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Study Designed to Evaluate the Effect of CimetrA in Patients Diagnosed With COVID-19

M

MGC Pharmaceuticals

Status and phase

Completed
Phase 2

Conditions

Corona Virus Infection
Covid19

Treatments

Diagnostic Test: PK parameters
Diagnostic Test: POST- COVID-19 Functional Status Scale:
Diagnostic Test: VAS scale
Diagnostic Test: Pregnancy test
Diagnostic Test: D-Dimer test (coagulation)
Diagnostic Test: Vital signs
Diagnostic Test: COVID-19-Related Symptoms assessment
Diagnostic Test: COVID-19-Impact on Quality-of-Life Questionnaire
Diagnostic Test: Inflammatory markers
Diagnostic Test: ECG
Diagnostic Test: SARS-CoV-2 test (PCR)
Diagnostic Test: Hematology blood test
Diagnostic Test: Biochemistry blood test
Diagnostic Test: WHO Ordinal Score
Drug: Treatment administration (twice a day)
Diagnostic Test: Physical examination

Study type

Interventional

Funder types

Industry

Identifiers

NCT05037162
MGC-009

Details and patient eligibility

About

Multi-center multinational-controlled study in Israel, Brazil, Spain, and South-Africa.

240 adult patients who suffer from moderate COVID-19 infection. Safety will be assessed through collection and analysis of adverse events, blood and urine laboratory assessments and vital signs.

After Screening visit, the study drug will be administrated twice a day morning and evening (every 12 hours) during (day 1 and day 2) The patients will be randomized in 1:1:1 ratio to study drug (CimetrA) in two dosages in addition to Standard of Care - Arm 1, 2 or (Placebo) in addition to Standard of Care- Arm 3.

Full description

A preparation of CimertA (Botanical Drug), comprising Curcumin, Boswellia, and Vitamin C in a nanoparticular formulation, is proposed as a treatment for the disease associated with the novel corona virus SARS-CoV-2. This initiative is presented under the urgent circumstances of the fulminant pandemic caused by this lethal disease, which is known as COVID-19 and has spread across the globe causing death and disrupting the normal function of modern society. The grounds for the proposal are rooted in existing knowledge on the components and pharmacological features of this formulation and their relevance to the current understanding of the disease process being addressed.

The breakout of a lethal pneumonia in the city of Wuhan, China, towards the end of 2019, has led to the characterization of the new coronavirus related disease COVID-19. Its prominent features include a high rate of person-to-person transmission, a substantial risk of developing a lethal respiratory syndrome and potential failure of additional organs. Risk factors for a life-threatening clinical course have been identified, including advanced age and assorted comorbidities, such as cardiovascular disease, diabetes mellitus, hypertension, cancer. However, individuals devoid of any of the recognized risk factors are not immune to the severe manifestation of the disease and once infected carry a certain risk of mortality which has been calculated in Italy at circa 2%.

CoV is an enveloped, positive-sense single-stranded RNA (ss-RNA) virus belonging to the Coronaviridae family. The severe acute respiratory syndrome associated coronavirus disease 2019 (COVID-19) illness is a syndrome of viral replication in concert with a host inflammatory response. The cytokine storm and viral evasion of cellular immune responses may play an equally important role in the pathogenesis, clinical manifestation, and outcomes of COVID-19. Systemic proinflammatory cytokines and biomarkers are elevated as the disease progresses towards its advanced stages, and correlate with worse chances of survival.

SARS-CoV-2 activates the innate immune system and results in a release of a large number of cytokines, including IL-6, which can increase vascular permeability and cause a migration of fluid and blood cells into the alveoli as well as the consequent symptoms such as dyspnea and respiratory failure. The higher mortality is being linked to the result of ARDS (acute respiratory distress syndrome) aggravation and the tissue damage that can result in organ-failure and/or death.

Serum cytokine levels that are elevated in patients with Covid-19-associated cytokine storm include interleukin-1β, interleukin-6, IP-10, TNF, interferon-γ, macrophage inflammatory protein (MIP) 1α and 1β, and VEGF. Higher interleukin-6 levels are strongly associated with shorter survival. The relative frequencies of circulating activated CD4+ and CD8+ T cells and plasma blasts are increased in Covid-19. In addition to the elevated systemic cytokine levels and activated immune cells, several clinical and laboratory abnormalities, such as elevated CRP and d-dimer levels, hypoalbuminemia, renal dysfunction, and effusions, are also observed in Covid-19, as they are in cytokine storm disorders. Laboratory test results reflecting hyperinflammation and tissue damage were found to predict worsening outcomes in Covid-19.

