Mode
Text Size
Log in / Sign up
Phase 1 N=40 Randomized Double-blind Treatment

Evaluate the Safety, Tolerability, and PK of EP547 in Healthy Subjects and Subjects With Cholestatic or Uremic Pruritus

Pruritus · Cholestasis · Kidney Failure

Enrolled (actual)
40
Serious AEs
0.0%
Results posted
Jun 2023
Primary outcome: Primary: Incidence of Adverse Events — 5; 5; 5; 3 participants

Study Design & Population

Study type
Interventional
Phase
Phase 1
Interventions
EP547 (Drug); Placebo (Drug)
Age
Adult, Older Adult · 18+ yrs
Sex
All
Sponsor
Escient Pharmaceuticals, Inc
Primary completion
Jul 2021

Outcome Measures

OutcomeResultp-value
PRIMARY
Incidence of Adverse Events
5; 5; 5; 3; 3; 4
SECONDARY
Maximum Plasma Concentration [Cmax] After Single Dose of EP547
1421.0; 6309.6; 17232.6; 27799.2; 36352.2; 1506.6
SECONDARY
Maximum Plasma Concentration [Cmax] After Multiple Doses of EP547
2834.7; 8760.7; 29613.1; 3421.0; 3192.7

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.

Eligibility Criteria

Inclusion Criteria

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

Exclusion Criteria

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)
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT04510090). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

Back to search