Zavegepant Intranasal Spray for the Acute Treatment of Episodic Cluster Headache
2026年7月14日 更新者:Mark J Burish、The University of Texas Health Science Center, Houston
Zavegepant Intranasal Spray for the Acute Treatment of Episodic Cluster Headache: A Prospective, Open-Label, Single-Arm, Interventional Pilot Study
The purpose of this study is to assess headache response rate for minimal pain at 30 minutes following zavegepant administration and to assess additional effectiveness and treatment failure endpoints at various timepoints after zavegepant administration
研究概览
研究类型
介入性
注册 (估计的)
40
阶段
- 阶段2
联系人和位置
本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。
学习联系方式
- 姓名:Mark J Burish, MD, PhD
- 电话号码:713-486-7771
- 邮箱:nctt.wec@uth.tmc.edu
学习地点
-
-
Texas
-
Houston、Texas、美国、77030
- The University of Texas Health Science Center at Houston
-
接触:
- Mark J Burish, MD,PhD
- 电话号码:(713) 704-3127
- 邮箱:Mark.J.Burish@uth.tmc.edu
-
-
参与标准
研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。
资格标准
适合学习的年龄
- 成人
- 年长者
接受健康志愿者
不
描述
Inclusion Criteria:
- A diagnosis of episodic cluster headache according to the International Classification of Headache Disorders 3rd edition
- A history of at least 2 prior headache bouts
- Onset of cluster headache before age 50 years
- Cluster headache attacks last a minimum duration of 45 minutes (if untreated)
- Evidence of signed informed consent (ICF) as described in the protocol, indicating compliance with the requirements and restrictions listed in the ICF and this protocol
Exclusion Criteria:
General exclusions
- Pregnant or breastfeeding patients.
- Inability to follow training instructions for use of nasal device.
- Unable to speak or read English.
- Unable to access the internet (for the Questionnaires / Case Report Forms).
- Females of childbearing potential, without the ability to use 2 acceptable methods of contraception to avoid pregnancy for up to 48 hours after each study drug administration, followed by 1 acceptable method for 28 days after the last administration of study treatment.
- Body mass index ≥ 35 kg/m2
- Prisoners or subjects who are involuntarily incarcerated.
- Subjects who are compulsorily detained for treatment of either a psychiatric or physical (e.g., infectious disease) illness.
- Have participated in another clinical research study with biological investigational agents (or other relevant agents) in the last 90 days.
- Positive drug screen for drugs of abuse at the investigator's discretion (e.g., positive amphetamines may be allowed when prescribed for an approved indication such as ADHD)
Past medical history exclusions:
- Co-existing disease or other characteristics that precludes appropriate diagnosis of cluster headache. Other headache and facial pain disorders are allowed as long as their attacks are distinguishable from cluster headache attacks
- Currently uncontrolled, unstable, or recently diagnosed cardiovascular or neurovascular disease, Raynaud's disease, uncontrolled hypertension, a history of myocardial infarction , Acute Coronary Syndrome (ACS), Percutaneous Coronary Intervention (PCI), cardiac surgery, stroke or Transient Ischemic Attack (TIA) in the prior 6 months
- A known history of severe hepatic impairment, or diagnosis of Gilbert's Syndrome or any other active hepatic or biliary disorder
- A history of Human Immunodeficiency Virus (HIV).
- Active drug or alcohol use or dependence that, in the opinion of the site investigator, would interfere with adherence to study requirements
- Response of "yes" to Question 4 or 5 for suicidal ideation, or any suicidal behavioral question on the Columbia Suicide Severity Rating Scale (C-SSRS) at screening (or up to 1 year prior to the screening, as assessed in the medical history), or any indication of serious risk of suicide in the opinion of the investigator
- Psychiatric disorders that, in the opinion of the site investigator, would interfere with adherence to study requirements. This includes participants who have confirmed but untreated psychiatric disorders, or have psychiatric disorders that, in the opinion of the site investigator, would make them unable to undergo an ECG, have laboratory testing, or administer the medication at the appropriate time. "Psychiatric disorders" refers specifically to the following Diagnostic and Statistical Manual of Mental Disorders, 5th Edition (DSM-5) classes of disorders: Schizophrenia Spectrum and Other Psychotic Disorders, Bipolar and Related Disorders, Depressive Disorders, Anxiety Disorders, Obsessive-Compulsive and Related Disorders, Trauma- and Stressor-Related disorders, Dissociative Disorders, Somatic Symptom and Related Disorders, Feeding and Eating Disorders, Disruptive, Impulse-Control and Conduct Disorders, Substance-Related and Addictive Disorders, or Neurocognitive Disorders
