search
Back to results

Evaluation of Efficacy of Levamisole and Formoterol+Budesonide in Treatment of COVID-19

Primary Purpose

COVID-19

Status
Unknown status
Phase
Phase 2
Locations
Iran, Islamic Republic of
Study Type
Interventional
Intervention
Levamisole Pill + Budesonide+Formoterol inhaler
Lopinavir/Ritonavir + hydoxychloroquine
Sponsored by
Fasa University of Medical Sciences
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for COVID-19

Eligibility Criteria

15 Years - 100 Years (Child, Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

Definitely positive COVID-19 patients

Exclusion Criteria:

Patients with acute respiratory problems including patients with:

  1. Spo2<60%
  2. Severe respiratory distress
  3. Heamodynamic instabilitty
  4. Acid base disturbance
  5. Severe Anemia Patients with severe hepatic diseases Patients with Nurvous system diseases

Sites / Locations

  • Vali-Asr HospitalRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Levamisole Pill + Budesonide+Formoterol inhaler+Standard care

Standard care

Arm Description

This group will take Levamisole + Budesonide/Formoterol along side with standard treatment regime.

This group will take standard treatment regime introduced by Ministry of health.

Outcomes

Primary Outcome Measures

Clear chest CT-scan
Chest Ct scan should be negative
PCR test
PCR test should be negative

Secondary Outcome Measures

Physical statues of patient
Patient should relief from signs of disease

Full Information

First Posted
March 30, 2020
Last Updated
April 9, 2020
Sponsor
Fasa University of Medical Sciences
search

1. Study Identification

Unique Protocol Identification Number
NCT04331470
Brief Title
Evaluation of Efficacy of Levamisole and Formoterol+Budesonide in Treatment of COVID-19
Official Title
Evaluation of Efficacy of Pharmacotherapy Treatment of COVID- 19 Infection Using Oral Levamisole and Formoterol+Budesonide Inhaler and Comparison of This Treatment Protocol With Standard National Treatment of the Disease
Study Type
Interventional

2. Study Status

Record Verification Date
April 2020
Overall Recruitment Status
Unknown status
Study Start Date
April 4, 2020 (Actual)
Primary Completion Date
April 20, 2020 (Anticipated)
Study Completion Date
May 20, 2020 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Fasa University of Medical Sciences

4. Oversight

Studies a U.S. FDA-regulated Drug Product
Yes
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
Yes
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
New Corona virus (COVID-19) has made a horrible situation for all of the countries. This disease is not only a health problem but also economy, culture and the whole entity of the countries is under attack by the virus. This disease seems to affect the body in two different pathology pathways. From one side virus can decrease activity of immune system in the blood stream and whole body and from other side it can attack the respiratory cells. Tissue biopsy shows that immune cells penetrate into the Lung tissue and we have accumulation and over activity of Immune cells in the lung. This inflammation in respiratory tract probably is the major cause of Cytokine storm and release of TNF-α and IL-6 into the blood. It seems that by three strategy disease can be treated. 1- By using systemic immune simulators. 2- By using topical anti-inflammatory drug in the respiratory system (Steroids or NSAIDs) 3- By inhibition of replication of the virus in the attacked cells.
Detailed Description
Looking at the pathology of this disease shows that COVID-19 virus binds to the Angiotensin converting enzyme II (ACE II) which is located on the surface of different cells in the body and specially on the cells of respiratory system. This enzyme is responsible to turn angiotensin II into angiotensin1-7. It is also turns angiotensin I into angiotensin 1-9. When ACEII would be blocked by virus level of angiotensin II will be increased and this enzyme along with vasoconstriction, makes cells to manufacture TNF α and IL-6 which are responsible for cytokine storm and Lymphopenia. Also presence of virus and virus shell on the surface of the infected cells make immune system to attack to the respiratory system hence effect of angiotensin II inside the cell causes fibrosis of the respiratory cells. This inflammation and tissue damage make Acute Respiratory Distress syndrome (ARDS) which is lethal for patients. There is a dilemma in treatment of this infection. From one side it doesn't make sense to decrease the immune response hence it will make the infection worse. And from other side stimulation of the immune response because of respiratory inflammation can expedite process of lethal ARDS. A new strategy for treatment of this disease which consists of local anti- inflammatory and systemic immune stimulant drugs can be considered as a reasonable strategy.As immunostimulator, Levamisole can increase Lymphocytes and empower the immunity of the body. This drug can also bind to Papaine Like Protease(PL-pro) of the shell of the virus which is necessary for virulence of COVID-19. It also can decrease level of TNF α and IL-6, and as a chemical adjutant can introduce the virus to the immune system. In addition to Levamisole, Formoterol+Budesonide inhaler can be used in this protocol. Budesonide is a steroid and can suppress the immune reaction locally in the respiratory system. Formoterol is β2 agonist and can open airways. It also can bind to PL-pro and can neutralize the virus according to the published articles.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
COVID-19

