Last updated on December 2019

A Study of KY1005 in Patients With Moderate to Severe Atopic Dermatitis


Are you eligible to participate in this study?

You may be eligible for this study if you meet the following criteria:

  • Conditions: ATOPIC DERMATITIS
  • Age: Between 18 - 75 Years
  • Gender: Male or Female

Inclusion Criteria:

  • Adults ( 18 years but < 75 years of age) with Atopic Dermatitis (AD) for 1 year or longer at Baseline (Day 1; prior to first administration of Investigational Medicinal Product (IMP)).
  • EASI of 12 or higher at the Screening Visit and 16 or higher at Baseline.
  • vIGA of 3 or 4 at Baseline.
  • AD involvement of 10 percent or more of BSA at Baseline.
  • Documented history, within 6 months prior to Baseline, of either inadequate response to topical treatments or inadvisability of topical treatments.
  • Must have applied a stable dose of topical bland emollient (simple moisturiser, no additives [e.g., urea]) at least twice daily for at least 7 consecutive days before Baseline.
  • Able and willing to comply with requested study visits/telephone visits and procedures.
  • Able and willing to provide punch biopsy of both lesional and non-lesional skin at Baseline.
  • Able and willing to provide written informed consent.

Exclusion Criteria:

  • Recent treatment within specific time windows before the baseline visit for the management of atopic dermatitis such as topical or systemic corticosteroids, biologic or investigational therapies and/or phototherapy.
  • Known history of or suspected significant current immunosuppression, including history of invasive opportunistic infections despite infection resolution or otherwise recurrent infections of abnormal frequency or prolonged duration.
  • Basal and squamous cell skin cancer in the last 3 years prior to Baseline. Any other malignancies in the last 5 years prior to Baseline (excluding in situ cervical carcinoma).
  • Severe concomitant illness that would in the Investigator's opinion inhibit the patient's participation in the study, including for example, but not limited to, renal disease, neurological conditions, heart failure and pulmonary disease.
  • Laboratory values at the Screening Visit:
  • a. Serum creatinine > 1.6 mg/dL (141 mol/L) in female patients and > 1.9 mg/dL (168 mol/L) in male patients;
  • b. Alanine aminotransferase (ALT) or aspartate aminotransferase (AST) > 1.5 upper limit of normal (ULN);
  • c. Platelet count < 100 10^9/L;
  • d. Haemoglobin (Hb): Male < 13.5g/dL and Female <12g/dL;
  • e. White blood cell count (WBCC) < 3.0 10^9/L;
  • f. Absolute neutrophil count < 2.0 10^9/L;
  • g. Absolute lymphocyte count < 0.5 10^9/L;
  • h. Total bilirubin > ULN.
  • Participation in any other clinical study, including non-interventional studies.

Recruitment Status: Open


Brief Description Eligibility Contact Research Team


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