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Registration Number.DRP-10827 GTIN Number.4806533601754

Study ClinicalTrials.gov NCT01280344 Type Phase II Subjects Postoperative ileus Key Finding Program discontinued after lack of efficacy signal for the POI endpoint

Research Protocol Summary Study Protocol: 0.25 mg AOD-9604 administered intra-articularly via ultrasound guidance Frequency: Weekly injections Duration: 4-7 weeks in research studies Combination Therapy: 6 mg hyaluronic acid co-administered for enhanced effects Assessment Timeline: Significant improvements observed by 8-9 weeks Note: These protocols are from animal research and have not been validated for human use