First Human Dose Study of Anti-IL-20 in Psoriasis: A Study of Safety, Tolerability and Early Signals of Biologic and Clinical Effects
| Status: | Terminated |
|---|---|
| Conditions: | Psoriasis |
| Therapuetic Areas: | Dermatology / Plastic Surgery |
| Healthy: | No |
| Age Range: | 18 - 75 |
| Updated: | 2/10/2017 |
| Start Date: | April 2008 |
| End Date: | January 2011 |
A Randomised, Double-blind, Placebo-controlled, Single and Multiple Dose, Dose-escalation Trial of Anti-IL-20 (109-0012) 100 mg/Vial in Psoriatic Subjects, Followed by an Expansion Phase
This trial is conducted in the United States of America (USA). The aim of this clinical
trial is evaluate the safety and tolerability of anti-IL-20 in patients with psoriasis and
to determine the preliminary efficacy in an expansion phase of this trial.
This trial consists of 3 parts: A single dose (SD) dose-escalation phase for 16 weeks, a
multiple dose (MD) dose-escalation phase for 22 weeks, and a MD expansion phase for 22
weeks.
Initiation of the MD expansion phase will depend on results from the SD and MD
dose-escalation phases and only if an acceptable safety profile is present. Subjects
participating in the expansion phase are not allowed to have participated in the previous
phases (SD and MD dose-escalation phases) of the trial.
trial is evaluate the safety and tolerability of anti-IL-20 in patients with psoriasis and
to determine the preliminary efficacy in an expansion phase of this trial.
This trial consists of 3 parts: A single dose (SD) dose-escalation phase for 16 weeks, a
multiple dose (MD) dose-escalation phase for 22 weeks, and a MD expansion phase for 22
weeks.
Initiation of the MD expansion phase will depend on results from the SD and MD
dose-escalation phases and only if an acceptable safety profile is present. Subjects
participating in the expansion phase are not allowed to have participated in the previous
phases (SD and MD dose-escalation phases) of the trial.
Inclusion Criteria:
- Subjects with moderate to severe stable chronic plaque psoriasis for at least 6
months, with or without psoriatic arthritis
- Affected body surface area (BSA) greater than or equal to 15%
- Physician's Global Assessment (PGA) score of 3 or more
- Female subjects of non-childbearing potential or postmenopausal for at least 1 year.
Male subjects must agree to use effective method of birth control
- Body Mass Index (BMI) less than or equal to 38.0 kg/m2
Exclusion Criteria:
- Concomitant anti-psoriatic treatment
- Infectious disease requiring systemic anti-infectious treatment within the 2 weeks
prior to administration of trial drug
- Known history of Human Immunodeficiency Virus (HIV)
- Hepatitis B and/or C (determined by test)
- Live virus or bacteria vaccines within the last month before drug administration
- Known active herpes/herpes zoster/cold sores
- Kidney insufficiency
- Liver insufficiency
- Lymphoproliferative disease
- History or signs of malignancy within the last 5 years
We found this trial at
14
sites
Click here to add this to my saved trials
Click here to add this to my saved trials
Click here to add this to my saved trials
Click here to add this to my saved trials
Click here to add this to my saved trials
Click here to add this to my saved trials
Click here to add this to my saved trials
Click here to add this to my saved trials
Click here to add this to my saved trials
Click here to add this to my saved trials
Click here to add this to my saved trials
Click here to add this to my saved trials
Click here to add this to my saved trials
Click here to add this to my saved trials