Prolectin-M in COVID-19 Patients Having Mild to Moderate Symptoms Not Requiring Oxygen Support.

COVID-19 Clinical Trial

— Prolectin-M  

Official title:

Effect of Prolectin-M; a (1-6)-Alpha-D-Mannopyranose on SarsCoV2 Viral Copy Numbers: A Proof of Concept, Open Label Randomized Controlled Trial

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT04512027
• Other study ID #: CIMED - 002- 2020
• Status: Completed
• Phase: N/A
• Start date: September 15, 2020
• Est. completion date: October 16, 2020

Study information

• Verified date: October 2020
• Source: Composite Interceptive Med Science
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

A randomised controlled trial of open label Prolectin-M; a (1-6)-alpha-D-Mannopyranose among patients with RT PCR positive COVID-19 patients.

Description:

SarsCoV2 has infected over 20 million people worldwide. The virus has a unique protein structure enabling it to rapidly infect and spread among the population. COVID19 is a global health emergency and has affected lives of all people irrespective of being infected. There are no proven therapies and a vaccine is yet to be approved for wide public usage.

Our study aims to test a hypothesis of physically blocking the spike protein from infecting the human cells, thus promoting its rapid excretion from the infected person.

We will randomise 10 subjects in this proof of concept trial and test the hypothesis by measuring the effect of Prolectin-M; a (1-6)-alpha-D-Mannopyranose in reducing the viral copy numbers over 5 days of treatment. The absolute copy numbers will be measured on digital droplet PCR developed by BioRad. A fall in copy numbers by 2-fold from baseline will be considered a positive treatment effect in this population. All standard care measures currently being practiced for these patients will be continued.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 10
• Est. completion date: October 16, 2020
• Est. primary completion date: September 19, 2020
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 45 Years

Eligibility

Inclusion Criteria:

• Symptomatic and laboratory-confirmed diagnosis of COVID-19.

• Age =18 years and =45 years, male and non-pregnant female

• Identified within 72 hours of testing positive on RT PCR.

• Able to give informed consent to stay in institutional care and undergo 3 times collection of throat and nasal swabs over 7-day period; Day 1, Day 3 and Day 5 since randomization.

Exclusion Criteria:

• Oxygen saturation at admission =96%.

• High temperature =100 deg F (=37.5 deg C) not controlled on oral doses of acetaminophen.

• Known history of diabetes on oral medications or insulin.

• IL-6 levels = 3times of laboratory reference range and / or significantly elevated levels of CRP, serum ferritin or d-dimer.

• Lymphocyte / monocyte ratio =3 or neutrophil / lymphocyte ratio =5 or platelet count =150,000 cells per microliter

• On any chronic medications for more than 4 weeks before randomization or active malignancy or having any co-morbidity that increases risk of rapid disease progression.

• Previously tested positive and recovered from COVID-19

Related Conditions & MeSH terms

• COVID-19

Intervention

Other:
• Prolectin-M; a (1-6)-alpha-D-Mannopyranose class
A treatment to decrease viral load, detected through digital droplet PCR, in mild to moderate cases of RT-PCR positive COVID-19
• Standard of Care
Currently approved standard of care for patients without symptoms requiring hospitalisation will be provided to all.

Locations

Country	Name	City	State
India	Mazumdar Shaw Medical Centre	Bangalore	Karnataka

Sponsors (2)

Lead Sponsor	Collaborator
Composite Interceptive Med Science	Pharmalectin Inc

Country where clinical trial is conducted

India, 

References & Publications (2)

http://medrxiv.org/lookup/doi/10.1101/2020.02.29.20029439

Suo T, Liu X, Feng J, Guo M, Hu W, Guo D, Ullah H, Yang Y, Zhang Q, Wang X, Sajid M, Huang Z, Deng L, Chen T, Liu F, Xu K, Liu Y, Zhang Q, Liu Y, Xiong Y, Chen G, Lan K, Chen Y. ddPCR: a more accurate tool for SARS-CoV-2 detection in low viral load specimens. Emerg Microbes Infect. 2020 Dec;9(1):1259-1268. doi: 10.1080/22221751.2020.1772678. — View Citation

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	SarsCoV2 viral copy number	Change in absolute viral copy number	7 days from randomisation
Secondary	b. Disease progression will be measured on a 7-point scale at 28 days. A 2-point change will be considered disease progression.	7-point severity score (ordinal scale): Not hospitalized, no limitations on activities; Not hospitalized, limitation on activities; Hospitalized, not requiring supplemental oxygen; Hospitalized, requiring supplemental oxygen; Hospitalized, on non-invasive ventilation or high flow oxygen devices; Hospitalized, on invasive mechanical ventilation or extracorporeal membrane oxygenation (ECMO); Death	28 days from randomisation