Study to Evaluate Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of AMG 181.



Status:Completed
Conditions:Colitis, Gastrointestinal, Crohns Disease
Therapuetic Areas:Gastroenterology
Healthy:No
Age Range:18 - 65
Updated:1/1/2014
Start Date:February 2011
End Date:December 2013
Contact:Amgen Call Center
Phone:866-572-6436

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A Phase 1, Randomized, Double-Blind, Placebo-controlled, Ascending Multiple Dose Study to Evaluate the Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of AMG 181 in Healthy Subjects, in Subjects With Active Ulcerative Colitis, and in Subjects With Active Crohn's Disease.

To assess the safety and tolerability of multiple subcutaneous doses of AMG 181 in healthy
subjects, in subjects with active ulcerative colitis, and in subjects with active Crohn's
disease.


Inclusion Criteria:

- Body Mass Index (BMI) between 18 and 34 kg/m2

- Normal physical and neurological examination, clinical laboratory values and ECG

- Ulcerative Colitis Disease Activity Index (UCDAI, aka Mayo score) score of 4 to 10
(inclusive), with a minimum sigmoidoscopy score of 1; (for subjects with ulcerative
colitis)

- Crohn's Disease Activity Index (CDAI) score of >150 and < 450 at screening (for
subjects with Crohn's disease)

- Additional inclusion criteria apply

Exclusion Criteria:

- 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 evaluations, procedures or completion

- History of malignancy of any type, other than in situ cervical cancer or surgically
excised non-melanomatous skin cancers within the past 5 years

- Underlying condition(s) that predisposes the subject to infections

- Disease limited to the rectum, i.e. within 10 cm of the anal verge (for subjects with
ulcerative colitis)

- Evidence of severe disease (as evidenced by an Hb concentration less or equal to
10g/dL; toxic megacolon, or an UCDAI score greater than 10) (for subjects with
ulcerative colitis)

- Subject has short bowel syndrome (for subjects with Crohn's disease)

- Presence of an ostomy (for subjects with Crohn's disease)

- Presence of a fistula (for subjects with Crohn's disease)

- Additional exclusion criteria apply
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