Pharmacokinetics of Dabrafenib in Subjects With Renal Impairment

NCT ID: NCT02852239

Last Updated: 2020-12-09

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE1
• Total Enrollment: 22 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2016-12-19
• Study Completion Date: 2019-09-27

Brief Summary

To characterize the pharmacokinetics and safety of dabrafenib following a single 100 mg oral dose in subjects with severe renal impairment and end stage renal disease not on dialysis.

Detailed Description

The main objective of this trial is to evaluate the pharmacokinetics of dabrafenib and metabolites after a single oral dose of dabrafenib in subjects with renal impairment as compared to healthy subjects with normal renal function.

This was a single-dose, open-label, parallel group single dose study to evaluate the pharmacokinetics (PK) and safety of a single oral dose of dabrafenib 100 mg in subjects with severe RI or ESRD compared to matched healthy subjects with normal renal function (control group).

The study consisted of a screening period, a treatment period and a follow-up period.

The Screening period started up to 28 days prior to dosing. Subjects who satisfied the inclusion/exclusion criteria at screening were admitted for baseline evaluations, which was done locally by the investigator. In the treatment period, subjects received a single 100 mg oral dose of dabrafenib administered as two 50 mg capsules with a whole glass of non-carbonated water (approximately 240 mL) in the morning of Day 1 following an overnight fast (minimum 10 hours). Subjects were confined to the study facility from Day -1 to Day 5, for collection of serial blood and urine samples. Subjects were discharged on Day 5.

In the follow-up period a telephone call was made to subjects 30 days post-dose to evaluate subject safety during the weeks after discharge from the facility. Adverse events occurring prior to Day 30 were followed until resolution or until judged to be permanent. Subjects returned to the clinic on Days 90 and 180 for the post-dose dermatological examination follow up.

For this study, the terms "investigational drug", "study drug" or "study treatment" refer to dabrafenib, administered as a single dose.

Conditions

Renal Impairment

Keywords

Renal impairment; Healthy volunteers; Clinical pharmacology study; DRB436; dabrafenib; normal renal function; impaired renal function

Study Design

• Allocation Method: NON_RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: BASIC_SCIENCE
• Blinding Strategy: NONE

Study Groups

Group 1 - Normal renal function

Subjects with normal renal function defined as GFR ≥ 90 mL/min at baseline and matching to the renal impaired subject based on gender, race, age, and weight.

Group Type: EXPERIMENTAL

dabrafenib

Intervention Type: DRUG

Single dose dabrafenib 100 mg

Group 2 - Severe renal function

Subjects with severe renal impairment defined as GFR of 15-29 mL/min at baseline.

Group Type: EXPERIMENTAL

dabrafenib

Intervention Type: DRUG

Single dose dabrafenib 100 mg

Group 3 - End stage renal disease (ESRD)

Subjects with end stage renal disease (ESRD), defined as GFR of \<15 mL/min at baseline.

Group Type: EXPERIMENTAL

dabrafenib

Intervention Type: DRUG

Single dose dabrafenib 100 mg

Interventions

dabrafenib

Single dose dabrafenib 100 mg

Intervention Type: DRUG

Other Intervention Names

DRB436

Eligibility Criteria

Inclusion Criteria

All subjects:

• Females must be of non-childbearing potential or must have negative pregnancy results at screening
• Good health as determined by lack of clinically significant findings
• Subjects must have a BMI between 18.0 kg/m2 and 38.0 kg/m2, with a body weight of at least 50 kg and no more than 140 kg
• Vitals signs within normal range
• Laboratory values at screening within local normal ranges or considered non-clinically significant

Additional criteria for renal impairment subjects:

-Stable renal disease without evidence of renal progression in the past 28 days prior to dosing

Additional criteria for healthy matched subjects:

• Matched to at least 1 renal impairment subject by race, age (+/-10 years), gender and weight (+/-10%)
• An absolute GFR of at least 90 ml/min

Exclusion Criteria

• Significant acute illness within the two weeks prior to dosing
• History or current diagnosis of cardiac disease indicating significant risk such as uncontrolled or significant cardiac disease or clinically significant ECG abnormalities
• Subjects will be screened for drugs of abuse
• History of drug or alcohol abuse within 6 months prior to dosing or evidence of such abuse as indicated by laboratory values at screening or baseline.
• Any surgical or medical condition which might significantly alter the absorption, distribution, metabolism or excretion of drugs.
• History of malignancy of any organ system, treated or untreated, within 5 years, regardless of where there is recurrence or metastases.
• Use of drugs known to prolong the QT interval within 4 weeks prior to dosing and for the duration of the study.
• Use of drugs know to affect CYP3A4 and/or CYP2C8 including both (strong or moderate) inhibitors and inducers, within 7 days prior to dosing or during the current study are prohibited

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 75 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

Novartis Pharmaceuticals

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Novartis Pharmaceuticals

Role: STUDY_DIRECTOR

Novartis Pharmaceuticals

Locations

Omega Research Consultants LLC

DeBary, Florida, United States

Hassman Research Institute

Berlin, New Jersey, United States

Wake Research Associates Oncology

Raleigh, North Carolina, United States

Countries

United States

Related Links

https://www.novctrd.com/ctrdweb/trialresult/trialresults/pdf?trialResultId=17675

CDRB436A2106 sudy results on the Novartis results database

Other Identifiers

CDRB436A2106

Identifier Type: -

Identifier Source: org_study_id