A Study to Evaluate the Pharmacokinetics of the Current Capsule Formulation of CORT125134 in Healthy Subjects

NCT06094790 | Completed Phase 1 FDA Drug

• 1 other identifier: CORT125134-453
• Study Type: interventional
• Target: 32
• Locations: 1 country
• Sites: 1

Brief Summary

A study designed to characterize the plasma pharmacokinetic (PK) profile of CORT125134 in healthy subjects receiving once-daily oral administration of the current capsule formulation of CORT125134 for 14 days.

Conditions

Healthy

Outcome Measures

Primary Outcomes (3)

• Area under the concentration-time curve over a dose-interval of plasma CORT125134 (AUCtau)

  Predose and at serial timepoints over a dose-interval following dosing on Days 1, 7, and 14

• Maximum concentration of plasma CORT125134 (Cmax)

  Predose and at serial timepoints up to 24 hours following Day 1 and Day 7 dosing, and at serial timepoints up to 120 hours following Day 14 dosing

• AUC from the time of dosing until 24 hours later of plasma CORT125134 (AUC0-24h)

  Statistical analysis of these data will be used to estimate the highest oral dose of CORT125134 current capsule formulation steady state AUC0-24h of plasma CORT125134.

  Predose and at serial timepoints up to 24 hours following dosing on Days 1, 7, and 14.

Study Arms (4)

Cohort 1

EXPERIMENTAL

Subjects will receive CORT125134 150 mg once daily for 14 days

Drug: CORT125134 150 mg

Cohort 2

EXPERIMENTAL

Subjects will receive CORT125134 250 mg once daily for 14 days

Drug: CORT125134 250 mg

Cohort 3

EXPERIMENTAL

Subjects will receive CORT125134 once daily for 14 days at a dose level decided based on evaluation of steady state exposure from Cohorts 1 and 2

Drug: CORT125134 dose to be determined

Cohort 4 (optional)

EXPERIMENTAL

Subjects will receive CORT125134 once daily for 14 days at a dose level decided based on evaluation of steady state exposure from Cohorts 1, 2, and 3, if it is considered that this cohort would aid achievement of the study objectives

Drug: CORT125134 dose to be determined

Interventions

CORT125134 150 mg DRUG

CORT125134 150 mg (3 X 50 mg current capsule formulation)

Cohort 1

CORT125134 250 mg DRUG

CORT125134 250 mg (5 X 50 mg current capsule formulation)

Cohort 2

CORT125134 dose to be determined DRUG

CORT125134 current capsule formulation, dose to be determined

Cohort 3; Cohort 4 (optional)

Eligibility Criteria

• Age: 18 Years - 65 Years
• Sex: all
• Healthy Volunteers: Yes
• Age Groups: Adult (18-64), Older Adult (65+)

You may qualify if:

• Give written informed consent
• Be healthy males or non-pregnant, non-lactating healthy females
• Must agree to use an adequate method of contraception as described in the study protocol
• Have a body mass index (BMI) of 18 to 32 kg/m\^2, inclusive and body weight more than 50 kg (110 pounds)
• Be willing to comply with study restrictions as described in study protocol
• Be able to comply with the requirements of the entire study
• Be judged to be in good health, based on the results of medical history, physical examination, vital signs, electrocardiogram (ECG), and clinical laboratory findings
• Have suitable veins for multiple venipuncture/cannulation

You may not qualify if:

• Be an employee or immediate family member of the Clinical Research Unit or Corcept
• Have been previously enrolled in this study
• Have multiple drug allergies, or be allergic to any of the components of study drug
• Have a condition that could be aggravated by glucocorticoid blockade (eg, asthma, any chronic inflammatory condition)
• In the 1 year before study drug administration, have a history of drug or alcohol abuse
• In the 6 calendar months before study drug administration, on average: have smoked more than 5 cigarettes/day, consumed more than 14 units (female) or 21 units (male) of alcohol/week (1 unit/drink = 5 ounces of wine, or 12 ounces of beer, or 1.5 ounces of hard liquor), consumed licorice or other glycyrrhetic acid derivatives regularly, in the judgement of the Investigator
• In the 2 calendar months before study drug administration, have donated/ lost blood or plasma in excess of 400 mL
• In the 30 days before study drug administration, have participated in another clinical trial of a new chemical entity or a prescription medicine
• Have a positive test for alcohol or drugs of abuse at Screening or admission
• Have a positive test for exogenous glucocorticoids at Screening
• Have clinically-relevant abnormal findings on vital signs, physical examination, laboratory screening tests, or 12-lead ECG, at Screening and/or before first dose
• Have any medical or social reasons for not participating in the study raised by their primary care physician
• Have any other condition that might increase the risk to the individual or decrease the chance of obtaining satisfactory data, as assessed by the Investigator
• Have taken any prohibited prior medication, as described in study protocol

Sponsors & Collaborators

• Corcept Therapeutics: lead

Study Sites (1)

Quotient Sciences, Miami, Inc.

Miami, Florida, 33126, United States

Location

MeSH Terms

Interventions

relacorilant

Study Officials

• Andreas Moraitis

  Corcept Therapeutics

  STUDY DIRECTOR

Study Design

• Study Type: interventional
• Phase: phase 1
• Allocation: RANDOMIZED
• Masking: NONE
• Purpose: OTHER
• Intervention Model: PARALLEL
• Sponsor Type: INDUSTRY
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: October 17, 2023
• First Posted: October 23, 2023
• Study Start: May 18, 2017
• Primary Completion: November 15, 2017
• Study Completion: November 15, 2017
• Last Updated: October 23, 2023

Record last verified: 2023-10

Data Sharing

• IPD Sharing: Will not share

Locations

US (1)