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A Real-World Medical Chart Review of Spinal Muscular Atrophy Patients Treated With Onasemnogene Abeparvovec in Saudi Arabia (SMA-REAL)

28. august 2026 oppdatert av: Novartis Pharmaceuticals

Spinal Muscular Atrophy Center-based REAL World Retrospective Medical Chart Review of Patient Treated With Onasemnogene Abeparvovec (Zolgensma®) in Saudi Arabia

The aim of this retrospective medical chart review is to describe the clinical outcomes, clinical characteristics, and demographics of patients with spinal muscular atrophy (SMA) type 1 treated with onasemnogene abeparvovec (OA) at a single clinical center in Saudi Arabia. The study will use secondary data collected from the electronic medical records of SMA type 1 patients.

Studieoversikt

Status

Har ikke rekruttert ennå

Studietype

Observasjonsmessig

Registrering (Antatt)

6

Kontakter og plasseringer

Denne delen inneholder kontaktinformasjon for de som utfører studien, og informasjon om hvor denne studien blir utført.

Studiekontakt

Studer Kontakt Backup

  • Navn: Novartis Pharmaceuticals

Deltakelseskriterier

Forskere ser etter personer som passer til en bestemt beskrivelse, kalt kvalifikasjonskriterier. Noen eksempler på disse kriteriene er en persons generelle helsetilstand eller tidligere behandlinger.

Kvalifikasjonskriterier

Alder som er kvalifisert for studier

  • Barn

Tar imot friske frivillige

Nei

Prøvetakingsmetode

Ikke-sannsynlighetsprøve

Studiepopulasjon

SMA type 1 patients receiving OA at a single clinical center in Saudi Arabia.

Beskrivelse

Inclusion criteria:

  1. Patients with a genetically confirmed diagnosis of SMA type 1 who were treated with OA.
  2. Availability of data on at least one visit before treatment initiation and two visits post-treatment is a must for inclusion.
  3. Patients who were treated with OA starting in January 2023.
  4. 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

Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.

Hvordan er studiet utformet?

Designdetaljer

Kohorter og intervensjoner

Gruppe / Kohort
OA Cohort
Patients with SMA type 1 who were treated with OA.

Hva måler studien?

Primære resultatmål

Resultatmål
Tidsramme
Proportion of SMA Type 1 Non-Sitters Patients Achieving Independent Sitting for ≥30 Seconds at Any Visit up to 12 Months After OA Administration
Tidsramme: Up to 12 months
Up to 12 months

Sekundære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Children's Hospital of Philadelphia Infant Test of Neuromuscular Disorders (CHOP-INTEND) Score
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: 12 months

Ability to thrive is defined as meeting the following criteria:

  • Ability to tolerate thin liquids, as demonstrated by a formal swallowing assessment, with tested consistency classified as "very thin" or "thin" and results recorded as "normal swallow," "functional swallow," or "safe for swallowing";
  • No requirement for nutritional support via mechanical feeding methods (e.g., feeding tube);
  • Maintenance of body weight at or above the 3rd percentile for age and sex, according to World Health Organization (WHO) child growth standards, appropriate for the child's age at assessment.
12 months
Number and Percentage of Patients Without Permanent Ventilatory Support or Death After OA Administration
Tidsramme: 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:

  • Tracheostomy, or
  • ≥16 hours per day of respiratory support (including non-invasive ventilation) for 14 or more consecutive days, in the absence of an acute reversible illness and excluding perioperative ventilation.
Up to approximately 3 years
Number and Percentage of Patients With Adverse Events
Tidsramme: Up to approximately 3 years
Up to approximately 3 years
Number and Percentage of Patients by Demographic and Clinical Characteristics
Tidsramme: Baseline

Demographic and clinical characteristics include:

  • Sex
  • City of residence
  • Preterm birth status
  • Functional classification
  • Developmental milestones achieved prior to treatment initiation
  • SMA-related symptoms
  • Comorbidities
  • CHOP-INTEND Score
  • HINE-2 Score
  • Ambulatory status
  • Swallowing assessment result
  • Feeding method
  • Anthropometric measures
Baseline
Age
Tidsramme: Baseline
Age, gestational age at birth, age at symptom onset, and age at SMA type 1 diagnosis.
Baseline
Duration Between Symptom Onset and Diagnosis
Tidsramme: Baseline
Baseline

Samarbeidspartnere og etterforskere

Det er her du vil finne personer og organisasjoner som er involvert i denne studien.

Etterforskere

  • Studieleder: Novartis Pharmaceuticals, Novartis Pharmaceuticals

Studierekorddatoer

Disse datoene sporer fremdriften for innsending av studieposter og sammendragsresultater til ClinicalTrials.gov. Studieposter og rapporterte resultater gjennomgås av National Library of Medicine (NLM) for å sikre at de oppfyller spesifikke kvalitetskontrollstandarder før de legges ut på det offentlige nettstedet.

Studer hoveddatoer

Studiestart (Antatt)

20. august 2026

Primær fullføring (Antatt)

20. november 2026

Studiet fullført (Antatt)

20. november 2026

Datoer for studieregistrering

Først innsendt

27. juli 2026

Først innsendt som oppfylte QC-kriteriene

27. juli 2026

Først lagt ut (Faktiske)

30. juli 2026

Oppdateringer av studieposter

Sist oppdatering lagt ut (Faktiske)

31. august 2026

Siste oppdatering sendt inn som oppfylte QC-kriteriene

28. august 2026

Sist bekreftet

1. august 2026

Mer informasjon

Denne informasjonen ble hentet direkte fra nettstedet clinicaltrials.gov uten noen endringer. Hvis du har noen forespørsler om å endre, fjerne eller oppdatere studiedetaljene dine, vennligst kontakt register@clinicaltrials.gov. Så snart en endring er implementert på clinicaltrials.gov, vil denne også bli oppdatert automatisk på nettstedet vårt. .

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