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BioWorld - Wednesday, December 31, 2025
Home » Topics » Regulatory » MHLW

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Inserting contact lens into eye

J&J wins Japan approval for first drug-releasing combination contact lenses for vision correction and allergic eye itch

March 29, 2021
By Gina Lee
HONG KONG – Johnson & Johnson Vision (J&J Vision) has received its first global approval from Japan for its Acuvue Theravision with Ketotifen contact lenses. The Japanese Ministry of Health, Labour and Welfare’s green light will help with patients with vision correction, while simultaneously alleviating ocular allergic symptoms for allergic conjunctivitis, while they wear the lenses.
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Eisai lands new MHLW approvals for lymphoma and carcinoma indications

March 26, 2021
By Gina Lee
HONG KONG – Eisai Co. Ltd. has received not one, but two approvals from Japan’s Ministry of Health, Labour and Welfare (MHLW), for its anticancer agent Remitoro (denileukin diftitox) and multiple receptor tyrosine kinase inhibitor Lenvima (lenvatinib mesylate). Both approvals, each for a rare disease indication, were granted based on phase II trial results, instead after the usual phase III trials.
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Cabometyx

Takeda wins additional indication for tyrosine kinase inhibitor Cabometyx

Dec. 8, 2020
By Gina Lee
HONG KONG – Takeda Pharmaceutical Co. Ltd. received approval from Japan’s Ministry of Health, Labor and Welfare (MHLW) for an additional indication for its tyrosine kinase inhibitor, Cabometyx (cabozantinib), clearing the firm to manufacture and market 20-mg and 60-mg tablets for patients with unresectable hepatocellular carcinoma that has progressed after prior systemic therapy.
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Pills and bottle

After years of effort, Japan slashes drug lag

Dec. 8, 2020
By Alfred Romann
TOKYO – Steadily over a decade and a half, Japan’s drugs and devices regulator has all but eliminated a huge drug lag that put the second largest drug market in the world well behind most others in terms of the time it took for approvals and patient access to innovative drugs.
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Pills and bottle

After years of effort, Japan slashes drug lag

Dec. 7, 2020
By Alfred Romann
TOKYO – Steadily over a decade and a half, Japan’s drugs and devices regulator has all but eliminated a huge drug lag that put the second largest drug market in the world well behind most others in terms of the time it took for approvals and patient access to innovative drugs.
Read More
Cabometyx

Takeda wins additional indication for tyrosine kinase inhibitor Cabometyx

Dec. 3, 2020
By Gina Lee
HONG KONG – Takeda Pharmaceutical Co. Ltd. received approval from Japan’s Ministry of Health, Labor and Welfare (MHLW) for an additional indication for its tyrosine kinase inhibitor, Cabometyx (cabozantinib), clearing the firm to manufacture and market 20-mg and 60-mg tablets for patients with unresectable hepatocellular carcinoma that has progressed after prior systemic therapy.
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Approved stamp

Cureapp wins approval for Cureapp SC, Japan’s first therapeutic app

Sep. 4, 2020
By Gina Lee
HONG KONG – Tokyo-based Cureapp Inc. has received the Ministry of Health, Labour and Welfare (MHLW)’s green light to manufacture and sell Cureapp SC [Smoking Cessation] Nicotine Addiction Treatment App and CO Checker, its therapeutics app to aid patients who are quitting smoking.
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Japanese flag

Japan’s MLWH ends June with string of approvals, looks set for busy 2H 2020

July 7, 2020
By Gina Lee
HONG KONG – Japan’s Ministry of Health, Labour and Welfare (MHLW) ended the first half of 2020 by handing out a flurry of approvals to both domestic and international companies across a wide spectrum of indications.
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Japan’s MLWH ends June with string of approvals, looks set for busy 2H 2020

July 2, 2020
By Gina Lee
HONG KONG – Japan’s Ministry of Health, Labour and Welfare (MHLW) ended the first half of 2020 by handing out a flurry of approvals to both domestic and international companies across a wide spectrum of indications.
Read More
Japanese shield and coronavirus

Japan advances fight against COVID-19 with four-day approval for remdesivir

May 12, 2020
By David Ho and Gina Lee
HONG KONG – Japan has become the first country in the world to approve Veklury (remdesivir), Gilead Sciences Inc.’s experimental drug, to treat COVID-19. The fast approval was based on U.S. data and that country’s emergency use of the drug to tackle the pandemic, although it is unclear whether the drug is safe or effective for treating COVID-19.
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