A trial platform to assess approved SARS-CoV-2 vaccines in immunocompromised patients: first sub-protocol for a pilot trial comparing the mRNA vaccines Comirnaty® and COVID-19 mRNA Vaccine Moderna®.

Details

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State: Public
Version: Final published version
License: CC BY 4.0
Serval ID
serval:BIB_B5A01BBEEB3D
Type
Article: article from journal or magazin.
Collection
Publications
Institution
Title
A trial platform to assess approved SARS-CoV-2 vaccines in immunocompromised patients: first sub-protocol for a pilot trial comparing the mRNA vaccines Comirnaty® and COVID-19 mRNA Vaccine Moderna®.
Journal
Trials
Author(s)
Speich B., Chammartin F., Smith D., Stoeckle M.P., Amico P., Eichenberger A.L., Hasse B., Schuurmans M.M., Müller T., Tamm M., Dickenmann M., Abela I.A., Trkola A., Hirsch H.H., Manuel O., Cavassini M., Hemkens L.G., Briel M., Mueller N.J., Rauch A., Günthard H.F., Koller M.T., Bucher H.C., Kusejko K.
Working group(s)
study groups from the Swiss HIV Cohort Study and the Swiss Transplant Cohort Study
ISSN
1745-6215 (Electronic)
ISSN-L
1745-6215
Publication state
Published
Issued date
21/10/2021
Peer-reviewed
Oui
Volume
22
Number
1
Pages
724
Language
english
Notes
Publication types: Clinical Trial Protocol ; Journal Article
Publication Status: epublish
Abstract
Late 2019, a new highly contagious coronavirus SARS-CoV-2 has emerged in Wuhan, China, causing within 2 months a pandemic with the highest disease burden in elderly and people with pre-existing medical conditions. The pandemic has highlighted that new and more flexible clinical trial approaches, such as trial platforms, are needed to assess the efficacy and safety of interventions in a timely manner. The two existing Swiss cohorts of immunocompromised patients (i.e., Swiss HIV Cohort Study (SHCS) and Swiss Transplant Cohort Study (STCS)) are an ideal foundation to set-up a trial platform in Switzerland leveraging routinely collected data. Within a newly founded trial platform, we plan to assess the efficacy of the first two mRNA SARS-CoV-2 vaccines that reached market authorization in Switzerland in the frame of a pilot randomized controlled trial (RCT) while at the same time assessing the functionality of the trial platform.
We will conduct a multicenter randomized controlled, open-label, 2-arm sub-study pilot trial of a platform trial nested into two Swiss cohorts. Patients included in the SHCS or the STCS will be eligible for randomization to either receiving the mRNA vaccine Comirnaty® (Pfizer/BioNTech) or the COVID-19 mRNA Vaccine Moderna®. The primary clinical outcome will be change in pan-lg antibody response (pan-Ig anti-S1-RBD; baseline vs. 3 months after first vaccination; binary outcome, considering ≥ 0.8 units/ml as a positive antibody response). The pilot study will also enable us to assess endpoints related to trial conduct feasibility (i.e., duration of RCT set-up; time of patient recruitment; patient consent rate; proportion of missing data). Assuming vaccine reactivity of 90% in both vaccine groups, we power our trial, using a non-inferiority margin such that a 95% two-sided confidence interval excludes a difference in favor of the reference group of more than 10%. A sample size of 380 (190 in each treatment arm) is required for a statistical power of 90% and a type I error of 0.025. The study is funded by the Swiss National Science Foundation (National Research Program NRP 78, "COVID-19").
This study will provide crucial information about the efficacy and safety of the mRNA SARS-CoV-2 vaccines in HIV patients and organ transplant recipients. Furthermore, this project has the potential to pave the way for further platform trials in Switzerland.
ClinicalTrials.gov NCT04805125 . Registered on March 18, 2021.
Keywords
Aged, COVID-19, COVID-19 Vaccines, Humans, Immunocompromised Host, Multicenter Studies as Topic, Pilot Projects, RNA, Messenger, Randomized Controlled Trials as Topic, SARS-CoV-2, Viral Vaccines, Organ transplant, Platform trial, Protocol, Randomized controlled trial, HIV, Vaccine
Pubmed
Web of science
Open Access
Yes
Create date
05/11/2021 18:48
Last modification date
23/11/2022 8:14
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