- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06190678
Study of Pirtobrutinib (LOXO-305) in Participants With Impaired Kidney Function and Healthy Participants
January 3, 2024 updated by: Eli Lilly and Company
An Open-label, Nonrandomized, Single-dose, Parallel-group, Safety, Tolerance, and Pharmacokinetic Study of LOXO-305 Administered to Fasted Renally Impaired Male and Female Subjects and Fasted Matched-control Healthy Subjects
The main purpose of this study is to measure how much of pirtobrutinib (LOXO-305) gets into the bloodstream and how long it takes the body to eliminate it in participants with impaired kidney function and healthy participants.
The side effects and tolerability of pirtobrutinib will also be evaluated.
Participation could last around 46 days.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
16
Phase
- Phase 1
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
California
-
Anaheim, California, United States, 92801
- Orange County Research Institute
-
-
Florida
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Edgewater, Florida, United States, 32132
- Riverside Clinical Research
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Miami, Florida, United States, 33014
- Clinical Pharmacology of Miami
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Orlando, Florida, United States, 32809
- Orlando Clinical Research Center
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Minnesota
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Saint Paul, Minnesota, United States, 55114
- Prism Research
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-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
- Males and females of non-childbearing potential.
- Within body mass index (BMI) range 18.5 to 40.0 kilograms per square meter (kg/m²).
- Participants will be in good health, based on medical history, physical examination findings, vital signs, 12 lead electrocardiogram (ECG), or clinical laboratory tests, as determined by the Investigator (or designee).
- Able to comply with all study procedures, including the 8-night stay at the Clinical Research Unit and follow-up phone call.
Exclusion Criteria:
History or presence of any of the following, deemed clinically significant by the Investigator (or designee), and/or Sponsor:
- liver disease
- pancreatitis
- peptic ulcer disease
- intestinal malabsorption
- gastric reduction surgery
- history or presence of clinically significant cardiovascular disease.
- Participants with out-of-range, at-rest vital signs.
- Abnormal laboratory values determined to be clinically significant by the Investigator (or designee).
- Clinically significant abnormality, as determined by the Investigator (or designee), from physical examination.
- Participation in any other investigational study drug trial involving administration of any investigational drug in the past 30 days or 5 half-lives, whichever was longer, prior to the first dose administration (Day 1).
- Use or intention to use any prescription or over-the-counter medications within 14 days prior to the first dose administration (Day 1) and through end of trial.
- History or presence, upon clinical evaluation, of any illness that, in the opinion of the Investigator, would interfere with the ability to provide informed consent or comply with study instructions, or that might confound the interpretation of the study results, or put the participant at undue risk.
- Donation of blood from 56 days prior to Screening, plasma or platelets from 4 weeks prior to Screening.
- Receipt of blood products within 2 months prior to Check-in (Day -1).
- Significant history of hypersensitivity, intolerance, or allergy to any drug compound, food, or other substance, unless approved by the Investigator (or designee).
