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SARS-CoV2 InfectionMAOi-COV19NCT04590222

Impact of a Monoamine Oxidase Inhibitor on the Phenotype of Blood Mononucleated Cells in Patients With COVID-19

An observational study of SARS-CoV2 Infection, run by Assistance Publique - Hôpitaux de Paris at 1 site in France.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record

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Trial summary

The principal objective is to determine the impact of phenelzine on the activation phenotype of T cells and myeloid cells during SARS-CoV2 infection Read more about this study

Who is it for?
Ages 18 years and older
Conditions the study is for
SARS-CoV2 Infection
What is being tested?
blood sample
How many people
51 participants
Where
1 siteFrance
Study dates
20 Nov 2020to 19 Jan 2022
Phase
Observational

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Study population: Patients will be recruited from the Bicêtre Hospital (followed in hospitalization and in ambulatory services)

Who may be able to join

  • 1. Individuals male or female ≥18 years of age at time of enrolment
  • 2.Subject (or legally authorized representative provides non opposition form prior to initiation of any study procedure.
  • 3. Understands and agrees to comply with planned study procedure. (Agrees to the collection of venous blood per protocol).
  • 4. Has laboratory-confirmed SARS-CoV-2 infection as determined by PCR, or other commercial or public health assay in any specimen<72hours prior to enrollment and/or a chest CT scan reported as highly likely SARS-CoV2 infection.
  • The different scales for severity are as follows:
  • 5. Non severe patients: Clinical assessment (evidence of rales/crackles on exam) or CT scan involvement AND SpO2> 94% on room air, or ≤ 94% on room air but > 94% with nasal Oxygen with a flow rate <= 3l O2/min
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  • For the severe infection's patients' group:
  • 6. Patients requiring mechanical ventilation and/or supplemental oxygen >= 6l O2/min
  • For the obese patients 'group:
  • 7. Obese patients will be defined as an BMI > 30
  • 8. Co inclusion in non-interventional researches is possible

Who cannot join

  • Pregnant and breast-feeding women
  • Patients previously treated by phenelzine (Nardil®)
  • Persons unable to give their no opposition
  • Persons under guardianship or curatorship
  • No affiliated to social insurance.

Trial locations and contacts

1 site in 1 country.

France1 site
  • CHU Bicêtre

    Le Kremlin-Bicêtre, 94270

Other trials in France

About this study

The principal objective is to determine the impact of phenelzine on the activation phenotype of T cells and myeloid cells during SARS-CoV2 infection

Read the detailed description

Investigators want to test in vitro (in France Stage 1), and in vivo in a phase 1b/2 clinical trial (Stage 2 in Australia) a widely used antidepressant (the monoamine oxidase inhibitor (MAOi) Phenelzine (Nardil*), repurposed as an antiviral drug to treat SARS-CoV-2. Indeed this proposal leverages extensive existing data on the epigenetic mechanism of action of phenelzine and new data suggesting that it has an anti-viral action against the SARS-CoV-2 virus.

Epigenetic drugs are promising antiviral treatments capable of modifying epigenetic tags and re-programming host and viral genomes. Epigenetic modulation could be useful at least at two steps: the entry of the virus, and the regulation of the immune response. The SARS-Cov-2 depends on ACE2 and TMPRSS2 to gain cellular entry. The reduction of the expression of these proteins could therefore be protective.

Recent clinical studies have demonstrated that, in addition to their effects on neurotransmitter regulation, anti-depressants also possess anti-inflammatory characteristics via impacting pro inflammatory cytokines production which are involved in the 'cytokines storm' during severe disease. (2). These patients also have fewer circulating functional T cells and NK cells and greater numbers of dysfunctional, exhausted CD8+ T cells (3). These abnormalities are probably deleterious and reduce the efficacy of anti-viral responses.

The in-depth and patented epigenetic, cellular, and structural analyses of human cell lines harbouring the SARS-CoV-2 infective machinery and capable of propagating the virus have shown that:

  • The epigenetic enzyme (histone demethylase) LSD1 directly regulates the SARS-CoV-2-binding domain of ACE2 and the protease active sites of TMPRSS2 (patented), which are critical for viral entry and propagation within the host.
  • MAOi, which target LSD1 activity, inhibit the ACE2/TMPRSS2 machinery, which investigators hypothesize will prevent viral entry into the host cell to reduce viral load, disease burden, and the emergence of cytokine storms. In support of novel dual targeting viral blockage strategy recent work have shown that targeting TMPRSS2 or ACE2 alone has anti-viral activity (4).

