Estudio de fase 1b/2a de NVG-291 en sujetos con lesión de la médula espinal
Un estudio de fase 1b/2a aleatorizado, doble ciego, controlado con placebo de NVG-291 en sujetos con lesión de la médula espinal
A Randomized, Double-Blind, Placebo-Controlled Phase 1b/2a Study of NVG-291 in Spinal Cord Injury Subjects
Descripción general del estudio
Estado
Estado
Condiciones
Condiciones
Intervención / Tratamiento
Intervención / Tratamiento
Descripción detallada
To evaluate the effect of NVG-291 on descending connectivity in subjects with subacute and chronic SCI (20 subjects per Cohort and results will be analyzed separately) using objective electrophysiological measures, in addition to clinical assessments. To evaluate safety and tolerability of NVG-291 in a SCI population, as measured by clinical assessments (Physical Examination, Vital Signs, ECG, etc.) as well as clinical laboratory measures. NOTE: Enrollment of the chronic cohort has been completed; approximately 20 individuals will be enrolled in the subacute group. For more information about the trial please visit www.connectscistudy.com.
Tipo de estudio
Tipo de estudio
Inscripción (Actual)
Inscripción
Fase
Fase
- Fase 2
- Fase 1
Contactos y Ubicaciones
Ubicaciones de estudio
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-
Illinois
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Chicago, Illinois, Estados Unidos, 60611
- Shirley Ryan AbilityLab
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-
Criterios de participación
Criterio de elegibilidad
Criterio de elegibilidad
Edades elegibles para estudiar
Acepta Voluntarios Saludables
Géneros elegibles para el estudio
Descripción
Inclusion Criteria:
- A subject must provide written informed consent in accordance with local regulations prior to initiation of any study-specific activities/procedures. A legally authorized representative (LAR) may be used to assist in signing the informed consent.
- Cervical spinal cord injury (SCI) resulting from acute physical trauma.
- Males and females.
- Age 18 to 75 years, inclusive.
- Cervical SCI, incomplete, with a neurological level of injury at C7 or higher.
- Had incomplete cervical SCI within the period from 1 year to 10 years inclusive (Chronic Cohort 1) OR within 20 days to 90 days inclusive (Subacute Cohort 2) at time of randomization.
- Chronic Cohort 1 only: Must be able to volitionally initiate at least one step on one leg (without body weight support).
- Must have a Walking Index for Spinal Cord Injury II (WISCI II) score as follows:
- Chronic Cohort 1: Less than or equal to Level 14.
- Subacute Cohort 2: Less than or equal to Level 10.
- Graded Redefined Assessment of Strength, Sensibility and Prehension (GRASSP) Prehension Ability score/hand grip strength as follows:
- Chronic Cohort 1:
- Must have a score of at least 2 on at least one of the Prehension Ability grasp patterns of the GRASSP assessment in at least one upper extremity.
- Must have no more than one Prehension Ability grasp pattern score = 4 in the upper extremity satisfying the criterion above.
- Subacute Cohort 2:
- Must have some voluntary (nonzero) force measured by grip dynamometry in at least one upper extremity.
- Must have no more than one Prehension Ability grasp pattern score = 3 in at least one upper extremity.
- Must not have a Prehension Ability grasp pattern score = 4 in the upper extremity satisfying the criterion above.
- Presence of Motor Evoked Potentials (MEPs):
- Chronic Cohort 1: In two specific target muscle groups.
- Subacute Cohort 2: In one specific target muscle group.
- Must be fluent in English.
- Must be willing and able to comply with scheduled visits, all sample collections, and other trial procedures.
Exclusion Criteria:
- Nontraumatic SCI (e.g., due to infection, ischemia, metabolic abnormality, congenital abnormality, malignancy, radiation injury, surgical complications, or other disease process).
- SCI due to gunshot wound or penetrating injury.
- Two or more (noncontiguous) spinal cord lesions.
- MRI or CT evidence of anatomically complete spinal cord transection.
- Any form of ventilatory dependence.
- Any condition that precludes adequate clinical assessment of all four extremities, such as contracture, peripheral nerve injury, or amputation.
- History of uncontrolled seizures, or:
- Chronic Cohort 1: Any seizure within the last 6 months.
- Subacute Cohort 2: Any seizure occurring 1 week or more after the SCI.
- Metal implant in the head that is likely to interfere with MRI analysis.
- Pregnant or breastfeeding.
- Any neurological condition that is considered to interfere with performance or likely confound assessment, such as multiple sclerosis, stroke, or progressive syringomyelia.
- History of substance abuse within 12 months prior to screening, based on medical records or self-report.
- Evidence of spinal instability or persistent spinal stenosis and/or compression related to the initial trauma.
- Prior treatment with cell therapy delivered into the central nervous system (intrathecal or intraparenchymal).
- Severe neuropathic pain inadequately controlled by medication.
- Body mass index (BMI) > 40 kg/m2.
- Received botulinum toxin injection(s) in an upper or lower extremity muscle in the prior 6 months.
- Received 4-aminopyridine within 7 days of first dose.
- Prior treatment with a protein tyrosine phosphatase sigma (PTPσ) mimetic peptide.
- Intrathecal opioid use.
- Currently participating in an interventional clinical trial.
