Pharmacological Studies in Hospitalized COVID-19 Patients in Belgium: We Could Do Better
- PMID: 35891407
- PMCID: PMC9320769
- DOI: 10.3390/v14071427
Pharmacological Studies in Hospitalized COVID-19 Patients in Belgium: We Could Do Better
Abstract
Belgium has actively participated in clinical research on severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) since the beginning of the pandemic to help identify effective and safe treatments for COVID-19. The objective of this review is to provide a picture of the clinical studies carried out in hospitalized patients with COVID-19 in Belgium. We collected data on all randomized, interventional trials in patients with COVID-19 that were registered on two recognized clinical trial registers, started enrollment before 31 December 2021, and included at least one patient in a Belgian center. Data were collected concerning the therapies investigated and the nature of the trials performed. Thirty-three hospitals (32% of all Belgian hospitals) participated in at least one of 28 trials (13 sponsored by the industry and 15 by academic centers) on therapeutics for COVID-19 in hospitalized patients: 7 (25%) evaluated antivirals, 17 (61%) immunomodulators, 2 (7%) anti-coagulants, and 1 (3%) nitric oxide to improve respiratory function. Nineteen (68%) were phase II trials. Only three (11%) of the trials were international platform trials. Despite numerous trials, less than 3% of all Belgian patients hospitalized with COVID-19 participated in a clinical trial on therapeutics. As in many other countries, more efforts could have been made to avoid running small, under-powered, mono- or bicenter trials, to create better collaboration between the different Belgian hospitals, and to participate in more international clinical trials, and more specifically in adaptive, platform trials.
Keywords: Belgium; adaptive platform trials; severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2).
Conflict of interest statement
M.H. is the co-leader of the DisCoVeRy trial, the national coordinator of the EU-SolidAct trial, and was the principal investigator of the COV-AID trial and the MIRAGE trial. She is a co-leader of the Belgian COVID-19 Therapeutics Guidelines for Hospitalized Adults, and is a member of the task force on COVID-19 therapeutics. She has received funding for COVID-19 clinical trials from Fonds Erasme-COVID-19, the KCE, and EU Horizon. She has received fees for presentations by Pfizer, and has benefitted from congress and travel expenses paid by Pfizer and Gilead. J.-L.V. has no conflicts of interest to declare.
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