The purpose of this clinical research study is to evaluate the safety and effectiveness of an investigational drug for post bunion removal surgery pain. Participation is completely voluntary.
Criteria:Subject scheduled to undergo a primary unilateral bunionectomy with distal first metatarsal osteotomy (i.e., Austin procedure) and internal fixation under regional anesthesia (Mayo and popliteal sciatic block).
Subjects (male or female) between the ages of 18 and 75 years, inclusive.
Body mass index (BMI) of 18.0 to 38.0 kg/m2 , inclusive.