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HCVax for Chronic Hepatitis C
Study Summary
This trial is to see if a new HCV immunotherapy is safe and if it causes an immune response in patients with chronic HCV.
- Chronic Hepatitis C
Timeline
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Trial Design
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Who is running the clinical trial?
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- You are not currently receiving treatment for hepatitis C with direct-acting antiviral medication.
- Group 1: Low dose group
- Group 2: High dose group
- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
Frequently Asked Questions
Could I potentially qualify to engage in this clinical experiment?
"To be eligible for this research, individuals must have hepatitis and fall within the age range of 18 to 60. A total of 30 participants will partake in the trial."
Does this research endeavor include individuals aged sixty and above?
"According to the criteria for participation, prospective patients must be aged 18-60. Those under 18 are eligible for 27 different studies and those over 65 can apply for 237 trials."
Are any new participants being welcomed into this research endeavor?
"According to the records available on clinicaltrials.gov, this research study is still accepting patient applications. The protocol was initially unveiled in April of 2021 and has been revised most recently at the end of September that same year."
How many individuals have been conscripted to take part in this research?
"Affirmative. Research hosted on clinicaltrials.gov indicates that this scientific investigation, which first appeared online on April 20th 2021, is currently searching for participants. 30 patients need to be sourced from two different medical facilities."
To what extent does HCVax pose a risk to human health?
"The data collected on HCVax's safety and efficacy is limited, thus giving it an overall score of 1."
Who else is applying?
What state do they live in?
How old are they?
What site did they apply to?
What portion of applicants met pre-screening criteria?
How many prior treatments have patients received?
Why did patients apply to this trial?
How responsive is this trial?
Typically responds via
Most responsive sites:
- Gastrointestinal Specialists of Georgia: < 24 hours
Average response time
- < 1 Day
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