Study on the Effects of S-217622 for Adults Hospitalized with COVID-19

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What is this study about?

This clinical trial is focused on studying the treatment of COVID-19, a respiratory infection caused by the SARS-CoV-2 virus. The trial will evaluate a new medication called S-217622, which is a type of drug known as a protease inhibitor. Protease inhibitors work by blocking a specific enzyme that the virus needs to multiply, potentially helping to reduce the severity of the infection. Participants in the study will receive either the S-217622 medication or a Placebo-B, which is a substance with no active ingredients, alongside the standard care they would normally receive in the hospital.

The purpose of this study is to determine if a 5-day treatment with S-217622 can improve the clinical outcomes for patients hospitalized with COVID-19. The study will involve patients who are admitted to the hospital with symptoms of a respiratory infection and have confirmed COVID-19. The trial will monitor participants over a period of 60 days to assess their recovery and overall health status. The main focus will be on how quickly patients recover, as well as their health condition at the end of the study period.

Throughout the study, researchers will also keep track of any serious health events or side effects that may occur. This will help ensure the safety of the participants and provide valuable information about the potential benefits and risks of using S-217622 as a treatment for COVID-19. The trial aims to provide insights into whether this new medication can be an effective addition to the current treatment options for hospitalized patients with COVID-19.

1 joining the trial

Upon joining the trial, you will be asked to provide informed consent. This means you agree to participate after understanding the trial’s purpose and procedures.

You must be at least 18 years old and have been admitted to the hospital with signs of a respiratory infection, confirmed as COVID-19.

2 randomization

You will be randomly assigned to receive either the S-217622 treatment or a placebo. A placebo is a tablet that looks like the treatment but does not contain the active substance.

This process ensures that the trial results are unbiased and reliable.

3 treatment administration

If assigned to the treatment group, you will receive S-217622 in the form of a tablet. The treatment lasts for 5 days.

The medication is taken orally, meaning you will swallow the tablet.

4 monitoring and follow-up

Your health will be monitored throughout the trial to assess your recovery and any side effects. This includes regular check-ups and assessments.

The primary outcome measured is the Days to Recovery Scale over a period of 60 days. This scale tracks your recovery progress.

5 completion of trial

At the end of the trial, your overall health and recovery status will be evaluated.

The trial aims to determine if the S-217622 treatment improves clinical outcomes for patients hospitalized with COVID-19.

Who Can Join the Study?

  • Must be 18 years or older.
  • Must provide informed consent to participate in the trial. This means you understand the trial and agree to take part.
  • Must be admitted to the hospital or waiting for hospital admission with signs or symptoms of a respiratory infection.
  • Must have a confirmed SARS-CoV2 infection (the virus that causes COVID-19) by a test done within the last 14 days.
  • The onset of symptoms related to the SARS-CoV2 infection must have started within 14 days before joining the trial.
  • Must be hospitalized for COVID-19 management, showing signs or symptoms that suggest a lower respiratory tract infection. This means the infection affects the lungs or airways.

Who Cannot Join the Study?

  • Patients who are not hospitalized for the management of COVID-19.
  • Patients who are not adults. The study is for adults only.
  • Patients who are not able to follow the study procedures or take the study medication as required.
  • Patients who have any medical condition that the study doctors believe would make it unsafe for them to participate.
  • Patients who are pregnant or breastfeeding.
  • Patients who are participating in another clinical trial that could interfere with this study.
  • Patients who have a known allergy or sensitivity to the study medication or its ingredients.

Where you can join this trial?

Verified and Recommended Sites

No sites found in this category

Verified Sites

Site Name City Country Status
Bispebjerg Hospital Copenhagen Denmark

Other Sites

Site Name City Country Status
Evangelismos S.A. Athens Greece
St Vincent’s University Hospital Dublin Ireland
Rigshospitalet Copenhagen Denmark
Gentofte Hospital Hellerup Denmark
Hospital Del Mar Barcelona Spain
Wojewodzki Szpital Zakazny W Warszawie SPZOZ Warsaw Poland
Zealand University Hospital, Department of Cardiology Roskilde Denmark
Thoracic General Hospital Of Athens I Sotiria Athens Greece
Nordsjaellands Hospital Hillerød Denmark
Democritus University Of Thrace Alexandroupoli Greece
Coun Ulwoxjikur Hflhcvlv Cork Ireland
Lzyoc Gajxpke Hcoegilw Oh Aqyokl Athens Greece
Ujfmvaataa Hxzxibtv Cebbfiz Cologne Germany
Hdctmikp Hriaulxk Hvidovre Denmark
Hfeslggw Uojcxpismonou Hmniwfvl Tllha y Peicqd Iidqvncd Cswebu dwpvyqrnthtnjomnk (wkad Badalona Spain
Ultmglogjp Gwaclig Hjnhutkp Alnashx Athens Greece

Want to learn more about this study or check if you can participate? Contact us.

Trial status

Country Status Recruitment Start
Denmark Denmark
Not recruiting
15.02.2023
Germany Germany
Not recruiting
15.02.2023
Greece Greece
Not recruiting
15.02.2023
Ireland Ireland
Not recruiting
15.02.2023
Poland Poland
Not recruiting
15.02.2023
Spain Spain
Not recruiting
15.02.2023

Trial locations

S-217622 is a medication being tested in this clinical trial. It is a protease inhibitor, which means it works by blocking a specific enzyme that the virus needs to multiply. By inhibiting this enzyme, the medication aims to reduce the amount of virus in the body, potentially leading to better outcomes for patients who are hospitalized with COVID-19. The trial is investigating whether a 5-day treatment with this medication, in addition to standard care, can improve the health of patients compared to those who do not receive it.

COVID-19 – COVID-19 is a respiratory illness caused by the SARS-CoV-2 virus. It primarily spreads through respiratory droplets when an infected person coughs, sneezes, or talks. The disease can start with mild symptoms such as fever, cough, and fatigue, but it may progress to more severe conditions like difficulty breathing and pneumonia. In some cases, it can lead to acute respiratory distress syndrome (ARDS) and multi-organ failure. The progression of the disease varies widely among individuals, with some experiencing mild symptoms and others developing severe complications. The course of the illness can last from a few days to several weeks, depending on the severity and the individual’s health condition.

Trial ID:
2022-501020-19-01
Protocol code:
INSIGHT 018
NCT ID:
NCT05605093
Trial Phase:
Therapeutic confirmatory (Phase III)

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