Rhinitis, Allergic, Perennial and Seasonal Clinical Trial
Official title:
Drug Use Investigation for XYZAL
Verified date | August 2015 |
Source | GlaxoSmithKline |
Contact | n/a |
Is FDA regulated | No |
Health authority | Japan: Pharmaceuticals and Medical Devices Agency |
Study type | Observational |
This post-marketing surveillance study (PMS) is conducted to collect safety and efficacy data among subjects with allergic rhinitis, urticaria, eczema, dermatitis, skin irritation, prurigo or pruritus cutaneous who have never been treated with levocetirizine tablets before.
Status | Completed |
Enrollment | 10728 |
Est. completion date | December 2013 |
Est. primary completion date | December 2013 |
Accepts healthy volunteers | No |
Gender | Both |
Age group | N/A and older |
Eligibility |
Inclusion Criteria: - Must be the first time for taking levocetirizine tablet Exclusion Criteria: - As this is PMS study, there are no exclusion criteria. |
Time Perspective: Prospective
Country | Name | City | State |
---|---|---|---|
n/a |
Lead Sponsor | Collaborator |
---|---|
GlaxoSmithKline |
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | The number of adverse events in Japanese subjects treated with levocetirizine tablets | 4 weeks | Yes |
Status | Clinical Trial | Phase | |
---|---|---|---|
Completed |
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