A Single Dose Evaluation of the Effects of Renal Impairment on Deflazacort Pharmacokinetics

This is a non-randomized, open-label, single-dose study to compare the PK of 21 desacetyl-DFZ
and, if data permits, deflazacort in 8 subjects with ESRD to that of 8 healthy matched
control subjects (age, body mass index [BMI], and gender).

All subjects with ESRD will be on hemodialysis (HD). Dosing of deflazacort followed by PK
evaluation of 21 desacetyl DFZ and, if data permits, deflazacort, will only be performed on a
non-HD day.

On Day 1, that will be scheduled on a non-HD day for subjects with ESRD, a single oral dose
of deflazacort will be administered followed by serial blood sampling for 24 hours to assess
the PK of 21 desacetyl-DFZ, and, if data permits, deflazacort.

Safety will be monitored throughout the study by repeated clinical and laboratory
evaluations.

Subjects will return to the Clinical Research Unit (CRU) 3 days (± 1 day) following study
drug administration to determine if any adverse events (AEs) have occurred since the last
study visit. Subjects who terminate the study early will be contacted if the Principal
Investigator (PI) deems necessary.

A total of sixteen (16) adult male and female subjects will be enrolled. Renal Impaired
Cohort: Eight (8) subjects with ESRD on HD. Healthy Match Control Cohort: Eight (8) healthy
subjects with estimated creatinine clearance (CLcr) ≥ 90 mL/min. Subjects will be matched for
age [± 15 years], BMI [± 15 %], and gender [1:1] to the subjects in the ESRD cohort.

Each subject will receive a single oral dose of 18 mg (3 X 6 mg tablets) deflazacort,
following an overnight fast.

Study drug will be administered orally with approximately 240 mL of water.

Inclusion Criteria:

- Continuous non-smokers or moderate smokers

- For a female of non-childbearing potential: must have undergone a sterilization
procedures or be postmenopausal with amenorrhea for at least 1 year prior to the first
dose and FSH serum levels consistent with postmenopausal status

- A non vasectomized, male subject must agree to use a condom with spermicide or abstain
from sexual intercourse during the study until 90 days

- If male, must agree not to donate sperm from dosing until 90 days Subject with ESRD on
Hemodialysis

- Adult male or female, 18 80 years of age

- BMI ≥ 18.5 and ≤ 40.0 kg/m2 - Subject is maintained on a stable regimen of HD at least
3 months Healthy Subject

- Healthy adult male and female subjects will be matched 1:1 to a specific subject in
the ESRD cohort based upon age, BMI, and gender [1:1]. The following criteria should
be fulfilled:

- 18 to 80 years of age. Age must be within ± 15 years of the matched subject's age
in the ESRD cohort

- BMI ≥ 18.5 and ≤ 40.0 kg/m2. BMI must be within ± 15% of the matched subject's
BMI in the ESRD cohort

- Has a CLcr ≥ 90 mL/min

Exclusion Criteria:

- Subject is mentally or legally incapacitated or has significant emotional problems at
the time of the screening visit or expected during the conduct of the study

- History or presence of hypersensitivity or idiosyncratic reaction to the study drugs
or related compounds (e.g., steroids or their formulations including lactose and corn
starh)

- History (within the last year prior to dosing) or presence of peptic ulcers

- History or presence of:

- Gastritis or esophagitis, diverticulitis, ulcerative colitis (if there is
probability of impending perforation), abscess or pyogenic infections, or fresh
intestinal anastomosis

- Previous corticoids-induced myopathy

- Ocular herpes simplex

- Symptomatic cardiomyopathy at screening

- Immunosuppression or other contraindications for corticosteroid treatment

- History of chronic systemic fungal or viral infections

- Galactose intolerance, Lapp lactose deficiency, or glucose-galactose
malabsorption

- Osteoporosis

- Myasthenia gravis

- Epilepsy

- Idiopathic hypocalcuria

- Seated blood pressure is less than 90/40 mmHg or greater than 170/100 mmHg

- Seated heart rate is lower than 40 bpm or higher than 99 bpm

- QTcF interval is > 500 msec

- Has received any live or live-attenuated vaccine within 30 days

- Has received any immunosuppressive agents, coal tar, and/or radiation therapies within
30 days

- Has received injectable corticoids in the 12 weeks prior to dosing or any oral form of
corticoids in 30 days

- Unable to refrain from or anticipates the use of:

- Any drug known to be moderate or strong inhibitors or inducers of cytochrome P450
(CYP) 3A or P-glycoprotein (P-gp) for 14 days or 28 days, respectively

- Any medication or substance which cannot be discontinued at least 14 days

- Female subjects of childbearing potential

- Female subjects who are pregnant or lactating

- Positive results at screening for HIV, HBsAg or HCV

- Has been on a diet incompatible with the on study diet within 28 days

- Donation of blood or significant blood loss within 56 days

- Plasma donation within 7 days

- Participation in another clinical trial within 28 days Subject with ESRD

- Is a regular user of any medication that would significantly alter glomerular
filtration rate, e.g., cimetidine

- Has presence of a renal carcinoma or acute renal disease caused by infection or drug
toxicity

- History of drug abuse within the past 2 years

- Has a positive urine/breath alcohol or urine/serum/saliva drug testing Normal Renal
Function

- History or presence of alcoholism or drug abuse within the past 2 years

- Positive urine drug or urine/breath alcohol results