Dolutegravir Plus Lamivudine Simplified Therapy

NCT03884673 · tracked via the Priya Life Science China tracker

Sponsor

Guangzhou 8th People's Hospital

Phase

Observational

Started

2019-01-01

Last updated

2022-09-14

Condition(s) studied

HIV/AIDS

Investigational drug(s) / intervention(s)

DTG+ 3TC →

DTG+ 3TC: It is a simplified therapy regimen study of dolutegravir combined with lamivudine for HIV-1 infected patients in the real world of China.

Study summary

Dolutegravir (DTG) is one type of integrase inhibitor, lamivudine (3TC) is one type of reverse transcriptase inhibitor, both of which are HIV medicine prevents HIV from self-multiplying, reduces the viral load. The data of the existing randomized controlled clinical studies show that the simplified two-drug DTG-based regimen is similar to the three-drug regimen in terms of efficacy, but there are no relevant data and reports on the efficacy and safety of DTG+3TC in HIV-infected patients in China so far. This project aims to explore the efficacy and safety of the DTG + 3TC regimen for HIV-infected patients in real clinical environment, to guide clinical application, and to provide a theoretical basis for the selection of simplified schemes for the formulation of guidelines.

This study was done to see if the combination of two anti-HIV medicines, dolutegravir (DTG, Tivicay) and lamivudine (3TC, Epivir) taken once a day, provide a safe, effective, and well-tolerated treatment for HIV.

Eligibility

Sex

ALL

Min age

18 Years

Max age

—

Healthy volunteers

Inclusion Criteria: 1. Age (\> 18 years), male and female; 2. HIV-1 infected; 3. Using a standard three-drug-based regimen for at least 24 weeks. Based on clinical decision making\* decide if patients can be treated with the DTG+3TC simplified scheme for a variety of reasons, such as (but not limited to): patients cannot tolerate the conventional three-drug treatment scheme, renal insufficiency, osteoporosis, bone marrow suppression and for other reasons patients cannot use the conventional three-drug treatment scheme; 4. Initial HIV-1 RNA viral load and CD4 cell count were unlimited. 5. CD4 can be monitored at least three times in the first year (including baseline, 24 weeks of treatment and 48 weeks of treatment). After the first year, CD4 can be detected at least once every six months. 6. State Informed Consent for Free Treatment has been signed; 7. Good compliance and signing Informed Consent (\* Reference criteria: Refer to APSIRE study, creatinine clearance rate (\> 50 mL/min), no DTG/3TC allergy history, HBsAg negative, no chronic liver disease, no severe liver damage, no pregnancy during the study) Exclusion Criteria: 1. Has participated in other clinical trials of HIV vaccine or other drug trials in the past three months; 2. Researchers decide if patients could/not complete the scheduled follow-up (factors to consider such as weak, poor compliance, etc.). 3. Has a clear history of DTG or 3TC allergy; 4. HBsAg and/or HBV-DNA positive; 5. Pregnancy during the study period.

Primary outcome measure(s)

Virus suppression rate — 96 weeks
ratio of HIV RNA \< 50 copies/mL at 48 and 96 weeks of treatment
Adverse events — 96 weeks
Rate of adverse events reported during the observational period

Trial sites (1)

Facility	City	Region	Status
Guangzhou 8th People's Hospital	Guangzhou	Guangdong	Recruiting

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT03884673 on ClinicalTrials.gov ↗ ← All trials in China