- ICH GCP
- Реестр клинических исследований США
- Клиническое испытание NCT07733934
Study of Teverelix DP on Prostate Volume, Urinary Function and Clinical Outcomes Following Acute Urinary Retention
A Randomized, Double-Blind, Placebo-Controlled, Multi-centre Study to Evaluate the Effects of Teverelix DP, a GnRH Antagonist, on Prostate Volume, Urinary Function and Clinical Outcomes in Men Following a First Episode of Acute Urinary Retention (AUR)
This randomized, double-blind, placebo-controlled Phase 2 study is evaluating Teverelix DP in men following a first episode of acute urinary retention (AUR) associated with benign prostatic hyperplasia (BPH), a population at risk of recurrent urinary retention and subsequent surgical or minimally invasive intervention.
The study is designed to evaluate the effects of Teverelix DP on total prostate volume and urinary function and to prospectively evaluate clinically meaningful outcomes including recurrent AUR, BPH-related surgical or minimally invasive intervention, protocol-defined treatment failure and clinical benefit.
Participants will be randomized to one of four treatment groups evaluating two active Teverelix DP regimens: 90 mg administered intramuscularly (IM) and 120 mg administered subcutaneously (SC) and their respective matched placebo controls.
The primary endpoint is percent change from baseline in total prostate volume (TPV) at Week 12. Participants will continue to be evaluated during the 28-week treatment period for urinary function and prospectively defined clinical outcomes, including recurrent AUR, BPH-related intervention, treatment failure and clinical benefit, and will be followed through Week 52 for protocol-defined longer-term assessments and safety follow-up.
The study is designed to characterize biological activity, urinary function, clinical outcomes, safety and the relative treatment effects of the two Teverelix DP regimens to inform dose and route selection and subsequent clinical development.
Обзор исследования
Статус
Подробное описание
Тип исследования
Регистрация (Оцененный)
Фаза
- Фаза 2
Контакты и местонахождение
Контакты исследования
- Имя: Ruhena Chowdhury, PhD
- Номер телефона: +4407491167075
- Электронная почта: rchowdhury@antev.co.uk
Критерии участия
Критерии приемлемости
Возраст, подходящий для обучения
- Взрослый
- Пожилой взрослый
Принимает здоровых добровольцев
Описание
Inclusion Criteria:
- Male aged 45 years or older
- Having given his written consent
- Successful TWOC as defined by successful voiding with a minimum residual volume
- Having had a first episode of spontaneous acute urinary retention within 6 days of study screening visit.
- Prostate volume >40 g (assessed by TRUS)
- Patients may initiate or continue alpha-blocker therapy at or before randomization. The same agent and dose should be continued throughout the treatment period where possible
Agrees to practice contraception during the entire study treatment period and for 3 months after the last dose of IMP is administered:
- Either by using double barrier contraception and in compliance with local guidelines,
- or, is truly sexually abstinent, when this is in line with the preferred and usual lifestyle of the patient
i. Note: Periodic abstinence [e.g. calendar, ovulation, symptothermal, postovulation methods for the female partner with childbearing potential] and withdrawal are not acceptable methods of contraception.
- Must be treatment naïve to GnRH analogues
Exclusion Criteria:
- Participated in another investigational study within 3 months before recruitment
- AUR due to i.e. postoperative retention following major abdominal/pelvis/spinal surgery
- Neurological related AUR
- Contraindication to the use of alpha blockers
- Previous prostate or urethral surgery
- Previous histological or clinical diagnosis of prostate cancer
- Any unstable co-existing medical condition
Has abnormal screening and/or baseline laboratory values that suggest a clinically significant underlying disease, or the following laboratory values:
- Liver function test (aspartate aminotransferase [ASAT/SGOT], alanine aminotransferase [ALAT/SGPT]), exceeding >2X the upper limit of the normal (ULN) range
- Total bilirubin exceeding >1.5X the upper limit of the normal (ULN) range
- An estimated glomerular filtration rate (eGFR) < 30 mL/min, based on creatinine clearance calculation by the Chronic Kidney Disease Epidemiology Collaboration (CKD-EPI) equation normalised to an average surface area of 1.73m2, at the screening visit.
