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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01294969
Other study ID # SMA-10-15
Secondary ID
Status Completed
Phase Phase 4
First received February 10, 2011
Last updated December 15, 2016
Start date September 2010
Est. completion date October 2011

Study information

Verified date October 2011
Source Alcon Research
Contact n/a
Is FDA regulated No
Health authority Korea: Food and Drug Administration
Study type Interventional

Clinical Trial Summary

To evaluate patient perceptions of Al-4943 in subjects with allergic conjunctivitis previously treated with a topical ocular anti-allergy leukotriene-release inhibitor medication.


Recruitment information / eligibility

Status Completed
Enrollment 47
Est. completion date October 2011
Est. primary completion date October 2011
Accepts healthy volunteers No
Gender Both
Age group 12 Years and older
Eligibility Inclusion Criteria:

- History of allergic conjunctivitis within last 24 months

- Active signs and symptoms of ocular allergies

Exclusion Criteria:

- Severe or serious ocular condition, ocular surgical intervention, ocular infection

Study Design

Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment


Intervention

Drug:
AL-4943A
Once daily topical ocular allergy medication used for 7 days

Locations

Country Name City State
Korea, Republic of Alcon Korea Ltd. Seoul

Sponsors (1)

Lead Sponsor Collaborator
Alcon Research

Country where clinical trial is conducted

Korea, Republic of, 

Outcome

Type Measure Description Time frame Safety issue
Primary Overall Patient satisfaction 7 days No
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