Abstract | BACKGROUND: The Phase 3 REsearch Evaluating Migraine Prophylaxis Therapy ( PREEMPT) trials demonstrated efficacy/tolerability of onabotulinumtoxinA for headache prevention in adults with chronic migraine. This post hoc analysis assessed time of onset of onabotulinumtoxinA after the first treatment in total and responder populations and consistency weekly through five treatment cycles. METHODS: In the 24-week, double-blind, placebo-controlled phase of PREEMPT, individuals were randomized 1:1 to onabotulinumtoxinA (155-195 U) or placebo every 12 weeks for two cycles. The primary pooled efficacy variable was change in headache days per 28 days at week 24. We assessed change in headache and migraine/probable migraine (hereafter migraine) days/week compared with baseline week 4. RESULTS: CONCLUSIONS: Treatment with onabotulinumtoxinA is associated with significant reductions in headache and migraine days/week at week 1, persisting after week 3, compared with placebo. Combined with earlier reports showing onabotulinumtoxinA treatment results in a persistent and progressive reduction in headache days over 56 weeks, it is suggested peak benefit may require multiple treatments. TRIAL REGISTRATION NUMBER: ClinicalTrials.gov: NCT00156910 and NCT00168428.
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Authors | David W Dodick, Stephen D Silberstein, Richard B Lipton, Ronald E DeGryse, Aubrey Manack Adams, Hans-Christoph Diener |
Journal | Cephalalgia : an international journal of headache
(Cephalalgia)
Vol. 39
Issue 8
Pg. 945-956
(Jul 2019)
ISSN: 1468-2982 [Electronic] England |
PMID | 31112399
(Publication Type: Journal Article, Multicenter Study, Randomized Controlled Trial)
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Chemical References |
- Botulinum Toxins, Type A
- onabotulinum toxin A
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Topics |
- Adult
- Botulinum Toxins, Type A
(therapeutic use)
- Chronic Disease
- Double-Blind Method
- Female
- Humans
- Male
- Middle Aged
- Migraine Disorders
(diagnosis, drug therapy)
- Time Factors
- Treatment Outcome
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