A Multi-Center, Open-Label Study

Withdrawn before enrolling · Phase 1

Conditions studied: Renal Disease, End Stage Renal Disease

In brief

This study will be an open-label, single-treatment, single-dose, parallel group study to evaluate the pharmacokinetics (PK) of droxidopa in subjects with mild, moderate, and severe renal dysfunction and End Stage Renal Disease (ESRD) after a single dose compared to matched healthy subjects with normal renal function. A total of 48 male or female subjects, 16 subjects with normal renal function (eGFR greater than 90 mL/min/1.73m²) and eight each (8) with mild (60 less than eGFR less than 89 mL/min/1.73m²), moderate (30 less than eGFR less than 59 mL/min/1.73m²), or severe (15 less than eGFR less than 29 mL/min/1.73m²) renal impairment or ESRD (eGFR \< 15 mL/min/1.73m² and requiring hemodialysis) will be selected according to the inclusion and exclusion criteria. The medical and laboratory examinations will take place within 28 days before dosing. A single dose of 600 mg of droxidopa as an investigational drug will be administered with 240 mL of water after an overnight fast (minimum 10 hours). Blood samples for the measurement of plasma concentrations of droxidopa and metabolites including but not limited to 3-OM-DOPS, NE, vanillic acid, and protocatechuic acid will be collected before and 0, .5, 1, 1.5, 2, 3, 4, 5, 6, 8, 10, 12, 24, 30, 36 hours after dosing for healthy volunteers and subjects with mild, moderate, and severe renal impairment and those with ESRD. For the latter, samples will be collected on both a non-hemodialysis and a hemodialysis visit. During dialysis, samples of dialysate, from the arterial and venous sides of the dialyzer will be collected at 30-minute intervals during the dialysis period. In addition, the entire dialysate will be collected, its volume recorded, and a sample retained for the measurement of droxidopa and metabolites including but not limited to 3-OM-DOPS, NE, vanillic acid, and protocatechuic acid concentrations. Urine samples for the measurement of urinary excretion of droxidopa and metabolites including but not limited to 3-OM-DOPS, NE, vanillic acid, and protocatechuic acid will be collected before and over the following intervals after dosing: 0 2, 2-4, 4-6, 6-8, 8-12, 12-24, and 24-36 hours for healthy volunteers and subjects with mild, moderate, and severe renal impairment. A post-study visit with physical examination and laboratory tests will take place within seven (7) days after the last PK blood sampling.

Key facts

Study ID

NCT01468259

Run by

Chelsea Therapeutics

People needed

0

Starts

2012-10-01

Expected to finish

2012-12-01

Last updated by the study team

2013-03-29

Who can join

Age: 18 and older, up to 79. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• Informed Consent
• Male or Female between 18 and 79 years
• Female subject of childbearing potential not surgically sterile or min 2 years postmenopausal must use approved contraceptives
• BMI 20 to 40 kg per m2
• Refrain from exercise
• eGFR per protocol for condition
• Sufficient venous access
• Stable medication dosing 14 days prior to and during study
• Healthy control subjects must show good general health per protocol
• Subjects will be matched Healthy to Renal Impaired by demographics data

You may not qualify if…

• Inability to complete study
• Insufficient venous access
• Clinically significant illness within 4 weeks of study
• History of clinically unstable disease except renal impairment in those subjects
• Medical or surgical conditions that may inhibit absorption of IP
• Laboratory value or medical issue which may interfere with study data or be hazardous for the subject
• Medication that may interfere with drug absorption or elimination process 4 weeks prior to study
• Consumption of grapefruit products within 7 days prior and after study
• Dose changes of medications 14 days prior to and during study
• Active alcohol abuse or drug addiction
• Positive alcohol test at screening or after
• Excessive xanthine consumption
• Positive serology test Hepatitis B or Hepatitis C or HIV
• Excessive nicotine usage
• Positive urine screen for drugs of abuse without prescription
• Clinically relevant abnormal 12 lead ECG
• Donation of bood or plasma or platelets within 30 days of study
• Clinical trial with another agent within 30 days or 5 half lives whichever is longer
• Informed consent unavailable or withdrawn
• Any condition the investigator feels would interfere with study data or subjects health
• Employee or relative of study center or center staff or investigator
• Any condition that may increase risk for subject
• Clinically significant lab value
• Clinically significant acute or chronic disease other than renal impairment in those subjects that may interfere with data or health
• Medication dose change within 14 days of study

Where it is running

• NOCCR — Knoxville, Tennessee, United States

Full record on ClinicalTrials.gov

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