Fasenra Pediatric Japan Post-Marketing Study(PMS)
The purpose of the investigation is to confirm the followings under the post-marketing actual use of Fasenra® Subcutaneous Injection 30 mg / 10mg Syringe (hereinafter referred to as Fasenra). 1. Development of unexpected related AEs\* 2. To grasp development of related AEs\* in the real-world post-marketing setting. 3.
| Condition(s) | Bronchial Asthma |
|---|---|
| Status | Recruiting |
| Study type | Observational |
| Summary | The purpose of the investigation is to confirm the followings under the post-marketing actual use of Fasenra® Subcutaneous Injection 30 mg / 10mg Syringe (hereinafter referred to as Fasenra). 1. Development of unexpected related AEs\* 2. To grasp development of related AEs\* in the real-world post-marketing setting. 3. Effectiveness (pulmonary function and asthma control) \* AEs investigator or MAH considers that there is a reasonable possibility that the experience may have been caused by the drug |
| Who can participate | Inclusion Criteria: The evaluable patients in children aged ≥6 years to \<15 years are those treated with Fasenra for the first time due to "Bronchial asthma (only the patients with intractable bronchial asthma which could not be controlled with the existing therapy) Exclusion Criteria: none |
| Sex | All |
| Lead sponsor | AstraZeneca |
| Locations | Aichi, Japan; Chiba, Japan; Hiroshima, Japan; Hokkaido, Japan; Hyōgo, Japan; Ibaraki, Japan (+7 more sites) |
| Start date | 2024-07-16 |
| NCT ID | NCT06427876 |
| Official listing | https://clinicaltrials.gov/study/NCT06427876 |