H+ Yangji Hospital
Seoul, South Korea
NCT Number: NCT07312799
To evaluate the pharmacokinetic interactions of AD-2321, AD-2322 in healthy adult volunteers.
Trial opening soon.
Get Notified19 year–64 year
All sexes
Interventional
Phase 1
Seoul, South Korea
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
AD-2321 Oral Tablet
AD-2322 Oral Tablet
AD-2321 Oral Tablet+AD-2322 Oral Tablet
Time frame: pre-dose (0hour) to 24 hours post-dose on Day 14
AUCτ,ss
Time frame: pre-dose (0hour) to 24 hours post-dose on Day 14
Contact information is provided by the study sponsor or research team.
Addpharma Inc.
Industry
A Two-arm, Open-label, Single-sequence, Multiple-dose Study to Evaluate the Pharmacokinetic Interaction and the Safety of AD-2321 and AD-2322 in Healthy Adult Volunteers
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
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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