Clinical Study to Evaluate the Treatment Effect and Safety of BAY1817080 in Patients With Overactive Bladder (OAB)

Overactive Bladder Clinical Trial

— OVADER  

Official title:

A Randomized, Placebo-controlled, Double-blind, Parallel-group, Multi-center, Proof-of-concept Study to Assess the Efficacy and Safety of BAY 1817080 in Patients With Overactive Bladder (OAB) Over a 12-week Treatment Period

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT04545580
• Other study ID #: 19733
• Secondary ID: 2019-002575-34
• Status: Completed
• Phase: Phase 2
• Start date: September 16, 2020
• Est. completion date: January 21, 2022

Study information

• Verified date: December 2022
• Source: Bayer
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The aim of the study is to determine how well the drug BAY1817080 works in OAB patients with urgency urinary incontinence (UUI), defined as involuntary leakage of urine, accompanied or immediately preceded by a sudden compelling desire to void. BAY1817080 is a new drug under development which blocks proteins expressed on the sensory nerves in the bladder. These nerves seem to overreact in OAB patients. This study will test if the treatment with BAY1817080 will reduce the frequency of OAB symptoms. The frequency of OAB symptoms before the treatment and the frequency after 4, 8 and 12 weeks of treatment will be compared. Another important objective of this study will be the assessment of BAY1817080 safety and tolerability in this patient population. BAY1817080 will be compared to a "placebo". A placebo tablet looks like the study drug but does not have any medicine in it. Using a placebo helps to learn if the study drug works. Each participant is expected to take part in the study for about 5 months (around 20-22 weeks).

Recruitment information / eligibility

• Status: Completed
• Enrollment: 99
• Est. completion date: January 21, 2022
• Est. primary completion date: December 22, 2021
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

at screening:

• Adults = 18 years of age at the time of signing the informed consent
• Have "wet" OAB symptoms (urgency, frequency and urinary incontinence) for = 3 months prior to screening visit
• Women of childbearing potential (WOCBP) must agree to use acceptable effective or highly effective contraceptive methods
• Capable of giving signed informed consent
• Willing and able to complete the electronic bladder diary and questionnaires

at baseline (to be checked at V3, prior to randomization):

• Completion of all 3 days of 3-day electronic bladder diary during run-in phase
• Compliance of =80% with intake of study intervention during run-in
• Frequency of micturition on average = 8 episodes/24 hours during the run-in phase according to 3-day electronic bladder diary
• Frequency of urgency urinary incontinence on average = 1 episode/24 hours during the run-in phase according to 3-day electronic bladder diary

Exclusion Criteria:

• Polyuria known or based on the clinical evidence during the run-in phase recorded in the 3-day electronic bladder diary and the investigator´s clinical judgement
• Significant stress incontinence or mixed stress/urgency incontinence
• Post-void residual volume (PVR) > 150 mL at Visit 1 or at Visit 3
• In need of catheterization (indwelling or intermittent)
• Clinically significant urinary outflow obstruction
• Previous pelvic radiation, or previous or current malignant disease of pelvic organs
• Neurogenic bladder
• Bladder pain syndrome/interstitial cystitis
• Recurrent and/or symptomatic bladder stones
• Current symptomatic or recent (within 30 days prior to Visit 1), or recurrent (2 or more infections within 6 months, or > 3 infections within 12 months) urinary tract infection
• Unexplained macro- or micro-hematuria
• Diabetes insipidus
• Diabetes mellitus with inadequate glycemic control as indicated by HbA1C result of > 8% at screening
• Clinically significant cardiovascular or cerebrovascular disease
• Systolic blood pressure = 160 mmHg and/or diastolic blood pressure = 100 mmHg
• Clinically significant abnormal electrocardiogram (ECG) at screening
• Moderate-to-severe hepatic impairment defined as Child-Pugh Class B or C
• Laboratory values outside the inclusion range (as specified in the laboratory manual and in the reports from the central laboratory) before start of study intervention, and considered clinically relevant
• At screening:
• ALT above 2xULN OR
• AST above 2xULN OR
• total bilirubin greater than ULN OR
• AP above 2x ULN OR
• INR greater than ULN (unless on vitamin K antagonist treatment) OR
• Positive hepatitis B virus surface antigen (HBsAg) OR
• Positive hepatitis C virus antibodies (anti-HCV) and detection of mRNA (HCV-mRNA, only tested if hepatitis C virus antibodies were detected)
• Severe renal impairment as defined by estimated glomerular filtration rate (eGFR) < 30 mL/min/1.73 m^2 calculated by Modification of Diet in Renal Disease (MDRD) formula
• Any other diseases or conditions that according to the investigator can compromise the function of the body systems and could result in altered absorption, excessive accumulation, impaired metabolism, or altered excretion of the study intervention (e.g., excessively low body weight, Chronic bowel disease, Crohn's disease and ulcerative colitis)
• Any severe or unstable diseases or medical conditions including psychiatric disorders that might interfere with the conduct of the study, or could jeopardize the safety of the participant, or the interpretation of the results
• History of major depression within 2 years prior to screening, or a history of other major psychiatric disorder at any time (e.g., schizophrenia, bipolar disorder)
• Concurrent malignancy or history of cancer (except for adequately treated basal cell or squamous cell carcinoma of the skin) within the last 5 years prior to screening
• Intake of prohibited medication due to potential drug-drug interaction Use of other treatments that might interfere with the conduct of the study or the interpretation of the results e.g.
• a) use of any drug treatment after start of study intervention intended for the OAB/UI symptoms other than the study intervention
• b) neuromodulation therapy and intravesical treatment - less than 12 months prior to screening or at any time during the study
• c) use of any treatment intended for other conditions but which can affect urinary bladder function during the study
• d) Non-drug treatment (e.g. physical treatment or acupuncture): permitted only if initiated =4 weeks prior to Screening and planned to be continued during the study)

