Japan’s cost-effectiveness assessment (CEA) panel has approved a revised handling policy for the CEA system for FY2026, with the health…
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- JCR’s MPS IIIA Drug Gets Orphan Tag in Europe
January 24, 2022
- Shipment Control Lifted for Pfizer's Methotrexate Injection After One Year
January 21, 2022
- Shionogi Submits PI Data for Oral COVID-19 Drug in Japan
January 21, 2022
- FunPep, EPS Group in Talks to Codevelop Peptide Drugs in China
January 21, 2022
- BMS’ Second CAR-T Therapy Abecma Approved in Japan
January 21, 2022
- Fuji Pharma Slapped with Biz Improvement Order over GMP Violations
January 20, 2022
- Daiichi Sankyo to Offload 8 US Assets to Cosette
January 20, 2022
- Katarzyna Maria Witkos Takes Helm at Alnylam Japan
January 20, 2022
- First Subject Enrolled in US PII/III of Anti-MTBR Tau Antibody for Alzheimer’s: Eisai
January 20, 2022
- AnGes/Vasomune's COVID-19 Med Enters PIIa for Severe Hospitalized Patients in US
January 20, 2022
- SymBio Seeks to Start PII Trial for Pediatric Adenovirus Infections in UK
January 19, 2022
- Mitsubishi Tanabe Earns Japan Rights for ADC Zynlonta
January 19, 2022
- Ono, Neurimmune Extend Drug Discovery Pact for Neurodegenerative Diseases
January 18, 2022
- Shionogi’s COVID-19 Vaccine Enters Japan PIII, AstraZeneca Jab as Control
January 18, 2022
- Nipro Grabs Rights for Nexium Authorized Generic, Filing Done in August
January 18, 2022
- Enhertu Accepted for FDA Review for Second-Line Breast Cancer Use
January 18, 2022
- MSD, Kyorin to Copromote Oral COVID-19 Med Lagevrio in Japan from Jan. 31
January 18, 2022
- CSL Behring Files Prophylactic Treatment for HAE Attacks in Japan
January 17, 2022
- Pfizer Files Oral COVID-19 Pill in Japan
January 14, 2022
- Mitsubishi Tanabe’s Oral Edaravone Accepted for FDA Review in ALS
January 14, 2022
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