Metabolic Cofactor Supplementation and Hydroxychloroquine Combination in Covid-19 Patients

COVID-19 Clinical Trial

Official title:

A Multi Centre, Randomised, Controlled, Open-Label Phase 2/3 Study to Evaluate The Efficacy, Tolerability and Safety of Metabolic Cofactor Supplementation and Hydroxychloroquine Combination in Covid-19 Patients

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT04573153
• Other study ID #: COVID-19-MCS
• Status: Recruiting
• Phase: Phase 2/Phase 3
• Start date: September 21, 2020
• Est. completion date: March 31, 2021

Study information

• Verified date: September 2020
• Source: ScandiBio Therapeutics AB
• Contact: Assoc. Prof. Levent DOGANAY, MD
• Phone: +90 505 525 04 91
• Email: ldoganay[@]hotmail.com
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This open label, randomized, controlled, investigator-initiated, multi-centre trial aims to establish metabolic improvements in COVID-19 subjects by dietary supplementation with cofactors N-acetylcysteine, L-carnitine tartrate, nicotinamide riboside and serine plus standard therapy. The primary objective is to assess the clinical efficacy of the combination of metabolic cofactors supplementation and hydroxychloroquine in COVID-19 patients.

Description:

Coronaviruses are a large family of ribonucleic acid viruses that cause mild to moderate upper respiratory diseases in humans. There is an urgent need for COVID-19 therapeutics due to the S-shaped curve expansion of the infections, widespread pandemic status, and global burden. Given the similarities between SARS-CoV-2 and other coronaviruses, and its relative ease of sample acquisition and study, it has been widely accepted that drug repositioning is a promising approach to make available an effective, safety-assured treatment in a timely manner.

This open label, randomized, controlled, investigator-initiated, multi-centre trial aims to establish metabolic improvements in COVID-19 subjects by dietary supplementation with cofactors N-acetylcysteine, L-carnitine tartrate, nicotinamide riboside and serine plus standard therapy. The investigational drug products, the mixture of the four co-factors will be administered as a powder with strawberry aroma to be dissolved in 200 ml of preferably cold still drinking water and be consumed within 5 minutes.

This study is planned as a Phase II / III clinical drug research to be conducted in patients diagnosed with COVID-19. Patients will be ambulatory and after the diagnosis/confirmation of diagnosis, will be sent home with their treatment. However, patients may be hospitalised during this initial examination period due to deterioration in their physical health or due to any medical condition which was not present at admission.

The primary objective is to assess the clinical efficacy of the combination of metabolic cofactors supplementation and hydroxychloroquine in COVID-19 patients. For the primary purpose, the proportion of patients who were hospitalised during the course of disease until 14 days after the initial diagnosis of Covid-19 disease will be compared. Patients who were hospitalised during the 14-day period, but at any time point after consenting will be evaluated as an end-point occurrence.

The secondary aim in this study is to evaluate the safety and tolerability of metabolic cofactors supplementation and hydroxychloroquine combination.

The initial part of the Phase II/III study is planned as a Phase II study which will enrol 100 patients and after an interim analysis it will conclude as a Phase III study (300 patients). Totally 400 COVID-19 disease patients will be randomized on a 3:1 basis to the combination metabolic cofactors supplementation and hydroxychloroquine or hydroxychloroquine+ placebo in eight clinical sites in Turkey.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 400
• Est. completion date: March 31, 2021
• Est. primary completion date: January 31, 2021
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Patients of both genders (females and males) over 18 years of age

• Written informed consent obtained from the subjects prior to any procedures related to the study

• Understand all procedures to be applied within the scope of the study protocol

• Ambulatory patients with symptoms diagnosed with COVID-19 with Chest tomography (CT) result positivity in the last 72 hours

• Patients with stable clinical course and who could be treated on an ambulatory basis.

