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The analysis was a phase-III trial, the final stage of human being testing normally required by the U.S. Food and Drug Administration before it will consider approving a drug. Based on the total results, an FDA advisory panel fulfilled on Sept. 6 and recommended the drug’s approval for the treatment of rheumatoid arthritis in cases in which standard therapy offers failed. Abatacept, marketed as Orencia, is manufactured by Bristol-Myers Squibb, which sponsored the study. The lead author, Tag Genovese, MD, Stanford associate professor of medicine , is certainly a paid consultant for the ongoing company. This drug works where others haven’t, said Genovese, who is also the associate chief of the medical school’s Division of Immunology and Rheumatology.