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TEZSPIRE (Tezepelumab) Asthma Japan Post-Marketing Study (PMS)
TEZSPIRE (Tezepelumab) Asthma Japan Post-Marketing Study (PMS)

NCT05729711

Active Not RecruitingN/A

Sponsor: AstraZeneca

Conditions: Bronchial Asthma (Only the Patients With Severe or Intractable Bronchial Asthma Which Could Not be Controlled With the Existing Therapy)

Countries: Japan

The purpose of the investigation is to confirm the followings under the post-marketing actual long-term use of Tezspire. 1. Development of related AEs 2. Contributing factors possibly having an impact on the safety and effectiveness 3. Development of unexpected related AEs

Eligibility overview

Sex: ALL

Healthy volunteers: No

Study type: OBSERVATIONAL

Eligibility criteria
Inclusion Criteria:

* The evaluable patients are those treated with Tezspire for the first time due to "Bronchial asthma (only the patients with severe or intractable bronchial asthma which could not be controlled with the existing therapy)

Exclusion Criteria:

None
Locations (33)
  • Aichi, Japan
  • Akita, Japan
  • Aomori, Japan
  • Chiba, Japan
  • Fukui, Japan
  • Fukuoka, Japan
  • Gifu, Japan
  • Gunma, Japan
  • Hiroshima, Japan
  • Hokkaido, Japan
  • Hyōgo, Japan
  • Ibaraki, Japan
  • Ishikawa, Japan
  • Kagawa, Japan
  • Kanagawa, Japan
  • Kumamoto, Japan
  • Kyoto, Japan
  • Mie, Japan
  • Miyagi, Japan
  • Nara, Japan
  • Numakunai, Japan
  • Okayama, Japan
  • Osaka, Japan
  • Ōita, Japan
  • Saitama, Japan
  • Shimane, Japan
  • Shizuoka, Japan
  • Tochigi, Japan
  • Tokyo, Japan
  • Wakayama, Japan
  • + 3 more on CT.gov