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
Bastrop, Louisiana 71220
1506
mi
from 91732
Bastrop, LA
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Birmingham, Alabama 35203
1785
mi
from 91732
Birmingham, AL
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Chattanooga, Tennessee 37421
1862
mi
from 91732
Chattanooga, TN
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Chesterfield, Michigan 48047
1983
mi
from 91732
Chesterfield, MI
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Chula Vista, California 91910
113
mi
from 91732
Chula Vista, CA
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Dothan, Alabama 36305
1899
mi
from 91732
Dothan, AL
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Great Neck, New York 11023
2446
mi
from 91732
Great Neck, NY
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Greensboro, North Carolina 27410
2146
mi
from 91732
Greensboro, NC
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Houston, Texas 77015
1368
mi
from 91732
Houston, TX
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Los Angeles, California 90036
19
mi
from 91732
Los Angeles, CA
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Miami, Florida 33122
2314
mi
from 91732
Miami, FL
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New York, New York 10018
2351
mi
from 91732
New York, NY
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North Little Rock, Arkansas 72117
1472
mi
from 91732
North Little Rock, AR
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Ogden, Utah 84405
590
mi
from 91732
Ogden, UT
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Poughkeepsie, New York 12601
2433
mi
from 91732
Poughkeepsie, NY
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Rochester, Minnesota 55905
1524
mi
from 91732
Rochester, MN
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Tampa, Florida 33607
2133
mi
from 91732
Tampa, FL
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Tucson, Arizona 85710
435
mi
from 91732
Tucson, AZ
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Urbana, Illinois 61801
1686
mi
from 91732
Urbana, IL
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Ventura, California 93003
74
mi
from 91732
Ventura, CA
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Webster, Texas 77598
1377
mi
from 91732
Webster, TX
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Winston-Salem, North Carolina 27103
2122
mi
from 91732
Winston-Salem, NC
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