The drug, Neupogen, is the first ever approved for the treatment of acute radiation injury.
The approval by the US Food and Drug Administration (FDA) came as a result of a research done by Professor Thomas J MacVittie and Assistant Professor Ann M Farese of University of Maryland School of Medicine.
The research was held in a non-human clinical model of high-dose radiation.
"Our research shows that this drug works to increase survival by protecting blood cells," MacVittie said.
"Neupogen is the first FDA-approved medical countermeasure to increase survival in patients exposed to myelosuppressive doses of radiation," a statement by FDA had earlier said.
"It was approved by FDA based on studies in animals (under the Animal Rule), as studies in humans could not be ethically conducted," it added.
Radiation damages the bone marrow, and as a result decreases production of infection-fighting white blood cells.
Neupogencounteracts these effects. The drug, which is made by Amgen, Inc, was first approved in 1991 to treat cancer patients receiving chemotherapy.
This planning is already under way. In 2013, the Biomedical Advanced Research and Development Authority (BARDA), an arm of the Department of Health and Human Services, bought USD 157 million worth of Neupogen for stockpiles around the country in case of nuclear accident or attack.
The research builds on 40 years of work that Dr MacVittie and his team have conducted in the field of radiation research, during which they have helped to define the field.
