Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of AMG 139 in Healthy Subjects and Subjects With Moderate to Severe Psoriasis
Primary Purpose
Psoriasis
Status
Completed
Phase
Phase 1
Locations
International
Study Type
Interventional
Intervention
AMG 139
Sponsored by

About this trial
This is an interventional treatment trial for Psoriasis focused on measuring Amgen, AMG 139
Eligibility Criteria
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
Sites / Locations
- Nucleus Network Limited
- Clinical Medical and Analytical eXcellence (CMAX)
- QPharm Pty Limited
- Auckland Clinical Studies Ltd
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Experimental
Arm Label
Part B
Part A
Arm Description
Four dose levels of AMG 139 administered as a single dose SC or IV in subjects with moderate-severe psoriasis (Part B).
Six dose levels of AMG 139 administered as a single dose SC or IV in healthy volunteers.
Outcomes
Primary Outcome Measures
Safety & tolerability: treatment-emergent AEs including clinically significant changes in physical examinations, safety lab tests, ECG, vital signs, or immunogenicity to AMG 139
Secondary Outcome Measures
Characterization of the pharmacokinetics (PK) of AMG 139
Psoriasis Activity and Severity Index (PASI) scores (Part B only)
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT01094093
Brief Title
Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of AMG 139 in Healthy Subjects and Subjects With Moderate to Severe Psoriasis
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
Study Type
Interventional
2. Study Status
Record Verification Date
May 2021
Overall Recruitment Status
Completed
Study Start Date
April 11, 2010 (Actual)
Primary Completion Date
July 26, 2011 (Actual)
Study Completion Date
July 26, 2011 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
AstraZeneca
4. Oversight
5. Study Description
Brief Summary
The purpose of this study is to assess the safety and tolerability of AMG 139 following single subcutaneous (SC) or intravenous (IV) dose administration in healthy subjects and subjects with moderate to severe psoriasis (PsO).
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Psoriasis
Keywords
Amgen, AMG 139
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 1
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
73 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Part B
Arm Type
Experimental
Arm Description
Four dose levels of AMG 139 administered as a single dose SC or IV in subjects with moderate-severe psoriasis (Part B).
Arm Title
Part A
Arm Type
Experimental
Arm Description
Six dose levels of AMG 139 administered as a single dose SC or IV in healthy volunteers.
Intervention Type
Drug
Intervention Name(s)
AMG 139
Intervention Description
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).
Primary Outcome Measure Information:
Title
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
Secondary Outcome Measure Information:
Title
Characterization of the pharmacokinetics (PK) of AMG 139
Time Frame
16-24 weeks
Title
Psoriasis Activity and Severity Index (PASI) scores (Part B only)
Time Frame
16-24 weeks
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
55 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
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
Facility Information:
Facility Name
Nucleus Network Limited
City
Melbourne
State/Province
Victoria
ZIP/Postal Code
3004
Country
Australia
Facility Name
Clinical Medical and Analytical eXcellence (CMAX)
City
Adelaide
ZIP/Postal Code
SA500
Country
Australia
Facility Name
QPharm Pty Limited
City
Herston
ZIP/Postal Code
4006
Country
Australia
Facility Name
Auckland Clinical Studies Ltd
City
Grafton
ZIP/Postal Code
1010
Country
New Zealand
12. IPD Sharing Statement
Learn more about this trial
Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of AMG 139 in Healthy Subjects and Subjects With Moderate to Severe Psoriasis
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