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Does a Nasal Instillation of Miglustat Normalize the Nasal Potential Difference in Cystic Fibrosis Patients ?

Primary Purpose

Cystic Fibrosis

Status
Completed
Phase
Phase 2
Locations
Belgium
Study Type
Interventional
Intervention
Miglustat
Placebo
Sponsored by
Cliniques universitaires Saint-Luc- Université Catholique de Louvain
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Cystic Fibrosis focused on measuring Cystic fibrosis, miglustat, nasal instillation, nasal potential difference

Eligibility Criteria

14 Years - undefined (Child, Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Cystic fibrosis patients homozygous for the F508del mutation as confirmed by genetic test
  • Aged 14 years and older
  • Male or female (non-pregnant women who are to remain non-pregnant for 3 months after the end of the study)
  • FEV1 > 50% of predicted normal

Exclusion Criteria:

  • Acute respiratory tract infection or pulmonary exacerbation requiring antibiotic intervention within 2 weeks of visit 1
  • Any condition prohibiting the correct measurement of the NPD such as respiratory tract infection
  • Active or passive smoking
  • Allergic chronic rhinitis
  • History of significant lactose intolerance
  • History of neuropathy
  • History of cataracts or known increased risk of cataract formation
  • Hypersensitivity to miglustat or any excipients
  • Planned treatment or treatment with another investigational drug or therapy within 1 month prior to randomisation

Sites / Locations

  • Cliniques Universitaires St Luc (Université Catholique de Louvain) 10 avenue Hippocrate

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

No Intervention

Active Comparator

Placebo Comparator

Arm Label

Baseline

Miglustat

Placebo

Arm Description

Visit 1

Nasal instillation of Miglustat (visit 2 or 3)

Nasal instillation of placebo (visit 3 or 2)

Outcomes

Primary Outcome Measures

change in response to Chloride-free solution and isoproterenol ( reflecting chloride transport)

Secondary Outcome Measures

change in basal voltage value and in amiloride response ( reflecting sodium transport)

Full Information

First Posted
July 23, 2009
Last Updated
August 9, 2011
Sponsor
Cliniques universitaires Saint-Luc- Université Catholique de Louvain
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1. Study Identification

Unique Protocol Identification Number
NCT00945347
Brief Title
Does a Nasal Instillation of Miglustat Normalize the Nasal Potential Difference in Cystic Fibrosis Patients ?
Official Title
Does a Nasal Instillation of Miglustat Normalize the Nasal Potential Difference in Cystic Fibrosis Patients Homozygous for the F508del Mutation? A Randomized, Double Blind Placebo-controlled Study.
Study Type
Interventional

2. Study Status

Record Verification Date
August 2011
Overall Recruitment Status
Completed
Study Start Date
July 2009 (undefined)
Primary Completion Date
May 2011 (Actual)
Study Completion Date
June 2011 (Actual)

3. Sponsor/Collaborators

Name of the Sponsor
Cliniques universitaires Saint-Luc- Université Catholique de Louvain

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The purpose of this study is to investigate within a short delay the effect of nasal instillation of Miglustat on nasal potential difference in cystic fibrosis patients homozygous for the F508del mutation.
Detailed Description
Miglustat is an inhibitor of α-glucosidases and other enzymes. Oral miglustat is currently marketed in Europa and US for the treatment of Gaucher type 1 patients for whom enzyme replacement treatment is not an option. Gastro-intestinal side effects are common with this formulation. This medication has been shown to have a beneficial effect both on Cl- an Na+ transports in cystic fibrosis epithelial cells. In addition, a single airway delivery of low-dose Miglustat normalizes nasal potential difference (NPD) in F508del cystic fibrosis mice. NPD abnormalities specific of CF patients are considered to reflect the primary defect of CFTR protein so that any curative treatment is expected to correct them at least partially. In the field of respiratory pharmacology, it is a general rule that the inhaled route is to be favoured whenever possible : it is usually more effective despite much lower doses and systemic absorption (which also implies lower costs and improved tolerance). The aim of this study is to investigate the effect of a single local administration of Miglustat on NPD measurements in CF patients homozygous for the F508del mutation.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cystic Fibrosis
Keywords
Cystic fibrosis, miglustat, nasal instillation, nasal potential difference

