U.S. FDA accepts
application for Indivior's new schizophrenia drug
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[December 12, 2017] (Reuters)
- U.S. Food and Drug Administration (FDA)
accepted Indivior's application for its new schizophrenia treatment, the
British drugmaker said on Tuesday, boosting hopes of marketing the drug
in the country.
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The London-listed company, which specializes in heroin addiction
treatment, said the FDA had accepted its application for RBP-7000,
an investigational once-a-month injectable to treat schizophrenia.
Earlier this month, the company's experimental drug to help fight
America's growing opioid addiction crisis was approved by the FDA,
boosting its sales prospects as competitors threaten revenue from an
older product.
Shares in Indivior were expected to rise about 3 percent at market
open.
(Reporting by Justin George Varghese in Bengaluru; editing by Jason
Neely)
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