A Real-world Study of Lamivudine and Dotiravir Sodium Tablets in the Treatment-naïve HIV-1 Infected Patients
NCT05332470 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 200
Last updated 2022-04-18
Summary
Actual update to the US Department of Health and Human Services treatment guidelines for HIV-1 infection and European AIDS Clinical Society guidelines indicate Dovato(Dolutegravir/lamivudine) as an initial treatment in HIV-naÏve patients. However there is no real- life data. The investigators' results in real life have encouraged us to conduct a multicenter cohort study in patients who have already started their first antiretroviral therapy with DTG (dolutegravir) + 3TC(lamivudine ), to verify efficacy and tolerance in real life. The investigators' hypothesis is that the data will be similar to those reported in clinical trials.
Conditions
Interventions
- DRUG
-
Lamivudine and Dotiravir Sodium Tablets
3TC (300 mg p.o. q 24 h) plus DTG (50 mg p.o. q 24 h)
Sponsors & Collaborators
-
Peking Union Medical College Hospital
lead OTHER
Principal Investigators
-
WEI Lyu · Department of Infectious Diseases, PekingUMCH
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2022-05-01
- Primary Completion
- 2022-06-01
- Completion
- 2025-05-31
- FDA Drug
- Yes
More Related Trials
-
Rapid Test and Treat Dolutegravir Plus Lamivudine Study in Newly Diagnosed Human Immunodeficiency Virus (HIV)-1 Infected Adults
NCT03945981 ·Status: COMPLETED ·Phase: PHASE3
-
Efficacy and Tolerability of DTG Plus 3TC in HIV Infected Adults With Virologically Suppression and TDF Toxicity
NCT05493969 ·Status: NOT_YET_RECRUITING ·Phase: PHASE4
-
A Study to Evaluate the Efficacy, Safety, and Tolerability of Using an Oral Once-daily 2 Drug Regimen Compared to an Oral Once-daily 3 Drug Regimen for the Treatment of Human Immunodeficiency Virus (HIV)-1 in Adults Who Have Not Previously Taken Antiretroviral Therapy
NCT05979311 ·Status: ACTIVE_NOT_RECRUITING ·Phase: PHASE3
-
Safety and Effectiveness of Lamivudine When Given Once a Day Versus Twice a Day in Combination With Other Anti-HIV Drugs in HIV-Infected Adults Who Have Never Received Anti-HIV Drugs
NCT00004852 ·Status: COMPLETED ·Phase: PHASE2
-
Efficacy of Efavirenz 400mg vs. 600mg Combined With Lamivudine and Tenofovir in Treatment Naive HIV Infection
NCT04463784 ·Status: UNKNOWN ·Phase: NA
-
A Study of Efavirenz in HIV-Infected Patients Who Have Never Taken Anti-HIV Drugs
NCT00002227 ·Status: COMPLETED ·Phase: PHASE2
-
The Safety and Effectiveness of Zidovudine Plus Lamivudine, Used With and Without 1592U89, in HIV-1 Infected Children Who Have Taken Anti-HIV-1 Drugs
NCT00002391 ·Status: COMPLETED ·Phase: PHASE3
-
Three Generic Nevirapine-Based Antiretroviral Treatments in Chinese Patients:Multicentric Observation Cohort
NCT00618176 ·Status: COMPLETED ·Phase: PHASE4
-
The Effectiveness of Indinavir Plus Zidovudine Plus Lamivudine in HIV-Infected Patients With No Symptoms of Infection
NCT00002179 ·Status: COMPLETED ·Phase: PHASE4
-
Optimization of Antiretroviral Therapy
NCT02935075 ·Status: COMPLETED ·Phase: PHASE4
-
A New Tablet Containing Two FDA-Approved Drugs In HIV-Infected Patients Who Have Not Received Prior Therapy
NCT00053638 ·Status: COMPLETED ·Phase: PHASE3
-
Elvucitabine/Efavirenz/Tenofovir Versus Lamivudine/Efavirenz/Tenofovir in Human Immunodeficiency Virus (HIV)-1 Infected, Treatment-naive Participants
NCT00350272 ·Status: COMPLETED ·Phase: PHASE2
-
Effectiveness and Safety of Two Forms of Stavudine in HIV-Infected Patients
NCT00005918 ·Status: COMPLETED ·Phase: PHASE3
-
Lamivudine/Dolutegravir in Virologically Suppressed Subjects With Expected or Confirmed Resistance to Lamivudine
NCT04880785 ·Status: COMPLETED ·Phase: PHASE2
-
A Study of Retrovir and Epivir Alone or in Combination With 141W94 in HIV-Infected Patients
NCT00002195 ·Status: COMPLETED ·Phase: PHASE3
-
Safety and Efficacy of a Switch to Doravirine, Tenofovir, Lamivudine (MK-1439A) in Human Immunodeficiency Virus (HIV-1)-Infected Participants Virologically Suppressed on an Anti-retroviral Regimen in Combination With Two Nucleoside Reverse Transcriptase Inhibitors (MK-1439A-024)
NCT02397096 ·Status: COMPLETED ·Phase: PHASE3
-
Safety and Effectiveness of Short-Term Anti-HIV Drug Therapy for Recent HIV-1 Infection
NCT00414518 ·Status: COMPLETED ·Phase: NA
-
Tenofovir Disoproxil Fumarate/Emtricitabine/Efavirenz Versus Combivir/Efavirenz in Antiretroviral-Naive HIV-1 Infected Subjects
NCT00112047 ·Status: COMPLETED ·Phase: PHASE3
-
A Study of Three Different Anti-HIV Drug Combinations in HIV-Infected Patients
NCT00002410 ·Status: COMPLETED ·Phase: PHASE3
-
Description of Real World Antiviral Effectiveness and Sustainability of the 2-Drug Regimen Dolutegravir + Lamivudine in Untreated and Pre-treated Patients in Routine Clinical Care in Germany
NCT03754803 ·Status: COMPLETED
-
Evaluation of Safety, Tolerability, Pharmacokinetics, and Antiretroviral Activity of Ulonivirine (MK-8507) in Human Immunodeficiency Virus (HIV-1)-Infected Participants (MK-8507-003)
NCT02174159 ·Status: COMPLETED ·Phase: PHASE1
-
A Clinical Trial to Evaluate the Safety, Tolerability, and Pharmacokinetics of PGDM1400LS Alone and in Combination With VRC07-523LS and PGT121.414.LS in Healthy, HIV-uninfected Adult Participants
NCT05184452 ·Status: COMPLETED ·Phase: PHASE1
-
The Safety and Effectiveness of Lamivudine Plus Zidovudine, Used With and Without 1592U89, in HIV-1 Infected Patients Who Have Never Taken Anti-HIV Drugs
NCT00002389 ·Status: COMPLETED ·Phase: PHASE3
-
Backup With Combivir or Single Dose (SD) Truvada in Order to Avoid Non-nucleoside Reverse Transcriptase Inhibitor (NNRTI) Resistance After SD Nevirapine for the Prevention of Mother-to-child Transmission (PMTCT)
NCT00346567 ·Status: COMPLETED ·Phase: NA
-
Efficacy and Safety of TDF+3TC+EFV in Adults With HIV/HBV Coinfection
NCT01751555 ·Status: COMPLETED ·Phase: PHASE4