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A Study of DWJ1248 in Prevention of COVID-19 Infection After the Exposure of SARS-COV-2

D

Daewoong Pharmaceutical

Status and phase

Terminated
Phase 3

Conditions

SARS-COV-2 Infection
Covid19

Treatments

Drug: DWJ1248
Drug: Placebo

Study type

Interventional

Funder types

Industry

Identifiers

NCT04721535
DW_DWJ1248303

Details and patient eligibility

About

To evaluate the prevention of SARS-COV-2 infection after administration of DWJ1248 in person who contact from COVID-19 confirmed patient compared to the placebo.

Enrollment

9 patients

Sex

All

Ages

19+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Adults over the age of 19 as of the signed date in written consent
  • Subjects in self-quarantine who contact from COVID-19 confirmed patient
  • Subjects who have COVID-19 negative RT-PCR result
  • Subjects with no symptoms of COVID-19

Exclusion criteria

  • Subjects who cannot orally administer the investigational products
  • Subjects who need administration of immunosuppressants
  • Subjects who are allergic or sensitive to investigational products or its ingredients
  • Subjects who have a history of drug and/or alcohol abuse within 12 months before screening
  • Subjects who have been identified with uncontrolled concomitant diseases or conditions, including significant mental illness and social conditions, that may affect compliance with clinical trial procedures according to the determination of the investigators

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

9 participants in 2 patient groups, including a placebo group

DWJ1248
Experimental group
Description:
Camostat mesilate 200mg
Treatment:
Drug: DWJ1248
Placebo
Placebo Comparator group
Description:
Placebo
Treatment:
Drug: Placebo

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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