A Phase 2 Randomized, Double-Blind, Placebo-controlled Trial of Oral Camostat Mesylate for Early Treatment of COVID-19 Outpatients Showed Shorter Illness Course and Attenuation of Loss of Smell and Taste.
Journal
medRxiv : the preprint server for health sciences
Titre abrégé: medRxiv
Pays: United States
ID NLM: 101767986
Informations de publication
Date de publication:
31 Jan 2022
31 Jan 2022
Historique:
pubmed:
9
2
2022
medline:
9
2
2022
entrez:
8
2
2022
Statut:
epublish
Résumé
Early treatment of mild SARS-CoV-2 infection might lower the risk of clinical deterioration in COVID-19. To determine whether oral camostat mesylate would reduce upper respiratory SARS-CoV-2 viral load in newly diagnosed outpatients with mild COVID-19, and would lead to improvement in COVID-19 symptoms. From June, 2020 to April, 2021, we conducted a randomized, double-blind, placebo-controlled phase 2 trial. Single site, academic medical center, outpatient setting in Connecticut, USA. Of 568 COVID-19 positive potential adult participants diagnosed within 3 days of study entry and assessed for eligibility, 70 were randomized and 498 were excluded (198 did not meet eligibility criteria, 37 were not interested, 265 were excluded for unknown or other reasons). The primary inclusion criteria were a positive SARS-CoV-2 nucleic acid amplification result in adults within 3 days of screening regardless of COVID-19 symptoms. Treatment was 7 days of oral camostat mesylate, 200 mg po four times a day, or placebo. The primary outcome was reduction of 4-day log Participants receiving camostat had statistically significant lower quantitative symptom scores (FLU-Pro-Plus) at day 6, accelerated overall symptom resolution and notably improved taste/smell, and fatigue beginning at onset of intervention in the camostat mesylate group compared to placebo. Intention-to-treat analysis demonstrated that camostat mesylate was not associated with a reduction in 4-day log The camostat group had more rapid resolution of COVID-19 symptoms and amelioration of the loss of taste and smell. Camostat compared to placebo was not associated with reduction in nasopharyngeal SARS-COV-2 viral load. Additional clinical trials are warranted to validate the role of camostat mesylate on SARS-CoV-2 infection in the treatment of mild COVID-19. Clinicaltrials.gov, NCT04353284 (04/20/20)(https://clinicaltrials.gov/ct2/show/NCT04353284?term=camostat+%2C+yale&draw=2&rank=1).
Identifiants
pubmed: 35132421
doi: 10.1101/2022.01.28.22270035
pmc: PMC8820673
pii:
doi:
Banques de données
ClinicalTrials.gov
['NCT04353284']
Types de publication
Preprint
Langues
eng
Subventions
Organisme : NCRR NIH HHS
ID : UL1 RR024139
Pays : United States
Organisme : NCATS NIH HHS
ID : UL1 TR001863
Pays : United States