Идёт набор NCT06927999

An Outpatient Study of the Efficacy of ARS-2 in Patients With Chronic Spontaneous Urticaria

Фаза II С лечением Urticaria Chronic

Ориентир для пациента и семьи

Простыми словами

Автоматическая сводка по структурированным данным реестра. Она помогает сориентироваться, но не заменяет официальный протокол или оценку врача.

Что изучают: В протоколе указаны: Placebo, 0.5 mg epinephrine, 1 mg epinephrine.
Кому может быть актуально: Состояния в реестре: Urticaria Chronic. Базовые параметры: 18 лет — 65 лет · Все.
Что важно проверить: Возраст, диагноз и пол — только базовые ориентиры. Предыдущее лечение, анализы и другие обязательные условия указаны ниже в критериях участия.
Где проводится: США, Германия
Следующий шаг: Сохраните исследование, покажите его лечащему врачу и уточните актуальный статус у исследовательского центра. Расходы, документы и поездка →

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Официальное название

An Outpatient, Randomized, Double-Blinded, Placebo-Controlled, Cross-Over Study of the Efficacy of ARS-2 in Patients With Chronic Spontaneous Urticaria

Обзор

This is a Phase 2b, outpatient, single-dose, randomized, double blind, placebo-controlled, three period crossover study that will consist of a screening period and three blinded treatment periods. Subjects enrolled will have CSU with a history of moderate to severe acute exacerbations (or flares).

Вмешательства

Препарат Placebo
Placebo solution nasal spray containing no active drug
Препарат 0.5 mg epinephrine
0.5 mg epinephrine per spray
Препарат 1 mg epinephrine
1 mg epinephrine per spray

Первичные конечные точки

Determine the effect of ARS-2 (0.5 mg or 1 mg) versus placebo on itch and hive [Срок оценки: 12 months]

Критерии участия

Критерии включения

Is a male or female between the ages of 18 and 65 years, inclusive.
Has been clinically diagnosed with CSU and experiences an acute flare of moderate to severe urticaria symptoms (itch and hive severity UAS score ≥ 2) approximately 1-2 times a month or every other month consistently during the past year while on a chronic treatment.
Has been on a daily chronic treatment for ≥ 6 weeks.
Is willing to use a smartphone study application to record study assessments and AEs.
Has body weight more than 15 kilogram (kg).
Has no medical history of clinically significant hypertension and cardiovascular disease in the last 10 years
If female, is not pregnant or breastfeeding based on a negative urine pregnancy test at baseline.
Is able to communicate clearly with the Investigator and staff; able to read, complete questionnaires, and perform study procedures on the smartphone study application.
Is willing and able to provide written informed consent prior to participating in the study.
Controlled hypertension without beta blocker confirmed by the Investigator is acceptable.
At screening, has stable vital signs in the following ranges (after 5 minutes of rest):

Systolic blood pressure (SBP) ≥90 and ≤140 milliliters of mercury (mmHg)
Diastolic blood pressure (DBP) ≥50 and ≤90 mmHg
Heart rate (HR) ≥45 and ≤100 beats per minute (bpm)

Критерии исключения

Has a history of clinically significant gastrointestinal, renal, hepatic, neurologic, hematologic, endocrine, oncologic, pulmonary, immunologic, psychiatric, or cardiovascular disease or any other condition which, in the opinion of the Investigator, would jeopardize the safety of the subject or impact the validity of the study results.
Has any clinically significant medical condition or PE finding as deemed inappropriate by the Investigator.
Has abnormal cardiovascular exam at screening including any prior history of myocardial infarction or clinically significant abnormal electrocardiogram (ECG)
Has had significant traumatic injury or major surgery within 30 days prior to study screening.
Known hypersensitivity to any compound in the test product, or any other closely related compound (e.g., dihydropyridine-derived molecules).
Has participated in a clinical trial within 30 days prior to the first dose of study drug.
Has an immediate family member of the Investigator, or an employee of the study center, with direct involvement in the proposed study, or other studies under the direction of the Investigator or study center or is in a dependent relationship with a study center employee who is involved in the conduct of this study (e.g., spouse, parent, child, sibling), or may consent under duress.

Критерии приведены из реестра в оригинале (на английском). Окончательную оценку соответствия проводит исследовательский центр.

Здоровые добровольцы: Нет