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Clinical Trial Summary

Phase 1b/2a, Randomized, Double-Blind, Placebo-Controlled, Multiple Ascending Dose Escalation Study of the Safety, Tolerability, and Efficacy of Intravenous AP SA02 as an Adjunct to Best Available Antibiotic Therapy Compared to Best Available Antibiotic Therapy Alone for the Treatment of Adults With Bacteremia Due to Staphylococcus aureus


Clinical Trial Description

This study will be conducted in two phases: Phase 1b will to evaluate the safety and tolerability of multiple ascending intravenous (IV) doses of AP-SA02 or placebo as an adjunct to best available therapy (BAT) compared to BAT alone in subjects with SA bacteremia (SAB). Phase 2a will evaluate the efficacy, safety, and tolerability of multiple doses of AP-SA02 or placebo as an adjunct to BAT compared to BAT alone in subjects with complicated SAB. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05184764
Study type Interventional
Source Armata Pharmaceuticals, Inc.
Contact Vicki White, BS
Phone 310-633-4566
Email [email protected]
Status Not yet recruiting
Phase Phase 1/Phase 2
Start date February 2022
Completion date December 2023

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