The Plecanatide Chronic Idiopathic Constipation (CIC) Study



Status:Completed
Conditions:Constipation
Therapuetic Areas:Gastroenterology
Healthy:No
Age Range:18 - 75
Updated:7/8/2018
Start Date:October 2011
End Date:December 2012

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Study SP304-20210: A Randomized, 12-Week, Double-Blind, Placebo-Controlled, Repeat-Dose, Oral, Dose-Ranging Study to Assess the Safety and Efficacy of Plecanatide in Patients With Chronic Idiopathic Constipation

This is a randomized, double-blind, placebo controlled, 12 week repeat oral dose, dose
ranging study to determine the efficacy and safety of 3 doses of plecanatide compared to
placebo in patients with Chronic Idiopathic Constipation (CIC).

This is a Phase IIb/III, randomized, double-blind, placebo-controlled, 12-Week, Repeat, Oral
Dose Ranging, study to determine the safety and efficacy of plecanatide in patients with
chronic idiopathic constipation (CIC). Subjects diagnosed with CIC via modified Rome III
criteria will be screened against the inclusion and exclusion criteria for the study and
enter a 2 Week pre treatment screening. During this phase patients will be required to call
in their bowel movements (BM diary) as they occur, and call at least once daily to complete a
patient diary of questions on their symptoms (Symptom Diary) associated with CC, as they will
throughout the trial. Patients who complete at least 5 days of dosing per week, 6 of each 7
day period of BM diary calls, and continue to have less than 3 complete spontaneous movements
per week (as well as meeting other inclusion and exclusion criteria) will be enrolled and
randomized to one of three plecanatide doses 0.3 mg, 1.0 mg, and 3.0 mg or placebo. 880
patients will be randomized with the intent of having 200 patients per treatment group (each
group the same size) included in efficacy analyses. All subjects receiving at least one dose
of plecanatide or matching placebo will be included in the safety analyses.

Inclusion Criteria:

- Male or female aged 18-75, inclusive

- Body Mass Index = 18-35 kg/m2, inclusive

- Meets modified Rome III criteria for functional chronic idiopathic constipation for at
least 3 months with symptom onset for at least 6 months. Note: For this trial,
patients with manual maneuvers required for >25% of defecations will not be eligible
for participation.

- Less than 3 CSBMs per week at baseline and during pretreatment

- Completed a colonoscopy in accordance with medical guidelines as appropriate, with no
clinically significant findings

- Patient is willing to discontinue use of supplemental fiber, laxatives, prescription
and nonprescription medications, herbal or dietary supplements intended to treat
constipation during the screening, pre-treatment, treatment and 2-week post-treatment
periods

- Willing to maintain a stable diet during the study.

- Patients with hemorrhoids and/or diverticulosis (NOT diverticulitis) CAN be entered
into the study.

Exclusion Criteria:

- Loose stool (mushy) or watery (Bristol score- 6 or 7) stool in the absence of any
laxative or prohibited medicine for > 25% of BMs during the 3 months prior to
screening visit OR during the 14 day treatment period

- Patient meets the Rome III criteria for Irritable Bowel Syndrome (IBS-C)

- Active peptic ulcer disease not adequately treated or not stable

- History of cathartic colon, laxative, enema abuse, or ischemic colitis.

- Fecal impaction within 3 months of screening

- Patient has had /has any: diseases or conditions associated with constipation (GI or
CNS), structural abnormality of the GI tract or gastric bypass surgery, pelvic floor
dysfunction, pseudo-obstruction, active infectious gastritis, diverticulitis, anal
fissures or any disease or condition that can affect GI motility or defecation or can
be associated with abdominal pain

- Unexplained and clinically significant "alarm symptoms" including lower GI bleeding,
iron-deficiency anemia, weight loss or systemic signs of infection or colitis.