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2, Phase 3
Interventional Study Model
Parallel Assignment
Model Description
Study is two armed , double blind, parallel, randomized clinical trial.
Masking
ParticipantOutcomes Assessor
Masking Description
All of the research team will be blind about the groups of study and position of patients in each group except of physician and main researcher. Files of patients which will be numbered using a random number table will be sent for analyzer of the study.Information about position of patients in the groups is masked from research team. Outcomes Assessor will receive the information of patients without any name in the file. Just when statistical analysis would be finished information of groups will be revealed.
Allocation
Randomized
Enrollment
30 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Levamisole Pill + Budesonide+Formoterol inhaler+Standard care
Arm Type
Experimental
Arm Description
This group will take Levamisole + Budesonide/Formoterol along side with standard treatment regime.
Arm Title
Standard care
Arm Type
Active Comparator
Arm Description
This group will take standard treatment regime introduced by Ministry of health.
Intervention Type
Drug
Intervention Name(s)
Levamisole Pill + Budesonide+Formoterol inhaler
Other Intervention Name(s)
Levamisole and Budesonide+Formoterol inhaler both are generic drugs.
Intervention Description
Levamisole 50 mg tablet has to be taken 1-2 tablets every 8 hours Budesonide+Formoterol has to be inhaled 1-2 puff every 12 hours
Intervention Type
Drug
Intervention Name(s)
Lopinavir/Ritonavir + hydoxychloroquine
Other Intervention Name(s)
Kaletra+ Generic Hydroxy Chloroquine( Generic Drug)
Intervention Description
Hydroxy Chloroquine 200mg single dise Lopinavir/Ritonavir 2 tablets every 12 hours
Primary Outcome Measure Information:
Title
Clear chest CT-scan
Description
Chest Ct scan should be negative
Time Frame
between 3-7 days
Title
PCR test
Description
PCR test should be negative
Time Frame
between 3-7 days
Secondary Outcome Measure Information:
Title
Physical statues of patient
Description
Patient should relief from signs of disease
Time Frame
Between 3-7 days

10. Eligibility

Sex
All
Minimum Age & Unit of Time
15 Years
Maximum Age & Unit of Time
100 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Definitely positive COVID-19 patients Exclusion Criteria: Patients with acute respiratory problems including patients with: Spo2<60% Severe respiratory distress Heamodynamic instabilitty Acid base disturbance Severe Anemia Patients with severe hepatic diseases Patients with Nurvous system diseases
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Siamack Afazeli, Pharm.D
Phone
+989121392982
Email
Dr.afazeli@gmail.com
First Name & Middle Initial & Last Name or Official Title & Degree
Mojtaba Farjaam, MD
Phone
+989177104789
Email
farjam.md@gmail.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Siamack Afazeli
Organizational Affiliation
Fasa University of Medical Sciences
Official's Role
Principal Investigator
Facility Information:
Facility Name
Vali-Asr Hospital
City
Fasa
State/Province
Fars
Country
Iran, Islamic Republic of
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Jalal Karimi, PhD
Phone
+987153314026
Email
info@fums.ac.ir
First Name & Middle Initial & Last Name & Degree
Yousef Gholampoor, PhD
Phone
+987153314021
Email
info@fums.ac.ir

