Intravesical Cidofovir for Hemorrhagic Cystitis

Study Drug Administration:

If you are found to be eligible to take part in this study, on Day 1, you may receive some
fluid for hydration by vein and then cidofovir will be put into your bladder through your
foley catheter. The catheter will be clamped shut for 2 hours to keep the drug inside your
bladder. After 2 hours, the catheter will be unclamped so that the drug may drain out. If
you were receiving bladder irrigation (where the bladder is flushed with water) as therapy
for hemorrhagic cystitis, this therapy will be restarted after your dose of cidofovir.

Pharmacokinetic (PK) Testing:

On Day 1, blood (about 2 teaspoons each time) will be drawn for PK testing approximately 1
hour (+/- 15 minutes) before the dose, and then again at 1 hour (+/- 15 minutes), 2 hours
(+/- 15 minutes), 4 hours (+/- 1 hour), 14 hours (+/- 1 hour) and 24 hours (+/- 1 hour)
after the dose. A PK sample will also be drawn on Day 14 (+- 2 days) after the dose. PK
testing measures the amount of study drug in the body at different time points.

Virus Testing:

During this study, urine and blood will be collected and used for research to test for
certain viruses, including the type of infection you had when you joined this study.

Before and after the cidofovir dose on Day 1, Day 3 (+/- 1 day), Day 7 (+/- 2 days) and
again on Day 14 (+/- 2 days) urine and blood (about 1 teaspoon) will be collected for virus
testing.

Length of Study Participation:

Your active study participation will be over after the Day 30 follow-up phone call (below).
If you experienced a side effect, the study staff will continue checking your medical
records until the side effect becomes stable or gets better.

Follow-Up:

On Day 3 (+/- 1 day):

- You will have a physical exam.

- Your vital signs will be measured, and you will be asked about any symptoms you may be
having.

- Urine will be collected for routine tests

- Blood (about 1 teaspoon) will be drawn for routine tests.

On Day 7 (+/- 2 days):

- You will have a physical exam.

- Your vital signs will be measured, and you will be asked about any symptoms you may be
having.

- Blood (about 1 teaspoon) will be drawn for routine tests.

- Urine will be collected for routine tests.

On Day 14 (+/- 2 days):

- You will be asked about any symptoms you may be having.

- Blood (about 1 teaspoon) will be drawn for routine tests.

- Urine will be collected for routine tests.

On Day 30 (+/- 2 days), you will be contacted by phone and asked about any side effects you
may be having. This call will take about 10 minutes.

This is an investigational study. Cidofovir given by injection is commercially available and
FDA approved to treat CMV in patients with HIV. Its use in this study is investigational.

Up to 6 patients will take part in this study. All will be enrolled at MD Anderson.

Inclusion Criteria:

1. Polyoma BK or adenovirus viruria has been established either by positive urine
cytology or by PCR for BK virus or by positive urine culture for adenovirus.

2. The patient has either gross hematuria and/or passes blood clots.

3. Signed informed consent form containing all potential serious adverse events related
to cidofovir use as given on the package insert.

4. Hospitalized patients with a Foley catheter.

5. Women of childbearing potential (Women who are postmenopausal greater than 1 year or
who have had a bilateral tubal ligation or hysterectomy) must agree to use 2
acceptable methods of birth control (e. g., barrier method (such and condom or
diaphragm) and another form, such as an IUD or hormonal birth control, during the
study period and for a period of 2 months afterward. Males must also agree to use an
acceptable method of birth control (barrier method) during the study period and for 2
months afterward.

Exclusion Criteria:

1. Serum creatinine >2 mg/dl and/or calculated creatinine clearance < 50 ml/min using
the Cockcroft-Gault Creatinine Clearance formula (CrCl). CrCl = {(140-Age) x Weight
(kgs) x 0.85 (if female)}/ {72x Serum Creatinine (mg/dl)}

2. Urine protein > 100 mg/dl (equivalent to > 2+ proteinuria)

3. Age less than 18 years.

4. Prior therapy with formalin or carboprost 1 mg/dL administered intravesically.

5. Hypersensitivity to cidofovir, probenecid or sulfa-containing medications

6. Patients who have received prior cidofovir therapy within 2 weeks

7. Prior enrollment in the study

8. Women who are pregnant or breast-feeding

9. Evidence of end-organ adenoviral infection