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NCT00354653

A Trial To Study The Effect Of Lamivudine In Adult Patients Who Suffer From Chronic Hepatitis B Alone

Completed Phase 4 Last updated 3 March 2020
What this trial tests

Phase 4 trial testing LAMIVUDINE in CHRONIC HEPATITIS B in 100 participants. Completed in 23 January 2007.

Timeline
9 February 2002
Primary endpoint
23 January 2007
23 January 2007

Quick facts

Lead sponsorViiV Healthcare
PhasePhase 4
StatusCompleted
Study typeINTERVENTIONAL
Allocationnon randomized
Designsingle group
Maskingnone
Primary purposetreatment
Enrollment100
Start date9 February 2002
Primary completion23 January 2007
Estimated completion23 January 2007
Sites1 location across Iran

Drugs / interventions tested

Conditions studied

Sponsor

ViiV Healthcare — full company profile →

Who can join

15 and older, any sex, with CHRONIC HEPATITIS B. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The efficacy of lamivudine in Hepatitis Be Antigen (HBeAg) positive Asian patients of chronic hepatitis has been well established.The evidence in HBeAg negative patients is limited. Limited sustained response was observed post-treatment following a one year treatment period. Whether these results can be applied to patients in Iran is uncertain. This study is therefore intended to further assess the efficacy profile after two years of open treatment in the adult Iranian population.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

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Other ViiV Healthcare trials

Trials by the same sponsor.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT00354653.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing