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Anti-Androgen Treatment for COVID-19

Anti-Androgen Treatment for COVID-19

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04446429
Enrollment
268
Registered
2020-06-24
Start date
2020-10-21
Completion date
2021-01-21
Last updated
2021-12-10

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Androgenetic Alopecia, Benign Prostatic Hyperplasia, COVID-19, Prostate Cancer, SARS-CoV2, SARS (Severe Acute Respiratory Syndrome)

Keywords

Anti-Androgen, Proxalutamide

Brief summary

This study is intended to explore the possible protective role of anti-androgens in SARS-CoV-2 infection

Detailed description

During the continuing SARS-CoV-2 (COVID-19) pandemic, several studies have reported a significant difference in the rate of severe cases between adult females and adult males (42% vs 58%).Among children under the age of 14, the rate of severe cases was reported to be extremely low. To explain this difference, several theories have been proposed including cigarette smoking and lifestyle habits. However, no theory fits both the gender difference in severe cases as well as reduced risk in pre-pubescent children. Our past research on male androgenetic alopecia (AGA) has led us to investigate an association between androgens and COVID-19 pathogenesis. In normal subjects, androgen expression demonstrates significant variation between men and women as well as between adults and pre-pubescent children. SARS-CoV-2 primarily infects type II pneumocytes in the human lung. SARS-CoV-2 enters pneumocytes, by anchoring to the ACE2 cell surface receptor. Prior to receptor binding, viral spike proteins undergo proteolytic priming by the transmembrane protease, serine 2 (TMPRSS2). TMPRSS2 inhibition or knock down reduces ability of SARS-CoV-1 (a related virus to SARS-CoV-2) to infect cells in vitro. Additionally, TMPRSS2 also facilitates entry of influenza A and influenza B into primary human airway cells and type II pneumocytes. The human TMPRSS2 gene has a 15 bp androgen response element and in humans, androgens are the only known transcription promoters for the TMPRSS2 gene. In a study of androgen-stimulated prostate cancer cells (LNCaP), TMPRSS2 mRNA expression increase was mediated by the androgen receptor. Further, the ACE2 receptor, also critical for SARS-CoV-2 viral infectivity, is affected by male sex hormones with higher activity found in males. Androgenetic alopecia (AGA), often referred to as male pattern hair loss, is the most common form of hair loss among men. The development of androgenetic alopecia is androgen mediated and is dependent on genetic variants found in the androgen receptor gene located on the X chromosome; thus, it is hypothesized that men with AGA would be more prone to severe COVID-19 disease. The investigators conducted a preliminary observational study of hospitalized COVID-19 patients at two Spanish tertiary hospitals between March 23-April 6, 2020 to test this theory. In total, 41 Caucasian males admitted to the hospitals with a diagnosis of bilateral SARS-CoV-2 pneumonia were analyzed. The mean age of patients was 58 years (range 23-79). Among them, 29 (71%) were diagnosed with AGA (16 (39%) were classified as severe AGA (Hamilton IV or above)) and 12 (29%) did not present clinical signs of AGA. The diagnosis of AGA was performed clinically by a dermatologist. The precise prevalence of AGA among otherwise healthy Spanish Caucasian males is unknown; however, based on published literature, the expected prevalence of a similar age-matched Caucasian population is approximately 31-53%. Based on the scientific rationale combined with this preliminary observation, the investigators propose to test an anti-androgen as a treatment for patients recently diagnosed with COVID-19. We have chosen the use of the novel second generation androgen receptor (AR) antagonist proxalutamide as a means for rapid reduction in AR activity. Proxalutamide (GT0918) demonstrates a dual mechanism of action. It is highly effective in inhibiting AR as well as exhibiting pharmacological effects of inducing the down-regulation of AR expression; the mechanism that is not present in bicalutamide and enzalutamide. Additionally, it has been reported that Proxalutamide lowers the expression of ACE2. Both would be beneficial for preventing SARS-CoV-2 entry into lung cells. This study is intended to explore the possible protective role of anti-androgens in SARS-CoV-2 infection. Provided anti-androgens are effective in reducing the rate of COVID-19 hospitalization, subjects enrolled in this study may experience a lower rate of hospitalization.

