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Post-Marketing Observational Study to Evaluate Safety Profile of Avamys Treatment in Chinese Patients

Post-Marketing Observational Study to Evaluate Safety Profile of Avamys Treatment in Chinese Patients

Status
Recruiting
Phases
Phase 4
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR-OPC-17013719
Enrollment
Unknown
Registered
2017-12-06
Start date
2016-11-30
Completion date
Unknown
Last updated
2017-12-11

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Unlimited

Interventions

Case series:Avamys

Sponsors

Children’s Hospital of Chongqing Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
2 Years to No maximum

Inclusion criteria

Inclusion criteria: Subjects who have been prescribed Avamys for appropriate medical use.

Exclusion criteria

Exclusion criteria: No ICF

Design outcomes

Primary

MeasureTime frame
Adverse evevt;

Countries

China

Contacts

Public ContactYun-tao Jia

Children's Hospital of Chongqing Medical University

32233125@qq.com+86 023-63625666

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026