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Post Marketing Surveillance To Observe Safety And Efficacy Of Enbrel In Pediatric Patients With Psoriasis

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Pfizer

Status

Withdrawn

Conditions

Pediatric Psoriasis

Treatments

Drug: Enbrel group

Study type

Observational

Funder types

Industry

Identifiers

NCT01432249
B1801135

Details and patient eligibility

About

Enbrel was first approved as new medicine on 06 Oct 2003 in Korea and the indication of Pediatric Psoriasis was approved on 23 Sep 2009. However, as required for any new indication approved by Korea Food and Drug Administration (KFDA), safety and efficacy information of new indication should be provided at minimum 600 subjects administered in the setting of routine practice during the initial 4 years after new indication approved.

Full description

All patients enrolled should meet the usual prescribing criteria for Enbrel in psoriasis as per the local product information for usage.

Sex

All

Ages

8 to 17 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Children and adolescents aged 8 years to 17 years at time of consent
  2. Chronic severe psoriasis patients who are inadequately controlled by, or are intolerant to, other systemic therapies or phototherapies

Exclusion criteria

  1. Patients with known hypersensitivity to Enbrel or any component of the product
  2. Patients with active infections including chronic or localized infections such as tuberculosis (Treatment of Enbrel should not be initiated)

Trial design

0 participants in 1 patient group

Enbrel
Description:
The patients who are prescribed Enbrel for pediatric psoriasis
Treatment:
Drug: Enbrel group

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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