Tubular Function in Asian-American Patients Receiving TDF or ETV for HBV Treatment

• 18-70 year-old Asian-American male or female patients with HBeAg+ or HBeAg-CHB
• On TDF or ETV mono-therapy for 12-24 months, not previously exposed to other oral HBV drugs, nor received any type of interferon treatment in the past 12 months
• Be willing to participate
• Continuation of HBV treatment is medically indicated. That is for HBeAg-positive subjects, HBeAg remain positive or HBeAg becomes negative but still has detectable DNA by the PCR method; and for HBeAg-negative subjects, HBV DNA is either detectable or undetectable by the PCR method
• No clinical or virologic evidence of anti-HBV resistance to TDF treatment at the time of entering tests

• Serum creatinine \< 1.5 mg/L and estimated glomerular filtration rate (creatinine clearance) ≥ 60 mL/min/1.73m2 by the Cockcroft-Gault equation:

  (140-age in years)(body weight [kg] )/((72)(serum creatinine [mg/dl]) ) [Note: multiply estimated rate 0. by 85 for women; use actual body weight]

• Adequate hematologic function (absolute neutrophil count ≥ 1,500/mm3; hemoglobin ≥ 10.0 g/dL)
• To assure all the subjects will be regularly followed per study protocol and minimize the drop off rate, the subjects have to have documented pre-treatment full evaluation and necessary blood tests, medical adherence to HBV treatment, and regular follow-up (i.e., on HBV treatment not missing HBV medication (TDF or ETV) for more than a week, with medical follow-up for HBV treatment at least every 6 month and had all the necessary labs performed.
• In the absence of exclusion criteria.

Exclusion Criteria:

• Ethnicity: Non-Asian CHB patients
• Age: >70 years old
• Body weight and height: BMI ≥ 30
• Concomitant nephrotoxic agents - record all prescription and nonprescription items including herbs and natural remedies, NSAIDs, acyclovir, statins, ACEI or ARBs, Valproate
• Any other antiretroviral meds, antibiotic exposure during study to be noted
• History of HCV, HDV, or HIV co-infection
• Prior history of clinical hepatic decompensation defined as direct (conjugated) bilirubin ≥ 1.2 ULN; PT ≥ 1.2 ULN, platelets ≤ 50,000/mm3, or serum albumin ≤ 3.5 g/dL, ascites, jaundice, encephalopathy, or variceal hemorrhage
• Serum α-fetoprotein ≥ 50 ng/mL
• Evidence of hepatocellular carcinoma (HCC)
• History of solid organ or bone marrow transplantation
• History of malignancies in the past 5 years
• Pregnant women, and women who are breast feeding or who believe they may wish to become pregnant during the course of the study.
• Males and females of reproductive potential who are not willing to use an effective method of contraception during the study. For males, condoms should be used and for females, a barrier contraception method should be used in combination with one other form of contraception.
• History of significant renal disease
• History of significant bone disease
• History of HTN or DM on medical treatment

• Ongoing therapy with any of the following:

  1. Nephrotoxic agents
  2. Parenteral aminoglycoside antibiotics
  3. Cidofovir
  4. Cisplatin
  5. Foscarnet
  6. IV amphotericin B
  7. IV pentamidine
  8. Oral or IV ganciclovir
  9. Cyclosporine
  10. Tacrolimus
  11. IV vancomycin
  12. Chronic daily non-steroidal anti-inflammatory drug therapy
  13. Competitors of renal excretion Systemic chemotherapeutic agents
  14. Systemic corticosteroids
  15. Interleukin-2 (IL-2) and other immunomodulating agents

• Investigational agents (except with the expressed approval of the lead investigators) Administration of any of the above medications must be discontinued at least 30 days prior to the Baseline Visit and for the duration of the study period.

  1. Known hypersensitivity to the study drugs, the metabolites or formulation excipients
  2. Any other condition (including alcohol or substance abuse) or prior therapy that, in the opinion of the Investigators, would make the subject unsuitable for the study or unable to comply with dosing requirements