Covid19
Conditions
Keywords
Covid-19 symptoms
Brief summary
Protocol STRI12 - Study to Reinforce Immunity (STRI) - A Phase 2 Double-Blind, Randomized, Placebo-Controlled Study to Investigate the Safety and Efficacy of STRI Formula in Non-Hospitalized Participants with COVID-19 (the Study)
Detailed description
The Study to Reinforce Immunity (STRI) Phase 2 Clinical Trial is a randomized, double-blind, placebo-controlled clinical trial protocol assessing the safety and efficacy of STRI Formula in non-hospitalized participants with COVID-19. STRI Formula is a combination of food-based substances designed specifically to combat SARS-CoV-2, the coronavirus that causes COVID-19. The primary objective of the Study is to assess the efficacy of STRI Formula in reduction of time from treatment initiation to initial meaningful clinical improvement in COVID-19 symptoms. Additional secondary objectives are as follows: 1. To assess the safety of STRI Formula 2. To assess the efficacy of STRI Formula in reduction of time to COVID-19 sustained symptom improvement 3. To assess the efficacy of STRI Formula in reduction of time to COVID-19 initial symptom resolution 4. To assess the efficacy of STRI Formula in reduction of time to COVID-19 sustained symptom resolution 5. To assess the efficacy of STRI Formula in reduction in need for hospitalization 6. To assess the efficacy of STRI Formula in reduction in rates of fever 7. To assess the efficacy of STRI Formula in reduction in rates of hypoxia
Interventions
DRUGSTRI Formula
STRI Formula is a combination of food based substances (botanicals, vitamins, minerals, and protein) with multiple, distinct, synergistic, direct and indirect antiviral effects against SARS-CoV-2
DRUGPlacebo
Placebo oral capsule
Sponsors
Eyecheck, Inc.
Study design
Allocation
RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
TRIPLE (Subject, Caregiver, Investigator)
Masking description
Double-blind
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
1. Adults residing in the United States aged 18 years or older. 2. Provision of documentation of positive SARS-CoV-2 testing (via RT-PCR, rapid antigen testing) performed less than 7 days before screening, either via direct upload or confirmation from PCP. 1. electronic secure document upload; 2. allowing STRI Personnel to contact the PCP to confirm diagnosis; or 3. allowing STRI Personnel to contact the laboratory where the RT-PCR analysis was performed 3. Initial date of onset of COVID-19 signs/symptoms 7 days or less from date of STRI Screening and Randomization (i.e., Day 0). 4. During screening (Day 0): 1. participant-reported response of Mild or Moderate in response to the question Overall, how severe were your infection symptoms today? (FLU-PRO Plus Global Additional Daily Diary Items Question 1) 2. During prescreening, participant self-reported response of A little worse or Somewhat worse or Much worse or About the same in response to the question Overall, how were your infection symptoms today compared to yesterday? (FLU-PRO Plus Global Additional Daily Diary Items Question 2) 3. During prescreening, participant-reported response of No in response to the question Have you returned to your usual health today? (FLU-PRO Plus Global Additional Daily Diary Items Question 6) 4. At least TWO participant self-reported responses of Somewhat, Quite A Bit, or Very Much in any FLU-PRO Plus domain other than smell and taste (i.e., nose, throat, eyes, chest/respiratory, head, gastrointestinal, or body/systemic domains) 5. Ability to self-measure and self-report body temperature, and peripheral oxygen saturation (with STRI provided thermometer and STRI provided pulse oximeter). 6. Provision of signed and dated electronic informed consent form (via 21 CFR Part 11 compliant platform). 7. Provision of participant's primary care physician (PCP) name and phone number. 8. Consent to allow STRI Personnel to contact PCP for any reason and discuss participant's medical history and/or obtain participant's medical records. 9. Stated willingness to comply with all study procedures and availability for the duration of the study, including intent to comply with lifestyle considerations throughout Study duration. 10. Ability to take oral medication and be willing to adhere to the STRI Intervention Product (STRI Formula or placebo as capsules) regimen. 11. Ability to use the internet daily and check email daily. 12. Ability and consent to send and receive SMS text messages via cellular phone. 13. Provision of information (name, email address, and cellular phone number) of an emergency contact (e.g., family member/friend/colleague) willing to communicate with STRI Personnel in case the participant deteriorates. 14. Willingness to discontinue any dietary supplement that contains any active ingredient in STRI Formula (ascorbic acid, cholecalciferol, zinc, copper, quercetin, hesperidin, caffeic acid, epigallocatechin gallate, bovine lactoferrin) for the duration of the Study. 15. For men and women with child-bearing potential (as defined below), willingness to use adequate contraception for at least 100 days after beginning the Study.