Has congenital long QT syndrome or ECG abnormalities at screening of:
- Q-wave infarction, unless identified ≥6 months before screening
- Fridericia corrected QT interval (QTcF interval) >480 msec. If QTcF is prolonged in a patient with a pacemaker, the patient may be enrolled in the study upon discussion with the project clinician
- If the QTcF interval is 450-480 msec, inclusive, in a patient with current use of medications with known effects on QT interval, the patient may be enrolled in the study following discussion with the Medical Lead
Note: Cardiac arrhythmia grading:
- Bradyarrhythmias (HR <60/min)
- Tachyarrhythmias (HR >100/min
- Supraventricular arrhythmias - arrhythmias that originate in the sinoatrial node, atrial myocardium or atrioventricular node (regular QRS complex)
- Ventricular arrhythmias - arrhythmias that originate below the atrioventricular node (wide QRS complex)
- History or current evidence of alcohol or drug abuse within the last 12 months
- Prostate Specific Antigen (PSA) greater than 20ng/ml
- Use of suprapubic catheterization after failed urethral catheterization
- Neurogenic bladder dysfunction, confirmed or suspected, irrespective of etiology
- Isolated bladder neck disease
- Acute or chronic prostatitis
- Confirmed or suspected urethral stricture
- Known bladder stones
Use of the following medications prior to and during study participation:
- Any other IMP (within 3 months of enrolment)
- Herbal medications known to have anti-androgenic effects (e.g. red reishi, licorice, white peony, green tea, spearmint, black cohosh, chaste tree, saw palmetto, etc) (within 3 months of enrolment)
- Anti-androgen therapy (within 3 months of enrolment)
- T replacement therapy (within 3 months of enrolment)
- 5α-reductase inhibitor treatment etc. (within 25 weeks prior to screening: dutasteride; within 12 weeks prior to screening: finasteride (and others))
- Bethanechol chloride
- Any other medication or herbal product that may affect hormone levels and might, therefore, confound interpretation of the study results (e.g. St. John's wort) (within 3 months of enrolment)
Учебный план
Как устроено исследование?
Детали дизайна
- Основная цель: Уход
- Распределение: Рандомизированный
- Интервенционная модель: Параллельное назначение
- Маскировка: Тройной
Оружие и интервенции
Группа участников / Армия |
Вмешательство/лечение |
|---|---|
|
Активный компаратор: Teverelix DP 90 mg IM
|
Single dose at Day 1 of 90 mg injection IM
Single dose at Day 1 of 120 mg injection SC
|
|
Активный компаратор: Teverelix DP 120 mg SC
|
Single dose at Day 1 of 90 mg injection IM
Single dose at Day 1 of 120 mg injection SC
|
|
Плацебо Компаратор: Teverelix DP placebo 90 mg IM
|
Single dose at Day 1 of 90 mg injection IM
Single dose at Day 1 of 120 mg injection SC
|
|
Плацебо Компаратор: Teverelix DP placebo 120 mg SC
|
Single dose at Day 1 of 90 mg injection IM
Single dose at Day 1 of 120 mg injection SC
|
Что измеряет исследование?
Первичные показатели результатов
Мера результата |
Мера Описание |
Временное ограничение |
|---|---|---|
|
Percent Change from Baseline in Total Prostate Volume (TPV) at Week 12
Временное ограничение: Change from baseline to Week 12
|
Percent change from baseline in total prostate volume as assessed by transrectal ultrasound.
|
Change from baseline to Week 12
|
Вторичные показатели результатов
Мера результата |
Мера Описание |
Временное ограничение |
|---|---|---|
|
To assess the AUR clinical benefit rate of Teverelix DP after a single dose
Временное ограничение: From dosing to week 52
|
The proportion of patients meeting all of the following criteria during the 28-week treatment period and the 52-week observation period:
|
From dosing to week 52
|
|
Evaluate the durability of prostate volume reduction following a single dose of Teverelix DP
Временное ограничение: Change from baseline to week 52
|
Percent change in total prostate volume
|
Change from baseline to week 52
|
|
Change from baseline in post-void residual volume (PVR) (mL), assessed by ultrasound.
