of regenerative medicine, experts at Bio Japan 2024 said, as the fruits of cell and gene therapy research come to fruition with new approvals.
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3D rendering of CAR T therapy in cell

By the numbers: US leads charge of cell and gene therapies

Oct. 22, 2024
By Marian (YoonJee) Chu
U.S. biotechs and regulators ushered in the era of gene therapy in 2023, experts at Bio Japan said, but medical reform is needed to pave the way for the “year of cell therapy” in 2024 and implement wider access to ultra-expensive cell and gene therapies.
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Conceptual image for brain cancer treatment

Oncolytic virus therapy may soon change glioma care: Bio Japan

Oct. 15, 2024
By Marian (YoonJee) Chu
Virus is associated with sickness, but oncolytic virus therapies, which harness viruses to attack and kill cancer cells, may soon change the standard of treatment for cancer, including those long deemed uncurable like malignant glioma.
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Ligachem, Ono Pharma ink two ADC deals worth max $700M

Oct. 15, 2024
By Marian (YoonJee) Chu
Ligachem Biosciences Inc., of Daejeon, South Korea, and Osaka, Japan-based Ono Pharmaceutical Co. Ltd. agreed to two antibody-drug conjugate (ADC) deals that could reach $700 million (₩943.5 billion) combined.
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Brain and DNA

Aviadobio, Astellas ink $2B+ frontotemporal dementia gene therapy deal

Oct. 8, 2024
By Nuala Moran
Aviadobio Ltd. has entered a potential $2.18 billion license and commercialization agreement for its frontotemporal dementia gene therapy, AVB-101, with Astellas Pharma Inc. Astellas is making a $20 million equity investment in London-based Aviadobio and will pay up to $30 million up front in advance of deciding whether or not to exercise the exclusive option to worldwide rights.
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New Japan drug approvals: cancer, insomnia, Alzheimer’s and more

Oct. 1, 2024
By Marian (YoonJee) Chu
Japan’s Ministry of Health, Labour and Welfare granted new drug approvals and expanded indications for conditions like cancer, insomnia and Alzheimer’s disease (AD) Sept. 24, including Eli Lilly and Co.’s Kisunla (donanemab) for early symptomatic AD.
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Renalys’ ¥6B series A to fund phase III IgAN trial in Japan

July 23, 2024
By Tamra Sami
Renalys Pharma Inc. completed a ¥6 billion (US$38.199 million) series A round that will enable it to complete a phase III trial for sparsentan for immunoglobulin A nephropathy (IgAN) in Japan. Tokyo-based Renalys in-licensed rights to sparsentan in January 2024 from Travere Therapeutics Inc. to develop the compound in Japan and 13 Asian countries to treat IgAN, a rare kidney disease.
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Takeda moves mezagitamab to phase III in thrombocytopenia

June 25, 2024
By Tamra Sami
Takeda Pharmaceutical Co. Ltd. is progressing mezagitamab to phase III trials after the CD38 monoclonal antibody showed rapid and sustained increases in platelet counts in patients with persistent or chronic primary immune thrombocytopenia (ITP) in a phase IIb trial.
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Global handshake silhouette

Asahi Kasei seeks global pharma growth via $1.1B Calliditas buy

May 28, 2024
By Nuala Moran
Japanese industrial conglomerate Asahi Kasei Corp. has made an offer to acquire Swedish rare diseases specialist Calliditas Therapeutics AB for SEK11.8 billion (US$1.1 billion). The offer, at an 83% premium to the closing share price of SEK113.60 on Monday, May 27, is recommended by the three biggest shareholders and the board of Calliditas, which said the company would benefit from “being part of a larger platform.”
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USTR seal

Usual players show up again in US trade report of bad actors

May 21, 2024
By Mari Serebrov
The U.S. Trade Representative (USTR) once again called out the usual cast of characters in this year’s Special 301 Report for not playing by the rules when it comes to protecting intellectual property. And once again, industry asked the USTR to go further by placing new players on the list.
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