Proxalutamide
DrugProxalutamide 300mg q.d
NCT Number: NCT04728802
The purpose of this study is to assess the efficacy and safety of Proxalutamide as a treatment for hospitalized COVID-19 male and female patients.
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Notify Me18 year and older
All sexes
Interventional
Phase 3
Hospital Regional José Mendes, Itacoatiara, Amazonas, Brazil
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Proxalutamide 300mg q.d
Placebo pill
Time frame: Day 14
Recovery rate defined as those reaching scores 1 or 2 over 14 days after randomization on the COVID-19 ordinal scale.
The ordinal scale is defined as follows:
Time frame: Day 28
Recovery rate defined as those reaching scores 1 or 2 over 28 days after randomization on the COVID-19 ordinal scale.
The ordinal scale is defined as follows:
Time frame: 28 days
All-cause mortality rate over 28 days post randomization.
Time frame: 28 days
Number of day post-randomization required to achieve live hospital discharge.
Applied Biology, Inc.
Industry
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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