- Hematologic or solid malignancy diagnosis within 5 years prior to the screening visit. Subjects with a history of localized basal cell or squamous cell skin cancer are eligible for the study if they are cancer-free prior to the screening visit
Nasal issues
- History of nasal surgery in the 6 months preceding the screening visit
- Nose piercings that might interfere with positioning of the study medication
- Evidence at screening of significant nasal conditions that may affect the administration or absorption of the nasal product (e.g., severe septum deviation, nasal deformity or blockage, inflammation, perforation, mucosal erosion or ulceration, polyposis, nasal trauma) as evaluated by the Investigator or medically qualified delegate
- Prominent nasal congestion or rhinorrhea associated with cluster headache attacks that, in the opinion of the study team, will interfere with ipsilateral absorption of a nasal spray
Laboratory and ECG abnormalities within 3 months of screening including:
- ECG abnormalities including Corrected QT interval (QTc) > 470 msec, Left Bundle Branch Block (LBB), Right Bundle Branch Block (RBB) with QRS>150 msec, or Intraventricular Conduction Defect with a QRS duration ≥ 150 msec
- History of stage 4 renal disease (creatinine clearance<30 mL/min)
- Any unacceptable findings on laboratory studies or physical examination including bilirubin >1.5x upper limit of normal(ULN), Neutrophil count ≤ 1000/uL (or equivalent), Aspartate Aminotransferase (AST) or Alanine Aminotransferase (ALT) >1.5x ULN
- Uncontrolled diabetes, defined as HbA1c ≥ 7.5%
Zavegepant-specific exclusions
- History of hypersensitivity reaction to zavegepant or to any of the components of zavegepant
- Previous use of zavegepant, or previously intolerant of zavegepant (if tried for noncluster headache reasons)
- Concomitant use of potent inhibitors/inducers of Organic Anion Transporting Polypeptide 1B3 (OATP1B3) or Sodium/Taurocholate Cotransporting Polypeptide (NTCP) transporters including atazanavir, clarithromycin, cyclosporine, estrone sulfate, lopinavir, gemfibrozil, rifampin, or ritonavir
学习计划
本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。
研究是如何设计的?
设计细节
- 主要用途:治疗
- 分配:不适用
- 介入模型:单组作业
- 屏蔽:无(打开标签)
武器和干预
参与者组/臂 |
干预/治疗 |
|---|---|
|
实验性的:Zavegepant
|
Participants will administer zavegepant 10 mg twice in quick succession (once into the left nostril, once into the right nostril, for a total of 20mg) to treat up to 3 separate cluster headache attacks maintaining a minimum interval of 48 hours between administrations.
|
研究衡量的是什么?
主要结果指标
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
Percentage of participants who achieve minimal pain at 30 minutes following their first administration of zavegepant 20mg.
大体时间:end of study (up to 70 days from baseline)
|
Minimal pain is defined as 0 or 1 on the 0-4 numerical rating scale.
|
end of study (up to 70 days from baseline)
|
次要结果测量
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
Percentage of participants who achieve minimal pain at 15 minutes following zavegepant administration
大体时间:end of study (up to 70 days from baseline)
|
Minimal pain is defined as 0 or 1 on the 0-4 numerical rating scale.
|
end of study (up to 70 days from baseline)
|
|
Percentage of participants who achieve pain freedom at 30 minutes following zavegepant administration
大体时间:end of study (up to 70 days from baseline)
|
Pain freedom is defined as 0 on the 0-4 numerical rating scale.
|
end of study (up to 70 days from baseline)
|
|
Percentage of participants who achieve pain freedom at 15 minutes following zavegepant administration
大体时间:end of study (up to 70 days from baseline)
|
Pain freedom is defined as 0 on the 0-4 numerical rating scale.
|
end of study (up to 70 days from baseline)
|
|
Percentage of participants who use rescue therapy between 30-180 minutes following zavegepant administration
大体时间:end of study (up to 70 days from baseline)
|
end of study (up to 70 days from baseline)
|
|
|
Treatment failure as assessed by the percentage of participants with cluster headache recurrence within 3 hours
大体时间:end of study (up to 70 days from baseline)
|
Pain recurrence is defined as both of the following: 1.
A pain intensity of 0 or 1 on a 0-4 numerical rating scale at 30 minutes post-dose, and 2. pain intensity of 3 or 4 (on a 0-4 numerical rating scale) at any point between 30 minutes post-dose and 180 minutes post headache onset
|
end of study (up to 70 days from baseline)
|
合作者和调查者
在这里您可以找到参与这项研究的人员和组织。
合作者
调查人员
- 首席研究员:Mark J Burish, MD, PhD、The University of Texas Health Science Center, Houston
研究记录日期
这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。
研究主要日期
学习开始 (估计的)
2026年10月1日
初级完成 (估计的)
2028年4月1日
研究完成 (估计的)
2028年5月1日
研究注册日期
首次提交
2026年7月14日
首先提交符合 QC 标准的
2026年7月14日
首次发布 (实际的)
2026年7月20日
研究记录更新
最后更新发布 (实际的)
2026年7月20日
上次提交的符合 QC 标准的更新
2026年7月14日
最后验证
2026年7月1日
更多信息
此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.