Scrip is part of Pharma Intelligence UK Limited

This site is operated by Pharma Intelligence UK Limited, a company registered in England and Wales with company number 13787459 whose registered office is 5 Howick Place, London SW1P 1WG. The Pharma Intelligence group is owned by Caerus Topco S.à r.l. and all copyright resides with the group.

This copy is for your personal, non-commercial use. For high-quality copies or electronic reprints for distribution to colleagues or customers, please call +44 (0) 20 3377 3183

Printed By

UsernamePublicRestriction

Japan Re-approves Thalidomide For Cancer Treatment

This article was originally published in PharmAsia News

Executive Summary

TOKYO - Japan's Ministry of Health, Labor and Welfare has approved re-listing thalidomide, which Japan banned in 1962 for causing serious human deformations, to be marketed by Fujimoto Pharmaceutical, officials of the ministry's Pharmaceutical and Food Bureau and the Insurance Bureau confirmed Oct. 7

You may also be interested in...



Japan To List Nine Composites For National Health Insurance Coverage

TOKYO - At its Dec. 3 plenary meeting, Chuikyo (the Central Social Insurance and Medical Council), the government-private body that sets Japan's medical and pharmaceutical policies, approved the listing of nine composites for 13 pharmaceutical products, including the relisting of Fujimoto's Thaled (thalidomide) for multiple myeloma

Japan To List Nine Composites For National Health Insurance Coverage

TOKYO - At its Dec. 3 plenary meeting, Chuikyo (the Central Social Insurance and Medical Council), the government-private body that sets Japan's medical and pharmaceutical policies, approved the listing of nine composites for 13 pharmaceutical products, including the relisting of Fujimoto's Thaled (thalidomide) for multiple myeloma

Japan’s Ministry Reviews Thalidomide For Multiple Myeloma

The Ministry of Health, Labor and Welfare began a review panel meeting Aug. 26 to consider thalidomide as a treatment for multiple myeloma, on condition that adverse event prevention methods are fully addressed. The MHLW panel will consider safety measures put forth by pharmaceutical companies, such as registration requirements for pharmacists, physicians and patients and establishment of a third party to monitor compliance. Upon completion of the review the drug could be launched as early as the end of the year. Japan has 13,000-14,000 multiple myeloma patients. Thalidomide is approved to treat multiple myeloma in 17 countries. (Click here for more - Japanese language)

Latest Headlines
See All
UsernamePublicRestriction

Register

SC067074

Ask The Analyst

Ask the Analyst is free for subscribers.  Submit your question and one of our analysts will be in touch.

Thank you for submitting your question. We will respond to you within 2 business days. my@email.address.

All fields are required.

Please make sure all fields are completed.

Please make sure you have filled out all fields

Please make sure you have filled out all fields

Please enter a valid e-mail address

Please enter a valid Phone Number

Ask your question to our analysts

Cancel