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临床试验/EUCTR2019-002843-81-FR
EUCTR2019-002843-81-FR进行中(未招募)1 期

Switch to Tenofovir Alafenamide (TAF), Emtricitabine (FTC), Bictegravir (BIC)(Biktarvy®) in HIV-1-infected patients over 65 years old at risk of polymedication - BILOLDER

IMEA0 个研究点目标入组 50 人开始时间: 2019年8月6日最近更新:
适应症
相关药物

试验速览

阶段
1 期
状态
进行中(未招募)
发起方
入组人数
50

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional clinical trial of medicinal product

入排标准

性别
All

入选标准

  • HIV-1-infected patient
  • Age > 65 years old
  • Plasma HIV RNA = 50 copies/mL for = 6 months: one blip between 50 et 200 cp/ml is allowed in the last 6 months before screening.
  • Currently receiving an antiretroviral regimen containing a booster, ritonavir or cobicistat
  • No resistance mutation to integrase inhibitors on cumulative HIV RNA genotype. The reverse transcriptase resistant mutations M184V plus one TAM are allowed.
  • If no genotype is available, DNA genotype will be performed at screening visit: no resistance mutation to integrase inhibitors, the reverse transcriptase resistant mutations M184V plus one TAM are allowed.
  • Patient enrolled in or a beneficiary of a Social Security program (State Medical Aid or AME is not a Social Security program)
  • Informed consent form signed by patient and investigator
  • Are the trial subjects under 18? no
  • Number of subjects for this age range:
  • F.1.2 Adults (18-64 years) no
  • F.1.2.1 Number of subjects for this age range
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range 50

排除标准

  • HIV-2 infection
  • Currently receiving one of the following drugs : Hypericum perforatum,
  • rifampicin, rifabutin, carbamazepine, oxcarbazepine, phenobarbital, phenytoin, sucralfate, cyclosporine, primidone, ténofovir et adéfovir.
  • Hemoglobin < 10g/dL
  • Platelets < 100 000/mm3
  • Hepatic transaminases AST and ALT > 3x upper limit of normal (ULN)
  • Severe hepatic insufficiency (Child Pugh Class C)
  • Creatininemia clairance < 30 mL/min (MDRD)
  • History or presence of allergy to the trial drugs or their components
  • Patients participating in another clinical trial including an exclusion period that is still in force during the screening phase
  • Patients under judicial protection due to temporarily and slightly diminished mental or physical faculties or under legal guardianship.

研究者

发起方
IMEA

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