Evaluation of the Efficacy and Safety of Bumetanide in Parkinson's Disease

Phase 2

• Conditions: Parkinson Disease
• Interventions: Drug: Bumetanide white, oblong, scored tablet; Drug: Placebo white, oblong, scored tablet

• Registration Number: NCT03899324
• Lead Sponsor: B&A Therapeutics

Brief Summary

This is multicentre, proof of concept, randomized, double-blind, parallel-group, placebo-control study in 40 Parkinson's Disease (PD) patients. Patients will be randomized in 2 groups receiving Bumetanide or placebo for 4 months:

* Group 1 (20 PD patients): bumetanide

* Group 2 (20 PD patients): placebo intake identically to group 1.

Detailed Description

Not available

Study Timeline

• Study First Submitted: 2019-03-29
• Study First Submitted QC: 2019-04-01
• Study First Posted: 2019-04-02
• Study Start: 2019-04-26
• Status Verified: 2019-07
• Last Update Submitted: 2019-07-22
• Last Update Posted: 2019-07-23
• Primary Completion: 2020-09
• Study Completion: 2021-08

Recruitment & Eligibility

• Status: UNKNOWN
• Sex: All
• Target Recruitment: 40

Inclusion Criteria

1. Idiopathic Parkinson's disease fulfilling the UK Parkinson's Disease Brain Bank (UKPDSBB) criteria (cf. Appendix VII)
2. 40 < Age < 80 years old
3. Hoehn & Yahr 1.5-4 (OFF stage)
4. Walking and balance or freezing ≥ 1in the MDS-UPDRS II
5. Motor fluctuation defined by a score ≥ 1 on the item "time spent in the OFF state" of the MDS-UPDRS IV
6. Dose of L-DOPA ≥ 150 mg/d (concomitant treatment)
7. PD medications regimen stable for at least 3 months
8. Patients expected to remain on stable doses of PD medications during all the study
9. Covered by Health Insurance System
10. Able to understand and to sign the informed consent prior to selection
11. Negative pregnancy test at screening
12. Blood Pressure (BP) and Heart Rate (HR) considered Non Clinicaly Significant (NCS) by investigators
13. Electrocardiogram (ECG) recording on a 12-lead ECG considered NCS by investigators
14. Laboratory parameters within the normal range of the laboratory. Individual values out of the normal range can be accepted if judged clinically non relevant by the Investigator

Exclusion Criteria

1. Atypical parkinsonism or drug-induced parkinsonism
2. Cognitive impairment (MMSE ≤ 24)
3. Active psychiatric disorder (mood disorders, hallucinations or delirium with strong functional impact and not controlled by medication or which happened during the last 3 months before inclusion)
4. Treatment by Deep Brain Stimulation or continuous infusion of apomorphin/dopa gel
5. Renal or hepatic insufficiency
6. Electrolyte disturbances
7. A corrected QT (QTcF) interval >450ms for male or >470ms for female on the electrocardiogram
8. Any medical condition that might interfere with the protocol except those defined in Section 5.3
9. Contraindications to bumetanide : persistent anuria, hepatic encephalopathy included coma
10. Women pregnant, nursing or of childbearing age without effective contraception. Patients should not be enrolled if they plan to become pregnant during the time of study participation
11. Patient unable to attend scheduled visits or to comply to the protocol
12. Patient under legal guardianship or judicial protection
13. Patient in the exclusion period of another protocol
14. No possibility of contact in case of emergency
15. Known allergic reactions induced by Burinex (Bumetanide)

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Group 1: Experimental Bumetanide	Bumetanide white, oblong, scored tablet	bumetanide with a titration period
Group 2: Placebo comparator	Placebo white, oblong, scored tablet	placebo intake identically to group 1

Primary Outcome Measures

Name	Time	Method
The primary endpoint of this study is the change from baseline (V2) to endpoint (V5) in the MDS-UPDRS III motor score, evaluated 1 hour after the intake of the study treatment (Bumetanide or placebo) in patients in the OFF state.	Between Day 1 and Day 120

Secondary Outcome Measures

Name	Time	Method
Stand-Walk-Sit test at D1 (V2), D30 (V3), D60 (V4) and D120 (V5).	Day 1, Day 30, Day 60, Day 120
Change from V2 to V5 of the MDS-UPDRS part III and part I measured in a patient in the ON state.	Between Day 1 and Day 120	Movement Disorder Society Unified Parkinson's Disease Rating Scale
Change of scores of the MDS-UPDRS part II, III and IV during the trial, at D1 (V2), D30 (V3), D60 (V4) and D120 (V5).	Day 1, Day 30, Day 60, Day 120	Movement Disorder Society Unified Parkinson's Disease Rating Scale
Number of adverse events collected at each visit and phone calls.	Throughout the completion of the study, from Day 1 to Day 135

Trial Locations

Locations (1)

Chu Nantes; 🇫🇷 Nantes, France