Exclusion criteria
1. Inability to comply with study or follow-up procedures, or provide regular updates to their health status when contacted by the STRI Personnel via email, SMS, or phone. 2. Any prior or current hospitalization for COVID-19 or any need for hospitalization for any reason. 3. Any prior or current treatment with any agent for COVID-19. 4. Any known allergies or known toxicities to any of the specific ingredients in STRI Formula (including ascorbic acid, vitamin D, zinc, copper, amla, caffeic acid, coffee, bovine lactoferrin, milk, quercetin, hesperidin, oranges, citrus fruits, and/or green tea) 5. Body Mass Index \> 40 based on participant-reported weight and participant-reported height. 6. Participant-reported weight of less than 35kg. 7. Any history of radiation or chemotherapy for cancer within the last 3 months. 8. Any history of cardiac arrythmias, hemochromatosis, renal (including any known GFR \< 60mL/min) or hepatic disease (including chronic liver disease). 9. Any history of chronic pulmonary disorders 10. Any history of any gastrointestinal surgery or disease (including bariatric surgery or gastrointestinal resection, inflammatory bowel disease, or chronic intestinal diseases, such as (but not limited to) eosinophilic enteritis or autoimmune enteritis). 11. Any history of mineral or vitamin overload or deficiency (including chronic iron overload states, copper overload states, or ascorbic acid, vitamin D, zinc, or copper deficiencies). 12. Any history of any adverse event to green tea extract or any herbal products. 13. Prescreening Alcohol Use Disorders Identification Test (AUDIT) score of 8 or more indicating hazardous or harmful alcohol consumption, or alcohol dependence. 14. Pregnant or nursing/breastfeeding participants or participants intending to become pregnant within the next 24 months. 15. Men or premenopausal women not using adequate contraception. 16. Any other factors as judged by the principal investigator that would cause harm or increased risk to the participant or preclude the participant's full adherence with or completion of the study.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Length of time from treatment initiation to initial meaningful clinical improvement as measured over 30 days. | 30 days |
Secondary
| Measure | Time frame |
|---|---|
| Proportion of participants with any recorded serious adverse events | 30 days |
| Proportion of participants with any new comprehensive metabolic panel abnormalities (including electrolyte levels, glucose levels, renal and liver function testing) related to STRI Intervention Product between baseline and 30 days. | 30 days |
| Proportion of participants with any new complete blood count abnormalities (including white blood cell, red blood cell, hemoglobin, and platelets) related to STRI Intervention Product between baseline and 30 days. | 30 days |
| Proportion of participants that develop fever (measured as body temperature of more than 100.4 degrees F using a participant self-recorded thermometer). | 30 days |
| Proportion of participants that develop hypoxia (measured as peripheral oxygen saturation of less than 93% using a participant self-recorded pulse oximeter). | 30 days |
| Length of time from treatment initiation to sustained meaningful clinical improvement. | 30 days |
| Length of time from treatment initiation to sustained clinical recovery. | 30 days |
| Proportion of participants requiring hospitalization. | 30 days |
| Proportion of participants with COVID-19 signs/symptoms. | 30 days |
| Proportion of participants with COVID-19 signs/symptoms | 60 days |
| Proportion of participants who have expired. | 30 days |
| Length of time from treatment initiation to initial clinical recovery. | 30 days |
Other
| Measure | Time frame |
|---|---|
| Proportion of participants with PCR positivity for SARS-CoV-2 at 5, 10, 15, and 30 in saliva samples (first-stage only) compared to Day 1 (before treatment initiation) | 30 days |
Countries
United States
Contacts
Primary ContactRama D Jager, MD
Backup ContactAmbika Sharma, BS
Outcome results
None listed