FDA delays decision on Salix's diarrhea drug
Sept 5 (Reuters) - Salix Pharmaceuticals Ltd said the U.S. Food and Drug Administration would take more time to review the drugmaker's new treatment for HIV-related diarrhea and it now expects a regulatory decision by the end of the first quarter of 2013.
The drug crofelemer aims to provide symptomatic relief of non-infectious diarrhea in patients with HIV/AIDS on anti-retroviral therapy.
"By taking no action at this time, the FDA has allowed for the currently ongoing dialogue between Salix and the FDA to continue," Salix's Chief Development Officer Bill Forbes said in a statement.
Salix and the FDA were primarily discussing the production and control of the crofelemer active pharmaceutical ingredient - "a complex mixture that is the first botanical product to be reviewed by the agency for oral use."
About 1.2 million people in the United States are living with HIV/AIDS and about 40 percent of those patients suffer from either episodic or chronic diarrhea, Salix said.
Salix shares closed at $43.95 on Tuesday on the Nasdaq.
- Tweet this
- Share this
- Digg this
- In his native Alabama, Apple CEO's announcement he is gay prompts discomfort for some
- Xiaomi moves into third place in global smartphone war
- Islamic State fighters kill 220 Iraqis from tribe that opposed them
- Nurse defies Ebola quarantine with bike ride; negotiations fail |
- U.S. nurse defies Ebola quarantine with bike ride; negotiations fail