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CPI-1189 for AIDS Dementia
Study Summary
This trial will test if it is safe and effective to give CPI-1189 to patients with AIDS dementia.
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 do not have serious conditions like mental disorders or AIDS-related infections.I am 18 years old or older.I experience symptoms like forgetfulness and loss of muscle control.I have been on a consistent HIV medication regimen for the last 6 weeks.
- 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
Where are patients able to participate in this clinical trial?
"Right now, there are 6 hospitals enrolling patients for this study. The locations include 3 cities- Baltimore, Rochester and Chicago- as well as 6 additional sites. If you choose to participate in the trial, try and select a location that is close to reduce travel burdens."
Who would be an appropriate candidate for this type of research?
"Sixty individuals that are infected with HIV and eighteen years or older can participate in this study. Most importantly, potential patients should meet the following guidelines: displaying symptoms related to AIDS dementia such as forgetfulness, muscle control loss, decreased concentration or slow mental processing; a positive HIV diagnosis; being on anti-HIV medication for at least six weeks prior to joining the study (if applicable)."
Will this experiment be testing its effects on middle-aged adults?
"To meet the requirements for this trial, applicants must be between 18 and 0 years old. Out of the 477 total clinical trials, 110 are for people under 18 while 367 are for seniors."
Does the FDA sanction this medication?
"While there is some evidence backing the safety of this treatment, it received a 2 because Phase 2 trials have not yet found data supporting efficacy."
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