Phase 1
Completed N=32
Disposition of Eslicarbazepine Acetate and Its Metabolites S-licarbazepine and R-licarbazepine
Source: ClinicalTrials.gov NCT02281591 ↗Enrolled (actual)
32
Serious AEs
0.0%
Results posted
Dec 2014
Primary outcomePrimary: Cmax - the Maximum Plasma Concentration — 15809; 10496; 10364; 437 ng/mL
Summary
Single centre, open-label, randomised study in four parallel groups of healthy volunteers
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Cmax - the Maximum Plasma Concentration |
15809; 10496; 10364; 437; 222; 8099 | — |
| PRIMARY Tmax - the Time of Occurrence of Cmax |
1.99; 1.01; 0.965; 10.7; 18.6; 1.41 | — |
| PRIMARY AUC0-∞ - the Area Under the Plasma Concentration Versus Time Curve From Time Zero to Infinity |
271191; 201409; 132724; 11003; 8816; 116884 | — |
| SECONDARY AUC0-t - the Area Under the Plasma Concentration-time Curve to Last Measurable Time Point |
268045; 198313; 130147; 9419; 6757; 114635 | — |
Eligibility Criteria
Inclusion Criteria
- Male or female subjects aged between 18 and 45 years, inclusive.
- Subjects of body mass index (BMI) between 19 and 30 kg/m2, inclusive.
- Subjects who were healthy as determined by pre-study medical history, physical examination, vital signs, neurological examination, and 12-lead ECG.
- Subjects who had clinical laboratory tests clinically acceptable at screening and admission.
- Subjects who had negative tests for HBsAg, anti-HCV Ab and HIV-1 and HIV-2 Ab at screening.
- Subjects who were negative for drugs of abuse and alcohol at screening and admission.
- Subjects who were non-smokers or who smoke < 10 cigarettes or equivalent per day.
- Subjects who are able and willing to give written informed consent.
- (If female) She was not of childbearing potential by reason of surgery or, if of childbearing potential, she used one of the following methods of contraception: double barrier, intrauterine device or abstinence.
- (If female) She had a negative pregnancy test at screening and admission to Phase A.
Exclusion Criteria
- Subjects who did not conform to the above inclusion criteria, OR
- Subjects who had a clinically relevant history or presence of respiratory, gastrointestinal, renal, hepatic, haematological, lymphatic, neurological, cardiovascular, psychiatric, musculoskeletal, genitourinary, immunological, dermatological, endocrine, connective tissue diseases or disorders.
- Subjects who had a clinically relevant surgical history.
- Subjects who had a clinically relevant family history.
- Subjects who had a history of relevant atopy.
- Subjects who had a history of relevant drug hypersensitivity (especially carbamazepine or oxcarbazepine).
- Subjects who had a history of alcoholism or drug abuse.
- Subjects who consumed more than 14 units of alcohol a week.
- Subjects who had a significant infection or known inflammatory process on screening or admission.
Data sourced from ClinicalTrials.gov (NCT02281591). 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.