Временное ограничение: Change from baseline to week 28
|
Change from baseline to week 28
|
|
|
Change from baseline in maximum urinary flow rate (Qmax) (mL/sec), using Uroflowmetry.
Временное ограничение: Change from baseline to week 28
|
Change from baseline to week 28
|
|
|
Explore the correlation between change prostate volume and change in post-void residual volume (PVR) (mL)
Временное ограничение: Change from baseline to week 28
|
Change from baseline to week 28
|
|
|
Explore the correlation between change prostate volume and change in maximum urinary flow rate (Qmax) (mL/sec)
Временное ограничение: Change from baseline to week 28
|
Change from baseline to week 28
|
|
|
Incidence of AUR recurrence according to Teverelix dose (90 mg vs 120 mg) and route of administration (IM vs SC)
Временное ограничение: From Day 1 through study completion (an average of 1 year)
|
Identifying the optimal dosing regimen and route of administration from the following; 90 mg or 120 mg of Teverelix DP and intramuscular (IM) or subcutaneous (SC).
|
From Day 1 through study completion (an average of 1 year)
|
|
To assess time to Post-void residual (PVR) >60% of total bladder volume, measured by ultrasound.
Временное ограничение: From Day 1 through study completion (an average of 1 year)
|
PVR volume measurements will be taken at various timepoints in the study to assess the time taken for PVR >60% of total bladder volume
|
From Day 1 through study completion (an average of 1 year)
|
|
Incidence of Treatment-Emergent Adverse Events (Safety and Tolerability) of Teverelix DP in men with AUR secondary to benign prostatic hyperplasia (BPH).
Временное ограничение: From Day 1 through study completion (an average of 1 year)
|
Safety and tolerability will be evaluated by the incidence, nature, severity, and relationship to study treatment of adverse events (AEs) and serious adverse events (SAEs), together with assessments of clinical laboratory parameters, vital signs, physical examinations, electrocardiograms (ECGs), concomitant medications, and any clinically significant findings observed throughout the study.
|
From Day 1 through study completion (an average of 1 year)
|
|
To assess progression of BPH-related symptoms.
Временное ограничение: Change from Day 1 through study completion (an average of 1 year)
|
The International Prostate Symptom Score (IPSS) will be used to assess progression of BPH-related symptoms.
The total IPSS score is calculated by summing the scores from all seven questions, giving a range of 0 to 35.
Change in IPSS score will be reviewed.
Lower scores indicate fewer or less severe urinary symptoms, and higher scores indicate more severe urinary symptoms.
|
Change from Day 1 through study completion (an average of 1 year)
|
|
To assess the incidence of BPH-related minimally invasive procedures or surgeries. Procedure/surgery review will completed at visits throughout the study.
Временное ограничение: From Day 1 through study completion (an average of 1 year)
|
From Day 1 through study completion (an average of 1 year)
|
Соавторы и исследователи
Спонсор
Даты записи исследования
Изучение основных дат
Начало исследования (Оцененный)
Первичное завершение (Оцененный)
Завершение исследования (Оцененный)
Даты регистрации исследования
Первый отправленный
Впервые представлено, что соответствует критериям контроля качества
Первый опубликованный (Действительный)
Обновления учебных записей
Последнее опубликованное обновление (Действительный)
Последнее отправленное обновление, отвечающее критериям контроля качества
Последняя проверка
Дополнительная информация
Термины, связанные с этим исследованием
Ключевые слова
Дополнительные соответствующие термины MeSH
Другие идентификационные номера исследования
- ANT-2111-02
Информация о лекарствах и устройствах, исследовательские документы
Изучает лекарственный продукт, регулируемый FDA США.
Изучает продукт устройства, регулируемый Управлением по санитарному надзору за качеством пищевых продуктов и медикаментов США.
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