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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02108288
Other study ID # 1085EL-13-004
Secondary ID
Status Completed
Phase Phase 1
First received March 27, 2014
Last updated April 2, 2015
Start date April 2014
Est. completion date August 2014

Study information

Verified date April 2015
Source Otsuka Pharmaceutical Co., Ltd.
Contact n/a
Is FDA regulated No
Health authority Japan: Ministry of Health, Labor and Welfare
Study type Interventional

Clinical Trial Summary

OPC-1085EL ophthalmic solution, carteolol long-acting ophthalmic solution or latanoprost ophthalmic solution are administered once daily for 7 days and the effect on the blood concentration of carteolol and latanoprost in OPC-1085EL ophthalmic solution by formulating the combination drug will be determined.


Recruitment information / eligibility

Status Completed
Enrollment 30
Est. completion date August 2014
Est. primary completion date May 2014
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Male
Age group 20 Years to 45 Years
Eligibility Inclusion Criteria:

- Subjects who are considered medically healthy per investigator's judgment

Exclusion Criteria:

- Subjects with ocular conditions as defined by the protocol

- Subjects with intraocular pressure: <10 or =22 mmHg

Study Design

Allocation: Randomized, Endpoint Classification: Pharmacokinetics Study, Intervention Model: Parallel Assignment, Masking: Open Label


Related Conditions & MeSH terms


Intervention

Drug:
OPC-1085EL ophthalmic solution

Carteolol long-acting ophthalmic solution

Latanoprost ophthalmic solution


Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Otsuka Pharmaceutical Co., Ltd.

Country where clinical trial is conducted

Japan, 

Outcome

Type Measure Description Time frame Safety issue
Primary Cmax of Carteolol Day 1 and Day 7 No
Primary Cmax of Latanoprost Acid Day 1 and Day 7 No
Secondary Tmax of Carteolol Day 1 and Day 7 No
Secondary Tmax of Latanoprost Acid Day 1 and Day 7 No
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