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National Health Research Institutes, Taiwan
Traitements, essais et publications liés.
Traitements2programmes
Essais1liés
Publications3liées
SourceDBlocale
Traitements
2| Molécule | Indication / population | Phase | Objectif | Pays | Résultat |
|---|---|---|---|---|---|
| Adefovir Dipivoxil and LamivudineResearch Objective and Study End Points To evaluate the anti-HBV as well as HCC recurrence reducing effects of standard (18 months) lamivudine treatment at time of HBV reactivation with hepatitis flare up (HBV DNA \> 105 copies/mL and ALT level \> 2.0 x UNL) or prophylactic, prolong (36 months) adefovir dipivoxil therapy in post-operative HBsAg(+),\< 5 cm HCC patients, and to compare the results of who group with historical controls (T1297, HBsAg+,\< 5 cm HCC cohort),in terms of the following endpoints. 1. Primary endpoint: the 3-years recurrence rate (excluding those recur within first year). 2. Secondary endpoints: the first 2 year tumor recurrence rates the recurrence-free survival the overall survival. anti-viral efficacy, i.e. biochemical response and viral response rate. to correlate the changes of viral titer with the clinical outcome in post- operative HCC patients with adjuvant lamivudine or adefovir therapy. | Cancer | À vérifier | À vérifier | Taiwan | À vérifier |
| Adefovir Dipivoxil and LamivudineResearch Objective and Study End Points To evaluate the anti-HBV as well as HCC recurrence reducing effects of standard (18 months) lamivudine treatment at time of HBV reactivation with hepatitis flare up (HBV DNA \> 105 copies/mL and ALT level \> 2.0 x UNL) or prophylactic, prolong (36 months) adefovir dipivoxil therapy in post-operative HBsAg(+),\< 5 cm HCC patients, and to compare the results of who group with historical controls (T1297, HBsAg+,\< 5 cm HCC cohort),in terms of the following endpoints. 1. Primary endpoint: the 3-years recurrence rate (excluding those recur within first year). 2. Secondary endpoints: the first 2 year tumor recurrence rates the recurrence-free survival the overall survival. anti-viral efficacy, i.e. biochemical response and viral response rate. to correlate the changes of viral titer with the clinical outcome in post- operative HCC patients with adjuvant lamivudine or adefovir therapy. | Cancer | À vérifier | À vérifier | Taiwan | À vérifier |
Essais cliniques
1| Molécule | Indication / population | Phase | NCT | Titre | Statut |
|---|---|---|---|---|---|
| Adefovir Dipivoxil and Lamivudine | Cancer | À vérifier | NCT00455091 | A Phase III Study in Post-operative HBV-related Hepatocellular Carcinoma | TERMINATED |
Publications
3| Molécule | Indication / population | Titre | Journal | Date |
|---|---|---|---|---|
| Adefovir Dipivoxil and Lamivudine | [Compare the effect of combined therapy between telbivudine plus adefovir dipivoxil and lamivudine plus adefovir dipivoxil corresponding to renal function in patients with hepatitis B virus infection]. | Zhonghua gan zang bing za zhi = Zhonghua ganzangbing zazhi = Chinese journal of hepatology | ||
| Adefovir Dipivoxil and Lamivudine | [Low-levels of HBsAg quantification at 48-week in HBeAg-negative chronic hepatitis B patients are the advantageous population for HBsAg clearance]. | Zhonghua gan zang bing za zhi = Zhonghua ganzangbing zazhi = Chinese journal of hepatology | ||
| Adefovir Dipivoxil and Lamivudine | Human Embryoid Body-Based Assays for Preclinical Screening of Potential Teratogenic Drugs: Antiviral Drugs for Hepatitis B Virus as Examples. | Stem cells and development |