Roche says Japan approves new formulation of arthritis drug
ZURICH (Reuters) - Roche Holding AG's Japanese subsidiary Chugai said on Monday that Japanese health regulators have approved a new formulation of its rheumatoid arthritis drug Actemra.
Japanese regulators have approved a subcutaneous formulation of Actemra which shortens the delivery time of the drug compared to an intravenous formulation and can be administered at home.
Actemra was first launched with intravenous formulation in Japan for Castleman's disease and was later approved for rheumatoid arthritis.
Roche has also submitted the subcutaneous formulation for approval in the United States and Europe, where Actemra is approved for use in rheumatoid arthritis patients who are either intolerant to or have failed to respond to other medicines to treat inflammation.
(Reporting by Caroline Copley)
- U.S. immigration protesters drop U.S. border blockade plan
- Exclusive: Angry with Washington, 1 in 4 Americans open to secession
- About 60,000 Syrian Kurds flee to Turkey from Islamic State advance |
- Exclusive: Iran seeks give and take on militants, nuclear program
- White House intruder was armed with knife: officials