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Crossover Assignment
Masking
ParticipantCare ProviderInvestigator
Allocation
Randomized
Enrollment
10 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Baseline
Arm Type
No Intervention
Arm Description
Visit 1
Arm Title
Miglustat
Arm Type
Active Comparator
Arm Description
Nasal instillation of Miglustat (visit 2 or 3)
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
Nasal instillation of placebo (visit 3 or 2)
Intervention Type
Drug
Intervention Name(s)
Miglustat
Intervention Description
Nasal instillation of miglustat
Intervention Type
Drug
Intervention Name(s)
Placebo
Intervention Description
Nasal instillation of placebo matching in appearance with the Miglustat instillation
Primary Outcome Measure Information:
Title
change in response to Chloride-free solution and isoproterenol ( reflecting chloride transport)
Time Frame
change from baseline ( visit 1) and placebo to miglustat instillation
Secondary Outcome Measure Information:
Title
change in basal voltage value and in amiloride response ( reflecting sodium transport)
Time Frame
change from baseline (visit1) and placebo to miglustat instillation

10. Eligibility

Sex
All
Minimum Age & Unit of Time
14 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Cystic fibrosis patients homozygous for the F508del mutation as confirmed by genetic test Aged 14 years and older Male or female (non-pregnant women who are to remain non-pregnant for 3 months after the end of the study) FEV1 > 50% of predicted normal Exclusion Criteria: Acute respiratory tract infection or pulmonary exacerbation requiring antibiotic intervention within 2 weeks of visit 1 Any condition prohibiting the correct measurement of the NPD such as respiratory tract infection Active or passive smoking Allergic chronic rhinitis History of significant lactose intolerance History of neuropathy History of cataracts or known increased risk of cataract formation Hypersensitivity to miglustat or any excipients Planned treatment or treatment with another investigational drug or therapy within 1 month prior to randomisation
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Patrick LEBECQUE, MD, PhD
Organizational Affiliation
Cliniques Universitaires St Luc (Université Catholique de Louvain )
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Teresinha LEAL, MD, PhD
Organizational Affiliation
Cliniques Universitaires St. Luc ( Université Catholique de Louvain)
Official's Role
Principal Investigator
Facility Information:
Facility Name
Cliniques Universitaires St Luc (Université Catholique de Louvain) 10 avenue Hippocrate
City
Brussels
ZIP/Postal Code
1200
Country
Belgium

12. IPD Sharing Statement

Citations:
PubMed Identifier
19299496
Citation
Lubamba B, Lebacq J, Lebecque P, Vanbever R, Leonard A, Wallemacq P, Leal T. Airway delivery of low-dose miglustat normalizes nasal potential difference in F508del cystic fibrosis mice. Am J Respir Crit Care Med. 2009 Jun 1;179(11):1022-8. doi: 10.1164/rccm.200901-0049OC. Epub 2009 Mar 19.
Results Reference
background
PubMed Identifier
16546175
Citation
Norez C, Noel S, Wilke M, Bijvelds M, Jorna H, Melin P, DeJonge H, Becq F. Rescue of functional delF508-CFTR channels in cystic fibrosis epithelial cells by the alpha-glucosidase inhibitor miglustat. FEBS Lett. 2006 Apr 3;580(8):2081-6. doi: 10.1016/j.febslet.2006.03.010. Epub 2006 Mar 10.
Results Reference
background
PubMed Identifier
18309088
Citation
Noel S, Wilke M, Bot AG, De Jonge HR, Becq F. Parallel improvement of sodium and chloride transport defects by miglustat (n-butyldeoxynojyrimicin) in cystic fibrosis epithelial cells. J Pharmacol Exp Ther. 2008 Jun;325(3):1016-23. doi: 10.1124/jpet.107.135582. Epub 2008 Feb 28.
Results Reference
background
PubMed Identifier
19131642
Citation
Norez C, Antigny F, Noel S, Vandebrouck C, Becq F. A cystic fibrosis respiratory epithelial cell chronically treated by miglustat acquires a non-cystic fibrosis-like phenotype. Am J Respir Cell Mol Biol. 2009 Aug;41(2):217-25. doi: 10.1165/rcmb.2008-0285OC. Epub 2009 Jan 8.
Results Reference
background
PubMed Identifier
33331662
Citation
Southern KW, Murphy J, Sinha IP, Nevitt SJ. Corrector therapies (with or without potentiators) for people with cystic fibrosis with class II CFTR gene variants (most commonly F508del). Cochrane Database Syst Rev. 2020 Dec 17;12(12):CD010966. doi: 10.1002/14651858.CD010966.pub3.
Results Reference
derived

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Does a Nasal Instillation of Miglustat Normalize the Nasal Potential Difference in Cystic Fibrosis Patients ?

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