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Phase 1 Completed N=40 Randomized Double-blind Treatment

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

Source: ClinicalTrials.gov NCT04510090 ↗
Enrolled (actual)
40
Serious AEs
0.0%
Results posted
Jun 2023
Primary outcomePrimary: Incidence of Adverse Events — 5; 5; 5; 3 participants

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.

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

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. Informational only — not medical advice.

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