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
All IPD that underlie results in a publication and is comply with ethics will be revealed.
IPD Sharing Time Frame
between 1 to 2 months after analyzing the raw data.
IPD Sharing Access Criteria
Results will be available in Journals.
IPD Sharing URL
http://journal.fums.ac.ir/en
Citations:
PubMed Identifier
32113704
Citation
Rothan HA, Byrareddy SN. The epidemiology and pathogenesis of coronavirus disease (COVID-19) outbreak. J Autoimmun. 2020 May;109:102433. doi: 10.1016/j.jaut.2020.102433. Epub 2020 Feb 26.
Results Reference
background
PubMed Identifier
32292689
Citation
Wu C, Liu Y, Yang Y, Zhang P, Zhong W, Wang Y, Wang Q, Xu Y, Li M, Li X, Zheng M, Chen L, Li H. Analysis of therapeutic targets for SARS-CoV-2 and discovery of potential drugs by computational methods. Acta Pharm Sin B. 2020 May;10(5):766-788. doi: 10.1016/j.apsb.2020.02.008. Epub 2020 Feb 27.
Results Reference
background
PubMed Identifier
29054532
Citation
Gruppen MP, Bouts AH, Jansen-van der Weide MC, Merkus MP, Zurowska A, Maternik M, Massella L, Emma F, Niaudet P, Cornelissen EAM, Schurmans T, Raes A, van de Walle J, van Dyck M, Gulati A, Bagga A, Davin JC; all members of the Levamisole Study Group. A randomized clinical trial indicates that levamisole increases the time to relapse in children with steroid-sensitive idiopathic nephrotic syndrome. Kidney Int. 2018 Feb;93(2):510-518. doi: 10.1016/j.kint.2017.08.011. Epub 2017 Oct 18.
Results Reference
background
PubMed Identifier
28208675
Citation
Lee KY. Pneumonia, Acute Respiratory Distress Syndrome, and Early Immune-Modulator Therapy. Int J Mol Sci. 2017 Feb 11;18(2):388. doi: 10.3390/ijms18020388.
Results Reference
background
PubMed Identifier
32007143
Citation
Chen N, Zhou M, Dong X, Qu J, Gong F, Han Y, Qiu Y, Wang J, Liu Y, Wei Y, Xia J, Yu T, Zhang X, Zhang L. Epidemiological and clinical characteristics of 99 cases of 2019 novel coronavirus pneumonia in Wuhan, China: a descriptive study. Lancet. 2020 Feb 15;395(10223):507-513. doi: 10.1016/S0140-6736(20)30211-7. Epub 2020 Jan 30.
Results Reference
background
PubMed Identifier
32157847
Citation
Chen J. [How to understand the histopathology of SARS and coronavirus disease-19 (COVID-19) associated with acute respiratory distress syndrome]. Zhonghua Bing Li Xue Za Zhi. 2020 Apr 8;49(4):289-290. doi: 10.3760/cma.j.cn112151-20200309-00185. Chinese.
Results Reference
background
PubMed Identifier
32094336
Citation
Xu H, Zhong L, Deng J, Peng J, Dan H, Zeng X, Li T, Chen Q. High expression of ACE2 receptor of 2019-nCoV on the epithelial cells of oral mucosa. Int J Oral Sci. 2020 Feb 24;12(1):8. doi: 10.1038/s41368-020-0074-x.
Results Reference
background
PubMed Identifier
23092879
Citation
Santos RA, Ferreira AJ, Verano-Braga T, Bader M. Angiotensin-converting enzyme 2, angiotensin-(1-7) and Mas: new players of the renin-angiotensin system. J Endocrinol. 2013 Jan 18;216(2):R1-R17. doi: 10.1530/JOE-12-0341. Print 2013 Feb.
Results Reference
background
PubMed Identifier
12410849
Citation
Ruiz-Ortega M, Ruperez M, Lorenzo O, Esteban V, Blanco J, Mezzano S, Egido J. Angiotensin II regulates the synthesis of proinflammatory cytokines and chemokines in the kidney. Kidney Int Suppl. 2002 Dec;(82):S12-22. doi: 10.1046/j.1523-1755.62.s82.4.x.
Results Reference
background
PubMed Identifier
10588224
Citation
