Status:
COMPLETED
Camostat Mesylate in COVID-19 Outpatients
Lead Sponsor:
Yale University
Conditions:
COVID-19
Eligibility:
All Genders
18+ years
Phase:
PHASE2
Brief Summary
The rationale of the present clinical trial is that an orally available drug given to outpatients that could reduce the viral burden in the upper respiratory tract could forestall complications of SAR...
Detailed Description
The study is designed as a double-blind randomized controlled clinical trial to test the hypothesis that camostat mesylate, a serine protease inhibitor shown to inhibit SARS-COV-2 replication in vitro...
Eligibility Criteria
Inclusion
- Be enrolled within 3 days of being notified of their first positive COVID-19 test result.
- Evidence of a recent active COVID-19 infection, as evidenced by the positive test results being associated with at least one COVID-19-compatible symptom such as fever, upper respiratory symptoms, cough, chills, loss of taste/smell, etc.(see COVID-19-PRO symptom score sheet), or a recent high-risk exposure to COVID-19
- Provision of informed consent.
- Stated willingness to comply with all study procedures and availability for the duration of the study.
- Diagnosed with COVID-19 within past 3 days and not exhibiting manifestations requiring hospitalization such as extreme shortness of breath or severe prostration. Nurses at the study site will assess such severe conditions requiring hospitalization, which would preclude enrollment.
- Ability to take oral medication and be willing to adhere to the camostat mesylate regimen.
- For females of reproductive potential: use of highly effective contraception for at least 1 month prior to screening and agreement to use such a method during study participation and for an additional 4 weeks after the end of the camostat mesylate administration.
- For males of reproductive potential: use of condoms or other methods to ensure effective contraception with partner.
- Agreement to adhere to Lifestyle Considerations (see section 5.3) throughout study duration.
- English and Spanish speaking subjects as well as patients speaking any language for which we can find appropriate translators will be enrolled. A short form with interpretation will be used for anyone speaking a language for which a translated informed consent form is not currently available in accordance with local site IRB policies, including developing certified translations as necessary.
Exclusion
- Presence of COVID-19 disease manifestations that would require referral for consideration of hospitalization.
- A previous positive COVID-19 test reported more than 7 days before, which would indicate likelihood of non-culturable, nonreplicating virus.
- A positive COVID-19 test without a known recent exposure that would indicate an active infection, hence an unknown chance of non-culturable, non-replicating virus being present (i.e., asymptomatic COVID-19 infection of unknown duration).
- Pregnancy or lactation.
- Known allergic reactions to components of camostat mesylate.
- With regard to inclusion or exclusion of women of child-bearing potential, women who report that they know they are pregnant are excluded. All women of child-bearing potential who test positive for pregnancy by urine test at first visit are excluded. A day 14 followup blood pregnancy test will be done on appropriate enrolled women (i.e. those who had a negative urine pregnancy test on day 0 for further safety assessment ).
Key Trial Info
Start Date :
June 9 2020
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
April 22 2021
Estimated Enrollment :
70 Patients enrolled
Trial Details
Trial ID
NCT04353284
Start Date
June 9 2020
End Date
April 22 2021
Last Update
March 24 2022
Active Locations (1)
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1
Yale University
New Haven, Connecticut, United States, 06511