Phase 1 Clinical Trial to Evaluate Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of DWP212525 in Healthy Volunteers

Trial statusRecruiting
Trial phasePhase 1
Trial typeInterventional
Biological sexAll
Age19-55
SponsorDaewoong Pharmaceutical Co. LTD.

About this trial

The safety and tolerability of single and multiple administration of DWP212525

Eligibility criteria

Qualifiers

Healthy adult volunteers aged 19 to 55 years

Those with a body weight ≥ 50.0 kg to ≤ 90.0 kg with a body mass index (BMI) of ≥ 18.0 kg/m2 to ≤ 30.0 kg/m2

Received a sufficient explanation on this study

Eligible as subjects in the study

Disqualifiers

History of diseases such as clinically significant disease of hepatobiliary

Following conditions applicable to clinically significant acute or chronic infections or the past history confirmed via an interview

Hemato-oncologic diseases, including malignant tumor diagnosis

Past history of tuberculosis infection or confirmed tuberculosis in the IGRA test and chest X-ray test

Trial design

Treatments tested in this trial

  • DWP212525 XXmg
  • DWP212525 placebo

Treatment groups

84 Participants
are divided into 11 treatment groups

11

Treatment groups

See each treatment group below.