Status:
UNKNOWN
Raltegravir-based Antiretroviral Therapy for Resistant HIV-1 Infection
Lead Sponsor:
Peking Union Medical College
Conditions:
AIDS/HIV PROBLEM
Eligibility:
All Genders
18-65 years
Phase:
NA
Brief Summary
This study is to evaluate the safety and efficacy of RAL-based regimen in treatment-experienced patients with resistant HIV infection
Detailed Description
In our study, both efficacy and safety of raltegravir(RAL)-based therapy will be assessed. 300 treatment-experienced patients with drug-resistant HIV will be randomized to two arms (2:1). Group A (n=2...
Eligibility Criteria
Inclusion
- Age between 18-65 years
- HIV seropositive and confirmed by western blot
- have taken first line antiretroviral therapy for over one year and have any one of the criteria listed below (viral load of all the patients meeting these criteria should be confirmed at PUMCH laboratory)
- Viral load more than 400 copies/ml
- Viral rebound (confirmed by HIV RNA more than 400 copies/ml after virologic suppression)
- When viral load cannot be monitored, patients experience immunologic failure who meet at least one of the criteria listed below will be enrolled:
- CD4 count equal to or lower than baseline level with first-line therapy,on two occasions over three months apart
- CD4 count with 50 percentage fall from the on-treatment peak value
- persistent CD4 count levels less than 100 cells/μl after over one-year antiretroviral therapy
Exclusion
- Previous use of protease inhibitors
- Previous use of integrase inhibitors
- Pregnancy and breastfeeding
- poor compliance and drug interaction,
- opportunistic infections or malignancy at recruitment; or opportunistic infections within three months but still unstable within 14 days prior to recruitment
- HBsAg positive
- patients with the any of the following test results during screening for inclusion: WBC count\<2000/μl, neutrophil count\<1000/μl, Hb\<9g/dl, platelet count\<75000/μl, serum creatinine\>1.5 ULN, transaminases or alkaline phosphatase \>3 ULN, total bilirubin\>2 ULN, serum creatinine kinase\>2 ULN
- CCr\<60 ml/min
- Current intravenous drug use
- Severe neuropathy or mental disorder
- history of alcohol abuse and unable to withdrawal
- Severe peptic ulcer
Key Trial Info
Start Date :
May 1 2013
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
December 1 2015
Estimated Enrollment :
300 Patients enrolled
Trial Details
Trial ID
NCT01844310
Start Date
May 1 2013
End Date
December 1 2015
Last Update
May 1 2013
Active Locations (1)
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1
Peking Union Medical College Hospital
Beijing, China, 100730