LSD1 inhibition with Phenelzine in recent, successfully completed phase 1B clinical demonstrate that Phenelzine reverses the dysfunctional T cell phenotype and restores durable memory responses in vivo in advanced, metastatic breast cancer patients. Importantly, no adverse impact on healthy volunteer immune systems was recorded as part of the phase 1B clinical trial (5). Preclinical data shows that aged individuals have exhausted T cells compared to young individuals and MAOi re-waken these T cells resembling younger people.

Thus, investigators propose that in patients with severe COVID-19 infection, who are predominantly elderly; where dysfunctional T cells is also a feature, Phenelzine would have additional benefits on their immune function without adverse effects.

Therefore, this proposal exploits a clear mechanism of action of Phenelzine: epigenetic regulation and is the first study to explore epigenetic mechanisms in SARS-CoV-2 infection. Modulation of the epigenetism could directly counteract the virus via an antiviral effect, and indirectly via the restoration of a functional immune response.

Phenelzine has been used for nearly 60 years to treat major depressive disorder. Its side-effects, most of which are minor, are well characterized, including in the elderly or immune vulnerable.

Investigators approach is highly flexible, since LSD1 inhibition targets two immune mechanisms - a specific viral uptake pathway and the efficacy of T cell responses. Give the safety and easy applicability of Phenelzine, it lends itself to combinatorial therapeutic approaches as and when other anti-viral show efficacy. From the mechanistic perspective, investigators epigenetic approach complements and contextualises genetic studies on COVID-19.

Being tested
blood sample
Keywords
SARS-CoV2 Infection, Monoamine Oxidase Inhibitor, Activation phenotype of T and myeloid cells
Medical subject headings
COVID-19

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • blood sampleOther

    One blood sample of 60 mL (EDTA)

Study groups in NCT04590222
Study groupRoleWhat they receive
Female, BMI≥30, mildFemales: Obese BMI≥30 With Mild infection n = 10
Receives: Other: blood sample
Female, BMI≥30, severeFemales: Obese BMI≥30 With severe infection n = 10
Receives: Other: blood sample
Female, BMI<30, mildFemales: Non-Obese BMI<30 With Mild infection n = 10
Receives: Other: blood sample
Female, BMI<30, severeFemales: Non-Obese BMI<30 With severe infection n = 10
Receives: Other: blood sample
male, BMI≥30, mildmales: Obese BMI≥30 With Mild infection n = 10
Receives: Other: blood sample
male, BMI≥30, severemales: Obese BMI≥30 With severe infection n = 10
Receives: Other: blood sample
male, BMI<30, mildmales: Non-Obese BMI<30 With Mild infection n = 10
Receives: Other: blood sample
male, BMI<30, severemales: Non-Obese BMI<30 With severe infection n = 10
Receives: Other: blood sample
Healthy donors from the EFS (Etablissement Français du Sang, St Louis)Healthy donors from the EFS (Etablissement Français du Sang, St Louis) including 5 men and 5 women
Receives: Other: blood sample

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. levels of lymphocytes T DR + CD38 + and of monocytes CD14 dim + CD16 +.

    evaluate the levels of the activation of T cells and myeloid cells after phenelzine exposure by the levels of the % of DR+ CD38+ T cells and CD14+dim CD16+ monocytes.

    Measured: through study completion, an average of 1 year

Secondary outcomes (5)
  1. level of immune checkpoints

    evaluate the levels of the expression of immune checkpoints on T cells by flow cytometry

    Measured: through study completion, an average of 1 year

  2. cytokine production and proliferation

    evaluate the modification of functional capacities of T cells by cytokines production, and proliferation, after mitogenic and antigen recall stimulations including SARS-CoV-2 antigens

    Measured: through study completion, an average of 1 year

  3. levels of neutrophils

    assess if there is an impact of phenelzine on the activation levels of neutrophils

    Measured: through study completion, an average of 1 year

  4. level of immune responses in obese patients

    Determine if the immune responses in obese patients (a strong risk factor for severe Covid19) can be modulated in the same way compared with lean patients

    Measured: through study completion, an average of 1 year

  5. level of immune responses for men and women

    Determine if the immune responses can be modulated in the same way in men and in women (men being affected by more severe disease)

    Measured: through study completion, an average of 1 year

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted19 Oct 2020
  2. Study start20 Nov 2020
  3. Primary completion19 Jan 2022
  4. Study completion19 Jan 2022

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Case-control
Time perspective
Prospective
Enrolment
51 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT04590222
Sponsor's protocol ID
APHP200989
Other IDs
2020-A02398-31
Acronym
MAOi-COV19
Status last verified
Mar 2026
First submitted
9 Oct 2020
Last updated
23 Apr 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

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