Not provided
| ID | Type | Description | Link |
|---|---|---|---|
| CHARISMA | Other Identifier | Gemma Bio, Inc. |
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
GB221 is a gene therapy that delivers a working SMN1 gene to the motor neurons of people with spinal muscular atrophy (SMA) Type 1. This study will evaluate the safety, tolerability and efficacy of GB221 in two groups:
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Cohort 1A, safety and exploratory efficacy of a single dose in symptomatic participants | Experimental | Symptomatic participants with SMA Type 1 (up to 3 copies of SMN2), who are either treatment naïve or receiving risdiplam, with onset of disease during the first 6 months of life, aged from 2 weeks to younger than 12 months at the time of dosing. |
|
| Cohort 1B, expansion phase for confirmatory testing in symptomatic participants | Experimental | Symptomatic participants with SMA Type 1 (up to 3 copies of SMN2), who are either treatment naïve or receiving risdiplam, with onset of disease during the first 6 months of life, aged from 2 weeks to younger than 12 months at the time of dosing. |
|
| Cohort 2A, safety and exploratory efficacy of a single dose in presymptomatic participants | Experimental | Presymptomatic participants (treatment naïve or receiving risdiplam) at risk of developing SMA Type 1 (up to 2 copies of SMN2), aged from 2 weeks to younger than 5 months (< 150 days) at the time of dosing. |
|
| Cohort 2B, expansion phase for confirmatory testing in presymptomatic participants | Experimental | Presymptomatic participants (treatment naïve or receiving risdiplam) at risk of developing SMA Type 1 (up to 2 copies of SMN2), aged from 2 weeks to younger than 5 months (< 150 days) at the time of dosing. |
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| GB221 | Biological | GB221 |
|
| Measure | Description | Time Frame |
|---|---|---|
| Number of participants with treatment-related adverse events (AEs) and serious adverse events (SAEs) at Grade 3 or higher as characterized by CTCAEv5.0 | Assess the number of treatment-related AEs and SAEs as characterized by CTCAEv5.0 | Up to 18 months across multiple visits |
| Number of Participants with Clinically Significant Changes in Physical Functions | Assess the number of participants with clinically significant changes in physical functions. | Up to 18 months across multiple visits |
| Number of Participants with Clinically Significant Changes in Neurological Functions | Assess the number of participants with clinically significant changes in neurological functions. | Up to 18 months across multiple visits |
| Number of Participants with Clinically Significant Changes in Vital signs | Assess the number of participants with clinically significant changes in vital signs. | Up to 18 months across multiple visits |
| Change in electrocardiogram results | ECG will measure RR interval, P Wave, PR interval, PR segment, QRS Complex, ST segment, T wave and QT Interval. | Up to 18 months across multiple visits |
| Change in serum cardiac troponin I levels | Up to 18 months across multiple visits | |
| Number of Participants with Clinically Significant Laboratory Abnormalities as Measured Using Hematology, Chemistry and Coagulation Tests |
| Measure | Description | Time Frame |
|---|---|---|
| Assess the number of participants who experience permanent ventilation or death | Up to 18 months across multiple visits | |
| Percentage of infants with improvement in the motor milestones categories in Section 2 of the Hammersmith Infant Neurological Examination (HINE), with the exclusion of voluntary grasp. |
Not provided
Inclusion Criteria:
Symptomatic Participants
Presymptomatic Participants
Exclusion Criteria:
Not provided
Not provided
Not provided
Not provided
| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Denise Reilly | Contact | 267-718-7654 | clinical_studies@gemmabiotx.com |
| Name | Affiliation | Role |
|---|---|---|
| May Orfali, MD | Gemma Biotherapeutics | Study Director |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Hospital de Clínicas de Porto Alegre | Recruiting | Porto Alegre | Rio Grande do Sul | 90035-903 | Brazil |
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
| ID | Term |
|---|---|
| D014897 | Spinal Muscular Atrophies of Childhood |
| ID | Term |
|---|---|
| D009134 | Muscular Atrophy, Spinal |
| D013118 | Spinal Cord Diseases |
| D002493 | Central Nervous System Diseases |
| D009422 | Nervous System Diseases |
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Assess the number of participants with clinically significant laboratory changes including hematology, serum chemistry, and coagulation tests. |
| Up to 18 months across multiple visits |
| Number of Participants with Clinically Significant Laboratory Abnormalities as Measured Using Urine and CSF Tests | Assess the number of participants with clinically significant laboratory changes including urine and CSF tests. | Up to 18 months across multiple visits |
| Change in markers of immunogenicity | Assessment of humoral (NAb and TAb titers) and T-cell (IFNγ ELISpot) immune responses to the AAVhu68 capsid and SMN transgene product in serum and CSF. | Up to 18 months across multiple visits |
| Baseline, 6 months and 18 months post dose. |
| Change from baseline in mean Children's Hospital of Philadelphia Infant Test of Neuromuscular Disorders (CHOP-INTEND) Score. | Assess 16 types of muscle movements, each given a score from zero (the person can't complete the movement) to 4 (the person can complete the movement on their own, without assistance) to produce a score of 0 to 64. | Baseline, 6 months and 18 months post dose. |
| D020271 | Heredodegenerative Disorders, Nervous System |
| D019636 | Neurodegenerative Diseases |
| D016472 | Motor Neuron Disease |
| D009468 | Neuromuscular Diseases |
| D030342 | Genetic Diseases, Inborn |
| D009358 | Congenital, Hereditary, and Neonatal Diseases and Abnormalities |