Gene Therapy Trial in Patients With LGMDR9

Título: 
Gene Therapy Trial in Patients With LGMDR9
Estado de reclutamiento: 
Estado se actualizó más recientemente: 
August 24 2022
Fenotipo(s) clínico(s): 
Propósito de estudio: 

Phase 1-2 study including a dose escalation safety and proof of concept phase (Stage 1, open label), followed by a double-blind, randomized, placebo-controlled confirmatory phase (Stage 2)

Intervención / tratamiento: 
Other: GNT0006 Other: Day 0: Placebo Other: Day 0: GNT0006 Other: Day 365 (year 1): Placebo Other: Day 365 (year 1): GNT0006
Fase: 
Descripción del estudio: 

Multicenter, Phase 1-2 study evaluating safety, pharmacodynamic, efficacy, and immunogenicity of GNT0006, an Adeno-Associated Virus (AAV) vector carrying the human FKRP transgene.

This study will consist of 2 phases: an open-label dose escalation phase (Stage 1) and a double-blind placebo controlled, randomized phase (Stage 2), both with long-term follow-up (LTFU) period.

Stage 1 Two dose cohorts will be enrolled sequentially and enrollment. An initial cohort of three (3) patients will receive a potentially effective dose, followed by a 2nd higher dose cohort of 3 patients.

Stage 2 After selection of the effective dose in Stage 1, thirty-three (33) ambulant patients will be randomized at the optimal selected dose and followed up to the primary efficacy timepoint, i.e., one year after investigational medicinal product (IMP) (or placebo) administration.

At one-year post-IMP administration (timepoint of primary interest for efficacy), patients enrolled in placebo group will receive active IMP while patients randomized in the active IMP group will receive a placebo infusion.

All subjects will be followed for up to 5 years after active IMP (GNT0006) administration.

Tipo de estudio: 
Título oficial: 
A Phase 1-2 Multicenter Study (2-stages) to Evaluate the Safety and Efficacy of Intravenous GNT0006, Adeno-associated Viral Vector Carrying the FKRP Gene, in Patients With FKRP-related Limb-girdle Muscular Dystrophy (LGMDR9, Formerly LGMD2I)
Fecha de inicio del estudio: 
August 10, 2022
Fecha de finalización del estudio: 
October 2030
Objetivo(s) principal(es): 

Percent change from baseline in Forced Vital Capacity at one year [ Time Frame: Baseline through 12 months ]

Primary endpoint

Objetivo(s) secundario(s): 

10-Meter Walk test (10MWT) [ Time Frame: Baseline through 12 months ]

Secondary endpoint



Timed Up and Go (TUG) test [ Time Frame: Baseline through 12 months ]

Secondary endpoint



Change from baseline in North Star Assessment for Neuromuscular Disorders (NSAD) scale (with a range from 0 to 54, the higher the score the better the ability) [ Time Frame: Baseline through 12 months ]

Scale to assess patient's abilities necessary to remain functionally ambulant



2-minute walk distance test [ Time Frame: Baseline through 12 months ]

Secondary endpoint



Cardiac MRI [ Time Frame: Baseline through 12 months ]

To measure cardiac function (left ejection fraction)



Muscle MRI [ Time Frame: Baseline through 12 months ]

To measure change from baseline in fat repartition fraction in thigh and leg skeletal muscles



Muscle Biopsy [ Time Frame: Baseline through 12 months ]

Quantification of FKRP positive muscle fibers



Muscle Biopsy [ Time Frame: Baseline through 12 months ]

Percentage of glycosylation



Patient reported outcome and quality of life assessment [ Time Frame: Baseline through 12 months ]

Quality of Life in genetic Neuromuscular Disease (QoL-gNMD), with a range from 0 to 78, the higher the score the worse the quality of life



Patient reported outcome and quality of life assessment [ Time Frame: Baseline through 12 months ]

ACTIVLIM, scale measuring level of limitation in performing daily activities (total score ranging from 0 to 44, with the lower score the highest limitation)

Elegibilidad: 

Ages Eligible for Study:      16 Years to 99 Years   (Child, Adult, Older Adult)

Sexes Eligible for Study:      All

Accepts Healthy Volunteers:      No

Criterios de inclusión: 

1. Female and male ambulant patients

2. Patients ≥ 16 years old

3. Documented LGMDR9 diagnosis based on clinical presentation and genotyping confirming the FKRP gene mutations

4. Moderate diaphragmatic muscle impairment

Criterio de exclusión: 

1. Detectable serum neutralizing antibodies against AAV9

2. Cardiomyopathy

Sitio(s) de estudio / Ubicacion(es): 



Denmark

Rigshospitalet, University of Copenhagen Blegdamsvej 9    Recruiting

Copenhagen, Denmark, 2100

Contact: John Vissing, Pr    +45 35452562    john.vissing@regionh.dk   



France

Institute of Myology Pitié-Salpêtrière Hospital 47 Bd de l'Hôpital    Recruiting

Paris, France, 75013

Contact: Tanya Stojkovic, Dr    +33 (0) 1 42 16 58 70    essais-adultes@institut-myologie.org   



United Kingdom

Royal Victoria Infirmary Queen Victoria Road Level 6 Leazes Wing    Not yet recruiting

Newcastle Upon Tyne, United Kingdom, NE1 4LP

Contact: Volker Straub, Pr    +44 (0) 191 241 8762    volker.straub@newcastle.ac.uk   

Patrocinadores y Colaboradores: 

Atamyo Therapeutics

Investigador(es) principal(es): 

N/A

Para obtener más información, por favor comuníquese con el Coordinador del estudio: 

Contact:  

Email: 

Phone: 

ID de ClinicalTrials.gov: 
NCT05224505