A Study to Assess the Relative Bioavailability of JNJ-42756493 Tablets

NCT02466815 | Completed Phase 1

• 3 other identifiers: CR10746042756493EDI10042015-001583-19
• Study Type: interventional
• Target: 12
• Locations: 1 country
• Sites: 1

Brief Summary

The purpose of this study is to assess the relative bioavailability of 2 prototype G-025 tablets compared with the current G-018 tablet.

Conditions

Healthy

Keywords

Healthy; JNJ-42756493

Outcome Measures

Primary Outcomes (4)

• Maximum Observed Plasma Concentration (Cmax) of JNJ-42756493

  The Cmax is the maximum observed plasma JNJ-42756493 concentration. Relative bioavailability will be calculated by Cmax based on total drug concentrations.

  Predose, 0.16 hour (hr),0.33, 0.5, 0.75, 1, 1.5, 2, 2.5, 3, 4, 6, 8, 12 hr post-dose on Day 1; 24 and 36 hr post-dose on Day 2; 48hr post-dose on Day 3; 72hr post-dose on Day 4; 96hr post-dose on Day 5; 120hr post-dose on Day 6; 144hr post-dose on Day 7

• Area Under the Plasma Concentration-time Curve From Time 0 to 24 Hours (AUC[0-24]) of JNJ-42756493

  AUC(0-24) is the area under the plasma JNJ-42756493 concentration-time curve from time 0 to 24 hours. Relative bioavailability will be calculated by AUC(0-24) based on total drug concentrations.

  Predose, 0.16 hour (hr),0.33, 0.5, 0.75, 1, 1.5, 2, 2.5, 3, 4, 6, 8, 12 hr post-dose on Day 1; 24 and 36 hr post-dose on Day 2; 48hr post-dose on Day 3; 72hr post-dose on Day 4; 96hr post-dose on Day 5; 120hr post-dose on Day 6; 144hr post-dose on Day 7

• Area Under the Plasma Concentration-time Curve From Time 0 to Time of the Last Observed Quantifiable Concentration (Clast) (AUC[0-last]) of JNJ-42756493

  AUC(0-last) is the area under the plasma JNJ-42756493 concentration-time curve from time 0 to time of the last observed quantifiable concentration (Clast). Relative bioavailability will be calculated by AUC(0-last) based on total drug concentrations.

  Predose, 0.16 hour (hr),0.33, 0.5, 0.75, 1, 1.5, 2, 2.5, 3, 4, 6, 8, 12 hr post-dose on Day 1; 24 and 36 hr post-dose on Day 2; 48hr post-dose on Day 3; 72hr post-dose on Day 4; 96hr post-dose on Day 5; 120hr post-dose on Day 6; 144hr post-dose on Day 7

• Area Under the Plasma Concentration-time Curve From Time 0 to Infinite Time AUC (infinity) of JNJ-42756493

  AUC (infinity) is the area under the plasma JNJ-42756493 concentration-time curve from time 0 to infinite time, calculated as the sum of AUC(0-last) and Clast/lambda(z), in which lambda(z) is the first-order rate constant associated with the terminal portion of the curve. Relative bioavailability will be calculated by AUC (infinity) based on total drug concentrations.

  Predose, 0.16 hour (hr),0.33, 0.5, 0.75, 1, 1.5, 2, 2.5, 3, 4, 6, 8, 12 hr post-dose on Day 1; 24 and 36 hr post-dose on Day 2; 48hr post-dose on Day 3; 72hr post-dose on Day 4; 96hr post-dose on Day 5; 120hr post-dose on Day 6; 144hr post-dose on Day 7

Secondary Outcomes (1)

• Number of Participants With Adverse Events (AEs) or Serious Adverse Events (SAEs)

  Screening up to end of study (up to 3 months)

Study Arms (6)

Treatment A, then Treatment B and then Treatment C

EXPERIMENTAL

Participants will receive treatment A (JNJ-42756493 10 milligram \[mg\] tablet, current clinical formulation \[G-018\] which uses milled active pharmaceutical ingredient \[API\]) in period 1, treatment B (JNJ-42756493 10 mg tablet, Prototype Formulation I \[G-025\] which uses coarser API) in period 2 and then treatment C (JNJ-42756493 10 mg tablet, Prototype Formulation II \[G-025\] which uses coarser API) in period 3.

Drug: JNJ-42756493 Current Clinical Formulation (G-018); Drug: JNJ-42756493 Prototype Formulation I (G-025); Drug: JNJ-42756493 Prototype Formulation II (G-025)

Treatment B, then Treatment C and then Treatment A

EXPERIMENTAL

Participants will receive treatment B in period 1, treatment C in period 2 and then treatment A in period 3.

Drug: JNJ-42756493 Current Clinical Formulation (G-018); Drug: JNJ-42756493 Prototype Formulation I (G-025); Drug: JNJ-42756493 Prototype Formulation II (G-025)

Treatment C, then Treatment A and then Treatment B

EXPERIMENTAL

Participants will receive treatment C in period 1, treatment A in period 2 and then treatment B in period 3.

Drug: JNJ-42756493 Current Clinical Formulation (G-018); Drug: JNJ-42756493 Prototype Formulation I (G-025); Drug: JNJ-42756493 Prototype Formulation II (G-025)

Treatment A, then Treatment C and then Treatment B

EXPERIMENTAL

Participants will receive treatment A in period 1, treatment C in period 2 and then treatment B in period 3.

