A Phase 3 Long-term Safety Extension Study of SHP647 in Subjects With Moderate to Severe Ulcerative Colitis (AIDA)
a study on Inflammatory Bowel Disease
The purpose of this study is to evaluate the safety and tolerability of long-term treatment with SHP647 in participants with moderate to severe Ulcerative Colitis (UC).
Study will enroll Participants from the maintenance study (SHP647-303) and non-responsive participants from induction studies (SHP647-301 and SHP647-302).
Ulcerative Colitis Immunosuppressants Mesalamine Gastroenteritis Colitis Ulcer Colitis, Ulcerative
You can join if…
Open to people ages 16–80
- Participants and/or their parent or legally authorized representative must have an understanding, ability, and willingness to fully comply with study procedures and restrictions.
- Participants must be able to voluntarily provide written, signed, and dated(personally or via a legally authorized representative) informed consent and/or assent, as applicable, to participate in the study.
- Participants must have been previously enrolled in study SHP647-301, SHP647-302, or
SHP647-303, and reached 1 of the following clinical trial milestones:
- Completed the Week 12 visit in induction study SHP647-301 or SHP647-302, and did NOT achieve a clinical response. Clinical response is defined as: 1) a decrease from baseline in the composite score of patient-reported symptoms using daily e-diary and centrally read endoscopy of at least 2 points and at least 30 percent (%), with an accompanying decrease in the subscore for rectal bleeding greater than equals to (≥) 1 point or a subscore for rectal bleeding less than equals to [≤] 1, OR 2) a decrease from the induction study (SHP647-301 or SHP647-302) baseline total Mayo score of at least 3 points and at least 30%, with an accompanying decrease in the rectal bleeding subscore of at least 1 point or an absolute rectal bleeding subscore of 0 or 1.
- Completed the Week 52 visit in maintenance study SHP647-303.
- Withdrew early from maintenance study SHP647-303 due to treatment failure, defined by an endoscopic subscore that has increased by at least 1 point over baseline in the maintenance study or a value ≥2 plus an increase in clinical subscore (stool frequency
- rectal bleeding score) of at least 2 points. Centrally read endoscopic subscores will be used to determine treatment failure.
- Participants receiving any treatment(s) for ulcerative colitis (UC) are eligible provided they have been, and are anticipated to be, on a stable dose for the designated period of time.
- Participants are males or nonpregnant, nonlactating females who, if sexually active,agree to comply with the contraceptive requirements of the protocol, or females of nonchildbearing potential. Males and females of reproductive potential who are sexually active must agree to use acceptable contraception for the duration of the study.
You CAN'T join if...
- Participants who had major protocol deviation(s) (as determined by the sponsor) in study SHP647-301, SHP647-302, or SHP647-303.
- Participants who permanently discontinued investigational product because of an adverse event (AE), regardless of relatedness to investigational product, in study SHP647-301, SHP647-302, or SHP647-303.
- Participants who are likely to require major surgery for UC.
- Female participants who became pregnant during study SHP647-301, SHP647-302, or SHP647-304, or who are planning to become pregnant during the study period.
- Male participants who are planning to donate sperm must agree not to do so for the duration of the study and through 16 weeks after last dose of investigational product.
- Participants who, in the opinion of the investigator or the sponsor, will be uncooperative or unable to comply with study procedures.
- Participants who have a newly-diagnosed malignancy or recurrence of malignancy (other than resected cutaneous basal cell carcinoma, squamous cell carcinoma, or carcinoma in situ of the uterine cervix that has been treated with no evidence of recurrence).
- Participants who have developed any major illness/condition or evidence of an unstable clinical condition (for example [e.g.] renal, hepatic, hematologic, gastrointestinal(except disease under study), endocrine, cardiovascular, pulmonary, immunologic [e.g.,Felty's syndrome], or local active infection/infectious illness) that, in the investigator's judgment, will substantially increase the risk to the participant if he or she participates in the study.
- Participants with any other severe acute or chronic medical or psychiatric condition or laboratory or electrocardiogram (ECG) abnormality that may increase the risk associated with study participation or investigational product administration or may interfere with the interpretation of study results and, in the judgment of the investigator, would make the participant inappropriate for entry into this study.
- Participants with known exposure to Mycobacterium tuberculosis (TB) since testing at screening in study SHP647-301 or SHP647-302 and who are without a generally accepted course of treatment.
- Participants who are investigational site staff members or relatives of those site staff members or participants who are sponsor employees directly involved in the conduct of the study.
- Participants who are participating in or plan to participate in other investigational studies (other than SHP647-301, SHP647-302, or SHP647-303) during long-term extension study SHP647-304.
- University of California San Francisco not yet accepting patients
San Francisco, California, 94143, United States
- VA Long Beach Healthcare System not yet accepting patients
Long Beach, California, 90822, United States
- Kindred Medical Institute for Clinical Trials, LLC not yet accepting patients
Corona, California, 92879, United States
Please contact me about this study
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If you do not hear from the study team, please call 888-689-8273 and tell them you’re interested in study number NCT03283085.