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Perampanel for adjunctive treatment of partial-onset seizures: A pooled dose-response analysis of phase III studies.

Authors :
Kramer, Lynn D.
Satlin, Andrew
Krauss, Gregory L.
French, Jacqueline
Perucca, Emilio
Ben‐Menachem, Elinor
Kwan, Patrick
Shih, Jerry J.
Laurenza, Antonio
Yang, Haichen
Zhu, Jin
Squillacote, David
Source :
Epilepsia (Series 4); Mar2014, Vol. 55 Issue 3, p423-431, 9p
Publication Year :
2014

Abstract

Objective To better understand the relationship between efficacy and perampanel dose, integrated actual (last) dose data from three phase III trials and an extension study (blinded Conversion Period; open-label Maintenance Period) were analyzed. Methods Seizure frequency data were analyzed in patients who were randomized to and completed the 13-week Maintenance Period of the phase III studies on perampanel 8 mg, and who received an actual (last) dose of 12 mg during (1) the extension 16-week blinded Conversion Period or (2) weeks 1-13 of the extension Maintenance Period. Due to a treatment-by-region interaction (p = 0.042), analyses excluded patients from the Latin America region (n = 162/1,480; 10.9% of the treated cohort). Results Of 372 patients randomized to 8 mg in the phase III studies, 273 completed the Maintenance Period at 8 mg and 267 entered the extension study. In patients who then had an actual (last) dose of 12 mg during the extension blinded Conversion Period (n = 217), median percent change in seizure frequency per 28 days improved from −32.4% (8 mg, phase III Maintenance Period) to −44.2% (12 mg, extension blinded Conversion Period); 50% responder rates increased slightly from 37.3% to 42.9%. In patients who completed the phase III studies on 8 mg and had an actual (last) dose of 12 mg during weeks 1-13 of the extension Maintenance Period (n = 181), median percent change in seizure frequency per 28 days improved from −34.1% (phase III Maintenance Period) to −46.0% (weeks 1-13 extension Maintenance Period); 50% responder rates were 39.2% and 46.4%. Seizure control remained substantially unchanged in patients who completed the phase III studies at 12 mg and continued on that dose during the extension. Significance Increasing perampanel dose from 8 to 12 mg can produce additional benefits in seizure control in at least some patients who tolerate the higher dose. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00139580
Volume :
55
Issue :
3
Database :
Complementary Index
Journal :
Epilepsia (Series 4)
Publication Type :
Academic Journal
Accession number :
94913756
Full Text :
https://doi.org/10.1111/epi.12527