Ezrin Peptide (HEP-1) for Treatment of Coronavirus Disease (COVID-19) Infection
Primary Purpose
Covid19, Treatment, Corona Virus Infection
Status
Unknown status
Phase
Phase 1
Locations
Iran, Islamic Republic of
Study Type
Interventional
Intervention
Human Ezrin Peptide 1 (HEP1)
Placebo
Sponsored by
About this trial
This is an interventional treatment trial for Covid19 focused on measuring COVID19, Treatment, Ezrin peptide, HEP-1
Eligibility Criteria
Inclusion Criteria:
- Patients hospitalized with a positive SARS-CoV-2 PCR test and presenting with one or more clear clinical symptoms of COVID-19 disease
- No contraindication to HEP-1
- Obtained informed consent
Exclusion Criteria:
- Patients who had received any immuno-modulator therapy
- Active or chronic kidney/ liver diseases,
- Oncological diseases
- Other viral infection including HIV and hepatitis.
- Any allergic reaction or sensitivity to HEP-1
- Breast feeding or pregnancy
Sites / Locations
- Shahid Beheshti University of Medical Sciences
Arms of the Study
Arm 1
Arm 2
Arm Type
Placebo Comparator
Experimental
Arm Label
No intervention:control group
Experimental:Intervention group
Arm Description
Outcomes
Primary Outcome Measures
Time to clinical improvement of disease symptoms
Duration of Hospitalization
Duration of artificial ventilation
Secondary Outcome Measures
CT Severity score
Range 0-40
CBC
IL-1
IL-6
TNF
CRP
Full Information
NCT ID
NCT04627233
First Posted
November 6, 2020
Last Updated
November 11, 2020
Sponsor
Shahid Beheshti University of Medical Sciences
Collaborators
praxisgemeinschaft für zelltherapie
1. Study Identification
Unique Protocol Identification Number
NCT04627233
Brief Title
Ezrin Peptide (HEP-1) for Treatment of Coronavirus Disease (COVID-19) Infection
Official Title
The Clinical Trial of Application of Ezrin Peptide (HEP-1) for Treatment of Coronavirus Disease (COVID-19) Infection
Study Type
Interventional
2. Study Status
Record Verification Date
November 2020
Overall Recruitment Status
Unknown status
Study Start Date
December 20, 2020 (Anticipated)
Primary Completion Date
March 1, 2021 (Anticipated)
Study Completion Date
April 1, 2021 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Shahid Beheshti University of Medical Sciences
Collaborators
praxisgemeinschaft für zelltherapie
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
5. Study Description
Brief Summary
Currently, SARS-CoV-2 the novel member of the corona virus family, affecting the world leading to COVID-19 disease. It can result life-threatening condition by developing severe acute respiratory distress syndrome (ARDS). Based on previous evidence a group of patients with severe COVID-19 develop a cytokine storm syndrome which leads to hyper-inflammation lung tissue damage. Supportive care is the current management of COVID-19 is and management of ARDS as a main cause of mortality has been remained challenging. Therefore, an urgent effective treatment of COVID-19 regarding hyper-inflammation mechanism is required. Currently, development of novel anti-viral agents and vaccines are the main issues. However, it needs long time, from months to years, until suitable new medications and vaccines have been developed. An immune-modulatory tetra deca peptide (14-mer peptide) named Human Ezrin Peptide 1 (HEP-1) (trade name Gepon) was introduced by the group of Ataullakhanov in Russia. Regarding its proved anti-viral and anti-inflammatory effect, Russian authorities approved Gepon for treatment of ulcerative colitis treatment and Hepatitis -C.
In this regard, it seems that Hep-1 is a very safe immune-modulatory agent which can be effective in the management of COVID-19 infection without any adverse effect for the patient.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Covid19, Treatment, Corona Virus Infection
Keywords
COVID19, Treatment, Ezrin peptide, HEP-1
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 1
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
20 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
No intervention:control group
Arm Type
Placebo Comparator
Arm Title
Experimental:Intervention group
Arm Type
Experimental
Intervention Type
Drug
Intervention Name(s)
Human Ezrin Peptide 1 (HEP1)
Intervention Description
HEP-1 will be administrated s.c. into the lower abdominal wall
induction dosage: 2 mg Ezrin in 2 ml physiological saline applied s.c.,one injection every 12 hours until symptoms disappear followed by
maintenance dosage: 0.2 mg Ezrin in 1 ml physiological saline solution s.c 1/day for 10 days
Intervention Type
Drug
Intervention Name(s)
Placebo
Intervention Description
placebo group received normal saline in a same volume to match corresponding HEP-1 doses. Study drug was administered by qualified staff in research clinic settings; injections were given to abdominal sites on rotating basis, by anatomic quadrant.
Primary Outcome Measure Information:
Title
Time to clinical improvement of disease symptoms
Time Frame
7 days
Title
Duration of Hospitalization
Time Frame
28 days
Title
Duration of artificial ventilation
Time Frame
28 days
Secondary Outcome Measure Information:
Title
CT Severity score
Description
Range 0-40
Time Frame
28 days
Title
CBC
Time Frame
28 days
Title
IL-1
Time Frame
28 days
Title
IL-6
Time Frame
28 days
Title
TNF
Time Frame
28 days
Title
CRP
Time Frame
28 days
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Patients hospitalized with a positive SARS-CoV-2 PCR test and presenting with one or more clear clinical symptoms of COVID-19 disease
No contraindication to HEP-1
Obtained informed consent
Exclusion Criteria:
Patients who had received any immuno-modulator therapy
Active or chronic kidney/ liver diseases,
Oncological diseases
Other viral infection including HIV and hepatitis.
Any allergic reaction or sensitivity to HEP-1
Breast feeding or pregnancy
Facility Information:
Facility Name
Shahid Beheshti University of Medical Sciences
City
Tehran
Country
Iran, Islamic Republic of
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Farzad Ashrafi
Email
farzad.ashrafi@sbmu.ac.ir
12. IPD Sharing Statement
Citations:
PubMed Identifier
9365271
Citation
Bretscher A, Reczek D, Berryman M. Ezrin: a protein requiring conformational activation to link microfilaments to the plasma membrane in the assembly of cell surface structures. J Cell Sci. 1997 Dec;110 ( Pt 24):3011-8. doi: 10.1242/jcs.110.24.3011.
Results Reference
background
PubMed Identifier
25746045
Citation
Pore D, Gupta N. The ezrin-radixin-moesin family of proteins in the regulation of B-cell immune response. Crit Rev Immunol. 2015;35(1):15-31. doi: 10.1615/critrevimmunol.2015012327.
Results Reference
background
PubMed Identifier
24043890
Citation
Pore D, Parameswaran N, Matsui K, Stone MB, Saotome I, McClatchey AI, Veatch SL, Gupta N. Ezrin tunes the magnitude of humoral immunity. J Immunol. 2013 Oct 15;191(8):4048-58. doi: 10.4049/jimmunol.1301315. Epub 2013 Sep 16.
Results Reference
background
PubMed Identifier
23185364
Citation
Millet JK, Kien F, Cheung CY, Siu YL, Chan WL, Li H, Leung HL, Jaume M, Bruzzone R, Peiris JS, Altmeyer RM, Nal B. Ezrin interacts with the SARS coronavirus Spike protein and restrains infection at the entry stage. PLoS One. 2012;7(11):e49566. doi: 10.1371/journal.pone.0049566. Epub 2012 Nov 21.
Results Reference
background
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Ezrin Peptide (HEP-1) for Treatment of Coronavirus Disease (COVID-19) Infection
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