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

27 lipca 2026 zaktualizowane przez: 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.

Przegląd badań

Status

Jeszcze nie rekrutacja

Warunki

Interwencja / Leczenie

Szczegółowy opis

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.

Typ studiów

Interwencyjne

Zapisy (Szacowany)

126

Faza

  • Faza 2

Kontakty i lokalizacje

Ta sekcja zawiera dane kontaktowe osób prowadzących badanie oraz informacje o tym, gdzie badanie jest przeprowadzane.

Kontakt w sprawie studiów

Kryteria uczestnictwa

Badacze szukają osób, które pasują do określonego opisu, zwanego kryteriami kwalifikacyjnymi. Niektóre przykłady tych kryteriów to ogólny stan zdrowia danej osoby lub wcześniejsze leczenie.

Kryteria kwalifikacji

Wiek uprawniający do nauki

  • Dorosły
  • Starszy dorosły

Akceptuje zdrowych ochotników

Nie

Opis

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)

Plan studiów

Ta sekcja zawiera szczegółowe informacje na temat planu badania, w tym sposób zaprojektowania badania i jego pomiary.

Jak projektuje się badanie?

Szczegóły projektu

  • Główny cel: Leczenie
  • Przydział: Randomizowane
  • Model interwencyjny: Przydział równoległy
  • Maskowanie: Potroić

Broń i interwencje

Grupa uczestników / Arm
Interwencja / Leczenie
Aktywny komparator: 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
Aktywny komparator: 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
Komparator placebo: 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
Komparator placebo: 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

Co mierzy badanie?

Podstawowe miary wyniku

Miara wyniku
Opis środka
Ramy czasowe
Percent Change from Baseline in Total Prostate Volume (TPV) at Week 12
Ramy czasowe: 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

Miary wyników drugorzędnych

Miara wyniku
Opis środka
Ramy czasowe
To assess the AUR clinical benefit rate of Teverelix DP after a single dose
Ramy czasowe: 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
Ramy czasowe: 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.
Ramy czasowe: 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.
Ramy czasowe: 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)
Ramy czasowe: 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)
Ramy czasowe: 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)
Ramy czasowe: 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.
Ramy czasowe: 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).
Ramy czasowe: 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.
Ramy czasowe: 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.
Ramy czasowe: From Day 1 through study completion (an average of 1 year)
From Day 1 through study completion (an average of 1 year)

Współpracownicy i badacze

Tutaj znajdziesz osoby i organizacje zaangażowane w to badanie.

Sponsor

Daty zapisu na studia

Daty te śledzą postęp w przesyłaniu rekordów badań i podsumowań wyników do ClinicalTrials.gov. Zapisy badań i zgłoszone wyniki są przeglądane przez National Library of Medicine (NLM), aby upewnić się, że spełniają określone standardy kontroli jakości, zanim zostaną opublikowane na publicznej stronie internetowej.

Główne daty studiów

Rozpoczęcie studiów (Szacowany)

1 września 2026

Zakończenie podstawowe (Szacowany)

1 maja 2028

Ukończenie studiów (Szacowany)

1 maja 2028

Daty rejestracji na studia

Pierwszy przesłany

15 lipca 2026

Pierwszy przesłany, który spełnia kryteria kontroli jakości

27 lipca 2026

Pierwszy wysłany (Rzeczywisty)

29 lipca 2026

Aktualizacje rekordów badań

Ostatnia wysłana aktualizacja (Rzeczywisty)

29 lipca 2026

Ostatnia przesłana aktualizacja, która spełniała kryteria kontroli jakości

27 lipca 2026

Ostatnia weryfikacja

1 lipca 2026

Więcej informacji

Terminy związane z tym badaniem

Inne numery identyfikacyjne badania

  • ANT-2111-02

Informacje o lekach i urządzeniach, dokumenty badawcze

Bada produkt leczniczy regulowany przez amerykańską FDA

Tak

Bada produkt urządzenia regulowany przez amerykańską FDA

Nie

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