Phase 1
Completed N=127
A Study of Abemaciclib in Healthy Participants
Healthy
Source: ClinicalTrials.gov NCT02672423 ↗
Enrolled (actual)
127
Serious AEs
0.0%
Results posted
Aug 2018
Primary outcomePrimary: Pharmacokinetics (PK): Area Under the Concentration Versus Time Curve From Zero to Infinity (AUC[0-∞]) — 3080; 2880; 3110; 3120 Nanograms*hour/milliliter (ng*hr/mL)
Summary
The purpose of this study is to measure how much abemaciclib gets into the blood stream and how long it takes the body to get rid of it when given as capsules versus a tablet(s). The effect of a high fat meal on the tablet formulation will also be evaluated. In addition, the tolerability of abemaciclib tablet and capsule formulations will be evaluated. Information about any side effects that may occur will also be collected.
This study has 3 parts. Parts A and C will last about 44 days including follow-up. Part B will last about 60 days including follow-up. Screening may occur up to 28 days before the first dose of study drug. Participants are only allowed to enroll in one part.
This study is for research purposes only and is not intended to treat any medical condition.
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Pharmacokinetics (PK): Area Under the Concentration Versus Time Curve From Zero to Infinity (AUC[0-∞]) |
3080; 2880; 3110; 3120; 3130; 4170 | — |
| PRIMARY PK: Maximum Observed Drug Concentration (Cmax) |
104; 101; 95.2; 97.7; 95.8; 130 | — |
Eligibility Criteria
Inclusion Criteria
- Healthy surgically sterile or postmenopausal females and sterile males
- Have a body mass index (BMI) 18 to 32 kilograms per square meter (kg/m²)
Exclusion Criteria
- Have known allergies to abemaciclib, related compounds, or any components of the formulation
- Regularly use known drugs of abuse and/or show positive findings on urinary drug screening
- Show evidence of human immunodeficiency virus (HIV) infection and/or positive human HIV antibodies
- Show evidence of hepatitis C and/or positive hepatitis C antibody
- Show evidence of hepatitis B and/or positive hepatitis B surface antigen
Data sourced from ClinicalTrials.gov (NCT02672423). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication. Informational only — not medical advice.