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Clinical Trials/NCT05354713
NCT05354713
Completed
Phase 1

An Clinical Trial to Evaluate the Pharmacokinetics and the Safety of NVP-1805 Compared to Coadministration of NVP-1805-R1 With NVP-1805-R2 in Healthy Adult Volunteers

NVP Healthcare1 site in 1 country58 target enrollmentNovember 5, 2022

Overview

Phase
Phase 1
Intervention
NVP-1805
Conditions
Healthy Volunteers
Sponsor
NVP Healthcare
Enrollment
58
Locations
1
Primary Endpoint
NVP-1805's Pharmacokinetics of plasma
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

The purpose of this study is to compare the pharmacokinetics of NVP-1805 and coadministration of NVP-1805-R1 with NVP-1805-R2

Detailed Description

Evaluate pharmacokinetics and safety of NVP-1805 compared to coadministration of NVP-1805-R1 with NVP-1805-R2

Registry
clinicaltrials.gov
Start Date
November 5, 2022
End Date
April 27, 2023
Last Updated
2 years ago
Study Type
Interventional
Study Design
Crossover
Sex
All

Investigators

Sponsor
NVP Healthcare
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Healthy adult subjects who signed informed consent
  • BMI of \>18.0 kg/m2 and \<30.0 kg/m2 subject, weight more than 50kg(45 kg or more for woman)

Exclusion Criteria

  • Subjects participated in another clinical trial within 6 months prior to administration of the study drug
  • Inadequate subject for the clinical trial by the investigator's decision
  • Subjects participated in another clinical trial within 6 months prior to administration of the study drug

Arms & Interventions

NVP-1805

orally, once daily on Period 1 and Period 3 (or Period 2 and Period 4) (NVP-1805 80/10/20.8mg)

Intervention: NVP-1805

NVP-1805-R1 and NVP-1805-R2

orally, once daily on Period 1 or Period 3 (or Period 2 and Period 4) (NVP-1805-R1 80mg, NVP-1805-R2 10/20.8mg)

Intervention: NVP-1805-R1 and NVP-1805-R2

Outcomes

Primary Outcomes

NVP-1805's Pharmacokinetics of plasma

Time Frame: 0hours - 72hours

AUCt

Pharmacokinetics of plasma

Time Frame: 0hours - 72hours

Cmax

Study Sites (1)

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