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
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

Auteurs

Geoffrey Chupp (G)

Section of Pulmonary, Critical Care, and Sleep Medicine, Department of Internal Medicine, Yale School of Medicine, New Haven, CT, USA.

Anne Spichler-Moffarah (A)

Section of Infectious Diseases, Department of Internal Medicine, Yale School of Medicine, New Haven, CT, USA.

Ole S Søgaard (OS)

Department of Clinical Medicine and Department of Infectious Diseases, Aarhus University, Aarhus, Denmark.

Denise Esserman (D)

Yale Center for Analytical Sciences, Yale School of Public Health, New Haven, CT, USA.

James Dziura (J)

Yale Center for Analytical Sciences, Yale School of Public Health, New Haven, CT, USA.

Lisa Danzig (L)

Amicitiam Partners, San Francisco, CA.

Reetika Chaurasia (R)

Section of Infectious Diseases, Department of Internal Medicine, Yale School of Medicine, New Haven, CT, USA.

Kailash P Patra (KP)

Section of Infectious Diseases, Department of Internal Medicine, Yale School of Medicine, New Haven, CT, USA.

Aryeh Salovey (A)

Section of Infectious Diseases, Department of Internal Medicine, Yale School of Medicine, New Haven, CT, USA.

Angela Nunez (A)

Yale Center for Clinical Investigation, Yale School of Medicine, New Haven, CT, USA.

Jeanine May (J)

Yale Center for Clinical Investigation, Yale School of Medicine, New Haven, CT, USA.

Lauren Astorino (L)

Yale Center for Clinical Investigation, Yale School of Medicine, New Haven, CT, USA.

Amisha Patel (A)

Section of Hematology, Department of Internal Medicine, Yale School of Medicine, New Haven, CT, USA.

Stephanie Halene (S)

Section of Hematology, Department of Internal Medicine, Yale School of Medicine, New Haven, CT, USA.

Jianhui Wang (J)

Department of Pathology, Yale School of Medicine New Haven, CT, USA.

Pei Hui (P)

Department of Pathology, Yale School of Medicine New Haven, CT, USA.

Prashant Patel (P)

Investigation Drug Service, Yale New Haven Hospital, New Haven, CT, USA.

Jing Lu (J)

Investigation Drug Service, Yale New Haven Hospital, New Haven, CT, USA.

Fangyong Li (F)

Yale Center for Analytical Sciences, Yale School of Public Health, New Haven, CT, USA.

Geliang Gan (G)

Yale Center for Analytical Sciences, Yale School of Public Health, New Haven, CT, USA.

Stephen Parziale (S)

Yale Center for Analytical Sciences, Yale School of Public Health, New Haven, CT, USA.

Lily Katsovich (L)

Yale Center for Analytical Sciences, Yale School of Public Health, New Haven, CT, USA.

Gary V Desir (GV)

Investigation Drug Service, Yale New Haven Hospital, New Haven, CT, USA.

Joseph M Vinetz (JM)

Section of Infectious Diseases, Department of Internal Medicine, Yale School of Medicine, New Haven, CT, USA.

Classifications MeSH