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Repeated Application of Gene Therapy in CF Patients

Primary Purpose

Cystic Fibrosis

Status

Completed

Phase

Phase 2

Locations

United Kingdom

Study Type

Interventional

Intervention

pGM169/GL67A

Placebo

About this trial

This is an interventional treatment trial for Cystic Fibrosis focused on measuring Cystic fibrosis, Gene therapy, CFTR gene, Gene expression, Non-viral, Multi dose

Eligibility Criteria

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

Inclusion Criteria:

Cystic fibrosis confirmed by sweat testing or genetic analysis
Males and females aged 12 years and above
Forced expiratory volume in the 1st second (FEV1) between 50 & 90% predicted inclusive (Stanojevic reference equations).
Clinical stability at screening defined by:
1. Not on any additional antibiotics (excluding routine, long-term treatments) for the previous 2 weeks
2. No increase in symptoms such as change in sputum production/colour, increased wheeze or breathlessness over the previous 2 weeks
3. No change in regular respiratory treatments over the previous 4 weeks
4. If any of these apply, entry into the study can be deferred
Prepared to take effective contraceptive precautions for the duration of their participation in the study and for 3 months thereafter (as stated in GTAC guidelines)
If taking regular rhDNase (pulmozyme) is willing, and considered able by independent medical carers, to withhold treatment for 24 hours before and 24 hours after the gene therapy dose (nebulised doses only)
Written informed consent obtained
Permission to inform their general practitioner of participation in study

Exclusion Criteria:

Infection with Burkholderia cepacia complex organisms, MRSA or M. abscessus
Significant nasal pathology including polyps, clinically-significant rhinosinusitis, or recurrent severe epistaxis (nose bleeds) (nasal cohort only)
Chloride secretory response on nasal PD of > 5 mV (nasal cohort only; will only be known after first measurement)
Acute upper respiratory tract infection within the last 2 weeks (entry can be deferred)
Previous spontaneous pneumothorax without pleurodesis (bronchoscopic subgroup only)
Recurrent severe haemoptysis (bronchoscopic subgroup only)
Current smoker
Significant comorbidity including:
1. Moderate/severe CF liver disease (varices or significant, sustained elevation of transaminases: ALT/ AST>100 IU/l)
2. Significant renal impairment (serum creatinine > 150 mmol/l)
3. Significant coagulopathy (bronchoscopic group only)
Receiving 2nd line immunosuppressant drugs such as methotrexate, cyclosporine, intravenous immunoglobulin preparations
Pregnant or breastfeeding

Sites / Locations

Western General Hospital
Royal Hospital for Sick Children
Royal Brompton Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Placebo Comparator

Arm Label

pGM169/GL67A (CFTR Gene/Lipid Vector)

Placebo

Arm Description

Outcomes

Primary Outcome Measures

Relative change in percent predicted FEV1 after 12 doses of gene product

Secondary Outcome Measures

EFFICACY

Relative change in other spirometric measures; lung clearance index; chest CT scan; Quality of Life Questionnaires; exercise capacity; activity monitoring; serum calprotectin; sputum culture; sputum weight, cell counts and inflammatory markers; frequency of antibiotics for increased chest symptoms

SAFETY

The above efficacy measures; clinical examination; transcutaneous oxygen saturation; serum inflammatory markers (CRP, white blood cell count,cytokines); renal and hepatic function; gas transfer; immune response markers (anti-nuclear and double-stranded DNA antibodies, CFTR-specific T cell responses); endobronchial histology (subgroup only)

GENE EXPRESSION(subgroups only)

Transgene mRNA expression in nasal and lower airway brushing samples; potential difference measurements in nose and bronchi.

Full Information

NCT ID

NCT01621867

First Posted

June 14, 2012

Last Updated

October 21, 2015

Sponsor

Imperial College London

Collaborators

University of Edinburgh, University of Oxford, Royal Brompton & Harefield NHS Foundation Trust

1. Study Identification

Unique Protocol Identification Number

NCT01621867

Brief Title

Repeated Application of Gene Therapy in CF Patients

Official Title

A Randomised, Double-blind, Placebo-controlled Phase 2B Clinical Trial of Repeated Application of Gene Therapy in Patients With Cystic Fibrosis

Study Type

Interventional

2. Study Status

Record Verification Date

November 2012

Overall Recruitment Status

Completed

Study Start Date

May 2012 (undefined)

Primary Completion Date

May 2014 (Actual)

Study Completion Date

May 2014 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title

Sponsor

Name of the Sponsor

Imperial College London

Collaborators

University of Edinburgh, University of Oxford, Royal Brompton & Harefield NHS Foundation Trust

4. Oversight

Data Monitoring Committee

Yes

5. Study Description

Brief Summary

Cystic fibrosis is a genetic condition where epithelial cells, including from the respiratory tract, have an abnormal function of a surface protein, the cystic fibrosis transmembrane conductance regulator (CFTR) protein resulting from abnormal gene expression. The trial will assess the clinical efficacy, safety & tolerability and gene expression following repeated nebulised doses of a gene product coding for a normal CFTR protein, with the primary outcome of the trial assessing lung function.

