Secutrelvir for COVID-19
What You Need to Know Before You Apply
What is the purpose of this trial?
This trial tests the effectiveness and safety of a treatment called secutrelvir for COVID-19. It focuses on individuals with COVID-19 symptoms who are at risk of severe illness but are not hospitalized. Participants will receive either secutrelvir or a placebo (a pill with no active medicine) to evaluate the treatment's effectiveness. Those with COVID-19 symptoms and a high risk of severe illness may be suitable candidates for this trial. As a Phase 3 trial, it represents the final step before FDA approval, providing participants an opportunity to contribute to a potentially groundbreaking treatment.
Will I have to stop taking my current medications?
The trial does not specify if you need to stop taking your current medications, but you cannot have taken certain COVID-19-specific therapies recently. It's best to discuss your current medications with the trial team.
Is there any evidence suggesting that secutrelvir is likely to be safe for humans?
Research has shown that secutrelvir is generally well-tolerated. In a previous study with over 3,000 patients in Japan, researchers found no new safety concerns, and participants did not report any unexpected side effects. Another study examined secutrelvir's mechanism in the body and supported its safety.
Since this trial is in a later phase, substantial safety data already exists. Earlier trials have demonstrated that secutrelvir is reasonably safe. While no treatment is without risks, existing research suggests secutrelvir is safe for treating COVID-19.12345Why do researchers think this study treatment might be promising for COVID-19?
Unlike the standard of care for COVID-19, which includes antivirals like remdesivir and treatments such as monoclonal antibodies, Secutrelvir works differently by targeting a unique viral component to inhibit replication. Researchers are excited about Secutrelvir because it introduces a novel mechanism of action, potentially offering a more effective way to stop the virus from multiplying. Additionally, Secutrelvir may work faster and be more efficient in reducing viral load compared to existing treatments, which is critical for managing symptoms and preventing severe disease progression.
What evidence suggests that secutrelvir might be an effective treatment for COVID-19?
Research has shown that secutrelvir, also known as ensitrelvir, holds promise in treating COVID-19. In this trial, participants will receive either secutrelvir or a placebo. One study found that taking ensitrelvir for five days reduced the risk of developing symptoms by 67% after exposure to the virus. Participants who took ensitrelvir were also less likely to require hospitalization compared to those who didn't receive any antiviral treatment. The treatment helped clear the virus from the body more quickly. However, that study noted it didn't significantly speed up the relief of COVID-19 symptoms compared to a placebo. Overall, ensitrelvir may help reduce the severity and spread of COVID-19.678910
Who Is on the Research Team?
Medical Director
Principal Investigator
Shionogi Inc.
Are You a Good Fit for This Trial?
This trial is for adults and teens with COVID-19 who have symptoms but are not in the hospital, and who are at high risk of their illness becoming severe.Inclusion Criteria
Exclusion Criteria
Timeline for a Trial Participant
Screening
Participants are screened for eligibility to participate in the trial
Treatment
Participants receive secutrelvir or placebo
Follow-up
Participants are monitored for safety and effectiveness after treatment
What Are the Treatments Tested in This Trial?
Interventions
- Secutrelvir
Trial Overview
The study compares a new drug called secutrelvir to a placebo (inactive treatment) to see if it helps prevent mild or moderate COVID-19 from getting worse. Participants are randomly assigned to receive either secutrelvir or placebo.
How Is the Trial Designed?
2
Treatment groups
Experimental Treatment
Placebo Group
Participants will receive secutrelvir.
Participants will receive placebo.
Find a Clinic Near You
Who Is Running the Clinical Trial?
Shionogi
Lead Sponsor
Dr. Isao Teshirogi
Shionogi
Chief Executive Officer since 2008
PhD in Pharmaceutical Sciences from the University of Tokyo
Dr. Takuko Sawada
Shionogi
Chief Medical Officer since 2022
MD from a recognized institution (specific details not found)
Citations
NCT07743580 | A Study of Secutrelvir in Participants With ...
The primary purpose of this study is to evaluate the efficacy and safety of secutrelvir in symptomatic nonhospitalized adult and adolescent participants ...
New England Journal of Medicine Publishes ...
A five-day course of ensitrelvir significantly reduced the risk of symptomatic COVID-19 by 67% in individuals following exposure to an infected ...
Real-World Effectiveness of Ensitrelvir in Reducing Severe ...
The study found that patients who received ensitrelvir had a lower risk of being hospitalized compared to those who did not receive any antiviral treatment.
Ensitrelvir for the treatment of COVID-19: Final analysis of a ...
In a phase 1 study, ensitrelvir was well tolerated … 5 days demonstrated a significant reduction in viral titer and viral RNA
Ensitrelvir for Covid-19 Postexposure Prophylaxis in ...
The point estimate of protective efficacy for ensitrelvir postexposure prophylaxis (67.0%) was numerically higher than those reported in trials ...
Coronavirus Disease 2019 (COVID-19) Vaccine Safety
COVID-19 vaccines underwent the most intensive safety analysis in U.S. history. COVID-19 vaccines continue to be monitored for safety,
Evaluation of the safety profile of COVID-19 vaccines - PMC
Available evidence indicates that eligible COVID-19 vaccines have an acceptable short-term safety profile. Additional studies and long-term population-level ...
8.
ausvaxsafety.org.au
ausvaxsafety.org.au/pfizer-covid-19-vaccine-adult-formulation/pfizer-covid-19-vaccine-safety-data-all-participantsPfizer COVID-19 vaccine safety data - All participants
Data on this page show the responses of all individuals aged 12 years and older who received the adult 30 microgram formulation of the Pfizer COVID-19 ...
9.
fda.gov
fda.gov/vaccines-blood-biologics/safety-availability-biologics/covid-19-vaccine-safety-surveillanceCOVID-19 Vaccine Safety Surveillance
This page describes the monitoring the safety of authorized COVID-19 vaccines through both passive and active safety surveillance systems.
All COVID-19 Updates
available data support the safety and effectiveness of PAXLOVIDTM (nirmatrelvir tablets and ritonavir tablets) for the treatment of mild-to-moderate COVID-19
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