drugset / Trial / NCT03913195

Study of the Safety of Trogarzo™ Administered as an Undiluted "IV Push" or an Intramuscular Injection

NCT03913195

Phase 3 Completed 43 enrolled TaiMed Biologics Inc. Westat · collab
Non-randomizedSequentialOpen-labelTreatment

Summary

This study is designed to assess the safety and pharmacokinetic profile of 800 mg Trogarzo once every two weeks administered via "IV Push" or intramuscular injection. An initial "Sentinel Group" of 5 participants will begin receiving 800mg Trogarzo on a gradual schedule of increasing concentration and decreasing administration time until undiluted IV Push over 30 seconds is achieved, while safety and pharmacokinetics are evaluated. If no safety signals are seen, the Core Group of 15 participants will be enrolled. The Core Group will receive 800mg Trogarzo via undiluted IV Push over 30 seconds while safety and pharmacokinetics are monitored. After completion of the IV Push portion of the study, a second group of 20 participants will be enrolled to evaluate the safety and pharmacokinetics of administration of 800mg via intramuscular injection.

Timeline

Start
2019-05-30
Primary completion
2022-10-17
Completion
2022-10-31

Drugs

EvaluationDrugModalityDoseRoute
Subject ibalizumab Monoclonal antibody 800 mg Intravenous