Ambrisentan in Single Ventricle

A. Purpose of the Study The purpose of the study is to evaluate the safety, pharmacokinetics
(PK) and pharmacodynamics (PD) of ambrisentan in children with single ventricle heart defects
that are undergoing Fontan (stage III) surgical palliation. This is a double blind, placebo
controlled study. The primary objective of this Phase I/II study is to assess the plasma PK,
safety and PD of oral ambrisentan in children with surgically palliated single ventricle
heart defects. A secondary objective will be to assess whether ambrisentan improves
post-operative outcomes including amount and duration of chest tube drainage and hospital
length of stay.

B. Background and Significance Complex congenital heart defects associated with
underdevelopment of a ventricle account for ~8% of congenital heart disease with a birth
incidence of 4-8/10000 live births. These single ventricle lesions are associated with high
morbidity and 5 year mortality rates that approach 50%. Staged surgical palliation directs
returning venous blood flow directly into the lungs so that pulmonary blood flow occurs
without the aid of a pumping chamber. The final stage of surgery (stage III - the Fontan
procedure) incorporates inferior caval blood flow directly into the pulmonary arteries.
Consequently pulmonary blood flow and cardiac output are directly related to pulmonary
vascular resistance and ventricular function. The limitations of single ventricle surgical
palliation often result in a prolonged post-operative course with pleural effusions a
particular concern. There is also continued long term attrition. Elevated pulmonary vascular
resistance and impaired systemic ventricular function are important risk factors for early
and late failure of single ventricle palliation.

Ambrisentan is an endothelin receptor antagonist that improves pulmonary and possibly
systemic endothelial function. Ambrisentan is approved for treatment of pulmonary arterial
hypertension in adults and is used off-label for treatment of pulmonary hypertension in
childen. Children with single ventricle heart defects demonstrate both pulmonary and systemic
endothelial dysfunction and may benefit from treatment with this drug. However
pharmacokinetics and hemodynamic efficacy of ambrisentan have not been studied in single
ventricle patients. The most widely used alternative agent, sildenafil, was recently
associated with increased mortality in children. There is now a Food and Drug Administration
(FDA) safety warning against use of sildenafil in children. The investigators have previously
demonstrated hemodynamic benefits with use of sildenafil in these patients but ambrisentan is
a potentially safer agent. Therefore this study would fill an unmet need to guide dosing and
evaluate efficacy of ambrisentan in this vulnerable population.

C. Design and Procedures

This is a single-center, randomized, blinded PK study of ambrisentan in children ages ≥ 24
months and ≤120 months with single ventricle anatomy. There will be up to 20 subjects
enrolled; 16 will receive ambrisentan and 4 will receive placebo. A small placebo control
group is warranted to ensure that any treatment effect is not a result of post-operative
improvement. Patients will be enrolled at the time of their routinely scheduled Fontan
surgery.

Initial Dose: Oral ambrisentan 2.5 - 5 mg, single dose, once daily (nasogastric and
gastrostomy tube administration will be considered only when a nasogastric or gastrostomy
tube is already in place as part of routine post-operative care).Subjects will be randomized
by Investigational Drug Services (IDS) to placebo (n=4) or oral ambrisentan (n=16) using
permuted blocks. Subjects will receive either an oral suspension (2.5 or 5mg) or a 5mg tablet
depending on their ability to swallow a tablet. To begin to ensure safety, the initial 5
subjects enrolled in the study (at least 4 active drug) will receive a dose of 2.5mg in a
liquid suspension prepared by IDS. After enrollment of these subjects the investigators will
perform a preliminary PK/safety analysis and evaluate ambrisentan exposure. If the drug is
well tolerated (no grade III or greater adverse events) and exposure is less than the target
exposure of 500-800ng/mL, then the investigators may increase the dose to 5mg/dL provided via
tablet in those able to take a tablet or suspension for all others. If drug exposure is less
than 100ng/mL then the investigators will enroll additional study subjects to ensure that at
least 16 study subjects achieve adequate drug exposure. If drug exposure is in the target
range then the investigators will continue to enroll study subjects to receive the 2.5mg
suspension.

The total study duration is expected to be approximately 24 months for enrollment of up to 20
subjects. Study participants will remain in the study until 1 month after discharge following
stage III surgery intervention or for 6 months - whichever is shorter. The subjects will
receive routine care before, during and immediately after surgery and after hospital
discharge. The investigators will record all in-hospital adverse events and tabulate by organ
system. One month after the last study drug administration (dose #3), the investigators will
contact patients by phone or evaluate in person if they remain hospitalized.

Plasma PK will be evaluated using a limited sampling scheme. A preliminary safety and PK
analysis will be performed after 5 subjects are enrolled. Ambrisentan PK will be evaluated
and dosing may be adjusted to achieve levels consistent with those reported in the adult and
pediatric literature.

