NCT02327663

Brief Summary

This study evaluates generic emtricitabine(FTC) in Chinese naive chronic hepatitis B patients. Patients were divided into 2 groups: HBeAg positive Chronic hepatitis B(CHB)group and HBeAg negative Chronic hepatitis B(CHB)group.

Trial Health

35
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
2,000

participants targeted

Target at P75+ for phase_4

Timeline
Completed

Started Dec 2014

Typical duration for phase_4

Status
unknown

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

December 1, 2014

Completed
22 days until next milestone

First Submitted

Initial submission to the registry

December 23, 2014

Completed
7 days until next milestone

First Posted

Study publicly available on registry

December 30, 2014

Completed
2.4 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

June 1, 2017

Completed
6 months until next milestone

Study Completion

Last participant's last visit for all outcomes

December 1, 2017

Completed
Last Updated

December 30, 2014

Status Verified

December 1, 2014

Enrollment Period

2.5 years

First QC Date

December 23, 2014

Last Update Submit

December 29, 2014

Conditions

Keywords

Hepatitis B, chronicEmtricitabineAdefovir dipivixilHBeAg

Outcome Measures

Primary Outcomes (1)

  • virological response rate

    HBV DNA \< 500 copies/ml

    week 96

Secondary Outcomes (10)

  • HBV DNA decrease level

    week24, 48, 72 and 96

  • HBV DNA negativity rate

    week 24, 48 and 72

  • biochemical response

    week 24,48,72 and 96

  • HBeAg loss

    week 24,48,72 and 96

  • HBeAg seroconversion

    week 24,48,72 and 96

  • +5 more secondary outcomes

Study Arms (2)

HBeAg positive CHB group

EXPERIMENTAL

1000 patients take generic emtricitabine capsule(200 mg one time per day) for 96 weeks,and for patients who have HBV DNA \> 500 copies/ml, adefovir dipivoxil were combined

Drug: Emtricitabine

HBeAg negativie CHB group

EXPERIMENTAL

1000 patients take generic emtricitabine capsule(200 mg one time per day) for 96 weeks,and for patients who have HBV DNA \> 500 copies/ml, adefovir dipivoxil were combined

Drug: Emtricitabine

Interventions

emtricitabine were given to each patients at baseline and respoonse guided therapy was adopted according HBV DNA level at week 24

Also known as: Brand name:Huierding
HBeAg negativie CHB groupHBeAg positive CHB group

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • HBsAg positive for more than 6 months
  • HBeAg positive patients: HBV DNA ≥ 5log10 copies/ml
  • HBeAg postive patients: ALT≥2×ULN;or liver biopsy G≥2;or liver biopsy S ≥2;or liver biopsy Knodell HAI ≥ 4
  • HBeAg negative patients: HBV DNA ≥ 4log10 copies/ml
  • HBeAg postive patients: ALT≥2×ULN;or liver biopsy G≥2;or liver biopsy S ≥2;or liver biopsy Knodell HAI ≥ 4
  • nucleoside/nucleotide naive paitents

You may not qualify if:

  • Diagnosed HCC with AFP and ultrasound, CT or MRI
  • Creatine \>130μmol/L or Ccr \< 70mL/min
  • Hemoglobin \<100g/L
  • Neutrophils \<1.5E+9/L
  • PLT\<80E+9/L
  • Coinfected with HAV,HEV,HCV,HDV or HIV
  • ANA \> 1:100
  • Uncontrolled cardiovascluar diseases, kidney diseases,lung diseases, neurological diseases, digestive diseases,metabolic disorders, immune-compromised diseases or cancer
  • Drug abuse or alcohal addiction
  • Previous history of taking agents of lamivudine, adefovir, tenofovir entecavir or telbivudine
  • Long-term use of immunosuppressor or immunomodulator 6 months before enrollment to this trial
  • Underwent liver transplantation or liver transplantation in schedule
  • Allergic to nucleoside or nucleotide analogues
  • Preganency or in breastfeeding

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Related Publications (2)

  • Lim SG, Ng TM, Kung N, Krastev Z, Volfova M, Husa P, Lee SS, Chan S, Shiffman ML, Washington MK, Rigney A, Anderson J, Mondou E, Snow A, Sorbel J, Guan R, Rousseau F; Emtricitabine FTCB-301 Study Group. A double-blind placebo-controlled study of emtricitabine in chronic hepatitis B. Arch Intern Med. 2006 Jan 9;166(1):49-56. doi: 10.1001/archinte.166.1.49.

    PMID: 16401810BACKGROUND
  • Gish RG, Leung NW, Wright TL, Trinh H, Lang W, Kessler HA, Fang L, Wang LH, Delehanty J, Rigney A, Mondou E, Snow A, Rousseau F. Dose range study of pharmacokinetics, safety, and preliminary antiviral activity of emtricitabine in adults with hepatitis B virus infection. Antimicrob Agents Chemother. 2002 Jun;46(6):1734-40. doi: 10.1128/AAC.46.6.1734-1740.2002.

MeSH Terms

Conditions

Hepatitis B, Chronic

Interventions

Emtricitabine

Condition Hierarchy (Ancestors)

Hepatitis BBlood-Borne InfectionsCommunicable DiseasesInfectionsHepadnaviridae InfectionsDNA Virus InfectionsVirus DiseasesHepatitis, Viral, HumanHepatitis, ChronicHepatitisLiver DiseasesDigestive System DiseasesChronic DiseaseDisease AttributesPathologic ProcessesPathological Conditions, Signs and Symptoms

Intervention Hierarchy (Ancestors)

DeoxycytidineCytidinePyrimidine NucleosidesPyrimidinesHeterocyclic Compounds, 1-RingHeterocyclic CompoundsDeoxyribonucleosidesNucleosidesNucleic Acids, Nucleotides, and Nucleosides

Study Officials

  • Jun Cheng, M.D.

    Asian Pacific Alliance of Liver Diseases, Beijing

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Study Design

Study Type
interventional
Phase
phase 4
Allocation
NON RANDOMIZED
Masking
NONE
Purpose
TREATMENT
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
chaireman of Asian-Pacific Alliance of Liver Diseas,Beijing

Study Record Dates

First Submitted

December 23, 2014

First Posted

December 30, 2014

Study Start

December 1, 2014

Primary Completion

June 1, 2017

Study Completion

December 1, 2017

Last Updated

December 30, 2014

Record last verified: 2014-12