A Study to Evaluate the Pharmacokinetics and Safety of HCP1704 in Healthy Subjects

Hanmi Pharmaceutical

Status and phase: Completed; Phase 1

Conditions: Health, Subjective

Treatments: Drug: HGP1810; Drug: HCP1704

Study type: Interventional

Funder types: Industry

Identifiers

NCT04081857

HM-VIME-102

Details and patient eligibility

About

An open-label, randomized, single-dose crossover study to evaluate the pharmacokinetics and safety of HCP1704 in healthy subjects.

Enrollment: 48 patients

Sex: All

Ages: 19 to 55 years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

1. Age 19~55 years in healthy volunteers
2. BMI is more than 18.5 kg/m^2 , no more than 24.9 kg/m^2
3. Subjects who have ability to comprehend the objectives, contents of study and property of study drug before participating in trial and have willingness to sign of informed consent in writing

Exclusion criteria

1. Presence of medical history or a concurrent disease that may interfere with treatment and safety assessment or completion of this clinical study, including clinically significant disorders in digestive system, neuropsychiatric system, endocrine system, liver, cardiovascular system
2. Subjects who judged ineligible by the investigator

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Crossover Assignment

Masking: None (Open label)

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48 participants in 2 patient groups

Sequence 1

Experimental group

Description:

Period 1 : Fasted state + HGP1810 Period 2 : Fasted state + HCP1704

Treatment:

Drug: HGP1810

Drug: HCP1704

Sequence 2

Experimental group

Description:

Period 1 : Fasted state + HCP1704 Period 2 : Fasted state + HGP1810

Treatment:

Drug: HGP1810

Drug: HCP1704