Related Conditions & MeSH terms

• Overactive Bladder
• Urinary Bladder, Overactive

Intervention

Drug:
• Placebo
Matching placebo for BAY1817080, will be taken twice daily orally as tablet(s)
• BAY1817080
BAY1817080 will be taken twice daily orally as tablet(s)

Locations

Country	Name	City	State
Australia	Emeritus Research	Botany	New South Wales
Australia	Emeritus Research	Camberwell	Victoria
Austria	Medizinische Universität Graz	Graz	Steiermark
Austria	Medizinische Universität Innsbruck	Innsbruck
Czechia	Afimed s.r.o	Benesov
Czechia	Gynekologie Cheb s.r.o.	Cheb
Czechia	G-Centrum Olomouc s.r.o. Dr. Skrivanek	Olomouc
Czechia	GynCare MUDr. Michael Svec s.r.o.	Plzen
Czechia	Urocentrum Praha, s.r.o.	Praha 2
Czechia	Androgeos - private center of urology and andrology	Praha 6
Czechia	Fakultní nemocnice Bulovka	Praha 8
Germany	Urologicum Duisburg - Praxis Walsum	Duisburg	Nordrhein-Westfalen
Germany	Praxis Hr. Dr. M. Markov	Halle	Sachsen-Anhalt
Germany	Urologicum	Lutherstadt Eisleben	Sachsen-Anhalt
Germany	Überörtliche Gemeinschaftspraxis "Urologie Neandertal"	Mettmann	Nordrhein-Westfalen
New Zealand	Canterbury Urology Research Trust	Christchurch
New Zealand	Tauranga Urology Research Limited	Tauranga
Poland	Medico Praktyka Lekarska	Krakow
Poland	NZOZ NOVITA, Specjalistyczne Gabinety Lekarskie S.C	Lublin
Poland	Centrum Urologiczne Sp. z o.o.	Myslowice
Poland	NZOZ Heureka	Piaseczno
Poland	Przychodnia Lekarska Eskulap	Skierniewice
Portugal	CHULN - Hospital Santa Maria	Lisboa
Portugal	Centro Hospitalar Universitario do Porto	Porto
Portugal	CHUSJ - Hospital Sao Joao	Porto
Singapore	KK Women's and Children's Hospital	Singapore
Sweden	Göteborgs Urologmottagning	Göteborg
Sweden	Urogyn	Solna

Sponsors (1)

Lead Sponsor	Collaborator
Bayer

Countries where clinical trial is conducted

Australia,  Austria,  Czechia,  Germany,  New Zealand,  Poland,  Portugal,  Singapore,  Sweden, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Average change from baseline over Week 4, 8 and 12 (end of treatment [EoT]) in mean number of urgency urinary incontinence (UUI) episodes/24 hours based on electronic bladder diary		From baseline up to 12 weeks
Secondary	Change from baseline to Week 12 (EoT) based on electronic bladder diary in mean number of UUI episodes/24 hours		From baseline up to 12 weeks
Secondary	Change from baseline to Week 12 (EoT) based on electronic bladder diary in mean number of urinary incontinence (UI) episodes/24 hours		From baseline up to 12 weeks
Secondary	Change from baseline to Week 12 (EoT) based on electronic bladder diary in mean number of micturition episodes/24 hours		From baseline up to 12 weeks
Secondary	Change from baseline to Week 12 (EoT) based on electronic bladder diary in mean number of urgency episodes (Grade 3 or 4)/24 hours		From baseline up to 12 weeks
Secondary	Change from baseline to Week 12 (EoT) based on electronic bladder diary in mean number of nocturia episodes/24 hours		From baseline up to 12 weeks
Secondary	Change from baseline to Week 12 (EoT) based on electronic bladder diary in mean volume voided per micturition		From baseline up to 12 weeks
Secondary	Incidence of adverse events		From the start of study intervention (at start of run-in) until the follow-up visit (up to 18 weeks)

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