Last updated: 11/07/2018 19:48:04
A comparison of the bioavailability of 100mg and 200mg lamotrigine (LAMICTAL) tablets in healthy volunteers.
Clinicaltrials.gov ID
Not applicable
EudraCT ID
Not applicable
EU CT Number
Not applicable
Trial status
Study complete
Study complete
Trial overview
Official title: A comparison of the bioavailability of 100mg and 200mg lamotrigine (LAMICTAL) tablets in healthy volunteers.
Trial description: A comparison of the bioavailability of 100mg and 200mg lamotrigine (LAMICTAL) tablets in healthy volunteers.
Primary purpose:
Not applicable
Trial design:
Not applicable
Masking:
Not applicable
Allocation:
Not applicable
Primary outcomes:
Not applicable
Secondary outcomes:
Not applicable
Interventions:
Not applicable
Enrollment:
Not applicable
Primary completion date:
Not applicable
Observational study model:
Not applicable
Time perspective:
Not applicable
Clinical publications:
Wootton R Soul-Lawton J Rolan PE Fook Sheung CTC Cooper JDH Posner J.Comparison of the pharmacokinetics of lamotrigine in patients with chronic renal failure and healthy volunteers.BR. J. CLIN. PHARMACOL. 1997;43(1):23-27.
Inclusion and exclusion criteria
Trial location(s)
This study does not involve prospective enrollment of participants.
Study documents
Scientific result summary
Available language(s): English
If you wish to request for full study report, please contact - [email protected]
Results overview
Not applicable
Recruitment status
Study complete
Actual primary completion date
Not applicable
Actual study completion date
1990-15-03
Plain language summaries
Plain language summaries of clinical trial results for Phase 2-4 clinical trials that were initiated on or after January 2022 will be posted by GSK within one year following study completion.
Additional information about the trial
Not applicable
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