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Efficacy and Safety of ASF-1096 Cream 0.5% in the Treatment of Discoid Lupus Erythematosus (DLE) Lesions (2)

A

Astion Pharma

Status and phase

Completed
Phase 2

Conditions

Discoid Lupus Erythematosus

Treatments

Drug: ASF 1096 placebo cream
Drug: ASF 1096 0.5 % cream

Study type

Interventional

Funder types

Industry

Identifiers

NCT00625157
ASF1096-203

Details and patient eligibility

About

Lupus Erythematosus (LE) is an autoimmune disorder that includes a broad spectrum of clinical forms. One of these forms, Discoid Lupus Erythematosus (DLE) is a chronic disfiguring disease confined to the skin.

The aim of this pivotal trial is to investigate the efficacy and safety of ASF-1096 cream 0.5% in the treatment of patients with DLE or SLE presenting newly developed discoid lesions.

Sex

All

Ages

18 to 70 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • A clinical diagnosis of either DLE or SLE
  • Histological results from biopsy confirming the diagnosis (biopsy can be taken at screening)
  • Is prepared to grant authorised persons access to the medical records
  • Has signed informed consent

Exclusion criteria

  • Has an active skin disease other than DLE or another progressive or serious disease that interferes with the study outcome
  • Has scarring at the target lesion
  • Systemic treatment of SLE

Trial design

0 participants in 2 patient groups, including a placebo group

1
Experimental group
Treatment:
Drug: ASF 1096 0.5 % cream
2
Placebo Comparator group
Treatment:
Drug: ASF 1096 placebo cream

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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