Effectiveness and Safety of New Oral Antivirals for COVID-19

COVID-19 Clinical Trial

— ESOA-19  

Official title:

Post-marketing Surveillance Study of the Effectiveness and Safety of New Oral Antivirals for Outpatients With Mild-moderate COVID-19

Clinical Trial Details — Status: Active, not recruiting

Administrative data

• NCT number: NCT05894603
• Other study ID #: ESOA-19
• Secondary ID: EUPAS48186
• Status: Active, not recruiting
• Start date: August 1, 2022
• Est. completion date: June 30, 2024

Study information

• Verified date: May 2023
• Source: Universidade do Porto
• Contact: n/a
• Is FDA regulated: No
• Study type: Observational

Clinical Trial Summary

There is an increased lack of short- and long-term real-life effectiveness and safety data on new oral antivirals authorised and commercialised to treat COVID-19. To date, only two clinical trials have been published with data on the efficacy and safety of the use of the Paxlovid® and Lagevrio®. Since there is a public health, political, social and economic pressure to prevent severity, hospitalisation and death from COVID-19, monitoring the effectiveness and safety of commercialised oral antiviral therapies against COVID-19 has become emergent pharmacovigilance and public health task. The objective of the study is to monitor the post-marketing safety and effectiveness of the new oral antivirals indicated for the treatment of COVID-19, namely Nirmatrelvir/Ritonavir (Paxlovid®) and Molnupiravir (Lagevrio®), having as holders of the Authorization of Market introduction to Pfizer Europe MA EEIG and Merck Sharp & Dohme B.V., respectively.

Description:

There is an increased lack of short- and long-term real-life effectiveness and safety data on new oral antivirals authorised and commercialised to treat COVID-19. To date, only two clinical trials have been published with data on the efficacy and safety of the use of the Paxlovid® and Lagevrio®. Since there is a public health, political, social and economic pressure to prevent severity, hospitalisation and death from COVID-19, monitoring the effectiveness and safety of commercialised oral antiviral therapies against COVID-19 has become emergent pharmacovigilance and public health task6. A real-life cohort event monitoring system allows for the monitoring of newly introduced oral antivirals, in addition to existing spontaneous reporting systems and healthcare database studies (i.e., secondary data), as it is complementary to these systems in several ways. First, it is better suited to capture the more frequent AE, including those that are not medically attended. It generates more comprehensive safety data, e.g. on disease course and the impact of the AE. Moreover, there is insufficient data on these new medicines in real clinical practice, particularly from large-scale studies on the long-term efficacy or safety. This work, with scientific and academic interest but, essentially, clinical and regulatory importance, constitutes a duty of the regional pharmacovigilance units. As such, it is also an obligation of the Pharmacy and Therapeutics Commissions, based on the legislation in force, to "collaborate in studies to monitor the safety and effectiveness of medicines promoted in the context of the National Pharmacovigilance System".

Recruitment information / eligibility

• Status: Active, not recruiting
• Enrollment: 211
• Est. completion date: June 30, 2024
• Est. primary completion date: January 31, 2024
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

Participants eligible to be included in the study are identified by medical prescribing of

one of the drugs under study, and either the medicine recipient or their proxy should:

1. Comply with the eligibility criteria for prescribing these drugs (including patients = 18 years old), according to Norm nr 005/2022 of the General Directorate of Health of Portugal*;

2. Enrol in the study within the first 72 hours after dispensing treatment;

3. Be able to understand the Portuguese language;

4. Available for follow-up during study time;

5. Provide informed consent.

• Compliance with the eligibility criteria for prescribing these drugs is the sole responsibility of the prescriber who assesses the patient, so the study centres only include patients referred by the prescriber. Exclusion Criteria:

Will be considered ineligible participants those who:

1. Are not available for follow-up and monitoring;

2. Participate in phase I, II, III or IV clinical trials;

3. Life expectancy is less than one month.

Related Conditions & MeSH terms

• COVID-19

Intervention

Drug:
• Nirmatrelvir/ritonavir
Nirmatrelvir/ritonavir
• Molnupiravir
Molnupiravir

Locations

Country	Name	City	State
Portugal	Hospital do Divino Espírito Santo de Ponta Delgada, EPE	Açores
Portugal	Centro Hospitalar de Lisboa Ocidental, EPE	Lisboa
Portugal	Centro Hospitalar de Vila Nova de Gaia/Espinho, EPE	Porto
Portugal	Centro Hospitalar e Universitário de São João, EPE	Porto
Portugal	Centro Hospitalar Universitário de Santo António, EPE	Porto
Portugal	Unidade de Saúde Familiar - Homem do Leme (ACES Porto Ocidental)	Porto

Sponsors (4)

Lead Sponsor	Collaborator
Universidade do Porto	Centro de Investigação em Tecnologias e Serviços de Saúde (CINTESIS), Faculty of Medicine (FMUP), Rede de Investigação em Saúde (RISE), Laboratório Associado

Country where clinical trial is conducted

Portugal, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Safety outcome	The incidence of AE (with particular focus on AE of special interest) that emerge during or after the treatment period, serious AE, and AE leading to discontinuation of the treatment, as coded according to the MedDRA. Incidence data will be provided for each treatment group within the safety analysis population, including all patients who received at least one drug dose.; The occurrence of AE will be asked in open question / unsolicited. For each reported AE, date of onset, outcome, duration of symptoms (if recovered), and severity/impact of the symptoms (including medical assistance & hospitalisation) will be asked.	6 days after onset treatment for both drugs.
Primary	Safety outcome	The incidence of AE (with particular focus on AE of special interest) that emerge during or after the treatment period, serious AE, and AE leading to discontinuation of the treatment, as coded according to the MedDRA. Incidence data will be provided for each treatment group within the safety analysis population, including all patients who received at least one drug dose.; The occurrence of AE will be asked in open question / unsolicited. For each reported AE, date of onset, outcome, duration of symptoms (if recovered), and severity/impact of the symptoms (including medical assistance & hospitalisation) will be asked.	39 days after treatment onset for nirmatrelvir/ritonavir cohort.
Primary	Safety outcome	The incidence of AE (with particular focus on AE of special interest) that emerge during or after the treatment period, serious AE, and AE leading to discontinuation of the treatment, as coded according to the MedDRA. Incidence data will be provided for each treatment group within the safety analysis population, including all patients who received at least one drug dose.; The occurrence of AE will be asked in open question / unsolicited. For each reported AE, date of onset, outcome, duration of symptoms (if recovered), and severity/impact of the symptoms (including medical assistance & hospitalisation) will be asked.	19 days after treatment onset for molnupiravir cohort.
Primary	Effectiveness outcome	The incidence of hospitalisation for any cause (defined as =24 hours of acute care in a hospital or any similar facility) or death for any cause through day 29.	29 days after treatment onset for both drugs.
Secondary	Adherence to treatment	Will be measured using the self-reported 7-item Measure Treatment Adherence (MTA) tool validated for the Portuguese Population. The MTA is a psychometric tool derived from the Morisky et al. questionnaire and evaluates the individuals' behaviour concerning the daily use of medication.	6 days after onset treatment for both drugs.