The U.S. Food and Drug Administration approved Thursday
GlaxoSmithKline PLC’s vaccine Rotarix, for the prevention of rotavirus, an
infection that causes gastroenteritis (vomiting and diarrhea) in infants and
children.
The approval follows a phase III trial on more than 15,000
healthy infants from ten Latin American countries conducted by researchers from
the
"This vaccine provides another option to combat and reduce a potentially severe illness that affects so many children," Jesse L. Goodman, M.D., M.P.H., director of FDA's Center for Biologics Evaluation and Research said on the FDA’s Web Site.
Rotavirus infection usually hits children before age five,
causing about 2.7 million cases in the
Rotarix will be given in a two-dose series to infants from 6
to 24 weeks of age and will protect them against rotavirus gastroenteritis
caused by G1, G3, G4 and G9 strains of rotavirus.
Rotarix will compete with Merck’s already marketed Rotateq,
a similar product, which is usually given in three doses over the course of six
months. Rotateq was Merck’s second-best selling vaccine last year with revenue
of $525 million.
“With only two doses, Rotarix allows infants to complete the vaccination series against rotavirus earlier than ever before, which may prevent many of the emergency department visits and hospitalizations that are a burden on families and the healthcare system,” said Barbara Howe, a company vice president.