ClinConnect ClinConnect Logo
Search / Trial NCT01318096

Safety and Efficacy of Raltegravir+TDF+3TC in HBV/HIV Co-infected Patients

Launched by YUNNAN AIDS CARE CENTER · Mar 17, 2011

Trial Information

Current as of August 02, 2025

Unknown status

Keywords

Safety Efficacy Raltegravir Hbv/Hiv Co Infection

ClinConnect Summary

There are in total more than 72939 HIV infected people reported in Yunnan, the largest number for any province in China. About 800 HIV inpatients are admitted to our hospital every year, amongst them about 10% co-infected with HBV. HIV and HBV co-infection patients must receive two drugs active against both HIV and HBV, for example Tenofovir disoproxil fumarate (TDF)+ lamivudine (3TC) or TDF+FTC. TDF and 3TC are nucleotide analogues that can inhibit both HIV and HBV DNA polymerases (Dore, Cooper et al. 2004). Combination therapy could decrease drug resistance. In China, TDF is a second-line...

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:
  • Ability and willingness to provide written informed consent
  • HIV-1 infection, documented in patient medical record. Acceptable forms of documentation include positive HIV antibody or detectable HIV RNA
  • HIV-1 antiretroviral therapy naïve
  • Chronic HBV infection, defined as HBsAg positive \>6 months. Both HBeAg positive and negative subjects will be eligible
  • Detectable HBV DNA ( \> 300 copies/ml)
  • Serum alpha-fetoprotein (AFP) of ≤ 50 ng/ml within 4 weeks of study entry, or if elevated \> 50 ng/ml, an imaging study demonstrating no evidence of hepatic tumor within 4 weeks of enrollment
  • Exclusion Criteria:
  • Allergy or sensitivity to study drug
  • Pregnancy, breastfeeding or unwillingness/inability to adhere to contraceptive methods for the duration of the study (Female study volunteers must not participate in a conception process (e.g., active attempt to become pregnant). If participating in sexual activity that could lead to pregnancy, the female study volunteer must use the following forms of contraception while receiving study-specific medication(s) and for 30 days after stopping the medication. One of the following methods MUST be used appropriately: (1)Condoms\* (male or female) with or without a spermicidal agent; (2)Diaphragm or cervical cap with spermicide; (3)IUD; (4)Hormonal-based method.Condoms are recommended because their appropriate use is the only contraception method effective for preventing HIV transmission.
  • Prisoners or subjects who are incarcerated
  • Receipt of the following drugs with anti-HBV activity within 90 days prior to study entry or anticipated receipt during the course of the study including: ADV, telbivudine, alpha interferon, and other investigational agents with anti-HBV activity
  • Active opportunistic infection
  • Other causes of chronic liver disease identified (autoimmune hepatitis, haemochromatosis, Wilsons disease, alfa-1-antitrypsin deficiency)
  • Concurrent malignancy requiring cytotoxic chemotherapy
  • Decompensated or Child's C cirrhosis
  • Any other condition which in the opinion of the investigator might interfere with compliance or outcome of the study

About Yunnan Aids Care Center

The Yunnan AIDS Care Center is a leading clinical trial sponsor dedicated to advancing research and treatment options for HIV/AIDS and related co-infections. Located in Yunnan province, China, the center focuses on improving patient care through innovative clinical studies, community engagement, and collaboration with global health organizations. With a commitment to evidence-based practices, the Yunnan AIDS Care Center aims to enhance the quality of life for individuals affected by HIV/AIDS while contributing to the global understanding of the epidemic.

Locations

Kunming, Yunnan Provice, China

Patients applied

0 patients applied

Trial Officials

Cheng Xi Wang, M.D.

Principal Investigator

Yunnan Provincial Hospital of Infectious Diseases/Yunnan AIDS Care Center

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported

Similar Trials