drugset / Trial / NCT04839965

Study of Intravenous Ampion in Adult COVID-19 Patients Requiring Supplemental Oxygen

NCT04839965 ↗

Phase 2 Terminated 36 enrolled Ampio Pharmaceuticals. Inc.
RandomizedParallel-groupDouble-blindTreatment

Summary

This is a Phase 2 randomized study to evaluate the safety and efficacy of IV Ampion in improving the clinical course and outcomes of adult COVID-19 patients requiring supplemental oxygen.

Timeline

Start
2021-07-05
Primary completion
2022-02-07
Completion
2022-04-04

Outcome

Outcome not reported

Stopped: “The AP-017 study was prematurely terminated by the sponsor after an interim analysis.”

Drugs

EvaluationDrugModalityDoseRoute
Subject ASPARTYL-ALANYL-DIKETOPIPERAZINE Protein / enzyme biologic — Intravenous

Indications