H Plus Yangji Hospita
Seoul, South Korea
NCT Number: NCT05354713
The purpose of this study is to compare the pharmacokinetics of NVP-1805 and coadministration of NVP-1805-R1 with NVP-1805-R2
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Notify Me19 year and older
All sexes
Interventional
Phase 1
Seoul, South Korea
Evaluate pharmacokinetics and safety of NVP-1805 compared to coadministration of NVP-1805-R1 with NVP-1805-R2
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
NVP-1805 (80/10/20.8mg)
coadministration of NVP-1805-R1(80mg) and NVP-1805-R2(10/20.8mg)
Time frame: 0hours - 72hours
AUCt
Time frame: 0hours - 72hours
Cmax
NVP Healthcare
Industry
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
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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