Mode
Text Size
Log in / Sign up
Phase 1 Completed N=32 Randomized Treatment

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

OutcomeResultp-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.
View full record on ClinicalTrials.gov →

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.

Back to search