- Major surgery within 60 days of screening.
We found this trial at
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Orange, California 92868
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3000 Hundertmark
Chaska, Minnesota 55318
952-556-2686
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4495 Hale Parkway
Denver, Colorado 80220
303-399-4067
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875 Military Trl # 210
Jupiter, Florida 33458
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707 Hollybrook Drive
Longview, Texas 75605
903-238-8854
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4301 NW 63rd Street
Oklahoma City, Oklahoma 73116
405-840-5971
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100 West Gore St # 202
Orlando, Florida 32806
(407) 426-9299
Compass Research LLC Compass Research is a clinical research company dedicated to testing new medications...
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401 Roxbury Road
Rockford, Illinois 61107
815-397-7340
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1045 East 3900 South
Salt Lake City, Utah 84124
801-261-2000
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6261 N. La Cholla Blvd
Tucson, Arizona 85741
520-219-6394
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1897 Palm Beach Lakes Boulevard
West Palm Beach, Florida 33409
561-689-0606
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1709 S Rock Rd
Wichita, Kansas 67207
316-689-6629
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Albuquerque, New Mexico 87108
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Albuquerque, New Mexico
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Anaheim, California 92801
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Augusta, Kansas 67010
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Baton Rouge, Louisiana 70809
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Baton Rouge, Louisiana 70809
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Boone, North Carolina 28607
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Boston, Massachusetts 02135
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Brooklyn, New York 11230
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Brooklyn, New York 11215
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6400 Laurel Canyon Boulevard
Burbank, California 91505
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Centerville, Ohio 45459
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Chapel Hill, North Carolina 27599
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Charlotte, North Carolina 28210
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Chattanooga, Tennessee 37421
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Chesterfield, Michigan 48098
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Chicago, Illinois 60603
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Christiansburg, Virginia 24073
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Chula Vista, California 91910
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Clive, Iowa 50325
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Columbia, South Carolina 29203
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Columbus, Ohio 43214
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Dallas, Texas 75230
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Dallas, Texas 75010
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Davidson, North Carolina 28036
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Eagle, Idaho 83616
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El Paso, Texas 79902
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Evansville, Indiana 47714
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Greensboro, North Carolina 27408
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Greensboro, North Carolina 27406
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3813 South Hamilton Road
Groveport, Ohio 43125
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Harrisburg, North Carolina 28075
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Henrico, Virginia 23233
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Hermitage, Tennessee 37076
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Hialeah, Florida 33012
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Hollywood, Maryland 20636
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Houston, Texas 77034
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Hutchinson, Kansas 67502
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Inverness, Florida 34452
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Jackson, Tennessee 37805
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Kalamazoo, Michigan 49009
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Kansas City, Missouri 64114
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Knoxville, Tennessee 37912
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Lee'S Summit, Missouri 64064
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Little Rock, Arkansas 72211
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Marlton, New Jersey 08053
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Mentor, Ohio 44060
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Meridian, Idaho 83642
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Miami, Florida 33186
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Miami, Florida 33165
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Miami, Florida 33174
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Mobile, Alabama 36608
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Morgantown, North Carolina 28655
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Nashville, Tennessee 37205
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New Orleans, Louisiana 70115
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Newton, Kansas 67114
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Oak Lawn, Illinois 60453
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10040 Regency Cir
Omaha, Nebraska 68114
(402) 934-0044
Quality Clinical Research, Inc. Welcome to Quality Clinical Research. We originated here in Omaha, NE...
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Owensboro, Kentucky 42303
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Pasadena, Texas 77504
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Plantation, Florida 33317
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243 N Rd
Poughkeepsie, New York 12601
(845) 471-9410
Premier Medical Group of the Hudson Valley Premier Medical Group offers comprehensive, integrated care providing...
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3100 Duraleigh Rd
Raleigh, North Carolina 27612
(919) 781-2514
Wake Research Associates, LLC Wake Research is an Organization of Unified Investigational Sites working closely...
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Redlands, California 92374
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Redlands, California 92373
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Ridgewood, New Jersey 07450
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Rochester, Michigan 48307
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Sacramento, California 95825
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Saint Louis, Missouri 63128
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Salt Lake City, Utah 84107
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