The South Proxa-Rescue AndroCoV Trial Against COVID-19

Sponsor

Corpometria Institute (Other)

Overall Status

Completed

CT.gov ID

NCT05126628

Collaborator

Hospital da Brigada Militar de Porto Alegre, Porto Alegre, Brazil (Other), Hospital Arcanjo Sao Miguel, Gramado, Brazil (Other), Hospital Unimed Chapeco, Chapeco, Brazil (Other)

133

Enrollment

Location

Arms

1.3

Actual Duration (Months)

101.2

Patients Per Site Per Month

Study Details

Study Description

Brief Summary

The purpose of this study is to investigate the efficacy of proxalutamide or hospitalized moderate-to-severe COVID-19 patients.

Condition or Disease	Intervention/Treatment	Phase
COVID-19	Drug: Proxalutamide Drug: Placebo	Phase 3

Study Design

Study Type:

Interventional

Actual Enrollment :

133 participants

Allocation:

Randomized

Intervention Model:

Parallel Assignment

Intervention Model Description:

This study is designed as a prospective, interventional, placebo controlled, double-blinded, randomized parallel assignment study.This study is designed as a prospective, interventional, placebo controlled, double-blinded, randomized parallel assignment study.

Masking:

Double (Participant, Care Provider)

Masking Description:

Double (Participant, Care Provider)

Primary Purpose:

Treatment

Official Title:

Proxalutamide Treatment for Hospitalized COVID-19 Patients in Southern Brazil - The South Proxa-Rescue AndroCoV Trial

Actual Study Start Date :

Mar 6, 2021

Actual Primary Completion Date :

Mar 16, 2021

Actual Study Completion Date :

Apr 15, 2021

Arms and Interventions

Arm	Intervention/Treatment
Active Comparator: Active Comparator: Proxalutamide + Usual Care Proxalutamide + usual care as determined by care provider	Drug: Proxalutamide Proxalutamide 300mg q.d.(3 tablets of 100mg each) for 14 days.
Placebo Comparator: Placebo Comparator: Placebo + Usual Care Placebo + usual care as determined by care provider	Drug: Placebo Placebo 3 tablets q.d. for 14 days

Arm

Intervention/Treatment

Active Comparator: Active Comparator: Proxalutamide + Usual Care

Proxalutamide + usual care as determined by care provider

Drug: Proxalutamide

Proxalutamide 300mg q.d.(3 tablets of 100mg each) for 14 days.

Placebo Comparator: Placebo Comparator: Placebo + Usual Care

Placebo + usual care as determined by care provider

Drug: Placebo

Placebo 3 tablets q.d. for 14 days

Outcome Measures

Primary Outcome Measures

14-Day Recovery Rate [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: 8. Death; 7. Hospitalized, on invasive mechanical ventilation or ECMO; 6. Hospitalized, on non-invasive ventilation or high flow oxygen devices; 5. Hospitalized, requiring supplemental oxygen; 4. Hospitalized, not requiring supplemental oxygen- requiring ongoing medical care (COVID-19 related or otherwise; 3. Hospitalized, not requiring supplemental oxygen - no longer requires ongoing medical care; 2. Not hospitalized, limitation on activities; 1. Not hospitalized, no limitations on activities

Secondary Outcome Measures

28-Day Recovery Rate [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: 8. Death; 7. Hospitalized, on invasive mechanical ventilation or ECMO; 6. Hospitalized, on non-invasive ventilation or high flow oxygen devices; 5. Hospitalized, requiring supplemental oxygen; 4. Hospitalized, not requiring supplemental oxygen- requiring ongoing medical care (COVID-19 related or otherwise; 3. Hospitalized, not requiring supplemental oxygen - no longer requires ongoing medical care; 2. Not hospitalized, limitation on activities; 1. Not hospitalized, no limitations on activities
14-Day All-Cause Mortality Rate [Day 14]
Treatment efficacy of proxalutamide relative to placebo as assessed by all-cause mortality rate over 14 days post randomization.
28-Day All-Cause Mortality Rate [Day 28]
Treatment efficacy of proxalutamide relative to placebo as assessed by all-cause mortality rate over 28 days post randomization.
Post-Randomization Time to Recover (Alive Hospital Discharge) [Day 28]
Treatment efficacy of proxalutamide relative to placebo as assessed by number of day post-randomization required to achieve live hospital discharge.
Proportion of subjects needing potent, large-spectrum antibiotics [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. (%)
Proportion of increased ultrasensitive C-reactive protein (usCRP) (defined as usRCP > 7 mg/L) [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.
Proportion of increased d-dimer (defined as d-dimer > 500 mg/dL) [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.

