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On a Phase 3 Obesity ProgramThe clinical phase 3 program Qnexa in more than 4,500 patient examined, among under a Special Protocol Assessment of U.S. FDA designed to and was composed of three studies:. INADEQUATE , EQUIP and Conquer The INADEQUATE study was an 28-week, randomized, double – blind, placebo-controlled, prospective study with patients who will be randomized once-daily treatment with mid – and full – doses Qnexa, of the respective constituents to phentermine and topiramate and placebo. The average baseline BMI study population amounted to 36.3 kg/m2 having an average output weight from 223 kilograms. EQUIP and Conquer the research was 56-week, randomized, double – blind, placebo – controlled, prospective study by patients who are randomized to receive once-daily treatment with a low-, mid-or full-dose Qnexa, or placebo. Lay to EQUIP the average baseline BMI of the study population, 42.1 kg/m2 an average output weight 256 pounds and conquer, next-generation baseline BMI of 36.6 kg/m2 study population with average output weight 227 pounds. All patients were asked, a reduced calorie diet , which followed by an 500-calorie/day advised advised to implement a simple lifestyle modified Programme.

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