Phase 1
Completed N=40
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
| Outcome | Result | p-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)
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.