At a glance
ClinicalIndex Comparison RecordPhase 3Completed· 65 enrolled
Drug / intervention
Biological: Experimental: Tezepelumabdrug
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.
Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.
A 52-Week, Open-Label, Multicentre Study to Evaluate the Safety of Tezepelumab in Japanese Adults and Adolescents With Inadequately Controlled Severe Asthma (NOZOMI)
In Brief
A Phase 3 clinical trial evaluating Biological: Experimental: Tezepelumab for Severe Asthma. Completed, enrolled 65 participants across 5 sites.
Detailed Summary
This is an open-label, single arm study designed to evaluate the safety of tezepelumab administered subcutaneously every 4 weeks in Japanese adult and adolescent subjects with inadequately controlled severe asthma.
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsSevere Asthma
CountriesJapan
CollaboratorsAmgen
Timeline
Phase 3CompletedFinished
2020202120222023202420252026
Enrollment StartJun 2019
First PostedAug 2019
Primary CompletionMar 2021
TodayJul 2026
First PostedAug 7, 2019
Enrollment StartJun 10, 2019
Primary CompletionMar 18, 2021
TodayJul 2, 2026
Enrollment to primary: 1.8 yearsPosted 6.9 years ago
Interventions
Biological: Experimental: Tezepelumabdrug
Tezepelumab subcutaneous injection every 4 weeks