Study Details

• Type: Interventional
• Disease: Covid 19 Surveillance of positive tests
• Primary Site: Fondazione Policlinico Gemelli
• Start: February 2021
• Population: Outpatient pulmonary adults with documented positive SARS-CoV-2 test
• Duration: Ongoing

Study Description

MONET study is a Phase 3, open-label, individually randomized study in patients with documented positive SARS-CoV-2 test and mild symptoms of COVID-19, not hospitalized and recruited in Italy. This study will assess the efficacy of multiple MoAbs cocktails compared to SoC for Treatment of COVID-19 in Outpatient Adults. The study will be conducted in 42 clinical centers across Italy.

Study Design & Method

The procedure to be followed is the randomized administration of 2 different MoAbs cocktails, all intravenously over one-hour infusion. Then there will be control and monitoring of the differences that will occur in the participants of the study. The adaptive design of the study is aimed to meet the most topical needs of translational medical research programs implemented during a massive epidemic emergency due to newly emergent pathogens, such as SARS-CoV-2.

All participants will use the Healthentia app to answer simple and composite questionnaires about their health status. Each organisation will monitor any symptoms that any user/participant may appear.

42 Centers involved in the study and is planned to be executed on 750 to 2350 subjects

Estimation of the efficacy of any MoAbs in the prevention of the composite endpoint of either severe COVID-19 or hospitalization or access in an emergency department or death

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Study Details

• Type: Multicentric
• Disease: Covid 19 Surveillance of positive tests
• Primary Site: Fondazione Policlinico Gemelli
• Start: March 2021
• Population: Outpatient pulmonary adults with documented positive SARS-CoV-2 test
• Duration: Ongoing

Study Description

IPF VACCINE is a study to record and monitor Idiopathic pulmonary fibrosis (IPF) patients of the Agostino Gemelli IRCCS University Hospital Foundation after the administration of their vaccination. Healthentia application will be used to collect through questionnaires, any side effects that occurred on the day of vaccination and the following seven days.

Study Design & Method

All participants will download Healthentia application and register. For a period of 7 days, the user is asked, through an agile questionnaire, to report any side effects that occurred on the day of vaccination and the next seven days.

Monitor reactions on IPF Patients

Categorize side effects present in
IPF Patient group

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