Study to Compare and Evaluate the Safety and Pharmacokinetics After Subcutaneous Injection of HUC2-676 or HUC2-676-R in Healthy Adult Subjects
NCT ID: NCT07337174
Last Updated: 2026-01-13
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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NOT_YET_RECRUITING
PHASE1
40 participants
INTERVENTIONAL
2026-01-25
2026-03-24
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
CROSSOVER
TREATMENT
NONE
Study Groups
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HUC2-676
HUC2-676
subcutaneous injection
HUC2-676-R
HUC2-676-R
subcutaneous injection
Interventions
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HUC2-676
subcutaneous injection
HUC2-676-R
subcutaneous injection
Eligibility Criteria
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Inclusion Criteria
* Subjects who have been fully informed of the details of this clinical trial, have fully understood the information, have voluntarily decided to participate, and have provided written informed consent to comply with all protocol requirements throughout the trial period.
Exclusion Criteria
* For females: Pregnant women (positive urine hCG) or nursing mothers.
19 Years
65 Years
ALL
Yes
Sponsors
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Huons Co., Ltd.
INDUSTRY
Responsible Party
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Principal Investigators
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Park
Role: PRINCIPAL_INVESTIGATOR
Chungbuk National University Hospital
Central Contacts
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Other Identifiers
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HUC2-676
Identifier Type: -
Identifier Source: org_study_id
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