Phase 2 HIV and AIDS Trial, Recruiting NCT03684655 Sponsor: CellSight Technologies, Inc. Condition: HIV and AIDS
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Phase 2 HIV and AIDS Trial, Recruiting

NCT03684655
Recruiting Phase 2

Who may be able to join

AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI

Who might be able to join this trial:

  • People who are over 18 years old
  • People who are able to read and understand a written consent form
  • People who have HIV, and who either: are currently taking a combination HIV treatment (ART) regimen, have never taken HIV treatment, or have taken HIV treatment in the past but stopped at least 1 week before the study's imaging session
  • People whose recent blood test results (taken within the last 60 days) show that platelet counts, white blood cell levels, liver function, kidney function, and immune cell counts (CD4+ T cells, for those with HIV) are all within the required ranges (confirm specific numbers with trial site)

Who may not be able to join:

  • People who cannot have an MRI scan — for example, those with a permanent pacemaker, metal implants or prosthetics, an aneurysm clip, a non-removable piercing, or severe claustrophobia
  • People with a medical condition that, in the opinion of the trial doctor, would affect the quality of the scan images
  • People who have received treatments that affect the immune system (other than an HIV DNA vaccine) within the past 60 days
  • People who are currently pregnant (pregnancy testing will be done before the imaging agent is given, and a positive result will mean the person cannot continue in the study)
  • People who are currently breastfeeding
  • Women who could become pregnant (meaning those who have had a period in the last 24 months, or have not had a hysterectomy and/or removal of both ovaries or both fallopian tubes) must have a negative pregnancy test at the first visit and again within 24 hours before the PET scan, and must use 2 forms of contraception (withdrawal or timing-based methods do not count)
  • People who have previously had a stem cell transplant or solid organ transplant from another person
  • People whose recent blood tests show platelet counts, white blood cell counts, red blood cell levels, kidney function, or liver function outside the required ranges (confirm specific values with trial site)
  • People who have been hospitalised or needed intravenous antibiotics for a serious illness within the past 3 months
  • People who currently have an active HIV-related opportunistic infection, such as a specific type of pneumonia, widespread bacterial infection, invasive fungal infection, a throat yeast infection, or a brain parasite infection (a mild oral yeast infection is acceptable)
  • People who have previously been diagnosed with a bone marrow disorder called myelodysplasia, or who have a history of a blood or lymph system cancer
  • People with a documented history of heart failure that required medication, or that needed medical management within the past year
  • People with an active Hepatitis C infection (people who were previously treated for Hepatitis C and have no remaining signs of the virus may still be eligible — confirm with trial site)
  • People with an active autoimmune disease affecting the whole body
  • People who have had a routine vaccination within the 14 days before entering the study

Important: Always verify eligibility with the trial site directly before applying.

Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 12 July 2026
Phase 2: approximately ~30% of drugs entering this phase reach regulatory approval, based on published industry-wide historical data. This is not specific to this trial.
Phase success rates shown are historical industry-wide averages based on published data. They are not a prediction for this specific trial or your individual situation.

Contact this trial

Principal Investigator: Timothy J Henrich, MD, University of California, San Francisco

Phone: 415-206-5518

Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.

GP referral letter

Print a one-page summary to share with your doctor.

Trial details

Status
Recruiting
Phase
Phase 2
Sponsor
CellSight Technologies, Inc.
Registry
ClinicalTrials.gov
Start date
21 September 2018
Est. completion
1 October 2025

Where this trial is recruiting

🇺🇸 United States

Primary endpoints

Anatomical distribution of [18F]F-AraG

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

Data last synced from ClinicalTrials.gov: 12 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov