Trial of IW-9179 in Patients With Diabetic Gastroparesis (DGP)



Status:Completed
Conditions:Gastrointestinal
Therapuetic Areas:Gastroenterology
Healthy:No
Age Range:18 - Any
Updated:4/21/2016
Start Date:October 2014
End Date:December 2015

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A Multicenter, Randomized, Double-blind, Placebo-controlled, Parallel-group, Phase 2a Study of Oral IW-9179 Administered Once and Twice Daily for 4 Weeks to Patients With Diabetic Gastroparesis

The objectives of this study are to evaluate the safety of IW-9179 in patients with diabetic
gastroparesis (DGP) and the effect of treatment on the cardinal symptoms of DGP.


Inclusion Criteria:

- Patient is a male or non-pregnant, non-breastfeeding female, and is age 18 years or
older at the time of the Screening Visit.

- Patient has a confirmed diagnosis of type 1 or type 2 diabetes mellitus.

- Patient has a diagnosis of DGP with no history or evidence of mechanical obstruction,
symptoms for at least 3 consecutive months preceding the Screening Visit, and delayed
gastric emptying of solids documented within 2 years of the Screening Visit.

- Patient has a normal EGD either during the Screening Period or within 2 years of the
Screening Visit, with no evidence of structural or organic disease that may explain
the patient's gastroduodenal symptoms.

- Patient is compliant with eDiary completion.

- Patient agrees to refrain from making any new, major lifestyle changes.

- Patient is fluent and literate in English.

Exclusion Criteria:

- Patient has a history or current symptoms of any organic or structural disease that,
in the opinion of the investigator, can cause abdominal pain or discomfort and may
confound the assessment of DGP symptoms.

- Patients with rumination syndrome, cyclic vomiting syndrome, anorexia nervosa, or
bulimia.

- Patient is currently using a gastric electric stimulator or has had endoscopic
pyloric injections of botulinum toxin within the 6 months prior to the Screening
Visit.

- Patient has been hospitalized within the 2 months prior to the Screening Visit for
uncontrolled diabetes mellitus, DGP, or associated malnutrition.

- Patient reports significant diarrhea during the four weeks prior to the Screening
Visit, or more than 2 days during either week of the Pretreatment Period.

- Patient has had surgery of the GI tract any time before the Screening Visit, an
appendectomy or cholecystectomy during the 3 months before the Screening Visit,
non-GI surgery of the abdomen, pelvis, or retroperitoneal structures during the 6
months, or other major non-GI surgery during the 30 days before the Screening Visit.

- Patient has a history of cancer (resected basal cell or squamous cell carcinoma of
the skin is acceptable).
We found this trial at
22
sites
North Little Rock, Arkansas 72117
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North Little Rock, AR
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Bastrop, Louisiana 71220
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Bastrop, LA
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Birmingham, Alabama 35203
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Birmingham, AL
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Chattanooga, Tennessee 37421
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Chattanooga, TN
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Chesterfield, Michigan 48047
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Chesterfield, MI
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Chula Vista, California 91910
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from
Chula Vista, CA
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Dothan, Alabama 36305
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Dothan, AL
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Great Neck, New York 11023
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from
Great Neck, NY
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Greensboro, North Carolina 27410
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Greensboro, NC
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Houston, Texas 77015
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Houston, TX
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Los Angeles, California 90036
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Los Angeles, CA
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Miami, Florida 33122
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Miami, FL
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New York, New York 10018
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from
New York, NY
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Ogden, Utah 84405
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Ogden, UT
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Poughkeepsie, New York 12601
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Poughkeepsie, NY
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Rochester, Minnesota 55905
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Rochester, MN
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Tampa, Florida 33607
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Tampa, FL
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Tucson, Arizona 85710
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Tucson, AZ
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Urbana, Illinois 61801
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Urbana, IL
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Ventura, California 93003
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Ventura, CA
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Webster, Texas 77598
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Webster, TX
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Winston-Salem, North Carolina 27103
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from
Winston-Salem, NC
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