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Basic Science
- Allocation: Non-Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Pirtobrutinib (Severe Renal Impairment)
Pirtobrutinib administered orally
|
Administered orally
Other Names:
|
Experimental: Pirtobrutinib (Normal Renal Function)
Pirtobrutinib administered orally
|
Administered orally
Other Names:
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Pharmacokinetics (PK): Maximum Observed Concentration (Cmax) of Pirtobrutinib
Time Frame: Pre-dose up to 168 hours post-dose
|
PK: Cmax of pirtobrutinib
|
Pre-dose up to 168 hours post-dose
|
PK: Time to Maximum Observed Plasma Concentration (Tmax) of Pirtobrutinib
Time Frame: Pre-dose up to 168 hours post-dose
|
PK: Tmax of pirtobrutinib
|
Pre-dose up to 168 hours post-dose
|
PK: Area Under the Concentration-time Curve, From Hour 0 to the Last Measurable Concentration (AUC0-t) of Pirtobrutinib
Time Frame: Pre-dose up to 168 hours post-dose
|
PK: AUC0-t of pirtobrutinib
|
Pre-dose up to 168 hours post-dose
|
PK: Area Under the Concentration-time Curve, From Hour 0 to Infinity (AUC0-inf) of Pirtobrutinib
Time Frame: Pre-dose up to 168 hours post-dose
|
PK: AUC0-inf of pirtobrutinib
|
Pre-dose up to 168 hours post-dose
|
PK: Percentage extrapolation for AUC0-inf (%AUCextrap) of Pirtobrutinib
Time Frame: Pre-dose up to 168 hours post-dose
|
PK: %AUCextrap of pirtobrutinib
|
Pre-dose up to 168 hours post-dose
|
PK: Apparent Terminal Elimination Rate Constant (λZ) of Pirtobrutinib
Time Frame: Pre-dose up to 168 hours post-dose
|
PK: λZ of pirtobrutinib
|
Pre-dose up to 168 hours post-dose
|
PK: Apparent Plasma Terminal Elimination Half-life (t½) of Pirtobrutinib
Time Frame: Pre-dose up to 168 hours post-dose
|
PK: t½ of pirtobrutinib
|
Pre-dose up to 168 hours post-dose
|
PK: Apparent Systemic Clearance (CL/F) of Pirtobrutinib
Time Frame: Pre-dose up to 168 hours post-dose
|
PK: CL/F of pirtobrutinib
|
Pre-dose up to 168 hours post-dose
|
PK: Apparent Volume of Distribution During the Terminal Phase (Vz/F) of Pirtobrutinib
Time Frame: Pre-dose up to 168 hours post-dose
|
PK: Vz/F of pirtobrutinib
|
Pre-dose up to 168 hours post-dose
|
PK: Mean Residence Time (MRT) of Pirtobrutinib
Time Frame: Pre-dose up to 168 hours post-dose
|
PK: MRT of pirtobrutinib
|
Pre-dose up to 168 hours post-dose
|
PK: Unbound Cmax (Cmax,u) of Pirtobrutinib
Time Frame: Predose (Within 30 mins prior to dosing) on Day 1
|
PK: Cmax,u of pirtobrutinib
|
Predose (Within 30 mins prior to dosing) on Day 1
|
PK: Unbound AUC0-t (AUC0-t,u) of Pirtobrutinib
Time Frame: Predose (Within 30 mins prior to dosing) on Day 1
|
PK: AUC0-t,u of pirtobrutinib
|
Predose (Within 30 mins prior to dosing) on Day 1
|
PK: Unbound AUC0-inf (AUC0-inf,u) of Pirtobrutinib
Time Frame: Predose (Within 30 mins prior to dosing) on Day 1
|
PK: AUC0-inf,u of pirtobrutinib
|
Predose (Within 30 mins prior to dosing) on Day 1
|
PK: Unbound CL/F (CL/F,u) of Pirtobrutinib
Time Frame: Predose (Within 30 mins prior to dosing) on Day 1
|
PK: CL/F,u of pirtobrutinib
|
Predose (Within 30 mins prior to dosing) on Day 1
|
PK: Unbound Vz/F (Vz/F,u) of Pirtobrutinib
Time Frame: Predose (Within 30 mins prior to dosing) on Day 1
|
PK: Vz/F,u of pirtobrutinib
|
Predose (Within 30 mins prior to dosing) on Day 1
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Collaborators
Investigators
- Study Director: Renée Ward, MD, PhD, Loxo Oncology
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
February 1, 2021
Primary Completion (Actual)
June 4, 2021
Study Completion (Actual)
June 4, 2021
Study Registration Dates
First Submitted
December 11, 2023
First Submitted That Met QC Criteria
January 3, 2024
First Posted (Actual)
January 5, 2024
Study Record Updates
Last Update Posted (Actual)
January 5, 2024
Last Update Submitted That Met QC Criteria
January 3, 2024
Last Verified
January 1, 2024
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- LOXO-BTK-20013
- J2N-OX-JZNG (Other Identifier: Eli Lilly and Company)
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Yes
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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