Gullestad L, Aukrust P, Ueland T, Espevik T, Yee G, Vagelos R, Froland SS, Fowler M. Effect of high- versus low-dose angiotensin converting enzyme inhibition on cytokine levels in chronic heart failure. J Am Coll Cardiol. 1999 Dec;34(7):2061-7. doi: 10.1016/s0735-1097(99)00495-7.
Results Reference
background
PubMed Identifier
26245758
Citation
Jin HY, Chen LJ, Zhang ZZ, Xu YL, Song B, Xu R, Oudit GY, Gao PJ, Zhu DL, Zhong JC. Deletion of angiotensin-converting enzyme 2 exacerbates renal inflammation and injury in apolipoprotein E-deficient mice through modulation of the nephrin and TNF-alpha-TNFRSF1A signaling. J Transl Med. 2015 Aug 6;13:255. doi: 10.1186/s12967-015-0616-8.
Results Reference
background
PubMed Identifier
22536270
Citation
Tikellis C, Thomas MC. Angiotensin-Converting Enzyme 2 (ACE2) Is a Key Modulator of the Renin Angiotensin System in Health and Disease. Int J Pept. 2012;2012:256294. doi: 10.1155/2012/256294. Epub 2012 Mar 20.
Results Reference
background
PubMed Identifier
29929959
Citation
Guignabert C, de Man F, Lombes M. ACE2 as therapy for pulmonary arterial hypertension: the good outweighs the bad. Eur Respir J. 2018 Jun 21;51(6):1800848. doi: 10.1183/13993003.00848-2018. Print 2018 Jun. No abstract available.
Results Reference
background
PubMed Identifier
25089563
Citation
Meng Y, Li T, Zhou GS, Chen Y, Yu CH, Pang MX, Li W, Li Y, Zhang WY, Li X. The angiotensin-converting enzyme 2/angiotensin (1-7)/Mas axis protects against lung fibroblast migration and lung fibrosis by inhibiting the NOX4-derived ROS-mediated RhoA/Rho kinase pathway. Antioxid Redox Signal. 2015 Jan 20;22(3):241-58. doi: 10.1089/ars.2013.5818. Epub 2014 Oct 2.
Results Reference
background
PubMed Identifier
31262387
Citation
Zhang BN, Xu H, Gao XM, Zhang GZ, Zhang X, Yang F. Protective Effect of Angiotensin (1-7) on Silicotic Fibrosis in Rats. Biomed Environ Sci. 2019 Jun;32(6):419-426. doi: 10.3967/bes2019.057.
Results Reference
background
PubMed Identifier
24776703
Citation
Jiang F, Yang J, Zhang Y, Dong M, Wang S, Zhang Q, Liu FF, Zhang K, Zhang C. Angiotensin-converting enzyme 2 and angiotensin 1-7: novel therapeutic targets. Nat Rev Cardiol. 2014 Jul;11(7):413-26. doi: 10.1038/nrcardio.2014.59. Epub 2014 Apr 29.
Results Reference
background
PubMed Identifier
10518844
Citation
Szefler SJ. Pharmacodynamics and pharmacokinetics of budesonide: a new nebulized corticosteroid. J Allergy Clin Immunol. 1999 Oct;104(4 Pt 2):175-83. doi: 10.1016/s0091-6749(99)70059-x.
Results Reference
background
Citation
Potential inhibitors against papain-like protease of novel coronavirus (COVID-19) from FDA approved drugs ,Rimanshee Arya1, Amit Das1, Vishal Prashar1,*, Mukesh Kumar1, 2,* 1Radiation Biology & Health Sciences Division, Bhabha Atomic Research Centre, Trombay, Mumbai-400085, India 2Homi Bhabha National Institute, Mumbai-400094, India
Results Reference
background
PubMed Identifier
32738928
Citation
Nicolau DV, Bafadhel M. Inhaled corticosteroids in virus pandemics: a treatment for COVID-19? Lancet Respir Med. 2020 Sep;8(9):846-847. doi: 10.1016/S2213-2600(20)30314-3. Epub 2020 Jul 30. No abstract available.
Results Reference
derived
Links:
URL
https://doi.org/10.1101/2020.02.23.20026690
Description
Potential inhibitors against papain-like protease of novel coronavirus (COVID-19) from FDA approved drugs

Learn more about this trial

Evaluation of Efficacy of Levamisole and Formoterol+Budesonide in Treatment of COVID-19

We'll reach out to this number within 24 hrs