Detailed Description

Cystic fibrosis (CF), a common, genetically inherited disease, is caused by mutations in the cystic fibrosis transmembrane conductance regulator (CFTR) gene. This gene encodes the CFTR protein, which is expressed on the apical surface of epithelial cells, and which has many functions, the most important of which is thought to be ion transport. Abnormal ion transport leads to thick secretions in the airways, infection, inflammation and eventually irreversible lung damage. There is currently no treatment that halts the natural progression of the disease; all available successful therapies merely slow the rate of decline in clinical condition. To date, no viral gene transfer agents retain efficacy upon repeated administration. Our study will assess the safety and efficacy of a lipid-mediated vector harbouring a normal CFTR gene in repeated nebulised administrations. We have completed a single dose safety study which evaluated the safety and gene expression of a single dose of pGM169/GL67A administered to the nose and lung of individuals with cystic fibrosis. This trial is will randomise 130-patients to receive either a gene product (pGM169/GL67A)encoding for CFTR or placebo in a double-blinded fashion. All subjects will receive 12 doses of nebulised gene therapy at intervals of 4 weeks over a 48 week period. After dose 12 there will be 2 formal follow up visits, at 14 and 28 days post-dose. In addition, patients will be followed up long-term. Subgroups of patients will be enrolled for gene expression measurement in both nose (at least n=20) and lower airway via bronchoscopy (at least n=20). The primary outcome of the trial is to evaluate the relative change in predicted Forced Expiratory Volume in 1-second (FEV1) after 12-doses. Secondary outcome measures will assess the efficacy of the gene product (by assessment of patients' physiological function, serological indices, radiological appearances of the lungs and self-reported assessment of quality of life), on the degree of gene expression and on the product safely.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study

Cystic Fibrosis

Keywords

Cystic fibrosis, Gene therapy, CFTR gene, Gene expression, Non-viral, Multi dose

7. Study Design

Primary Purpose

Treatment

Study Phase

Phase 2

Interventional Study Model

Single Group Assignment

Masking

ParticipantInvestigator

Allocation

Randomized

Enrollment

130 (Actual)

8. Arms, Groups, and Interventions

Arm Title

pGM169/GL67A (CFTR Gene/Lipid Vector)

Arm Type

Active Comparator

Arm Title

Placebo

Arm Type

Placebo Comparator

Intervention Type

Drug

Intervention Name(s)

pGM169/GL67A

Intervention Description

5ml Gene Product/Lipid Vector pGM169/GL67A nebulised; 2ml nasal application of pGM169/GL67A in addition to 5ml nebulised gene product (Nasal Subgroup)

Intervention Type

Drug

Intervention Name(s)

Placebo

Intervention Description

5ml Nebulised non-active placebo; 2ml nasal administration of non-active placebo (nasal subgroup)

Primary Outcome Measure Information:

Title

Relative change in percent predicted FEV1 after 12 doses of gene product

Time Frame

12-months

Secondary Outcome Measure Information:

Title

EFFICACY

Description

Time Frame

12-months

Title

SAFETY

Description

Time Frame

12-months

Title

GENE EXPRESSION(subgroups only)

Description

Transgene mRNA expression in nasal and lower airway brushing samples; potential difference measurements in nose and bronchi.

Time Frame

12-months

10. Eligibility

Sex

All

Minimum Age & Unit of Time

12 Years

Accepts Healthy Volunteers

Eligibility Criteria

Inclusion Criteria: Cystic fibrosis confirmed by sweat testing or genetic analysis Males and females aged 12 years and above Forced expiratory volume in the 1st second (FEV1) between 50 & 90% predicted inclusive (Stanojevic reference equations). Clinical stability at screening defined by: Not on any additional antibiotics (excluding routine, long-term treatments) for the previous 2 weeks No increase in symptoms such as change in sputum production/colour, increased wheeze or breathlessness over the previous 2 weeks No change in regular respiratory treatments over the previous 4 weeks If any of these apply, entry into the study can be deferred Prepared to take effective contraceptive precautions for the duration of their participation in the study and for 3 months thereafter (as stated in GTAC guidelines) If taking regular rhDNase (pulmozyme) is willing, and considered able by independent medical carers, to withhold treatment for 24 hours before and 24 hours after the gene therapy dose (nebulised doses only) Written informed consent obtained Permission to inform their general practitioner of participation in study Exclusion Criteria: Infection with Burkholderia cepacia complex organisms, MRSA or M. abscessus Significant nasal pathology including polyps, clinically-significant rhinosinusitis, or recurrent severe epistaxis (nose bleeds) (nasal cohort only) Chloride secretory response on nasal PD of > 5 mV (nasal cohort only; will only be known after first measurement) Acute upper respiratory tract infection within the last 2 weeks (entry can be deferred) Previous spontaneous pneumothorax without pleurodesis (bronchoscopic subgroup only) Recurrent severe haemoptysis (bronchoscopic subgroup only) Current smoker Significant comorbidity including: Moderate/severe CF liver disease (varices or significant, sustained elevation of transaminases: ALT/ AST>100 IU/l) Significant renal impairment (serum creatinine > 150 mmol/l) Significant coagulopathy (bronchoscopic group only) Receiving 2nd line immunosuppressant drugs such as methotrexate, cyclosporine, intravenous immunoglobulin preparations Pregnant or breastfeeding

Overall Study Officials: