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BioWorld - Friday, January 30, 2026
Home » Topics » Regulatory » PMDA

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Pill with Japanese flag

Why many global drugs never reach Japan

Jan. 29, 2026
By Tamra Sami
No Comments
For years, Japan’s “drug lag” was shorthand for slow regulatory reviews and delayed approvals compared with the U.S. and Europe. But even as regulatory timelines have shortened, review capacity has expanded and international alignment has improved, Japanese patients still face gaps in access to innovative drugs.
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F-med prototype mini robot

F.Med redefines the future of microsurgical robotics

Jan. 21, 2026
By Tamra Sami
Microsurgery is performed to connect small human vessels, but the technical difficulty required to conduct this type of surgery is quite specialized and limits the number of surgeons who can perform microsurgery.
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Rakuten

Rakuten closes $100M series F round, teams with Lotte Biologics

Jan. 20, 2026
By Marian (YoonJee) Chu
Rakuten Medical Inc. raised $100 million in a series F round to support late-stage clinical development of ASP-1929, its Alluminox-derived photoimmunotherapy being tested with Keytruda (pembrolizumab) as a first-line treatment for recurrent head and neck cancer.
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Japanese flag

PMDA makes case for Japan as a haven for innovation

Oct. 15, 2025
By Mark McCarty
Japan has long been one of the premier markets for medical technology, but this market has suffered from a reputation for slow adoption of technologies outside the cardiovascular device space, a problem the Pharmaceuticals and Medical Devices Agency is keen to address.
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Head and neck anatomy

Real-world data illuminates Rakuten's Alluminox solid tumor platform

Sep. 26, 2025
By Marian (YoonJee) Chu
No Comments
Rakuten Medical Inc. is advancing a pipeline of solid tumor therapeutics built on its Alluminox platform worldwide, having gained conditional early approval of ASP-1929, an Alluminox-derived photoimmunotherapy, in Japan in 2020.
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PMDA U.S. office in Washington D.C.
Asia-Pacific in the spotlight

PMDA more open to use of clinical data from other nations

Sep. 23, 2025
By Mark McCarty
Japan’s Pharmaceuticals and Medical Devices Agency has traditionally been less than receptive to clinical data from other nations, but that aversion is slowly giving way. Ames Gross of Pacific Bridge Medical told BioWorld that a trial conducted in another nation with significant representation of those of Japanese ancestry can go a long way toward obviating the need for a trial conducted in Japan.
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PMDA U.S. office in Washington D.C.
Asia-Pacific in the spotlight

PMDA more open to use of clinical data from other nations

Sep. 16, 2025
By Mark McCarty
Japan’s Pharmaceuticals and Medical Devices Agency has traditionally been less than receptive to clinical data from other nations, but that aversion is slowly giving way. Ames Gross of Pacific Bridge Medical told BioWorld that a trial conducted in another nation with significant representation of those of Japanese ancestry can go a long way toward obviating the need for a trial conducted in Japan.
Read More
Coronavirus, lungs

Healios posts more upbeat data on Multistem cell therapy for ARDS

March 18, 2025
By Marian (YoonJee) Chu
Latest findings on Healios K.K.’s stem cell therapy to treat acute respiratory distress syndrome (ARDS), coined Multistem (invimestrocel; HLCM-051), found the regenerative medicine effective in reducing the number of patient days on ventilator treatment, as well as mortality benefits.
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Coronavirus, lungs

Healios posts more upbeat data on Multistem cell therapy for ARDS

March 14, 2025
By Marian (YoonJee) Chu
Latest findings on Healios K.K.’s stem cell therapy to treat acute respiratory distress syndrome (ARDS), coined Multistem (invimestrocel; HLCM-051), found the regenerative medicine effective in reducing the number of patient days on ventilator treatment, as well as mortality benefits.
Read More

Dimerix licenses phase III kidney disease drug to Fuso for ¥10.5B

Jan. 7, 2025
By Tamra Sami
Dimerix Ltd. and Fuso Pharmaceutical Industries Ltd. signed a license agreement for the development and commercialization of Dimerix’s phase III candidate, DMX-200, for the treatment of focal segmental glomerulosclerosis in Japan for ¥10.5 billion (US$66.5 million) plus royalties.
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