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A Phase 1 Clinical Trial to Evaluate the Safety and Pharmacokinetics of DW4421 and DW4421S in Healthy Adult Volunteers

Daewon Pharmaceutical logo

Daewon Pharmaceutical

Status and phase

Invitation-only
Phase 1

Conditions

Healthy Adult Volunteer

Treatments

Drug: DW4421S
Drug: DW4421

Study type

Interventional

Funder types

Industry

Identifiers

NCT07364877
DW4421-104

Details and patient eligibility

About

Safety and pharmacokinetic characteristics evaluation of DW4421 and DW4421S

Enrollment

38 estimated patients

Sex

All

Ages

19 to 50 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Healthy adult aged 19 to 50 (inclusive) years
  • Subjects weighing between 50 kg and 90 kg with BMI between 18 and 27 kg/m2 (inclusive)

Exclusion criteria

  • clinical significant liver, kidney, nervous system, respiratory, endocrine, hematology and oncology, cardiovascular, urinary, and mental diseases or past history

Trial design

Primary purpose

Basic Science

Allocation

Randomized

Interventional model

Crossover Assignment

Masking

None (Open label)

38 participants in 2 patient groups

Sequence A
Experimental group
Description:
cross-over
Treatment:
Drug: DW4421
Drug: DW4421S
Sequence B
Experimental group
Description:
Cross-over
Treatment:
Drug: DW4421
Drug: DW4421S

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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