- Received a non-permitted medication within 5.5 half-lives or 7 days, whichever is longer, prior to randomization.
- Receiving any treatment intended to enhance neuroplasticity (e.g., electrical stimulation, acute intermittent hypoxia) at the time of consent or within 4 weeks of randomization, whichever is longer.
- Any implanted internal spinal cord stimulator.
- Currently receiving neuromuscular stimulation.
- Currently receiving vagal or phrenic nerve stimulation.
- Chronic Cohort 1 only: Any contraindication to baseline and on-study MRIs, such as:
- History of a cardiac pacemaker or pacemaker wires.
- Ferromagnetic metallic particles in the body.
- Baclofen pump.
- Vascular clips in the head.
- Prosthetic heart valves.
- Severe claustrophobia impeding ability to participate in an imaging study.
- Malignancy within 5 years prior to screening, except for non-melanoma skin cancers or cervical or breast ductal carcinoma in situ.
- History of medically significant hepatic disease or evidence of impaired liver function based on initial laboratory testing.
- Severe renal insufficiency, defined as eGFR < 30 mL/min/1.73m2.
- Any disease, concomitant injury (such as significant traumatic brain injury), or condition that could interfere with the performance or interpretation of the protocol-specified assessments, in the opinion of the investigator.
- Any other social or medical condition (e.g., uncontrolled diabetes, unstable hypertension) which, in the opinion of the investigator, would make the subject unsuitable for study participation.
Plan de estudios
¿Cómo está diseñado el estudio?
Detalles de diseño
- Propósito principal: Tratamiento
- Asignación: Aleatorizado
- Modelo Intervencionista: Asignación paralela
- Enmascaramiento: Cuadruplicar
Número de brazos
Armas e Intervenciones
Grupo de participantes/brazoGrupo de participantes/brazo |
Intervención / TratamientoIntervención / Tratamiento |
|---|---|
|
Experimental: NVG-291 for SC Injection
NVG-291 administered by subcutaneous injection once daily for 12 weeks, with cetirizine pretreatment. |
A once daily injection |
|
Comparador de placebos: Placebo for SC Injection
Matching placebo administered by subcutaneous injection once daily for 12 weeks, with cetirizine pretreatment. |
A once daily injection |
¿Qué mide el estudio?
Medidas de resultado primarias
Medidas de resultado primarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
|
Electrophysiological
Periodo de tiempo: 12 weeks
|
MEP amplitudes (corticospinal contribution) in key target muscle groups |
12 weeks
|
Medidas de resultado secundarias
Medidas de resultado secundarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
|
10mWT time
Periodo de tiempo: 12 weeks
|
Walking speed |
12 weeks
|
|
9-HPT time
Periodo de tiempo: 12 weeks
|
Upper extremity dexterity |
12 weeks
|
|
Dynamometry testing (pinch grip, Chronic cohort 1; hand grip, Subacute cohort 2)
Periodo de tiempo: 12 weeks
|
Recorded force |
12 weeks
|
|
Graded and Redefined Assessment of Strength, Sensibility, and Prehension Test
Periodo de tiempo: 12 weeks
|
Hand function Max Score 116 points |
12 weeks
|
|
Lower extremity motor score (LEMS)
Periodo de tiempo: 12 weeks
|
Lower extremity Max Score 50 points |
12 weeks
|
|
Upper extremity motor score (UEMS)
Periodo de tiempo: 12 weeks
|
Upper extremity Max Score 50 points |
12 weeks
|
|
Incidences of Treatment Emergent Adverse Events (Safety and Tolerability)
Periodo de tiempo: 16 Weeks
|
incidences of treatment emergent adverse events |
16 Weeks
|
|
Plasma Concentration of Study Drug
Periodo de tiempo: 12 Weeks
|
initial and steady state predose and peak plasma drug concentrations |
12 Weeks
|
Colaboradores e Investigadores
Patrocinador
Patrocinador
Investigadores
Investigadores
- Director de estudio: Randall Kaye, M.D., NervGen Pharma
Publicaciones y enlaces útiles
Enlaces Útiles
Fechas de registro del estudio
Fechas importantes del estudio
Inicio del estudio (Actual)
Inicio del estudio
Finalización primaria (Actual)
Finalización primaria
Finalización del estudio (Actual)
Finalización del estudio
Fechas de registro del estudio
Enviado por primera vez
Enviado por primera vez
Primero enviado que cumplió con los criterios de control de calidad
Primero enviado que cumplió con los criterios de control de calidad
Publicado por primera vez (Actual)
Publicado por primera vez
Actualizaciones de registros de estudio
Última actualización publicada (Actual)
Última actualización publicada
Última actualización enviada que cumplió con los criterios de control de calidad
Última actualización enviada que cumplió con los criterios de control de calidad
Última verificación
Última verificación
Más información
Términos relacionados con este estudio
Palabras clave
Términos MeSH relevantes adicionales
Otros números de identificación del estudio
Otros números de identificación del estudio
- NVG-291-201
Plan de datos de participantes individuales (IPD)
¿Planea compartir datos de participantes individuales (IPD)?
Información sobre medicamentos y dispositivos, documentos del estudio
Estudia un producto farmacéutico regulado por la FDA de EE. UU.
Estudia un producto de dispositivo regulado por la FDA de EE. UU.
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