Exclusion Criteria:

• Patients who has partial oxygen saturation below 93% and require immediate hospitalisation after diagnosis

• Patients, upon initial examination, decided to be hospitalised at the intensive care-unit

• Inability or unwillingness to give written informed consent

• At physicians decision, the trial involvement will not be in patients' best interest, or any condition that does not allow the protocol to be followed safely

• Patients considered as inappropriate for this study for any reason

• Active participation in another clinical study

• Uncontrolled Type 1 or type 2 diabetes

• Severe liver disease (e.g. Child Pugh score = C, AST>5 times upper limit)

• Patients with known severe renal impairment (estimated glomerular filtration rate =30 mL/min/1.73 m2) or receiving continuous renal replacement therapy, hemodialysis, peritoneal dialysis

• Significant cardiovascular co-morbidity (i.e. heart failure)

• Patients with phenylketonuria (contraindicated for NAC)

• Known allergy for substances used in the study

• Pregnant or breastfeeding patients, or patients with positive pregnancy test in a pre-dose examination

• Receipt of any experimental treatment for COVID-19 within the 30 days prior to the time of the screening evaluation.

Related Conditions & MeSH terms

• COVID-19

Intervention

Drug:
• Hydroxychloroquine + Metabolic cofactor supplementation
Treatment arm will include dietary supplement consisting of serine, L-carnitine tartrate, N-acetylcysteine and nicotinamide riboside + standard therapy (hydroxychloroquine).
• Hydroxychloroquine + Sorbitol
Placebo comparator will include sorbitol as placebo + standard therapy (hydroxychloroquine).

Locations

Country	Name	City	State
Turkey	University of Health Sciences Istanbul Ümraniye Training and Research Hospital	Istanbul

Sponsors (10)

Lead Sponsor

Collaborator

ScandiBio Therapeutics AB

Alanya Alaaddin Keykubat University Alanya Training and Research Hospital, Bagcilar Training and Research Hospital, Bakirkoy Dr. Sadi Konuk Research and Training Hospital, Canakkale 18 Mart University Health Research and Application Hospital, Dr. Lutfi Kirdar Kartal Training and Research Hospital, Istanbul Medipol University Hospital, Istanbul Umraniye Training and Research Hospital, Kanuni Sultan Suleyman Training and Research Hospital, Monitor CRO

Country where clinical trial is conducted

Turkey, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	The evaluation of clinical efficacy of the combination of metabolic cofactor supplementation and hydroxychloroquine	The clinical efficacy will be evaluated by comparing the proportion of patients who were hospitalised during the course of disease until 14 days after the initial diagnosis of Covid-19.	14 days
Secondary	Adverse Event (AE), Serious Adverse Event (SAE) and discontinuation of treatment	Number/characteristics of Adverse Event (AE), Serious Adverse Event (SAE) and discontinuation of treatment due to study drug from baseline until the end of study.	14 days
Secondary	Chest Tomography	Chest imaging will be documented at baseline visit.	1 day
Secondary	ECG Measurement	Change in heart rate will be measured at baseline visit.	1 day
Secondary	Change of complete blood count from baseline	Complete blood count includes number of blood cells and concentration of hemoglobin. Complete blood count will be performed to measure possible toxic effects of the metabolic cofactors supplementation and hydroxychloroquine combination on hematological system.	14 days
Secondary	Changes in alanine aminotransferase (ALT) levels from baseline	Clinical evaluation of ALT levels from baseline until the end of study.	14 days
Secondary	Changes in aspartate aminotransferase (AST) levels from baseline	Clinical evaluation of AST levels from baseline until the end of study.	14 days
Secondary	Changes in C-reactive protein (CRP) levels from baseline	Clinical evaluation of CRP levels from baseline until the end of study.	14 days
Secondary	Changes in creatinine levels from baseline	Clinical evaluation of creatinine levels from baseline until the end of study.	14 days
Secondary	Changes in D-dimer levels from baseline	Clinical evaluation of D-dimer levels from baseline until the end of study.	14 days
Secondary	Changes in ferritin levels from baseline	Clinical evaluation of ferritin levels from baseline until the end of study.	14 days
Secondary	Changes in triglycerides levels from baseline	Clinical evaluation of triglycerides levels from baseline until the end of study.	14 days
Secondary	Changes in LDH levels from baseline	Clinical evaluation of LDH levels from baseline until the end of study.	14 days