In a first, the Food and Drug Administration recently gave fast-track approval for a cancer drug for children to begin selling even before testing in adults is finished. The drug, Clolar, is to treat relapsed leukemia. FDA's drug chief, Dr. Janet Woodcock, says she's open to speeding through more child-first cancer treatments whenever those smallest patients have no good options.

A stark new report from the influential Institute of Medicine urges government and drug makers to cut children's waiting time for access to experimental therapies ---- and for the NCI to actually develop those medicines if industry sees too little profit to do so.

A "near absence" of pediatric cancer drug research "threatens to halt the progress in childhood cancer treatment achieved during the past four decades," the report warns.
 


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