Skip to main content
Clinical Trials/NCT05043766
NCT05043766
Completed
Phase 1

A Phase 1b, Randomized 2-Part Single-Center Study to Evaluate the PK and Safety of Multiple Ascending Oral Doses of PF614 and the Food Effect and BA/BE of Single Oral Doses of PF614 Relative to OxyContin in Healthy Adult Subjects

Ensysce Biosciences1 site in 1 country84 target enrollmentSeptember 8, 2021

Overview

Phase
Phase 1
Intervention
PF614
Conditions
Healthy Volunteers
Sponsor
Ensysce Biosciences
Enrollment
84
Locations
1
Primary Endpoint
Incidence of Treatment-Emergent Adverse Events [Safety and Tolerability]
Status
Completed
Last Updated
3 years ago

Overview

Brief Summary

This is a single-center study incorporating 2 parts: A Multiple Ascending Dose Study (Part A) and a comparative Bioavailability/Bioequivalence and Food Effect study (Part B). Both parts of the study will be conducted in healthy adult subjects.

Detailed Description

This study is intended to evaluate the pharmacokinetics of OxyContin (oxycodone ER) and PF614, as well as PF614 fragments, following administration of multiple ascending doses of PF614, and to compare to steady-state pharmacokinetics to those of OxyContin. (Part A) In addition, oral bioavailability of oxycodone derived from single doses of PF614 of the to-be-marketed capsule formulation will be compared to that of the reference drug, OxyContin, in the fasted and fed condition. A pivotal food effect assessment will be incorporated into the study to determine the impact of a high fat meal on the bioavailability of oxycodone, following oral single-dose administration of PF614 (Part B).

Registry
clinicaltrials.gov
Start Date
September 8, 2021
End Date
March 21, 2022
Last Updated
3 years ago
Study Type
Interventional
Study Design
Crossover
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Males or females, ages 18-50 years in good general health,
  • BMI between 18 and 32 kg/m (inclusive)
  • Subjects must have a negative screen for drugs of abuse, nicotine, alcohol, Hepatitis B, Hepatitis C, and HIV.
  • Female subjects of child bearing potential must have a negative serum pregnancy test at randomization
  • Females must be of non-child bearing potential (e.g. postmenopausal) or of childbearing potential and agree to use a highly effective form of contraception from the time of screening to two weeks after last dose of study medication.
  • Subjects must have normal findings in a physical examination and 12 lead ECG and normal Vital Signs
  • Clinical laboratory values must be Within Normal limits as defined by the clinical laboratory
  • Subjects must be able to provide coherent written informed consent
  • Subjects must be willing and able to follow study instructions and be likely to complete all study requirements.

Exclusion Criteria

  • History of allergy or sensitivity to oxycodone
  • History of loud snoring or sleep apnea
  • History of medical problems encountered with opioid therapy
  • Urinary cotinine levels indicative of smoking or history of smoking or regular tobacco use with 2 months prior to screening
  • History of alcoholism or drug abuse
  • Use of prescription medications within 14 days of study drug administration with exception of contraceptives used by female subjects
  • Use of any opioid within 30 days prior to screening
  • History of allergy or sensitivity to naltrexone
  • History of allergy or sensitivity to naloxone
  • Donation of blood within 30 days prior to screening

Arms & Interventions

PF614

Part A will utilize a randomized, open-label, multiple-ascending dose design with up to 3 separate dose groups of 8 subjects. Within each dose group, subjects will be randomized to receive repeated BID doses, planned to be 12 hours apart over a 5 day period, for a total of 9 doses. Dose escalation to Dose Groups 2 and 3 will follow a review of pharmacokinetic, safety and tolerability data up to Day 10 of the preceding group. The doses or dosing regimen for Dose groups 2 and 3 may be modified based on a review of the data.

Intervention: PF614

PF614

Part A will utilize a randomized, open-label, multiple-ascending dose design with up to 3 separate dose groups of 8 subjects. Within each dose group, subjects will be randomized to receive repeated BID doses, planned to be 12 hours apart over a 5 day period, for a total of 9 doses. Dose escalation to Dose Groups 2 and 3 will follow a review of pharmacokinetic, safety and tolerability data up to Day 10 of the preceding group. The doses or dosing regimen for Dose groups 2 and 3 may be modified based on a review of the data.

Intervention: Naltrexone Hydrochloride

Part B Compare Bioavailability and Bioequivalence

Part B will utilize an open-label, single-dose, randomized, 4-way crossover design. Following confirmation of eligibility, subjects will be randomized to receive each of the single oral doses of study drugs (one at each treatment period). PF614 100 mg administered under fasted conditions; PF614 100 mg administered under fed conditions; OxyContin 40 mg administered under fasted conditions; OxyContin 40 mg administered under fed conditions

Intervention: PF614

Part B Compare Bioavailability and Bioequivalence

Part B will utilize an open-label, single-dose, randomized, 4-way crossover design. Following confirmation of eligibility, subjects will be randomized to receive each of the single oral doses of study drugs (one at each treatment period). PF614 100 mg administered under fasted conditions; PF614 100 mg administered under fed conditions; OxyContin 40 mg administered under fasted conditions; OxyContin 40 mg administered under fed conditions

Intervention: Naltrexone Hydrochloride

Part B Compare Bioavailability and Bioequivalence

Part B will utilize an open-label, single-dose, randomized, 4-way crossover design. Following confirmation of eligibility, subjects will be randomized to receive each of the single oral doses of study drugs (one at each treatment period). PF614 100 mg administered under fasted conditions; PF614 100 mg administered under fed conditions; OxyContin 40 mg administered under fasted conditions; OxyContin 40 mg administered under fed conditions

