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Taking people in ChinaPhase 1

The Effect of Chimeric Antigen Receptor (CAR)-T Cell Therapy on the Reconstitution of HIV-specific Immune Function

Key facts

Where
Guangzhou, ChinaSee the site
Phase
Phase 1

Could this be for you?

Answer for yourself. This is not a decision: only the study team can say whether you can take part.

  • Are you between 18 and 60 years old?

Where in China

  • Guangzhou 8th People's HospitalGuangzhou, ChinaTaking people

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?
Print a page for my doctor

Trial details

Who runs it
Guangzhou 8th People's Hospital
Trial code
NCT03240328
Record updated
14 September 2022
Original description
To study the safety and effectiveness of CAR-T Cell therapy on HIV patients whose plasma HIV has been successfully suppressed after cART, which is expected to enhance the res-constitution of HIV-specific immune function to assist the eradication of HIV reservoir.Read full original descriptionShow less

The Effect of CAR-T Cell Therapy on the Reconstitution of HIV-specific Immune Function

To study the safety and effectiveness of CAR-T Cell therapy on HIV patients whose plasma HIV has been successfully suppressed after cART, which is expected to enhance the res-constitution of HIV-specific immune function to assist the eradication of HIV reservoir.

Inclusion: HIV infection confirmed; Receiving cART more than 12 months; HIV viral-load < 50 copies/ml and CD4 cell count more than 350 cells/ul; Without serious liver, heart, liver and kidney diseases; The subjects know about the study and volunteer to attend the research and sign the informed consent.

Exclusion: With active HBV or HCV infection, or serious opportunistic infections; With serious chronic disease such like diabetes, the mental illness,et al; History of suffering from pancreatitis during cART; Pregnant or breast-fed; With poor adherence; Unable to complete follow up.

ClinicalTrials.gov NCT03240328