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Clinical Trial Details — Status: Temporarily not available

Administrative data

NCT number NCT01889745
Other study ID # 2013_0361
Secondary ID
Status Temporarily not available
Phase N/A
First received June 20, 2013
Last updated June 20, 2013

Study information

Verified date June 2013
Source Biotoxtech Co., Ltd
Contact n/a
Is FDA regulated No
Health authority Korea: Food and Drug Administration
Study type Expanded Access

Clinical Trial Summary

This study is designed to multiple dose and dose escalation study


Description:

A Phase I Clinical Study, Randomized, Single-blind, Placebo-controlled, Single Dose Escalation Study of the Safety, Tolerabiluty, and Pharmacokinetics of HX-1171 in Healthy Male Subjects


Recruitment information / eligibility

Status Temporarily not available
Enrollment 0
Est. completion date
Est. primary completion date
Accepts healthy volunteers
Gender Male
Age group 20 Years to 40 Years
Eligibility Inclusion Criteria:

- Adult males aged 20 to 40 years at screening.

- Be able to comply with the requirement of the study. Subject must provide written informed consent prior to study participation.

Exclusion Criteria:

- History or presence of liver, kidney, or nervous system disease, respiratory disorders, endocrinological disorders, hemato-oncologic, cardiovascular or psychiatric or gastrointestinal disorders.

- History of known hypersensitivity to drugs including HX-1171.

Study Design

N/A


Related Conditions & MeSH terms


Intervention

Drug:
HX-1171
Anti-oxidatant, Anti-inflamation

Locations

Country Name City State
Korea, Republic of Asan Medical Center Special City of Seoul

Sponsors (1)

Lead Sponsor Collaborator
Biotoxtech Co., Ltd

Country where clinical trial is conducted

Korea, Republic of, 

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