Effect of 7 Days of Dosing With a 10 mg Rectal Suppository of NRL001in Patients With Faecal Incontinence

NCT ID: NCT01175941

Last Updated: 2012-11-05

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE1
• Total Enrollment: 14 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2010-08-31
• Study Completion Date: 2011-12-31

Brief Summary

This is a study to examine the effect of alpha adrenergic stimulation of the anal canal and rectum on parameters affecting the control of defecation in subjects with faecal incontinence. The study will investigate the effects of rectal suppositories containing 10 mg NRL001 given for seven days, once daily. Rectal compliance and median anal resting pressure will be considered the primary objective of the study. A pharmacokinetic evaluation plus safety and tolerability assessment including monitoring of electrocardiograms (ECGs), blood pressure and heart rate will also be evaluated as secondary objectives.

Conditions

Fecal Incontinence

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: CROSSOVER
• Primary Study Purpose: TREATMENT
• Blinding Strategy: TRIPLE

Study Groups

NRL001

10 mg NRL001 in a 2 g suppository

Group Type: EXPERIMENTAL

NRL001

Intervention Type: DRUG

10 mg NRL001 in a 2 g suppository, administered once daily for 7 days

Placebo

Matched placebo control

Group Type: PLACEBO_COMPARATOR

Placebo control

Intervention Type: DRUG

Matched placebo - administered as a 2 g suppository, once daily for 7 days

Interventions

NRL001

10 mg NRL001 in a 2 g suppository, administered once daily for 7 days

Intervention Type: DRUG

Placebo control

Matched placebo - administered as a 2 g suppository, once daily for 7 days

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

• Male or female patient volunteers aged 40 to 85 years without clinically significant or uncontrolled cardiovascular, renal or hepatic disease (as determined by medical history, physical examination, laboratory test values, vital signs, and electrocardiograms [ECGs] at screening)
• Patients with mild/moderate passive faecal incontinence based on clinical symptomology and demonstrating the following criteria:
• ARP ≥20mmHg and ≤80mmHg
• Intact IAS as demonstrated by endoanal ultrasound
• Rectal capacity ≥150ml
• Cleveland Clinic Score ≥6 and ≤ 15
• Body mass index (BMI) ≥ 16 and ≤ 32
• Able and willing to receive rectal treatments
• Able to voluntarily provide written informed consent to participate in the study
• Must understand the purposes and risks of the study and agree to follow the restrictions and schedule of procedures as defined in the protocol
• Female volunteers must be either postmenopausal (for at least one year and confirmed by serum FSH at screening), or surgically sterile, practising true sexual abstinence, or using Investigator-approved methods of contraception throughout the study until after post study physical examination and have a negative pregnancy test at screening
• Must be willing to consent to have data entered into The Over-Volunteering Prevention System

Exclusion Criteria

• Patients with FI related to anatomical and/or traumatic sphincter defects
• Presence of any significant or uncontrolled cardiovascular, pulmonary, hepatic, renal, immunologic, neurological or psychiatric disease
• Concomitant ano-rectal conditions or diseases assessed as potentially interfering with the study medication by the Investigator (e.g. concomitant haemorrhoids, anal fissures). Conditions considered not interfering with the study medication are allowed
• Clinically relevant ECG-abnormalities with evident QTc prolongation and/or acute arrhythmia
• Current or history of drug or alcohol abuse
• Use of any disallowed concomitant medication, including over-the-counter items within 30 days prior to study drug administration until the end of the study
• Use of any medication in the last 30 days applied via the rectum
• Use of any medication currently or within the last 30 days which the investigator believes may affect the study participation or results
• Unstable regimen of any statin, hypertensive or diuretic medication (patient volunteers must be on a stable regimen for at least 2 months)
• Participation in a clinical drug study during the 90 days preceding the initial dose in this study
• History of any allergy to nifedipine or any alpha-adrenoceptor antagonist or latex
• Consumption of alcoholic beverages within 24 hours prior to each dosing
• Patient volunteers who are considered not competent to consent to the trial or score less than 25 on the MMSE®
• Volunteers who, in the opinion of the Investigator, are unsuitable for participation in the study

• Minimum Eligible Age: 40 Years
• Maximum Eligible Age: 85 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Norgine

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Jonathan A Simpson, MD

Role: PRINCIPAL_INVESTIGATOR

Nottingham University Hospital

Locations

Queens Medical Centre

Nottingham, Nottinghamshire, United Kingdom

Countries

United Kingdom

Other Identifiers

NRL001-01/2010 (MANO)

Identifier Type: -

Identifier Source: org_study_id