drugset / Trial / NCT05293236

ApTOLL for the Treatment of COVID-19

NCT05293236 ↗

RandomizedSequentialTriple-blindTreatment

Summary

There is a clear and urgent medical need of developing new medicinal products for COVID-19 since there are poor pharmacological tools to block the progression of patients to cytokine storm syndrome (CSS). To this aim, this Phase Ib clinical study (APTACOVID) pretends to determine whether ApTOLL, in combination with the standard of care, is safe and shows any biological effect) in those patients infected with SARS-CoV-2 who are not developed CSS yet.

Timeline

Start
2022-01-14
Primary completion
2022-12-31
Completion
2022-12-31

Outcome

Outcome not reported

Stopped: “Lack of patients due to reduced incidence in the COVID-19 infected population in Spain”

Drugs

EvaluationDrugModalityDoseRoute
Subject ApTOLL Aptamer 0.05 mg/kg Intravenous
Subject ApTOLL Aptamer 0.1 mg/kg Intravenous
Subject ApTOLL Aptamer 0.2 mg/kg Intravenous

Indications