Status:
COMPLETED
The Impact of Camostat Mesilate on COVID-19 Infection
Lead Sponsor:
University of Aarhus
Conditions:
Corona Virus Infection
Eligibility:
All Genders
18-110 years
Phase:
PHASE1
PHASE2
Brief Summary
SARS-CoV-2, one of a family of human coronaviruses, was initially identified in December 2019 in Wuhan city. This new coronavirus causes a disease presentation which has now been named COVID-19. The v...
Detailed Description
Cohort 1 - enrolment into the cohort of hospitalized patients has been completed (31 Dec 2020). Study results are publicly available at EClinicilMedicine, see link https://www.thelancet.com/journals/e...
Eligibility Criteria
Inclusion
- Cohort 1)
- Documented COVID-19 infection as evidenced by positive PCR (or comparable clinical assay) for SARS-CoV-2
- Less than 48 hours since time of hospital admission OR if hospital-acquired COVID-19 is suspected, less than 48 hrs since onset of symptoms
- Adolescents and adults age \>=18 years
- Subject or legally authorized representative able to give informed consent
- Admitted to hospital
- Cohort 2)
- Documented COVID-19 infection as evidenced by positive PCR (or comparable clinical assay) for SARS-CoV-2
- One or more of the following symptoms of COVID-19 infection: fever, cough, expectoration, shortness of breath, myalgia, fatigue, or head ache
- No more than 5 days since the beginning of symptom onset
- Adolescents and adults age \>=18 years
- Subject (or legally authorized representative, for Cohort 1 only) able to give informed consent
- Do not require immediate hospitalization (newly diagnosed COVID-19 patients who are discharged within 24 hrs of hospital admission are eligible for enrollment)
- Must be willing to fill out a daily symptom diary
- Must be available for a daily phone call
- Must be willing to take their own temperature at least once a day
- Exclusion criteria
- Any condition that, in the Investigator's opinion, will prevent adequate compliance with study therapy (e.g. the patient is considered to be moribund within the next 72 hrs or has uncontrolled substance abuse that prevents adherence to study medication). Patients needing ventilator treatment are eligible to be enrolled if they fulfill the other in/exclusion criteria.
- The following laboratory values at baseline (Day 0):
- Serum total bilirubin ≥3 ULN
- Estimated glomerular filtration rate (eGFR) ≤30 mL/min (based on serum creatinine)
- Known hypersensitivity to Camostat Mesilate
- Women who are pregnant or breastfeeding, or with a positive pregnancy test as determined by a positive urine or blood beta- human chorionic gonadotropin test during screening or women of child bearing potential\* who are unwilling or unable to use an acceptable method of contraception (combined estrogen and progestogen hormonal contraception (oral, intravaginal or transdermal), progesteron-only hormonal contraception (oral, injectable or implantable), intrauterine device or intrauterine hormone-releasing system) to avoid pregnancy during the study. Sexual abstinence will only be accepted in cases where this reflect the usual lifestyle.
Exclusion
Key Trial Info
Start Date :
April 4 2020
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
May 1 2023
Estimated Enrollment :
206 Patients enrolled
Trial Details
Trial ID
NCT04321096
Start Date
April 4 2020
End Date
May 1 2023
Last Update
April 18 2025
Active Locations (11)
Enter a location and click search to find clinical trials sorted by distance.
1
Region Hospital North Jutland
Hjørring, Region Nord, Denmark
2
Department of Infectious Diseases
Aalborg, Denmark
3
Department for Infectious Diseases, Aarhus University Hospital
Aarhus N, Denmark, 8200
4
Bispebjerg hospital
Copenhagen, Denmark, 2400