Corpometria Institute
Brasília, Federal District, 70390-150, Brazil
NCT Number: NCT05126628
The purpose of this study is to investigate the efficacy of proxalutamide or hospitalized moderate-to-severe COVID-19 patients.
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Notify Me18 year and older
All sexes
Interventional
Phase 3
Brasília, Federal District, 70390-150, Brazil
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Proxalutamide 300mg q.d.(3 tablets of 100mg each) for 14 days.
Placebo 3 tablets q.d. for 14 days
Time frame: Day 14
Treatment efficacy of proxalutamide relative to placebo as assessed by 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
Treatment efficacy of proxalutamide relative to placebo as assessed by 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: Day 14
Treatment efficacy of proxalutamide relative to placebo as assessed by all-cause mortality rate over 14 days post randomization.
Time frame: Day 28
Treatment efficacy of proxalutamide relative to placebo as assessed by all-cause mortality rate over 28 days post randomization.
Time frame: Day 28
Treatment efficacy of proxalutamide relative to placebo as assessed by number of day post-randomization required to achieve live hospital discharge.
Time frame: Day 28
Defined as the number of subjects who have required vancomycin, meropenem or polymyxin B allocated to each arm divided by the number of subjects randomized to that specific arm (%). Treatment efficacy of proxalutamide relative to placebo arm as assessed by the proportion of subjects needing vancomycin, meropenem or polymyxin B in each arm. (%)
Time frame: Day 7
Treatment efficacy of proxalutamide relative to placebo arm as assessed by the rate between the percentage of subjects presenting increased ultrasensitive C-reactive protein (usCRP) at Day 7 after randomization allocated in each arm.
Time frame: Day 7
Treatment efficacy of proxalutamide relative to placebo arm as assessed by the rate between the percentage of subjects presenting increased d-dimer at Day 7 after randomization allocated in each arm.
Corpometria Institute
Other
Proxalutamide Treatment for Hospitalized COVID-19 Patients in Southern Brazil - The South Proxa-Rescue AndroCoV Trial
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