The overall purpose of this research is to develop and use a blood test to better understand how quickly the viral drug ganciclovir works to clear infection with the CMV virus (Cytomegalovirus) when it occurs. This test will potentially let doctors know early in the course of therapy when a virus is not responding well to the therapy and could therefore be resistant to the drug. The target population of this study will be primarily kidney and lung transplant patients with CMV detected in the blood, although other patients may also be included if they meet criteria. The study will be divided into two phases. Phase I will evaluate a small number of exploratory patients initiating ganciclovir therapy and will require frequent blood sampling to obtain detailed information regarding the kinetic response of the virus to therapy. This information will be analyzed to help guide decisions regarding the number and frequency of blood samples needed in the larger phase II portion of the study. Strains will be characterized using phenotypic and genotypic methods to determine the presence or absence of mutations potentially responsible for the resistance.

Condition	Treatment or Intervention
Cytomegalovirus Infections	Drug: ganciclovir

Ages Eligible for Study:  18 Years and above,  Genders Eligible for Study:  Both

Criteria

Inclusion Criteria:

• Patients affiliated with Barnes-Jewish Hospital with CMV blood infection requiring antiviral therapy
• All patients will have a positive qualitative CMV PCR or viral culture before starting therapy
• Patients will receive treatment with ganciclovir at a dose and duration to be determined by the provider
• It is anticipated that most subjects will be organ transplant recipients but this is not a requirement of the study

Exclusion Criteria:

• Critically ill patients
• Patients with profound leukopenia or abnormal renal function that make a change in the antiviral drug dosage likely during the duration of the study
• Anemia (HGB < 8 g/dl) that would contraindicate the extra blood draws required by this study
• Problems with vascular access that would interfere with obtaining blood samples required by this study
• Residence outside of the St. Louis metropolitan area during the period of ganciclovir therapy
• Patients who are unable to provide informed consent because of diminished capacity related to illness, dementia, or other reasons

Missouri
      Infectious Diseases Division, St. Louis,  Missouri,  63110,  United States

Study ID Numbers:  NCRR-M01RR00036-0728; M01RR00036
Record last reviewed:  November 2001
Last Updated:  October 13, 2004
Record first received:  February 18, 2000
ClinicalTrials.gov Identifier:  NCT00004573
Health Authority: United States: Federal Government
ClinicalTrials.gov processed this record on 2005-04-08