Assessment of Efficacy of KAN-JANG® in Mild COVID-19
Launched by SWEDISH HERBAL INSTITUTE AB · Apr 14, 2021
Trial Information
Current as of May 12, 2025
Unknown status
Keywords
ClinConnect Summary
Rationale. Pathogenesis and progression of COVID-19 is a multistep process, which requires correct therapeutic strategy on various steps of initiation of overall defense response to pathogen and its resolution. Consequently, effective treatment of COVID-19 requires pharmaceutical corrections of many components innate, adaptive immune system, phases I-III metabolizing enzymes of detoxifying and repairing systems, and the SARS-Cov-2 virus' life cycle and proliferation.
It can be achieved by multitarget pharmaceutical intervention of herbal preparations with polyvalent and pleiotropic actions...
Gender
ALL
Eligibility criteria
- Inclusion Criteria:
- • Laboratory confirmed (SARS-Cov-2 PCR-positive test) mild COVID-19 infection (in the last three days),
- • COVID-19 patient in stable, moderate condition (i.e., not requiring Intensive Care Unit (ICU) admission).
- • Subjects must be under observation or admitted to a controlled facility or hospital (home quarantine is not sufficient).
- • Able to take medication alone
- • Able to give informed consent.
- Exclusion Criteria:
- • Pulmonary diseases
- • Chronic pulmonary diseases
- • Chronic rhinosinusitis
- • Patient admitted already under invasive mechanical ventilation;
- • The patient admitted with the severe acute respiratory syndrome and diagnosed with an etiologic agent other than Covid 19;
- • Renal failure requiring dialysis or creatinine ≥ 2.0mg/dl;
- • Tube feeding or parenteral nutrition.
- • Respiratory decompensation requiring mechanical ventilation.
- • Uncontrolled diabetes type 2.
- • Hypertension stage 3,
- • Autoimmune disease.
- • Pregnant or lactating women.
- • Patients are taking antibiotics for a reason other than COVID-19 at enrollment.
- • Has a chronically weakened immune system (AIDS, lymphoma, chemo-radio- corticosteroid therapy, immunosuppressive pathology);
- • Patients treated with chemo-radio-corticosteroid therapy in the last six months.
- • Patients with active cancer.
- • Taking immunosuppressive drugs (e.g., anti-rejection treatment after organ transplant);
- • Already participating in another clinical trial;
- • Has any other condition that would prevent safe participation in the study.
About Swedish Herbal Institute Ab
Swedish Herbal Institute AB is a pioneering organization dedicated to the research and development of herbal-based therapies and natural health products. With a focus on leveraging traditional knowledge and modern scientific methodologies, the Institute conducts rigorous clinical trials to evaluate the efficacy and safety of its herbal formulations. Committed to enhancing public health through innovation, Swedish Herbal Institute AB collaborates with healthcare professionals, academic institutions, and regulatory bodies to ensure the highest standards of quality and compliance in its research initiatives.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Tbilisi, , Georgia
Patients applied
Trial Officials
Levan Ratiani, PhD, MD
Principal Investigator
The First University Clinic of Tbilisi State Medical University
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported
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