Status:
COMPLETED
Effects of Rec 0/0438 in Patients With Neurogenic Detrusor Overactivity Due to Spinal Cord Injury
Lead Sponsor:
RECORDATI GROUP
Conditions:
Neurogenic Detrusor Overactivity
Eligibility:
All Genders
18-65 years
Phase:
PHASE1
PHASE2
Brief Summary
Study to investigate the safety, tolerability, pharmacokinetics and pharmacodynamics of Rec 0/0438 in subjects with neurogenic detrusor overactivity due to spinal cord injury
Detailed Description
Multicentre, double-blind, randomised, parallel groups, placebo-controlled study to be conducted in specialized centres in Europe to investigate the safety, tolerability, pharmacokinetics and pharmaco...
Eligibility Criteria
Inclusion
- Male and female subjects aged ≥18 years and ≤65 years.
- Female subjects must be either sterile or, if with child-bearing potential, must have a pregnancy test negative and commit to the use of a highly effective method of birth control (see Appendix 15.6) for the duration of the study, and until at least 1 month after the last dose of study medication. Male subjects must be willing to use male contraception (condom) to avoid pregnancies of their female partner of childbearing potential throughout the entire duration of the study, and for 3 months after the last dose of study medication.
- Suffering from NDO due to SCI at upper motor neuron level (below C6) and emptying the bladder performing clear intermittent self-catheterization (CISC).
- Subjects classified in group A, B, or C, of the ASIA (American Spinal Injury Association) impairment scale.
- Stable therapy for NDO in the last thirty days (Subjects should maintain the therapy stable for the duration of the study).
- At least 1 incontinence episode/day despite current treatment, according to what is reported in the Bladder Diary filled in by the subject.
- Subjects with diastolic blood pressure values between 60 and 99 mmHg (both inclusive), and systolic blood pressure values between 90 and 159 mmHg (both inclusive). Blood pressure measurement must be performed in subjects with an empty bladder.
- Subjects with stable concomitant medication treatment at baseline.
- Written informed consent must be given by subjects before any study related investigational procedures is performed.
Exclusion
- Breastfeeding women.
- Treatment with injection of botulinum toxin, unless in the opinion of the Investigator the bladder activity has returned to pre-treatment level.
- Use of prohibited concomitant medications, such as drugs that could affect immunoassay testing (systemic corticosteroids: prednisone, budesonide, prednisolone; calcineurin inhibitors: cyclosporine, tacrolimus; mTOR inhibitors: sirolimus, everolimus; IMDH inhibitors: azathioprine, leflunomide, mycophenolate; biologics: abatacept, adalimumab, anakinra , certolizumab, etanercept, golimumab, infliximab, ixekizumab, natalizumab, rituximab, secukinumab, tocilizumab, ustekinumab, vedolizumab; monoclonal antibodies: basiliximab, daclizumab, muromonab) or initiation of therapy with drugs affecting lower urinary tract symptoms (such as alpha-blockers, tadalafil 5 mg oad). If already present at Screening visit, therapy with drugs affecting lower urinary tract symptoms must be maintained stable through the study period (Note: occasional treatment with PDE-5 inhibitors for erectile dysfunction should be avoided between Screening visit and Day 8 and between Day 25 and 28).
- History of cerebro- or cardio-vascular diseases (TIA, stroke, hypertensive encephalopathy, angina pectoris, MI, cardiac by-pass, CHF NYHA classes III and IV).
- Uncontrolled type 1 or type 2 diabetes (Hb A1c \>8 %).
- Moderate to severe renal impairment (estimated creatinine clearance \<60 mL/min by the Cockcroft-Gault equation).
- Moderate to severe liver impairment (any liver function test: AST, ALT, GGT, Bilirubin \>2.5 times the upper limit of normal).
- Hemodynamically significant valve disease, including aortic stenosis or clinically significant ventricular or supraventricular arrhythmia, heart rate \>100 beats/min.
- Clinically important abnormal laboratory findings during the run-in period, including: Haemoglobin \<10 g/dL; Serum Potassium \>5.5 mmol/L; Serum Sodium \<132 mmol/L.
- Symptomatic active urinary tract infection (i.e. cloudy and/or malodorous urine, chills, fever, increased muscle spasticity or increased autonomic dysreflexia, letargy, hypotension, malaise).
- Evidence of any neoplastic disease.
- History of allergy, hypersensitivity or intolerance to drugs.
- Participation in an investigational drug study within 30 days prior to the screening assessment.
- Any other diseases or conditions, that according to the Investigator's opinion, make the subject unable to comply with protocol requirements, or unable to complete the study or increases the risk to the subject or which prevents optimal participation in achieving the objectives of the study.
Key Trial Info
Start Date :
June 7 2018
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
March 27 2019
Estimated Enrollment :
42 Patients enrolled
Trial Details
Trial ID
NCT03482037
Start Date
June 7 2018
End Date
March 27 2019
Last Update
January 29 2021
Active Locations (9)
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1
Recordati Investigative Site
Prague, Czechia
2
Department of Urology, Academic hospital Pitié-Salpêtrière, Assistance Publique-Hôpitaux de Paris, Pierre et Marie Curie Medical School, Sorbonne Universités
Paris, France, 75013
3
Centre Hospitalier Lyon Sud Unité de Pharmacie Clinique Oncologique (essai clinique) Pavillon Marcel Bérard - Bât. 1G
Pierre-Bénite, France, 69495
4
Recordati Investigative Site
Rouen, France