- ICH GCP
- Amerikanska kliniska prövningsregistret
- Klinisk prövning NCT07737756
A Real-World Medical Chart Review of Spinal Muscular Atrophy Patients Treated With Onasemnogene Abeparvovec in Saudi Arabia (SMA-REAL)
Spinal Muscular Atrophy Center-based REAL World Retrospective Medical Chart Review of Patient Treated With Onasemnogene Abeparvovec (Zolgensma®) in Saudi Arabia
Studieöversikt
Status
Betingelser
Studietyp
Inskrivning (Beräknad)
Kontakter och platser
Studiekontakt
- Namn: Novartis Pharmaceuticals
- Telefonnummer: +41613241111
- E-post: novartis.email@novartis.com
Studera Kontakt Backup
- Namn: Novartis Pharmaceuticals
Deltagandekriterier
Urvalskriterier
Åldrar som är berättigade till studier
- Barn
Tar emot friska volontärer
Testmetod
Studera befolkning
Beskrivning
Inclusion criteria:
- Patients with a genetically confirmed diagnosis of SMA type 1 who were treated with OA.
- Availability of data on at least one visit before treatment initiation and two visits post-treatment is a must for inclusion.
- Patients who were treated with OA starting in January 2023.
- Patients with at least 3 months of follow-up following the treatment with OA.
Exclusion criteria:
1. Any patient who does not fulfill any of the inclusion criteria listed above.
Studieplan
Hur är studien utformad?
Designdetaljer
Kohorter och interventioner
Grupp / Kohort |
|---|
|
OA Cohort
Patients with SMA type 1 who were treated with OA.
|
Vad mäter studien?
Primära resultatmått
Resultatmått |
Tidsram |
|---|---|
|
Proportion of SMA Type 1 Non-Sitters Patients Achieving Independent Sitting for ≥30 Seconds at Any Visit up to 12 Months After OA Administration
Tidsram: Up to 12 months
|
Up to 12 months
|
Sekundära resultatmått
Resultatmått |
Åtgärdsbeskrivning |
Tidsram |
|---|---|---|
|
Children's Hospital of Philadelphia Infant Test of Neuromuscular Disorders (CHOP-INTEND) Score
Tidsram: Up to approximately 3 years
|
CHOP-INTEND is a validated motor function assessment for infants with SMA.
The total score ranges from 0 to 64, with higher scores indicating better motor function.
Scores are derived from 16 items assessing spontaneous movement, strength, and motor abilities.
An increase in score reflects improvement in motor function.
|
Up to approximately 3 years
|
|
Change From Baseline in CHOP-INTEND Score
Tidsram: Baseline, up to approximately 3 years
|
CHOP-INTEND is a validated motor function assessment for infants with SMA.
The total score ranges from 0 to 64, with higher scores indicating better motor function.
Scores are derived from 16 items assessing spontaneous movement, strength, and motor abilities.
An increase in score reflects improvement in motor function.
|
Baseline, up to approximately 3 years
|
|
Hammersmith Infant Neurological Examination-Section 2 (HINE-2, Motor Milestones) Score
Tidsram: Up to approximately 3 years
|
The HINE-2 is a motor milestone assessment evaluating developmental abilities in infants.
The total score ranges from 0 to 26, with higher scores indicating greater achievement of motor milestones.
The scale assesses milestones such as head control, sitting, rolling, crawling, standing, and walking.
Higher scores correspond to more advanced motor development.
|
Up to approximately 3 years
|
|
Change From Baseline in HINE-2 Score
Tidsram: Baseline, up to approximately 3 years
|
The HINE-2 is a motor milestone assessment evaluating developmental abilities in infants.
The total score ranges from 0 to 26, with higher scores indicating greater achievement of motor milestones.
The scale assesses milestones such as head control, sitting, rolling, crawling, standing, and walking.
Higher scores correspond to more advanced motor development.
|
Baseline, up to approximately 3 years
|
|
Percentage of Patients who Maintain the Ability to Thrive at 12 Months After OA Treatment
Tidsram: 12 months
|
Ability to thrive is defined as meeting the following criteria:
|
12 months
|
|
Number and Percentage of Patients Without Permanent Ventilatory Support or Death After OA Administration
Tidsram: Up to approximately 3 years
|
Event-free survival of patients without permanent ventilatory support or death after OA administration. Permanent ventilatory support is defined as the requirement for either:
|
Up to approximately 3 years
|
|
Number and Percentage of Patients With Adverse Events
Tidsram: Up to approximately 3 years
|
Up to approximately 3 years
|
|
|
Number and Percentage of Patients by Demographic and Clinical Characteristics
Tidsram: Baseline
|
Demographic and clinical characteristics include:
|
Baseline
|
|
Age
Tidsram: Baseline
|
Age, gestational age at birth, age at symptom onset, and age at SMA type 1 diagnosis.
|
Baseline
|
|
Duration Between Symptom Onset and Diagnosis
Tidsram: Baseline
|
Baseline
|
Samarbetspartners och utredare
Sponsor
Utredare
- Studierektor: Novartis Pharmaceuticals, Novartis Pharmaceuticals
Studieavstämningsdatum
Studera stora datum
Studiestart (Beräknad)
Primärt slutförande (Beräknad)
Avslutad studie (Beräknad)
Studieregistreringsdatum
Först inskickad
Först inskickad som uppfyllde QC-kriterierna
Första postat (Faktisk)
Uppdateringar av studier
Senaste uppdatering publicerad (Faktisk)
Senaste inskickade uppdateringen som uppfyllde QC-kriterierna
Senast verifierad
Mer information
Termer relaterade till denna studie
Nyckelord
Ytterligare relevanta MeSH-villkor
Andra studie-ID-nummer
- COAV101A1SA01
Plan för individuella deltagardata (IPD)
Planerar du att dela individuella deltagardata (IPD)?
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