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

Healthy Clinical Trial

Official title:

An Open-Label, Repeat-Dose Study to Evaluate the Pharmacokinetics of Orally Administered CORT125134 Using the Current Capsule Formulation in Healthy Subjects

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT06094790
• Other study ID #: CORT125134-453
• Status: Completed
• Phase: Phase 1
• Start date: May 18, 2017
• Est. completion date: November 15, 2017

Study information

• Verified date: October 2023
• Source: Corcept Therapeutics
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial 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.

Description:

Initially, subjects will be enrolled into 2 cohorts each of 8 subjects (Cohort 1 and Cohort 2) to receive CORT125134 at 150 mg or 250 mg, respectively. Data from Cohorts 1 and 2 will be evaluated to select dose levels for Cohort 3 and optional Cohort 4.

The secondary objective of the study is to characterize the plasma PK profile of CORT125134 metabolites in healthy subjects receiving once-daily oral administration of the current capsule formulation of CORT125134.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 32
• Est. completion date: November 15, 2017
• Est. primary completion date: November 15, 2017
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 18 Years to 65 Years

Eligibility

Inclusion Criteria:

• 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

Exclusion Criteria:

• 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

Related Conditions & MeSH terms

• Healthy

Intervention

Drug:
• CORT125134 150 mg
CORT125134 150 mg (3 X 50 mg current capsule formulation)
• CORT125134 250 mg
CORT125134 250 mg (5 X 50 mg current capsule formulation)
• CORT125134 dose to be determined
CORT125134 current capsule formulation, dose to be determined

Locations

Country	Name	City	State
United States	Quotient Sciences, Miami, Inc.	Miami	Florida

Sponsors (1)

Lead Sponsor	Collaborator
Corcept Therapeutics

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	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
Primary	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
Primary	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.