ஸ்டெம் செல் ஆராய்ச்சி மற்றும் சிகிச்சை இதழ்

சுருக்கம்

History of Development and Regulations for Regenerative Medicines in Japan

Hanayuki Okura and Akifumi Matsuyama

Regenerative medicinal products were dealt with fewer than two categories only, pharmaceutical products and medical devices in the previous Pharmaceutical Affairs Law (PAL). Because regenerative medicinal products could not fully fit within the conventional regulatory contexts for pharmaceuticals, they were less available to the public. To overcome this issue, the Japanese parliament has legislated Laws for the Promotion of Comprehensive Measures to Facilitate Swift Distribution and Safe Use of Regenerative Medicines available to the Public (Regenerative Medicine Promotion Act). The Japanese government has changed the regulatory framework for regenerative medicinal products, 1) upgrading of directives for human stem cell-based clinical research to the Law concerning the Establishment of Safety of Regenerative Medicine Materials (Regenerative Medicine Safety Assurance Act), and 2) setting a new category for regenerative medicinal products in the Pharmaceutical and Medical Device Act (PMD Act), the latest revised PAL. It is noteworthy that the PMD Act permits expedited, conditional, and time-limited marketing approval as an exception for non-homogeneous regenerative medicinal products when efficacy is anticipated while safety is demonstrated. With these revisions of the regulatory framework for regenerative medicinal products, two tracks have become available for societal contribution to regenerative medicines. Japan is the only country where society has these two tracks, and social experiments on regenerative medicines in spectacular proportion are launched for societal contribution. We review here the history of the struggle to accelerate the availability of regenerative medicinal products for patients in Japan.