Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of AMG 139 in Healthy Subjects and Subjects With Moderate to Severe Psoriasis
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ClinicalTrials.gov Identifier: NCT01094093 |
Recruitment Status :
Completed
First Posted : March 26, 2010
Last Update Posted : May 10, 2021
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Condition or disease | Intervention/treatment | Phase |
---|---|---|
Psoriasis | Drug: AMG 139 | Phase 1 |
Study Type : | Interventional (Clinical Trial) |
Actual Enrollment : | 73 participants |
Allocation: | Randomized |
Intervention Model: | Parallel Assignment |
Masking: | Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor) |
Primary Purpose: | Treatment |
Official Title: | A Randomized, Double-Blind, Placebo-Controlled, Ascending Single-Dose Study to Evaluate the Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of AMG 139 in Healthy Subjects and Subjects With Moderate to Severe Psoriasis |
Actual Study Start Date : | April 11, 2010 |
Actual Primary Completion Date : | July 26, 2011 |
Actual Study Completion Date : | July 26, 2011 |
Arm | Intervention/treatment |
---|---|
Experimental: Part B
Four dose levels of AMG 139 administered as a single dose SC or IV in subjects with moderate-severe psoriasis (Part B).
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Drug: AMG 139
Six dose levels of AMG 139 administered as a single dose SC or IV in healthy volunteers (Part A) and subjects with moderate-severe psoriasis (Part B). |
Experimental: Part A
Six dose levels of AMG 139 administered as a single dose SC or IV in healthy volunteers.
|
Drug: AMG 139
Six dose levels of AMG 139 administered as a single dose SC or IV in healthy volunteers (Part A) and subjects with moderate-severe psoriasis (Part B). |
- Safety & tolerability: treatment-emergent AEs including clinically significant changes in physical examinations, safety lab tests, ECG, vital signs, or immunogenicity to AMG 139 [ Time Frame: 16-24 weeks ]
- Characterization of the pharmacokinetics (PK) of AMG 139 [ Time Frame: 16-24 weeks ]
- Psoriasis Activity and Severity Index (PASI) scores (Part B only) [ Time Frame: 16-24 weeks ]

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Ages Eligible for Study: | 18 Years to 55 Years (Adult) |
Sexes Eligible for Study: | All |
Accepts Healthy Volunteers: | Yes |
Inclusion Criteria:
Part A - Healthy Volunteers:
- Healthy male or female of non-reproductive potential subjects between 18 to 45 years-of-age
- Body mass index (BMI) between 18 and 32 kg/m2
- Normal or clinically acceptable physical examination, clinical laboratory values, and ECG
- Additional inclusion criteria apply
Part B - Psoriasis Subjects:
- Male or female of non-reproductive potential subjects with PsO between 18 to 55 years-of-age
- Body mass index (BMI) between 18 and 32 kg/m2
- Normal or clinically acceptable physical examination (PE), clinical laboratory values, and ECG; clinically acceptable PE includes evidence of moderate to severe plaque PsO
- Diagnosis of plaque PsO for at least 6 months
- Moderate to severe plaque PsO defined by:
- A minimum PASI score of ≥ 10
- Psoriasis involving ≥ 10% of the Body Surface Area (BSA)
- Additional inclusion criteria apply
Exclusion Criteria:
Parts A - Healthy Volunteers:
- History or evidence of a clinically significant disorder (including psychiatric), condition or disease that would pose a risk to subject safety or interfere with the study evaluation, procedures or completion;
- Recent or on-going infection(s)
- Underlying condition(s) that predisposes the subject to infections
- History of malignancy of any type, other than in situ cervical cancer or surgically excised non-melanomatous skin cancers in past 5 years
- Additional exclusion criteria apply
Part B - Psoriasis Subjects:
- History or evidence of a clinically significant disorder (including psychiatric), condition or disease that would pose a risk to subject safety or interfere with the study evaluation, procedures or completion;
- Recent or on-going infection(s)
- Underlying condition(s) that predisposes the subject to infections
- Guttate, pustular, or other non-plaque forms of PsO
- Evidence of skin conditions other than PsO (eg, eczema) that would interfere with evaluations of the effect of investigational product on psoriasis
- History of malignancy of any type, other than in situ cervical cancer or surgically excised non-melanomatous skin cancers in past 5 years
- Additional exclusion criteria apply

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01094093
Australia, Victoria | |
Nucleus Network Limited | |
Melbourne, Victoria, Australia, 3004 | |
Australia | |
Clinical Medical and Analytical eXcellence (CMAX) | |
Adelaide, Australia, SA500 | |
QPharm Pty Limited | |
Herston, Australia, 4006 | |
New Zealand | |
Auckland Clinical Studies Ltd | |
Grafton, New Zealand, 1010 |
Responsible Party: | AstraZeneca |
ClinicalTrials.gov Identifier: | NCT01094093 |
Other Study ID Numbers: |
20080767 |
First Posted: | March 26, 2010 Key Record Dates |
Last Update Posted: | May 10, 2021 |
Last Verified: | May 2021 |
Amgen AMG 139 |
Psoriasis Skin Diseases, Papulosquamous Skin Diseases |