Clinical Trial of Mycobacterium w in COVID-19 Positive Patients, Hospitalized But Not Critically Ill

COVID-19 Clinical Trial

Official title:

A Randomized, Double-blind, Two Arm, Controlled Clinical Trial to Compare the Efficacy and Safety of Mycobacterium w (Mw) Administered Along With Standard of Care Versus Placebo Administered Along With Standard of Care, in Adult, COVID 19 Positive Patients Hospitalized But Not Critically Ill.

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT04358809
• Other study ID #: CRSC20006
• Status: Recruiting
• Phase: Phase 3
• Start date: June 30, 2020
• Est. completion date: April 30, 2021

Study information

• Verified date: December 2020
• Source: Cadila Pharnmaceuticals
• Contact: Anil Avhad, MBBS
• Phone: 919833454044
• Email: anil.avhad[@]cadilapharma.co.in
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This is a randomized, double blind, two arms, placebo controlled, clinical trial to study to evaluate the the safety and efficacy of Mycobacterium w in combination with standard of care versus placebo with standard of care for preventing the progression of COVID-19 disease and for reduction in transfer to ICU in COVID-19 infected patients admitted to the hospital.

Description:

Total 480 hospitalized adult eligible patients will be randomized in 1:1 ratio to receive either Mw+SOC or placebo+SOC for first 3 days post-randomization.

Daily clinical evaluation of patient will be performed till discharge from hospital or till ICU admission.

Study duration for each patient will be approximately up to 28 days, or discharge from hospital or transfer to ICU, whichever is earlier.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 480
• Est. completion date: April 30, 2021
• Est. primary completion date: February 28, 2021
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• COVID-19 positive patients with ordinal scale score of 3.

• Patients of either gender, age = 18 years at the time of enrollment.

• Female patients who are currently using reliable methods of contraception (barrier methods and intrauterine contraceptive device), with a negative urine pregnancy test during screening and agree to informed compliance of contraceptive method until at least 3 months post-dosing.

• The patients must be able and willing to comply with the study protocol, available and willing to complete all the study assessments and must have signed an Informed Consent Form.

Exclusion Criteria:

• Patient with ordinal scale of =4 at the time of hospital admission and randomization.

• Pregnant and / or lactating female patients.

• A family history of congenital or hereditary immunodeficiency.

• Any disease condition requiring ICU admission.

• History of dialysis, silicosis, solid organ transplantation such as renal or cardiac transplants, and disorders of the heart, or nervous system, or other metabolic inflammatory conditions, psychiatric, occupational problems that make it unlikely that the patients will comply with the protocol as determined by the investigator.

• History of administration of any immunoglobulins, any immunotherapy (antineoplastic chemotherapy, radiation therapy, immunosuppressants to induce tolerance to transplants, and corticosteroids use) and/or any blood products within the 3 months preceding study dosing, or planned future administrations during the study period.

• History of allergic reactions or anaphylaxis to Mw or its component.

• Presence of any severe systemic/autoimmune disorders as determined by medical history and/or physical examination at the time of screening, which in the judgment of the Investigator would compromise the patient's health or is likely to result nonconformance to the protocol or a patient's ability to give written informed consent.

Related Conditions & MeSH terms

• COVID-19
• Critical Illness
• Mycobacterium Infections

Intervention

Drug:
• Suspension of heat killed (autoclaved) Mycobacterium w
Suspension of heat killed (autoclaved) Mw along with Standard of care (SOC) treatment for COVID-19

Other:
• Placebo
Placebo along with Standard of care (SOC) treatment for COVID-19

Locations

Country	Name	City	State
India	All India Institute of Medical Sciences, Bhopal	Bhopal
India	Post Graduate Institute of Medical Education and Research	Chandigarh
India	All India Institute of Medical Sciences, Delhi	Delhi
India	All India Institute of Medical Science, Raipur	Raipur	Chhattisgarh

Sponsors (2)

Lead Sponsor	Collaborator
Cadila Pharnmaceuticals	Council of Scientific and Industrial Research, India

Country where clinical trial is conducted

India, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Number of patients with increased disease severity	To compare the difference in proportion of patients with increased disease severity	From baseline to Day 3, Day 7, Day 14, Day 21, Day 28 or at any time during the study till 28 days post first dosing.
Secondary	Incidence of adverse events and serious adverse events (Safety)	To evaluate safety of Mw in COVID-19 patients admitted to hospital	Till day 28
Secondary	Number of COVID-19 patients discharged from hospital	To compare the proportion of patients discharged from hospital	From baseline to Day 3, Day 7, Day 14, Day 21, Day 28 or at any time during the study till 28 days post first dosing.
Secondary	Number of COVID-19 patients transfer to ICU	To compare the proportion of patients transfer to ICU	From baseline to Day 3, Day 7, Day 14, Day 21, Day 28 or at any time during the study till 28 days post first dosing.
Secondary	Number of COVID-19 patients with reduction in disease severity by 1 ordinal scale	To compare the proportion of patients with reduction in disease severity by 1 ordinal scale	From baseline to Day 3, Day 7, Day 14, Day 21, Day 28 or at any time during the study till 28 days post first dosing.
Secondary	Number of of symptom free patients	To compare the proportion of symptom free patients	From baseline to Day 3, Day 7, Day 14, Day 21, Day 28 or at any time during the study till 28 days post first dosing.