Relative Bioavailability of BMS-931699 From Prefilled Syringe Compared to Drug in Vial

Inclusion Criteria: * Healthy participants as determined by no clinically significant deviation from normal in medical history, physical examination, electrocardiograms, and clinical laboratory determinations * All participants must have hemoglobin, hematocrit, and platelets within normal limits at screening * All participants must have activated partial thromboplastin time, prothrombin time, and international normalized ratio within normal limits at screening Exclusion Criteria: * Any current or past history or risk for tuberculosis: * Active tuberculosis requiring treatment within the previous 3 years. All participants will be required to have a QuantiFERON tuberculosis Gold or T-SPOT tuberculosis test performed at screening. Also excluded are participants with evidence of a past tuberculosis infection without documented adequate therapy. Participants with a positive QuantiFERON tuberculosis Gold or T-SPOT tuberculosis test at screening will not be eligible for the study. A QuantiFERON tuberculosis Gold or T-SPOT tuberculosis test performed within 4 weeks of dosing on Day 1 is acceptable as long as there is documentation of a negative result. * Current clinical, radiographic, or laboratory evidence of active tuberculosis * A history of herpes zoster