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Pharmacokinetics and Safety Profiles After Administration of DA-5211 and Co-administration of DA-5211-R1 and DA-5211-R2 in Healthy Adult Volunteers

D

Dong-A ST

Status and phase

Completed
Phase 1

Conditions

Healthy

Treatments

Drug: DA-5211
Drug: DA-5211-R1 + DA-5211-R2

Study type

Interventional

Funder types

Industry

Identifiers

NCT05132049
DA5211_BE_I

Details and patient eligibility

About

Pharmacokinetics and safety Profiles after administration of DA-5211 and co-administration of DA-5211-R1 and DA-5211-R2 in healthy adult volunteers

Enrollment

42 patients

Sex

All

Ages

19+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Healthy volunteers
  • BMI between 18 and 30 kg/m2
  • Body weight: Male≥50kg, Female≥45kg
  • Subjects who have signed an informed consent themselves after receiving detailed explanation about clinical study

Exclusion criteria

  • Subjects with allergy or drug hypersensitivity
  • Subjects with clinically significant medical history
  • Subjects with history of drug abuse or addicted

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Crossover Assignment

Masking

None (Open label)

42 participants in 2 patient groups

Sequence A
Experimental group
Treatment:
Drug: DA-5211-R1 + DA-5211-R2
Drug: DA-5211
Sequence B
Experimental group
Treatment:
Drug: DA-5211-R1 + DA-5211-R2
Drug: DA-5211

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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