Evaluate the Safety, Tolerability, and PK of EP547 in Healthy Subjects and Subjects With Cholestatic or Uremic Pruritus
- Registration Number
- NCT04510090
- Lead Sponsor
- Escient Pharmaceuticals, Inc
- Brief Summary
This first in human, Phase 1/1b trial will evaluate the safety, tolerability, and pharmacokinetics of single and multiple ascending doses of EP547 in healthy subjects and subjects with cholestatic or uremic pruritus.
- Detailed Description
This study consists of both single and multiple ascending doses in healthy subjects and in subjects with cholestatic or uremic pruritus.
Up to 48 healthy subjects will receive a single dose of EP547 or placebo. There will be a screening period of up to 28 days prior to the first dose, and a follow up visit 7 days after dosing is completed.
24 healthy subjects will receive multiple doses of EP547 or placebo for 7 days. There will be a screening period of up to 28 days prior to the first dose, and a follow up visit 7 days and then 14 days after dosing is completed.
6 subjects with cholestatic disease will receive a single dose of EP547. There will be a screening period of up to 28 days prior to the first dose, and a follow up visit 7 days after dosing is completed.
Up to 16 subjects with cholestatic pruritus will receive multiple doses of EP547 or placebo for 7 days. There will be a screening period of up to 28 days prior to the first dose, and a follow up visit 7 days and then 14 days after dosing is completed.
6 subjects with uremic disease will receive a single dose of EP547. There will be a screening period of up to 28 days prior to the first dose, and a follow up visit 7 days after dosing is completed.
Up to 16 subjects with uremic pruritus will receive multiple doses of EP547 or placebo for 7 days. There will be a screening period of up to 28 days prior to the first dose, and a follow up visit 7 days and then 14 days after dosing is completed.
12 healthy subjects will receive two doses of EP547 under fasted or fed condition.
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 89
Healthy Subjects:
- Age 18 to 60 years, inclusive
- Body mass index greater than or equal to 19 to less than or equal to 35 kg/m2
- Medically healthy with no clinically significant medical history, physical examination, vital sign, standard 12- lead ECG, chemistry, hematology, urinalysis, or coagulation results at Screening as deemed by the Investigator
- Male and female subjects must use adequate birth control and agree not to donate sperm or eggs for the time periods specified in the protocol
Subjects with Cholestatic Pruritus:
- Age 18 to 80 years, inclusive
- Has a cholestatic disorder
- Has experienced daily or near-daily moderate to severe pruritus for greater than 4 weeks before Screening and at study entry has itch scores indicative of moderate to severe pruritus
- If currently taking medications to treat the cholestatic disorder, must be on a stable dose for greater than 12 weeks before Screening and plans to maintain the regimen throughout the study
- If currently taking medications known to impact pruritus, must be on a stable dose for greater than 4 weeks before Screening and plans to maintain the regimen throughout the study
- Male and female subjects must use adequate birth control and agree not to donate sperm or eggs for the time periods specified in the protocol
Subjects with Uremic Pruritus
- Age 18 to 80 years, inclusive
- Has ESRD and is receiving hemodialysis 3× per week
- Has experienced daily or near-daily moderate to severe pruritus for greater than 4 weeks before Screening and at study entry has itch scores indicative of moderate to severe pruritus
- If currently taking medications known to impact pruritus, must be on a stable dose for greater than 4 weeks before Screening and plans to maintain the regimen throughout the study
- Male and female subjects must use adequate birth control and agree not to donate sperm or eggs for the time periods specified in the protocol
Healthy Subjects:
- Any prescription medications within 14 days of Screening
- Positive result for HIV HBV, or HCV at Screening
- History of malignancy within the past 5 years
- Tobacco product or electronic cigarette use within 90 days of Day -1
- Positive drug, alcohol, or cotinine screen results at Screening or Day -1
- Significant history of abuse of drugs, solvents, or alcohol in the past 2 years
Subjects with Cholestatic Pruritus:
- Scheduled to receive a liver transplant during the study (placement on a transplant waiting list is not exclusionary)
- Is receiving ongoing UVB treatment or anticipates receiving such treatment during the study
- Pruritus is secondary to biliary obstruction
- History or presence of hepatocellular carcinoma, hepatic abscess, or acute portal vein Thrombosis
Subjects with Uremic Pruritus:
- Scheduled to receive a kidney transplant during the study (placement on a transplant waiting list is not exclusionary)
- Is receiving ongoing UVB treatment or anticipates receiving such treatment during the study
- Known noncompliance with hemodialysis treatment that, in the opinion of the Investigator, would impede completion or validity of the study
- Pruritus is attributed mainly to any disease unrelated to kidney disease, is only present during the hemodialysis sessions, or is attributed to a skin disorder that occurs in this population with associated itch (eg, acquired perforating dermatosis)
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description EP547 Single Dose EP547 Single doses of EP547 EP547 Multiple Doses EP547 Multiple doses of EP547 Placebo Single Dose Placebo Single doses of placebo Placebo Multiple Doses Placebo Multiple doses of placebo
- Primary Outcome Measures
Name Time Method Incidence of Adverse Events Measured from Day 1 to End of Study or Early Termination (up to 3 weeks) To assess safety and tolerability of EP547 following single and multiple oral administration
- Secondary Outcome Measures
Name Time Method Maximum Plasma Concentration [Cmax] After Single Dose of EP547 Pre-dose, 0.25, 0.5, 1, 1.5, 2, 2.5, 3, 4, 6, 9, and 12 hours post-dose on Day 1 To evaluate the pharmacokinetics of single dose of EP547
Maximum Plasma Concentration [Cmax] After Multiple Doses of EP547 Pre-dose, 0.25, 0.5, 1, 1.5, 2, 2.5, 3, 4, 6, 9, 12, and 24 hours post-dose on Day 7 To evaluate the pharmacokinetics of multiple doses of EP547
Trial Locations
- Locations (4)
CMAX Clinical Research
🇦🇺Adelaide, South Australia, Australia
Monash Medical Centre
🇦🇺Clayton, Victoria, Australia
The Alfred Hospital
🇦🇺Melbourne, Victoria, Australia
Auckland Clinical Studies (ACS)
🇳🇿Grafton, Auckland, New Zealand