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Study of Teverelix DP on Prostate Volume, Urinary Function and Clinical Outcomes Following Acute Urinary Retention

2026年7月27日 更新者:Antev Ltd.

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.

調査の概要

詳細な説明

An interim analysis of the primary endpoint will be conducted after at least 50% of patients have completed their 12-week visit. The interim analysis may also be used to inform future development strategy for Teverelix DP. Should the interim data demonstrate supportive safety and pharmacodynamic trends, the Sponsor may consider expansion of the clinical development program into a confirmatory Phase 3 trial.

研究の種類

介入

入学 (推定)

126

段階

  • フェーズ2

連絡先と場所

このセクションには、調査を実施する担当者の連絡先の詳細と、この調査が実施されている場所に関する情報が記載されています。

研究連絡先

参加基準

研究者は、適格基準と呼ばれる特定の説明に適合する人を探します。これらの基準のいくつかの例は、人の一般的な健康状態または以前の治療です。

適格基準

就学可能な年齢

  • 大人
  • 高齢者

健康ボランティアの受け入れ

いいえ

説明

Inclusion Criteria:

  1. Male aged 45 years or older
  2. Having given his written consent
  3. Successful TWOC as defined by successful voiding with a minimum residual volume
  4. Having had a first episode of spontaneous acute urinary retention within 6 days of study screening visit.
  5. Prostate volume >40 g (assessed by TRUS)
  6. 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
  7. Agrees to practice contraception during the entire study treatment period and for 3 months after the last dose of IMP is administered:

    1. Either by using double barrier contraception and in compliance with local guidelines,
    2. 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.

  8. Must be treatment naïve to GnRH analogues

Exclusion Criteria:

  1. Participated in another investigational study within 3 months before recruitment
  2. AUR due to i.e. postoperative retention following major abdominal/pelvis/spinal surgery
  3. Neurological related AUR
  4. Contraindication to the use of alpha blockers
  5. Previous prostate or urethral surgery
  6. Previous histological or clinical diagnosis of prostate cancer
  7. Any unstable co-existing medical condition
  8. Has abnormal screening and/or baseline laboratory values that suggest a clinically significant underlying disease, or the following laboratory values:

    1. Liver function test (aspartate aminotransferase [ASAT/SGOT], alanine aminotransferase [ALAT/SGPT]), exceeding >2X the upper limit of the normal (ULN) range
    2. Total bilirubin exceeding >1.5X the upper limit of the normal (ULN) range
    3. 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.
  9. Has congenital long QT syndrome or ECG abnormalities at screening of:

    1. Q-wave infarction, unless identified ≥6 months before screening
    2. 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
    3. 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)
  10. History or current evidence of alcohol or drug abuse within the last 12 months
  11. Prostate Specific Antigen (PSA) greater than 20ng/ml
  12. Use of suprapubic catheterization after failed urethral catheterization
  13. Neurogenic bladder dysfunction, confirmed or suspected, irrespective of etiology
  14. Isolated bladder neck disease
  15. Acute or chronic prostatitis
  16. Confirmed or suspected urethral stricture
  17. Known bladder stones
  18. Use of the following medications prior to and during study participation:

    1. Any other IMP (within 3 months of enrolment)
    2. 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)
    3. Anti-androgen therapy (within 3 months of enrolment)
    4. T replacement therapy (within 3 months of enrolment)
    5. 5α-reductase inhibitor treatment etc. (within 25 weeks prior to screening: dutasteride; within 12 weeks prior to screening: finasteride (and others))
    6. Bethanechol chloride
    7. 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)

研究計画

このセクションでは、研究がどのように設計され、研究が何を測定しているかなど、研究計画の詳細を提供します。

研究はどのように設計されていますか?

デザインの詳細

  • 主な目的:処理
  • 割り当て:ランダム化
  • 介入モデル:並列代入
  • マスキング:トリプル

武器と介入

参加者グループ / アーム
介入・治療
アクティブコンパレータ: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
アクティブコンパレータ: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
プラセボコンパレーター: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
プラセボコンパレーター: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

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
Percent Change from Baseline in Total Prostate Volume (TPV) at Week 12
時間枠: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

二次結果の測定

結果測定
メジャーの説明
時間枠
To assess the AUR clinical benefit rate of Teverelix DP after a single dose
時間枠: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:

  • No relapse of AUR;
  • No need or indication for surgical intervention; and
  • No occurrence of treatment failure (PVR >300 mL with Qmax <10 mL/sec).
From dosing to week 52
Evaluate the durability of prostate volume reduction following a single dose of Teverelix DP
時間枠: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.
時間枠: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.
時間枠: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)
時間枠: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)
時間枠: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)
時間枠: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.
時間枠: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).
時間枠: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.
時間枠: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.
時間枠:From Day 1 through study completion (an average of 1 year)
From Day 1 through study completion (an average of 1 year)

協力者と研究者

ここでは、この調査に関係する人々や組織を見つけることができます。

スポンサー

研究記録日

これらの日付は、ClinicalTrials.gov への研究記録と要約結果の提出の進捗状況を追跡します。研究記録と報告された結果は、国立医学図書館 (NLM) によって審査され、公開 Web サイトに掲載される前に、特定の品質管理基準を満たしていることが確認されます。

主要日程の研究

研究開始 (推定)

2026年9月1日

一次修了 (推定)

2028年5月1日

研究の完了 (推定)

2028年5月1日

試験登録日

最初に提出

2026年7月15日

QC基準を満たした最初の提出物

2026年7月27日

最初の投稿 (実際)

2026年7月29日

学習記録の更新

投稿された最後の更新 (実際)

2026年7月29日

QC基準を満たした最後の更新が送信されました

2026年7月27日

最終確認日

2026年7月1日

詳しくは

本研究に関する用語

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

はい

米国FDA規制機器製品の研究

いいえ

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