D. Study Interventions:

Baseline/Pre-Dose Assessment

After the parent or legally authorized representative has signed the Internal Review Board
(IRB) - approved informed consent form, and after it has been determined that the patient
satisfies all inclusion and exclusion criteria, the following evaluations will be performed
and recorded in the case report form (CRF):

1. Baseline demographics, medical history and medical baseline conditions.

2. Physical examination.

3. Preoperative laboratory assessment (obtained as part of usual clinical care for
pre-operative assessment:

1. Hematology: hematocrit, hemoglobin, white blood cell count with differential,
platelet count.

2. Serum chemistry: creatinine, blood urea nitrogen, sodium, potassium, calcium.

3. Liver function tests: aspartate transaminase (AST), alanine transaminase (ALT),
alkaline phosphatase, total bilirubin, conjugated bilirubin, serum albumin.

Study Procedures

1. Record the start and stop time of ambrisentan administration and all concomitant drugs.

2. Hemodynamic evaluation performed prior to initiation of study drug and at 0-1,1-6,18-30
and 40-60hrs after administration of the first ambrisentan dose (blood samples will be
collected only if central monitoring lines remain or if they can be timed with a routine
lab collection)

1. Record Fontan, common atrial, and systemic arterial pressures from existing central
lines that are placed as part of routine post-operative care.

2. Collect study labs (coincident with scheduled PK levels - see below):

i. plasma samples for biomarkers (endothelin 1 [ET1], brain natriuretic peptide [BNP]).

c. Record oxygen saturation from routinely collected arterial and venous blood gases.

d. Perform study echocardiogram at baseline and at one time point in the following
72hours at least 2 hours after ambrisentan administration.

3. PK blood samples (500 µL, up to 7 per patient) and pressure measurements will be
obtained at baseline and at 1-2, 3-4, 5-6, 8-12, 12-16, 24, and 48-84 hours post-initial
drug administration.

4. Adverse events will be collected during and for 1 month after the last study drug
administration. Results will be tabulated by organ system.

5. Physical examination will be performed within 24 hours after administration of study
drug and once daily during study enrollment.

6. Record all AEs and SAEs.

7. Record all concomitant medication administered 24 hours after administration of study
drug.

8. Up to 4 scavenge samples will be obtained from the clinical laboratory from samples
collected in the 24 hours following ambrisentan administration. Scavenged samples are
left over heparinized plasma samples from these children that are collected from the
clinical laboratory prior to discarding.

PK Sampling A limited PK sampling scheme will be employed such that no more than 3500 μl (7
samples, 500 μl per sample) of blood is obtained.

Hospitalization Procedures

1. Any of the following clinical laboratories performed as standard of care during the
study will be recorded. The investigators will use the laboratory values closest to
study dose if there have been multiple tests.

1. Hematology: hematocrit, hemoglobin, white blood cell count with differential,
platelet count

2. Serum chemistry: creatinine, blood urea nitrogen, sodium, potassium, calcium

3. Liver function tests: aspartate transaminase (AST), alanine transaminase (ALT),
alkaline phosphatase, total bilirubin, conjugated bilirubin

2. Physical examination will be performed daily during the post-operative hospitalization.

3. Record all Adverse Events (AEs) for 24 hours after the last dose of study drug

4. Record all Serious Adverse Events (SAEs) for 1 month after the last dose of study drug

5. Record duration of mechanical ventilation

6. Record hospital length of stay

7. Record intensive care unit length of stay

8. Record duration and volume of chest tube drainage

Inclusion Criteria:

1. Age ≥ 24 months; ≤120 months.

2. History of congenital heart disease with severe hypoplasia of a right or left
ventricle.

3. Undergoing Fontan surgery as part of standard clinical care.

4. Availability and willingness of the parent/legally authorized representative to
provide written informed consent and, as appropriate, assent from the child.

Exclusion Criteria:

1. History of serious adverse event related to ambrisentan administration.

2. History of ambrisentan exposure within 48 hours of the study.

3. Presence of pulmonary venous obstruction.

4. Treatment with cyclosporin.

5. Any of the following - as determined by the attending physician

- Significant hemodynamic instability

- Sepsis.

- Need for ECMO support.

6. Renal failure defined as serum creatinine > 2 times higher than the upper limit of
normal.

7. Liver dysfunction defined as alanine aminotransferase or aspartate aminotransferase >
3 times higher than the upper limit of normal.

8. Thrombocytopenia defined as a platelet count < 50 000 cells/µL.

9. Leukopenia defined as white blood cells < 2500 cells/µL.

10. Anemia defined as hemoglobin < 8mg/dL.

11. Atrial hypertension (mean LA pressure > 12mm Hg).