Eligibility Criteria

Criteria

Ages Eligible for Study:

18 Years and Older

Sexes Eligible for Study:

All

Accepts Healthy Volunteers:

Inclusion Criteria:

Admitted to the hospital with symptoms of COVID-19 within 7 days
Male and females age ≥18 years old
Laboratory confirmed positive SARS-CoV-2 rtPCR test
Clinical status on the COVID-19 Ordinal Scale (defined in Section 5.1) of 3, 4, 5, or 6
Coagulation: INR ≤ 1.5×ULN, and APTT ≤ 1.5×ULN
Subject (or legally authorized representative) gives written informed consent prior to performing any study procedures
Subject (or legally authorized representative) agree that subject will not participate in another COVID-19 trial while participating in this study

Exclusion Criteria:

Subject enrolled in a study to investigate a treatment for COVID-19
Requires mechanical ventilation
Subject taking an anti-androgen of any type including: androgen depravation therapy, 5-alpha reductase inhibitors, etc…
Patients who are allergic to the investigational product or similar drugs (or any excipients);
Subjects who have malignant tumors in the past 5 years, with the exception of completed resected basal cell and squamous cell skin cancer and completely resected carcinoma in situ of any type
Subjects with known serious cardiovascular diseases, congenital long QT syndrome, torsade de pointes, myocardial infarction in the past 6 months, or arterial thrombosis, or unstable angina pectoris, or congestive heart failure which is classified as New York Heart Association (NYHA) class 3 or higher, or left ventricular ejection fraction (LVEF) < 50%, QTcF > 450 ms
Subjects with uncontrolled medical conditions that could compromise participation in the study(e.g. uncontrolled hypertension, uncontrolled hypothyroidism, uncontrolled diabetes mellitus)
Known diagnosis of human immunodeficiency virus(HIV) , hepatitis C, active hepatitis B, treponema pallidum (testing is not mandatory）
Alanine Transaminase (ALT) or Aspartate Transaminase (AST) > 5 times the upper limit of normal.
Estimated glomerular filtration rate (eGFR) < 30 ml/min
Severe kidney disease requiring dialysis
Women of child-bearing potential, defined as all women physiologically capable of becoming pregnant, unless they are using highly effective contraception, as shown below, throughout the study and for 3 months after stopping GT0918 treatment. Highly effective contraception methods include:
Total Abstinence (when this is in line with the preferred and usual lifestyle of the patient. Periodic abstinence (e.g. calendar, ovulation, symptothermal, post-ovulation methods) and withdrawal are not acceptable methods of contraception, or
Use of one of the following combinations (a+b or a+c or b+c):

Use of oral, injected or implanted hormonal methods of contraception or other forms of hormonal contraception that have comparable efficacy (failure rate < 1%), for example hormone vaginal ring or transdermal hormone contraception.
Placement of an intrauterine device (IUD) or intrauterine system (IUS) ;
Barrier methods of contraception: Condom or Occlusive cap (diaphragm or cervical/vault caps) with spermicidal foam/gel/film/cream/vaginal suppository ;

Female sterilization (have had prior surgical bilateral oophorectomy with or without hysterectomy) or tubal ligation at least six weeks before taking study treatment. In case of oophorectomy alone, only when the reproductive status of the woman has been confirmed by follow-up hormone level assessment ;
Male sterilization (at least 6 months prior to screening). For female patients on the study, the vasectomized male partner should be the sole partner for that patient;
In case of use of oral contraception women should have been stable for a minimum of 3 months before taking study treatment. Women are considered post-menopausal and not of child bearing potential if they have had 12 months of natural (spontaneous) amenorrhea with an appropriate clinical profile (e.g. age appropriate, history of vasomotor symptoms) or have had surgical bilateral oophorectomy (with or without hysterectomy) or tubal ligation at least six weeks ago. In the case of oophorectomy alone, only when the reproductive status of the woman has been confirmed by follow up hormone level assessment, is she considered not of child bearing potential;
Sexually active males that do not to use a condom during intercourse while taking the drug and for 3 months after stopping GT0918 treatment and should not father a child in this period. A condom is required to be used also by vasectomized men in order to prevent delivery of the drug via seminal fluid.
Subject likely to transfer to another hospital within the next 28 days
Subject (or legally authorized representative) not willing or unable to provide informed consent