Interventions

200 mg q.d.

OTHERStandard of Care

Standard of care as determined by the PI

Sponsors

Applied Biology, Inc.
Lead SponsorINDUSTRY

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Intervention model description

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

Eligibility

Sex/Gender
MALE
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

1. Male age ≥18 years old 2. Laboratory confirmed positive SARS-CoV-2 rtPCR test within 7 days prior to randomization 3. Clinical status on the COVID-19 8-point Ordinal Scale of 1 or 2 4. Coagulation: INR ≤ 1.5×ULN, and APTT ≤ 1.5×ULN 5. Subject (or legally authorized representative) gives written informed consent prior to any study screening procedures 6. Subject (or legally authorized representative) agree that subject will not participate in another COVID-19 trial while participating in this study

Exclusion criteria

1. Subject enrolled in a study to investigate a treatment for COVID-19 2. Subject taking an anti-androgen of any type including: androgen depravation therapy, 5-alpha reductase inhibitors, etc… 3. Patients who are allergic to the investigational product or similar drugs (or any excipients); 4. 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 5. 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 6. Subjects with uncontrolled medical conditions that could compromise participation in the study(e.g. uncontrolled hypertension, hypothyroidism, diabetes mellitus) 7. Known diagnosis of human immunodeficiency virus(HIV) , hepatitis C, active hepatitis B, treponema pallidum (testing is not mandatory) 8. Alanine Transaminase (ALT) or Aspartate Transaminase (AST) \> 5 times the upper limit of normal. 9. Estimated glomerular filtration rate (eGFR) \< 30 ml/min 10. Severe kidney disease requiring dialysis 11. Subject unlikely to return for day 15 site visit for reasons other then remission 12. Subject (or legally authorized representative) not willing or unable to provide informed consent

Design outcomes

Primary

MeasureTime frameDescription
COVID-19 Hospitalization30 daysPercentage of subjects hospitalized due to COVID-19

Countries

Brazil

Participant flow

Participants by arm

ArmCount
Usual Care
Usual care as determined by the PI Usual Care: Care as determined by the PI
134
Proxalutamide + Usual Care
Proxalutamide + usual care as determined by the PI Proxalutamide: 200 mg q.d.
134
Total268

Withdrawals & dropouts

PeriodReasonFG000FG001
Overall StudyLost to Follow-up60

Baseline characteristics

CharacteristicTotalUsual CareProxalutamide + Usual Care
Age, Continuous44.5 years
STANDARD_DEVIATION 7.7
45 years
STANDARD_DEVIATION 10.8
44.2 years
STANDARD_DEVIATION 14
Coexisting conditions49 Participants20 Participants29 Participants
Race/Ethnicity, Customized
Mixed ethnicity (Brazil)
268 Participants134 Participants134 Participants
Region of Enrollment
Brazil
268 participants134 participants134 participants
Sex: Female, Male
Female
0 Participants0 Participants0 Participants
Sex: Female, Male
Male
268 Participants134 Participants134 Participants

Adverse events

Event typeEG000
affected / at risk
EG001
affected / at risk
deaths
Total, all-cause mortality
2 / 1340 / 134
other
Total, other adverse events
78 / 13445 / 134
serious
Total, serious adverse events
35 / 1343 / 134

Outcome results

Primary

COVID-19 Hospitalization

Percentage of subjects hospitalized due to COVID-19

Time frame: 30 days

Population: All randomized patients were included. 6 patients from the placebo arm lost to follow-up were assumed to be non-hospitalized (COVID-19 8-point ordinal scale 1) and were included in the intention-to-treat analysis.

ArmMeasureValue (COUNT_OF_PARTICIPANTS)
Usual CareCOVID-19 Hospitalization35 Participants
Proxalutamide + Usual CareCOVID-19 Hospitalization3 Participants

Source: ClinicalTrials.gov · Data processed: Feb 17, 2026