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Full eligibility criteria for NCT02632474
Ages eligible for Study
18 Years to 65 Years
Genders eligible for Study
Accepts Healthy Volunteers
HIV antibody positive
HIV RNA below 10*E5 copies/ml
CD4 T cell count above 200 cells/ml
Provision of written informed consent
HIV genotyping resistant to investigating drug
Pregnant, breastfeeding, or lactating
Any serious or active medical or psychiatric illness which, in the opinion of the Investigator, would interfere with treatment, assessment, compliance with the protocol, or subject safety. This would include any active clinically significant renal, cardiac, pulmonary, vascular, or metabolic (thyroid disorders, adrenal disease) illness, or malignancy
Medical or psychiatric condition or occupational responsibilities that may preclude compliance with the protocol
Laboratory blood values:
Haemoglobin <7.0 grams/decilitre (g/dL)
Neutrophil count <500/mm3
Platelet count <50,000/mm3
Aspartate aminotransferase or Alanine transaminase >5 times Upper Limit of Normal
Subjects with an estimated creatinine clearance of <50 mL/minute
All locations for NCT02632474
Shanghai Public Health Clinical Center
Shanghai, Shanghai, China, 201508
View full eligibility
Tris trial is registered with FDA with number: NCT02632474. The sponsor of the trial is Shanghai Public Health Clinical Center and it is looking for 10 volunteers for the current phase.
Official trial title: ART Drug Dosage Adjustment Using FSCII in Chinese HIV-infected Population
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