Management of Migraine Using Enerumab and Traditional Therapy at the Time of COVID-19
調査の概要
詳細な説明
Migraine is a debilitating disorder that affects 37 million people in the United States. Recently, three new injectables calcitonin gene-related peptide (CGRP) receptor antagonists-erenumab, fremanezumab, and galcanezumab-were FDA approved for prophylactic treatment of migraine in adults, that plays a key role in migraine pathophysiology. By blocking the receptor function of CGRP, these agents can reduce the total number of headache days per month and limit the need for using multiple medications. In clinical trials, these agents, which have no drug interactions and minimal adverse reactions, reduced headache days per month by as much as 50% in patients experiencing multiple migraine days each month. These new biologics, however, are more expensive for the patient compared with other prophylactic treatments
The rational of this study was to assess the efficacy of erenumab on frequency of monthly migraine days in adults at baseline, 3 months and 6 months, disability in patients with chronic migraine and on post covid migraine severity
研究の種類
入学 (実際)
連絡先と場所
研究場所
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Fayoum、エジプト、63111
- Marwa Kamal Ahmed Tolba
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参加基準
適格基準
就学可能な年齢
健康ボランティアの受け入れ
受講資格のある性別
サンプリング方法
調査対象母集団
Migraine prevention is an area of a large unmet medical need, with existing prophylactic therapies often having modest efficacy and poor tolerability. Calcitonin gene-related peptide (CGRP) receptor antagonism is a novel approach to migraine preventive therapy. Erenumab is a human monoclonal antibody against CGRP receptor. The present study is a phase 3 trial intended to assess the efficacy and safety of erenumab for prevention of migraine in Egyptian adults with chronic migraine (CM).
The study consists of a screening period (up to 24 weeks, including at baseline period), a 12-week period and a 24-week period ,.
説明
Inclusion Criteria:
- -Ages Eligible for Study: 18 Years to 65 Years (Adult, Older Adult)
- Sexes Eligible for Study: All
History of at least 5 attacks of migraine
-≥ 15 headache days of which ≥ 8 headache days meet criteria as migraine days during the baseline period
- chronic migraineurs with failure to more than 2 preventive treatments
- chronic migraineurs without any preventive treatments
- Naive to anti CGRP monclonal antibodies
Exclusion Criteria:
Participants are excluded from the study if any of the following criteria apply:
• unable to understand the study requirements, the informed consent, or complete headache records as required per protocol;
- History of cluster or hemiplegic headache
- Evidence of seizure or major psychiatric disorder Cardiac or active hepatic disease
- pregnant, actively trying to become pregnant, or breast-feeding;
- episodic migraineurs,
- Other headache types
- allergy to latex;
- received nerve blocks or trigger point injections in the previous 8 weeks or plans to receive them during the study;
- prior exposure in the last 6 months to biologics or drugs specifically targeting the calcitonin gene-related peptide (CGRP) pathway;
- a psychiatric condition, that may affect the interpretation of efficacy and safety data or contraindicates the participant's participation in the study
研究計画
研究はどのように設計されていますか?
デザインの詳細
- 観測モデル:コホート
- 時間の展望:断面図
この研究は何を測定していますか?
主要な結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
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mean number of migraine days
時間枠:6 months
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The primary end point was the change from baseline to months 4 through 6 in the mean number of migraine days per month.
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6 months
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changes on migraine severity during COVID-19 infection
時間枠:during the 6 months
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measuring the severity of migraine attacks on a numerical scale
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during the 6 months
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二次結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
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reduction in migraine days
時間枠:during the 6 months
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Secondary end points were a 50% or greater reduction in mean migraine days per month
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during the 6 months
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rate of using migraine medications
時間枠:during the 6 months
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change in the number of days of use of acute migraine-specific medication
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during the 6 months
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assessment of migraine effect on physical activity
時間枠:during the 6 months
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change in scores on the physical-impairment and everyday-activities domains of the Migraine Physical Function Impact Diary (scale transformed to 0 to 100, with higher score
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during the 6 months
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協力者と研究者
スポンサー
出版物と役立つリンク
一般刊行物
- Schoenen J, Manise M, Nonis R, Gérard P, Timmermans G. Monoclonal antibodies blocking CGRP transmission: An update on their added value in migraine prevention. Rev Neurol (Paris). 2020 Dec;176(10):788-803. doi: 10.1016/j.neurol.2020.04.027. Epub 2020 Aug 2. Review.
- Garland SG, Smith SM, Gums JG. Erenumab: A First-in-Class Monoclonal Antibody for Migraine Prevention. Ann Pharmacother. 2019 Sep;53(9):933-939. doi: 10.1177/1060028019835166. Epub 2019 Feb 27. Review.
研究記録日
主要日程の研究
研究開始 (実際)
一次修了 (実際)
研究の完了 (実際)
試験登録日
最初に提出
QC基準を満たした最初の提出物
最初の投稿 (実際)
学習記録の更新
投稿された最後の更新 (実際)
QC基準を満たした最後の更新が送信されました
最終確認日
詳しくは
本研究に関する用語
キーワード
追加の関連 MeSH 用語
その他の研究ID番号
- Erenumab in migraine
個々の参加者データ (IPD) の計画
個々の参加者データ (IPD) を共有する予定はありますか?
医薬品およびデバイス情報、研究文書
米国FDA規制医薬品の研究
米国FDA規制機器製品の研究
この情報は、Web サイト clinicaltrials.gov から変更なしで直接取得したものです。研究の詳細を変更、削除、または更新するリクエストがある場合は、register@clinicaltrials.gov。 までご連絡ください。 clinicaltrials.gov に変更が加えられるとすぐに、ウェブサイトでも自動的に更新されます。
Erenumabの臨床試験
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University of Maryland, BaltimoreAmgen終了しました