Drug: JNJ-42756493 Current Clinical Formulation (G-018); Drug: JNJ-42756493 Prototype Formulation I (G-025); Drug: JNJ-42756493 Prototype Formulation II (G-025)

Treatment B, then Treatment A and then Treatment C

EXPERIMENTAL

Participants will receive treatment B in period 1, treatment A in period 2 and then treatment C in period 3.

Drug: JNJ-42756493 Current Clinical Formulation (G-018); Drug: JNJ-42756493 Prototype Formulation I (G-025); Drug: JNJ-42756493 Prototype Formulation II (G-025)

Treatment C, then Treatment B and then Treatment A

EXPERIMENTAL

Participants will receive treatment C in period 1, treatment B in period 2 and then treatment A in period 3.

Drug: JNJ-42756493 Current Clinical Formulation (G-018); Drug: JNJ-42756493 Prototype Formulation I (G-025); Drug: JNJ-42756493 Prototype Formulation II (G-025)

Interventions

JNJ-42756493 Current Clinical Formulation (G-018) DRUG

JNJ-42756493 10 milligrams (2 tablets of 5 mg each) will be administered as current clinical formulation (G-018) in treatment A in either period 1, 2 or 3 as per treatment sequence.

Treatment A, then Treatment B and then Treatment C; Treatment A, then Treatment C and then Treatment B; Treatment B, then Treatment A and then Treatment C; Treatment B, then Treatment C and then Treatment A; Treatment C, then Treatment A and then Treatment B; Treatment C, then Treatment B and then Treatment A

JNJ-42756493 Prototype Formulation I (G-025) DRUG

JNJ-42756493 10 milligrams (2 tablets of 5 mg each) will be administered as Prototype Formulation I (G-025) in treatment B in either period 1, 2 or 3 as per treatment sequence.

Treatment A, then Treatment B and then Treatment C; Treatment A, then Treatment C and then Treatment B; Treatment B, then Treatment A and then Treatment C; Treatment B, then Treatment C and then Treatment A; Treatment C, then Treatment A and then Treatment B; Treatment C, then Treatment B and then Treatment A

JNJ-42756493 Prototype Formulation II (G-025) DRUG

JNJ-42756493 10 milligrams (2 tablets of 5 mg each) will be administered as Prototype Formulation II (G-025) in treatment C in either period 1, 2 or 3 as per treatment sequence.

Treatment A, then Treatment B and then Treatment C; Treatment A, then Treatment C and then Treatment B; Treatment B, then Treatment A and then Treatment C; Treatment B, then Treatment C and then Treatment A; Treatment C, then Treatment A and then Treatment B; Treatment C, then Treatment B and then Treatment A

Eligibility Criteria

• Age: 18 Years - 55 Years
• Sex: all
• Healthy Volunteers: Yes
• Age Groups: Adult (18-64)

You may qualify if:

• Participants should be willing to adhere to the prohibitions and restrictions specified in this protocol
• Woman must be either: postmenopausal (greater than (\>) 45 years of age with amenorrhea for at least 2 years, or any age with amenorrhea for at least 6 months and a serum follicle stimulating hormone (follicle stimulating hormone \[FSH\]) \>40 international unit per litre \[IU/L\]); surgically sterile
• Woman must have a negative serum beta-human chorionic gonadotropin (hCG) pregnancy test at screening and a negative urine pregnancy test on Day -1 of each treatment period
• Woman must agree not to donate eggs (ova, oocytes) for the purposes of assisted reproduction during the study and for 3 months after receiving the last dose of study drug.
• Man who is sexually active with a woman of childbearing potential and has not had a vasectomy, must agree to use a highly effective method of contraception as deemed appropriate by the investigator and to not donate sperm during the study and for 3 months after receiving the last dose of study drug

You may not qualify if:

• Participants with history of or current clinically significant medical illness including (but not limited to) cardiac arrhythmias or other cardiac disease, hematologic disease, coagulation disorders (including any abnormal bleeding or blood dyscrasias), lipid abnormalities, significant pulmonary disease, including bronchospastic respiratory disease, diabetes mellitus, hepatic or renal insufficiency, thyroid disease, neurologic or psychiatric disease, infection, or any other illness that the investigator considers should exclude the subject or that could interfere with the interpretation of the study results
• Participants with history or current evidence of ophthalmic disorder, such as central serous retinopathy or retinal vein occlusion, active wet age related macular degeneration, diabetic retinopathy with macular edema, uncontrolled glaucoma, corneal pathology such as keratitis, keratoconjunctivitis, keratopathy, corneal abrasion, inflammation or ulceration
• Participants with clinically significant abnormal values for hematology, clinical chemistry, or urinalysis at screening or at Day -1 of Period 1 as deemed appropriate by the investigator
• Participants with clinically significant abnormal physical examination, vital signs, or 12-lead electrocardiogram (ECG) at screening or at Day -1 of Period 1 as deemed appropriate by the investigator
• Participants with use of any prescription or nonprescription medication (including vitamins and herbal supplements), except for paracetamol and hormonal replacement therapy within 14 days before the first dose of the study drug is scheduled until completion of the study

Sponsors & Collaborators

• Janssen Research & Development, LLC: lead

Study Sites (1)

Unknown Facility

Merksem, Belgium

Location

Study Officials

• Janssen Research & Development, LLC Clinical Trial

  Janssen Research & Development, LLC

  STUDY DIRECTOR

Study Design

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

Study Record Dates

• First Submitted: June 5, 2015
• First Posted: June 9, 2015
• Study Start: June 1, 2015
• Primary Completion: August 1, 2015
• Study Completion: August 1, 2015
• Last Updated: February 3, 2025

Record last verified: 2025-01

Locations

BE (1)