CimetrA, comprising Curcumin, Boswellia, and Vitamin C in a nanoparticular formulation, was studied on patients with the novel corona virus SARS-CoV-2 in randomized double blind control Phase II study (MGC-006 - under a previous product name - ArtemiC). The study product demonstrated excellent safety and efficacy profiles.

In the in vitro clinical trial CimetrA demonstrated the ability to reduce cytokines elevation in PBMC induced cell tissue.

Enrollment

240 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Confirmed by PCR test SARS-CoV-2 infection (according to nationally authorized laboratory criteria)
  2. Hospitalized patient with COVID-19 of moderate stable or worsening severity not requiring ICU admission (defined by NIH criteria - fever, cough, dyspnea, fast breathing, but no signs of severe pneumonia, including SpO2 ≥ 94% on room air).
  3. Age: 18 years old and above.
  4. Subjects must be hospitalized
  5. Ability to receive treatment by spray into the oral cavity

Exclusion criteria

  1. Tube feeding or parenteral nutrition.
  2. Patients with scores 5 or above per the Ordinal Scale for Clinical Improvement published by the WHO. (i.e., who need oxygen supply beyond use of nozzles or simple mask)
  3. Need for admission to ICU during the present hospitalization at any time prior to completion of the recruitment to the study.
  4. Any condition which, in the opinion of the Principal Investigator, would prevent full participation in this trial or would interfere with the evaluation of the trial endpoints.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Triple Blind

240 participants in 3 patient groups, including a placebo group

Arm 1 - CimetrA-1
Experimental group
Description:
CimetrA-1, with a total dose containing a combination of Curcumin 40 mg, Boswellia 30 mg and Vitamin C 120 mg in spray administration - divided in 4 separate doses given as an add on therapy, total of 4 doses over 48 hours (day 1 and day 2), twice a day (morning and evening).
Treatment:
Diagnostic Test: Hematology blood test
Diagnostic Test: WHO Ordinal Score
Diagnostic Test: Physical examination
Drug: Treatment administration (twice a day)
Diagnostic Test: Vital signs
Diagnostic Test: Biochemistry blood test
Diagnostic Test: COVID-19-Related Symptoms assessment
Diagnostic Test: COVID-19-Impact on Quality-of-Life Questionnaire
Diagnostic Test: Inflammatory markers
Diagnostic Test: ECG
Diagnostic Test: PK parameters
Diagnostic Test: Pregnancy test
Diagnostic Test: D-Dimer test (coagulation)
Diagnostic Test: POST- COVID-19 Functional Status Scale:
Diagnostic Test: VAS scale
Diagnostic Test: SARS-CoV-2 test (PCR)
Arm 2 - CimetrA-2
Experimental group
Description:
CimetrA-2, with a total dose containing a combination of Curcumin 28 mg, Boswellia 21 mg and Vitamin C 84 mg in spray administration - divided in 4 separate doses given as an add on therapy, total of 4 doses over 48 hours (day 1 and day 2), twice a day (morning and evening).
Treatment:
Diagnostic Test: Hematology blood test
Diagnostic Test: WHO Ordinal Score
Diagnostic Test: Physical examination
Drug: Treatment administration (twice a day)
Diagnostic Test: Vital signs
Diagnostic Test: Biochemistry blood test
Diagnostic Test: COVID-19-Related Symptoms assessment
Diagnostic Test: COVID-19-Impact on Quality-of-Life Questionnaire
Diagnostic Test: Inflammatory markers
Diagnostic Test: ECG
Diagnostic Test: PK parameters
Diagnostic Test: Pregnancy test
Diagnostic Test: D-Dimer test (coagulation)
Diagnostic Test: POST- COVID-19 Functional Status Scale:
Diagnostic Test: VAS scale
Diagnostic Test: SARS-CoV-2 test (PCR)
Arm 3 - Placebo
Placebo Comparator group
Description:
Placebo, composed of the same solvent but without active ingredients, given as an add on therapy in spray administration, total of 4 doses over 48 hours (day 1 and day 2), twice a day (morning and evening).
Treatment:
Diagnostic Test: Hematology blood test
Diagnostic Test: WHO Ordinal Score
Diagnostic Test: Physical examination
Drug: Treatment administration (twice a day)
Diagnostic Test: Vital signs
Diagnostic Test: Biochemistry blood test
Diagnostic Test: COVID-19-Related Symptoms assessment
Diagnostic Test: COVID-19-Impact on Quality-of-Life Questionnaire
Diagnostic Test: Inflammatory markers
Diagnostic Test: ECG
Diagnostic Test: PK parameters
Diagnostic Test: Pregnancy test
Diagnostic Test: D-Dimer test (coagulation)
Diagnostic Test: POST- COVID-19 Functional Status Scale:
Diagnostic Test: VAS scale
Diagnostic Test: SARS-CoV-2 test (PCR)

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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