lamivudine / Generic mfg.  >>  Phase N/A
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6 Trials

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Trial + Data / EventsStatusPhNRegionInterventionsSponsorConditionsPrimary complStudy compl
lamivudine / Generic mfg.
ChiCTR-TRC-09000638: A Study on the viral kinetics of different regimes of Pegylated Interferon and Lamivudine combination therapy in HBeAg Positive Chronic Heptatitis B

Completed
N/A
30
 
PEG-Intron A 100mcq sc once weekly, Lamivudine 100mg QD treatment period 104 weeks (include 32 doses of PEG-Intron A and 96 or 104 weeks Lamivudine) versus one year treatment of Lamivudine 100mg QD
Schering-Plough; None, Hepatitis Research Fund
Viral Diseases
 
 
ChiCTR-TRC-12002962: A clinical study on Diwuyanggan capsule in treating HBeAg-negative chronic hepatitis B

Completed
N/A
144
 
Diwuyanggan capsule orally taken three times daily ;Antiviral treatment group:the nucleoside analogues (Entikawei, Adefovir Dipivoxil Tablets, Lamivudine and so on) ;Diwuyanggan capsule and the nucleoside analogues
Hubei province hospital of Traditional Chinese Medicine; Hubei province hospital of traditional Chinese medical, National Natural Science Foundation of China, State Administration of Traditional Chinese Medicine
Chronic hepatitis B
 
 
ChiCTR-OCH-14004522: Treatment effect and drug-resistant mutations in Chinese AIDS patients switching to second-line antiretroviral therapy

Completed
N/A
195
 
Tenofovir (TDF) + Kaletra (ritonavir and lopinavir mixture) + lamivudine (3TC)combination antiretroviral therapy ;Tenofovir (TDF) + Kaletra (ritonavir and lopinavir mixture) + lamivudine (3TC)combination antiretroviral therapy
Key Laboratory of AIDS Immunology of National Health and Family Planning Commission, Department of Laboratory Medicine, The First Affiliated Hospital, China Medical University; Disease Prevention and Control Center of Henan Province, the Twelfth Five-Year Project on Tackling Key Problems of National Science and Technology (2012ZX10001002-002-013)
AIDS
 
 
ChiCTR1900024611: Dual therapy with lopinavir/ritonavir plus lamivudine could be an effective alternative for antiretroviral-therapy-naive adults with HIV-1 infection in resource-limited settings: planned 144 week, a randomized, open-label and non-inferiority study from China

Recruiting
N/A
200
 
Dual-therapy of lopinavir/ritonavir (LPV/r) plus 3TC (DT group) ;triple-therapy regimen containing tenofovir (TDF), 3TC plus efavirenz (EFV)
Guangzhou Eighth People's Hospital; Level of the institution:, no
AIDS
 
 
ChiCTR1900028166: Bioequivalence Study of Combination-ACC007 Tablets in Human

Completed
N/A
48
 
Tablet; Specification: Each tablet contains 150 mg of ACC007, 300 mg of lamivudine and 300 mg of tenofovir fumarate; it is orally administered on an empty stomach, 1 tablet per cycle, 2 cycles in total. ;Tablet; Specification: ACC007 2 tablets + lamivudine 1 tablet + tenofovir fumarate 1 tablet; oral administration on an empty stomach, 2 tablets per cycle, 2 cycles in total.
Nanjing Drum Tower Hospital, the Affiliated Hospital of Nanjing University Medical School; Jiangsu Aidea Pharmaceutical Co., Ltd., Self-financing
HIV/ADIS
 
 
NCT00476606: A Prospective Cohort of Children With HIV Infection

Active, not recruiting
N/A
500
RoW
Zidovudine, Stavudine, Didanosine, Lamivudine, Nevirapine, Efavirenz, LPV/r, Saquinavir, Indinavir, Ritonavir, Nelfinavir
The HIV Netherlands Australia Thailand Research Collaboration, Khon Kaen University
HIV Infections
06/24
06/24

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