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Low-doses Melphalan Inhalation in Patients With COVID-19 (CoronavIrus Disease 2019) Pneumonia (MICOV)

F

Federal State Budgetary Institution, Pulmonology Scientific Research Institute

Status and phase

Unknown
Phase 2

Conditions

COVID-19
Viral Pneumonia

Treatments

Other: Standard of care
Drug: Melphalan

Study type

Interventional

Funder types

Other

Identifiers

NCT04380376
PSRI05-20

Details and patient eligibility

About

This single-center, prospective, open-label, comparator study, blind for central accessor evaluates the efficacy, safety of inhalations of low-doses of melphalan in patients with pneumonia with confirmed or suspected COVID-19. All patients will receive 0,1 mg of melphalan in 7-10 daily inhalations 1 time per day.

Full description

It was previously shown that in ultra-low (more than 100 times lower than conventional therapeutic) doses inhalations of alkylating drug (melphalan) are effective in severe steroid-resistant bronchial asthma, a form of the disease often characterised by neutrophilic type of inflammation. The exacerbation frequency reduced after the treatment, steroid-sparing effect was shown, morphological signs of bronchial epithelial regeneration were revealed and quality of life of asthmatic patients, treated with ultra-low doses of melphalan, improved. In preclinical studies and studies with volunteers, it was found that inhalations of ultra-low doses of melphalan do not have cytotoxic properties, but have local and systemic anti-inflammatory effects and decrease the activation of lymphocytes due to blockade of heavy β-chain of the interleukin (IL)-2 surface receptor. In addition, in ultra-low concentrations, alkylating agents are able to disrupt the cell signalling through the receptor for tumor necrosis factor (TNF), thereby exerting a protective effect from the cytotoxic activity of TNF-α, which leads to the anti-inflammatory response.

Taking into account, that severe cases of COVID are characterised with hyperergic inflammatory response (and in some cases even with the development of "cytokine storm") it can be assumed that the inhalation use of low-doses of melphalan due to its anti-inflammatory properties can be effective treatment for patients with COVID-associated pneumonia.

Enrollment

60 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Age ≥18 years
  2. A patient must have confirmed the diagnosis of bi-lateral moderate / severe pneumonia ( viral or viral-bacterial with confirmed of suspected COVID-19).
  3. Presence new infiltrates or increase already available infiltrates of pulmonary infiltrates on lung CT within 48 hours before baseline.
  4. A patient has as minimum one of the following symptoms:

fever >38 degrees Celsius, cough, dyspnea, SaO2 (arterial oxygen saturation) <95% (with room air)

Exclusion criteria

  1. Informed consent is withdrawn by the patient.
  2. The patient doesn't follow the instructions of the research staff regarding the requirements of the research protocol.
  3. Unable to contact the patient.
  4. The researcher believes that participation in the study is not in the interests of the patient and / or further participation in the study is unsafe for the patient's health.
  5. There is a violation of the criteria for inclusion and / or non-inclusion in the study.
  6. The patient has developed an adverse event, which, according to the researcher, makes further participation in the study unsafe for the patient.
  7. The licensing authority or ethics committee, for any reason, decides to discontinue the entire study or close this research center.
  8. A female patient becomes pregnant, is planning a pregnancy, or is breastfeeding while participating in this study.

Trial design

Primary purpose

Treatment

Allocation

Non-Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

60 participants in 2 patient groups

Melphalan inhalations
Experimental group
Description:
Inhalations with Melphalan 0,1 mg dissolved in 2 ml sodium chloride (NaCl) 0,9% 1 per day for 7-10 consequent days
Treatment:
Drug: Melphalan
Standard of care group
Other group
Description:
Patients assigned to the standard of care group will not receive any additional therapy.
Treatment:
Other: Standard of care

Trial contacts and locations

2

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Central trial contact

Evgeny Sinitsyn; Kiril A Zykov, Prof

Data sourced from clinicaltrials.gov

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