Intervention: OxyContin

Outcomes

Primary Outcomes

Incidence of Treatment-Emergent Adverse Events [Safety and Tolerability]

Time Frame: 30 days

Adverse Events, Significant Adverse Events, Adverse Events leading to discontinuation

Pharmacokinetics t1/2 [Half-life]

Time Frame: PK sampling time points 0, 30 minutes; 1, 2, 3, 4, 6, 8, and 12 hours

Terminal elimination half-life

Pharmacokinetics Ctrough [Minimum Plasma Concentration before next dose]

Time Frame: Prior to dosing on Days 2, 3, and 4

Concentrations prior to dosing

Pharmacokinetics Part B Cmax

Time Frame: PK sampling time points 0, 30 minutes; 1, 2, 3, 4, 6, 8, and 12 hours

Maximum (peak) plasma concentration in fed vs fasted state

Bioavailability and Bioequivalence

Time Frame: PK sampling time points 0, 30 minutes; 1, 2, 3, 4, 6, 8, and 12 hours

Bioavailability and Bioequivalence of single oral doses of PF614 prodrug and oxycodone derived from from PF614 vs. oxycodone derived from OxyContin in healthy adult subjects (Part B)

Pharmacokinetics AUC [Area Under the Curve]

Time Frame: Full PK sampling time points will be 0, 30 minutes; 1, 2, 3, 4, 6, 8, and 12 hours

Area under the concentration-time curve from the time of dosing to the start of the next dosing interval using PF614 concentrations and oxycodone concentrations in plasma.

Pharmacokinetics Cmax [Maximum Plasma Concentration]

Time Frame: PK sampling time points will be 0, 30 minutes; 1, 2, 3, 4, 6, 8, and 12 hours

Maximum (peak) plasma concentration first dose

Pharmacokinetics Tlag [Time to first measurable plasma concentration]

Time Frame: PK sampling time points will be 0, 30 minutes; 1, 2, 3, 4, 6, 8, and 12 hours

Time prior to the time corresponding to the first measurable (non-zero) concentration

Pharmacokinetics Vz/F [Volume of Distribution]

Time Frame: PK sampling time points 0, 30 minutes; 1, 2, 3, 4, 6, 8, and 12 hours

Apparent volume of distribution during the terminal-elimination phase

Pharmacokinetics Tmax [Time to maximum plasma concentration]

Time Frame: PK sampling time points 30 minutes; 1, 2, 3, 4, 6, 8, and 12 hours

Time to maximum plasma concentration on Day 1 (first dose)

Pharmacokinetics CL/F [Clearance]

Time Frame: PK sampling time points 0, 30 minutes; 1, 2, 3, 4, 6, 8, and 12 hours

Apparent total systemic clearance

Pharmacokinetics Part B AUC

Time Frame: PK sampling time points 0, 30 minutes; 1, 2, 3, 4, 6, 8, and 12 hours

Area under the concentration-time curve from the time of dosing extrapolated to time infinity in fed vs fasted state

Pharmacokinetics AUC, Steady State

Time Frame: PK sampling time points 0, 30 minutes; 1, 2, 3, 4, 6, 8, and 12 hours

Steady-state (Day 5) area under the concentration-time curve from the time of dosing extrapolated to time infinity

Pharmacokinetics Cmax, Steady State

Time Frame: PK sampling time points 0, 30 minutes; 1, 2, 3, 4, 6, 8, and 12 hours

Maximum (peak) plasma concentration at steady-state on Day 5

Pharmacokinetics elimination rate

Time Frame: PK sampling time points 0, 30 minutes; 1, 2, 3, 4, 6, 8, and 12 hours

Terminal elimination rate/constant

Pharmacokinetics Tmax, Steady State

Time Frame: PK sampling time points 0, 30 minutes; 1, 2, 3, 4, 6, 8, and 12 hours

Time to maximum plasma concentration on Day 5

Pharmacokinetics Part B AUC 0-t

Time Frame: PK sampling time points 0, 30 minutes; 1, 2, 3, 4, 6, 8, and 12 hours

Area under the concentration-time curve from the time of dosing to the last measurable concentration in fed vs fasted state

Secondary Outcomes

  • Pharmacokinetics Part B Terminal elimination rate(PK sampling time points 0, 30 minutes; 1, 2, 3, 4, 6, 8, and 12 hours)
  • Pharmacokinetics Part B Tmax(PK sampling time points 0, 30 minutes; 1, 2, 3, 4, 6, 8, and 12 hours)
  • Plasma Concentration of inactive metabolic fragment #1(PK sampling time points 0, 30 minutes; 1, 2, 3, 4, 6, 8, and 12 hours)
  • Plasma Concentration of inactive metabolic fragment #2(PK sampling time points 0, 30 minutes; 1, 2, 3, 4, 6, 8, and 12 hours)
  • Pharmacokinetics Part B CL/F(PK sampling time points 0, 30 minutes; 1, 2, 3, 4, 6, 8, and 12 hours)
  • Pharmacokinetics Part B pAUC(PK sampling time points 0, 30 minutes; 1, 2, 3, 4, 6, 8, and 12 hours)
  • Pharmacokinetics Part B Tlag(PK sampling time points 0, 30 minutes; 1, 2, 3, 4, 6, 8, and 12 hours)
  • Pharmacokinetics Part B Vz/F(PK sampling time points 0, 30 minutes; 1, 2, 3, 4, 6, 8, and 12 hours)
  • Pharmacokinetics Part B t1/2(PK sampling time points 0, 30 minutes; 1, 2, 3, 4, 6, 8, and 12 hours)

Study Sites (1)

Loading locations...

Similar Trials