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An Open Study to Evaluate the Sustained Effect in Patients Showing Virological Responses With Muscle-related Symptom of Chronic Hepatitis B Patients Who Received Clevudine

Bukwang Pharmaceutical logo

Bukwang Pharmaceutical

Status

Completed

Conditions

Chronic Hepatitis B

Study type

Observational

Funder types

Industry

Identifiers

NCT01264107
CLV-409

Details and patient eligibility

About

An Open Study to Evaluate the Sustained Effect in Patients Showing Virological Responses With Muscle-related Symptom of Chronic Hepatitis B Patients Who Received Clevudine.

Enrollment

37 patients

Sex

All

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Patients is currently clevudine treatment.
  2. Patients with HBV DNA < 300 cpoies/mL and ALT normal Showing Muscle-related Symptom Who received Clevudine
  3. Patient who is able to give written informed consent prior to study start and to comply with the study requirements.

Exclusion criteria

  1. Patient is currently receiving antiviral, immunomodulatory, cytotoxic or corticosteroid therapy.
  2. Patient is pregnant or breast-feeding.
  3. Patient has a significant gastrointestinal, renal, decompensated liver, bronchopulmonary, neurological, cardiac, oncologic(except HCC)or allergic disease.
  4. Patient, in the opinion of the investigator, unsuitable for the study.
  5. Showing Muscle-related Symptom who any other evidence.

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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