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Generated: September 17, 2019

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CLINICAL TRIALS PROFILE FOR TELBIVUDINE

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Clinical Trials for Telbivudine

Trial ID Title Status Sponsor Phase Summary
NCT00051090 Treatment of Hepatitis B Virus (HBV) Before Beginning Anti-HIV Drugs in Patients With Both HBV and HIV Withdrawn National Institute of Allergy and Infectious Diseases (NIAID) N/A This study will evaluate the drug telbivudine (LdT) for treatment of hepatitis B virus (HBV) in HIV infected patients. Patients will take telbivudine alone for 24 weeks, add anti-HIV drugs for 24 weeks, then stop taking telbivudine while continuing their anti-HIV drug regimen. To enroll in this study, patients must not be taking any anti-HIV drugs and cannot have taken more than 31 days of treatment with lamivudine (3TC), protease inhibitors (PIs), or nonnucleoside reverse transcriptase inhibitors (NNRTIs).
NCT00057265 A Randomized, Double Blind Trial of LdT (Telbivudine) Versus Lamivudine in Adults With Compensated Chronic Hepatitis B Completed Novartis Pharmaceuticals Phase 3 This study is being conducted to compare the safety and effectiveness of the investigational medication, LdT (Telbivudine) with Lamivudine, a drug currently approved by the US, European and Asian Health Authorities for the treatment of hepatitis B infection. The results for patients taking LdT will be compared to results for patients taking Lamivudine.
NCT00057265 A Randomized, Double Blind Trial of LdT (Telbivudine) Versus Lamivudine in Adults With Compensated Chronic Hepatitis B Completed Novartis Phase 3 This study is being conducted to compare the safety and effectiveness of the investigational medication, LdT (Telbivudine) with Lamivudine, a drug currently approved by the US, European and Asian Health Authorities for the treatment of hepatitis B infection. The results for patients taking LdT will be compared to results for patients taking Lamivudine.
NCT00076336 Telbivudine Versus Lamivudine in Adults With Decompensated Chronic Hepatitis B and Evidence of Cirrhosis Completed Novartis Pharmaceuticals Phase 3 This research study was conducted to compare the safety and effectiveness of the investigational medication, LdT (Telbivudine) versus Lamivudine, a drug currently approved by the US, European and Asian Health Authorities for the treatment of Hepatitis B infection. The results for patients taking LdT will be compared to results for patients taking lamivudine.
NCT00115245 Telbivudine Versus Adefovir Dipivoxil in Adults With HBegAg-Positive, Compensated Chronic Hepatitis B Completed Novartis Pharmaceuticals Phase 3 This research study is being conducted to compare the safety and effectiveness of the investigational medication, LdT (telbivudine) versus adefovir dipivoxil, a drug approved by the Food and Drug Administration (FDA) for the treatment of hepatitis B infection. The results for patients taking LdT will be compared to results for patients taking adefovir dipivoxil.
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Clinical Trial Conditions for Telbivudine

Condition Name

Condition Name for Telbivudine
Intervention Trials
Chronic Hepatitis B 32
Hepatitis B, Chronic 14
Hepatitis B 9
HBV-related Liver Cirrhosis 2
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Condition MeSH

Condition MeSH for Telbivudine
Intervention Trials
Hepatitis B 69
Hepatitis 69
Hepatitis B, Chronic 59
Hepatitis A 59
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Clinical Trial Locations for Telbivudine

Trials by Country

Trials by Country for Telbivudine
Location Trials
China 65
United States 45
Korea, Republic of 14
Taiwan 10
Spain 8
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Trials by US State

Trials by US State for Telbivudine
Location Trials
California 9
New York 5
Texas 4
Florida 2
Arizona 2
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Clinical Trial Progress for Telbivudine

Clinical Trial Phase

Clinical Trial Phase for Telbivudine
Clinical Trial Phase Trials
Phase 4 41
Phase 3 16
Phase 2/Phase 3 1
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Clinical Trial Status

Clinical Trial Status for Telbivudine
Clinical Trial Phase Trials
Completed 36
Unknown status 15
Withdrawn 7
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Clinical Trial Sponsors for Telbivudine

Sponsor Name

Sponsor Name for Telbivudine
Sponsor Trials
Novartis Pharmaceuticals 22
Novartis 15
Yonsei University 4
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Sponsor Type

Sponsor Type for Telbivudine
Sponsor Trials
Other 76
Industry 48
NIH 2
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