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Study Summary
This trial will test the safety of tucaresol in HIV patients also taking HAART, as well as its effect on viral load.
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowTimeline
Treatment Details
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Who is running the clinical trial?
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- I am unable to understand and give consent for treatment.I have hepatitis B or C.I have been on anti-HIV medication for at least 6 months without issues.I am currently on anti-HIV medication.My HIV viral load is under 50 copies/ml on my current treatment.I have a history of heart, sickle cell, anemia, or lung conditions.I am currently taking abacavir or medications that affect my immune system.I have been vaccinated within the last 30 days.I am 18 years old or older.I can attend weekly doctor visits.I have a history of tumors.I do not plan to change my HIV treatment during the study.
- 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
Are geriatric patients accepted in this trial?
"This medical trial welcomes adults of any age above 18 years and below 65."
Are any additional participants being accepted at this time for the clinical trial?
"Per the information on clinicaltrials.gov, this trial is not currently accepting participants. Initially posted in June 2000 and last edited in 2005, it has been inactive for some time; however, there are 484 other medical studies actively enrolling patients presently."
Is my eligibility sufficient to partake in this endeavor?
"This clinical trial seeks to recruit 24 individuals living with HIV between the ages of 18 and 0. To be eligible, patients must meet the following criteria: being at least 18 years old, having a current positive diagnosis for HIV, possessing more than 300 CD4 T cells per microlitre upon screening, taking specific anti-HIV medications successfully for six months or longer without expectation to change their therapy during the study period, having plasma viral load below 50 copies/ml while on treatment prior to enrolment in this trial as well as undetectable levels throughout all screenings and baseline tests; additionally they need to commit to weekly visits."
Has this procedure been granted endorsement from the FDA?
"This is an early stage trial, so the safety of this treatment has been rated a 1 due to insufficient evidence backing its efficacy and security."
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