drugset / Trial / NCT01831427

Study to Evaluate the Safety, Tolerability, Pharmacokinetics and Efficacy of GS-5745 (Andecaliximab) in Adults With Moderate to Severe Active Ulcerative Colitis

NCT01831427

Phase 1 Completed 74 enrolled Gilead Sciences
RandomizedSequentialTriple-blindTreatment

Summary

The primary objectives of this study are as follows: * To assess the safety and tolerability of escalating single and multiple doses of GS-5745 (andecaliximab) in participants with moderate to severe ulcerative colitis (UC) as assessed by adverse events (AEs) and laboratory abnormalities * To assess the pharmacokinetics (PK) of GS-5745 (andecaliximab) in participants with moderate to severe UC.

Timeline

Start
2013-03-28
Primary completion
2015-01-05
Completion
2015-02-06

Publications

  • Results Bhandari BR, Fogel R, Onken J, Yen EH, Kanwar B, Subramanian GM, McHutchison GJ, et al. Safety and Efficacy of GS-5745 an Anti-Matrix Metalloproteinase 9 (MMP) Monoclonal Antibody in Patients with Moderately to Severely Active Ulcerative Colitis. Gastroenterology 2015;148 (4): S-1196.

Drugs

EvaluationDrugModalityDoseRoute
Subject Andecaliximab Monoclonal antibody 0.3 mg/kg Intravenous
Subject Andecaliximab Monoclonal antibody 1 mg/kg Intravenous
Subject Andecaliximab Monoclonal antibody 2.5 mg/kg Intravenous
Subject Andecaliximab Monoclonal antibody 5 mg/kg Intravenous
Subject Andecaliximab Monoclonal antibody 150 mg Intravenous

Indications