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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00421746
Other study ID # BMI 001 / SMR-1389
Secondary ID
Status Completed
Phase Phase 2
First received January 11, 2007
Last updated August 2, 2007
Start date January 2006
Est. completion date July 2007

Study information

Verified date August 2007
Source Bio-Medisinsk Innovasjon
Contact n/a
Is FDA regulated No
Health authority Norway: Norwegian Medicines AgencyDenmark: Danish Medicines AgencyUnited Kingdom: Medicines and Healthcare Products Regulatory Agency
Study type Interventional

Clinical Trial Summary

The purpose of this study is to determine whether piboserod, a serotonin-4 receptor antagonist, is effective for the treatment of patients with congestive heart failure.


Description:

Despite intensive research for decades, mortality and morbidity in chronic heart failure remains quite high. There is an obvious need for new drugs, especially drugs which may have a different mode of action than the existing ones on the market.

The purpose of this trial is to evaluate whether a new drug candidate, piboserod, has beneficial biological effects in stable outpatients with symptomatic heart failure receiving evidence based treatment for heart failure and to assess safety and tolerability of this treatment.


Recruitment information / eligibility

Status Completed
Enrollment 137
Est. completion date July 2007
Est. primary completion date
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 80 Years
Eligibility Inclusion Criteria:

- Clinical diagnosis of CHF (NYHA class II-IV)

- Locally determined LVEF < 0.35 (by CMR, echocardiography, LV angiography, or radionuclide cardioangiography)

- Stable sinus rhythm

- Stable evidence based pharmacological treatment for CHF.

Exclusion Criteria:

- Unstable patients hospitalised within last 2 weeks

- Baseline prolongation of QTc interval

- Atrial fibrillation at randomisation

- MI or re-vascularisation last 3 months

- Stroke last 3 months.

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double-Blind, Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Drug:
Piboserod


Locations

Country Name City State
Denmark Amager Hospital Copenhagen
Denmark Bispebjerg Hospital Copenhagen
Denmark Rigshospitalet Copenhagen
Denmark Frederiksberg Hospital Frederiksberg
Denmark Amtsygehuset i Herlev Herlev
Denmark Hvidovre Hospital Hvidovre
Denmark Odense Universitets Hospital Odense
Denmark Svendborg Sygehus Svendborg
Norway Østlandske Hjertesenter Moss
Norway Fana Hjertesenter Nesttun
Norway Rikshospitalet Oslo
Norway Ullevål Universitetssykehus Oslo
Norway Stavanger Universitetssjukehus Stavanger
Norway St. Olavs Hospital Trondheim
United Kingdom Bridlington and District General Hospital Bridlington
United Kingdom Castel Hill Hospital Cottingham East Yorkshire
United Kingdom Western Infirmary Glasgow

Sponsors (2)

Lead Sponsor Collaborator
Bio-Medisinsk Innovasjon Smerud Medical Research International AS

Countries where clinical trial is conducted

Denmark,  Norway,  United Kingdom, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change from baseline to end-of-therapy in Left Ventricular Ejection Fraction, as measured using CMR imaging 6 months
Secondary Change in LV systolic and diastolic volume (and/or diameter) by CMR 6 months
Secondary Change in NYHA functional class 6 months
Secondary Change in various biomarkers for heart failure 6 months
Secondary Change in QoL-scores 6 months
Secondary Change in 6-minute walk distance 6 months
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