Evaluation of the Efficacy, Durability, Safety, and Tolerability of RP-G28 in Patients With Lactose Intolerance



Status:Active, not recruiting
Conditions:Food Studies
Therapuetic Areas:Pharmacology / Toxicology
Healthy:No
Age Range:18 - 75
Updated:3/23/2019
Start Date:June 26, 2018
End Date:July 2019

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A Phase 3, Multicenter, Randomized, Double-blind, Placebo-controlled, Parallel-group Study to Evaluate the Efficacy, Durability, Safety, and Tolerability of RP-G28 in Patients With Lactose Intolerance

This is a multicenter, randomized, double-blind, placebo-controlled, parallel-group study
conducted in the United States (US) to assess the efficacy of RP-G28 compared to placebo on
symptom reduction related to lactose intolerance.


Inclusion Criteria:

- Patient is 18-75 years of age, inclusive, at screening;

- Intolerance to milk and other dairy products;

- Patient agrees to refrain from all other treatments and products used for lactose
intolerance, to follow diet modifications required during periods of the study that
include abstinence from all dairy in some periods and consuming dairy in other
periods;

- Patient meets the defined minimum lactose intolerance symptom composite score; and

- Patient has positive Hydrogen Breath Test (HBT) results for lactase deficiency.

Exclusion Criteria:

- Patient has a disorder associated with abnormal gastrointestinal motility such as
gastroparesis (from any cause), amyloidosis, neuromuscular diseases (including
Parkinson's disease), collagen vascular diseases, uremia, or malnutrition;

- Patient has undergone bowel preparation for endoscopic or radiologic investigation
within 4 weeks of Screening (example, colonoscopy preparation);

- Patient has a history of surgery that alters the normal function of the
gastrointestinal tract including, but not limited to: fundoplication, gastrointestinal
bypass surgery, bariatric surgery, gastric banding, colostomy, vagotomy, pyloroplasty,
colectomy or other surgery for Crohn's disease or ulcerative colitis; and

- Patient has received antibiotic treatment, or had a high colonic enema, colonic
irrigation, colonic hydrotherapy, or colonic cleaning within 30 days prior to or
during Screening.
We found this trial at
34
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Chula Vista, California 91910
Phone: 619-518-7535
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Albuquerque, New Mexico
Principal Investigator: Ellen Kim
Phone: 505-224-7407
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Bellevue, Washington 98007
Phone: 425-454-4768
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Berlin, New Jersey 08009
Phone: 856-753-7335
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Birmingham, Alabama
Principal Investigator: David DeAtkine, MD
Phone: 205-327-1077
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Birmingham, AL
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Brooklyn, New York 11215
Phone: 929-251-3456
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Charleston, South Carolina 29412
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Cincinnati, Ohio
Phone: 513-671-8080
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Colorado Springs, Colorado 80910
Principal Investigator: Kari T Uusinarkaus
Phone: 719-226-8020
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Dayton, Ohio 45409
Principal Investigator: Steven Folkerth
Phone: 937-297-8999
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Fairfax, Virginia 22031
Principal Investigator: Kenneth Mirkin
Phone: 703-689-9860
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Gainesville, Florida 32610
Principal Investigator: Bruce K Branin, DO
Phone: 352-538-5407
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Great Neck, New York 11021
Principal Investigator: Michael J Goldstein, MD
Phone: 516-482-5976
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Hartsdale, New York
Principal Investigator: Michael Gerdis, MD
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Honolulu, Hawaii
Principal Investigator: Pantea Shoja
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Houston, Texas
Principal Investigator: Francisco D Velazquez, MD
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Huntington Park, California 90255
Phone: 323-588-1968
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Knoxville, Tennessee 37920
Principal Investigator: Evelyne M Davidson, MD
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Lampasas, Texas
Phone: 512-556-4130
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Lincoln, California 95648
Principal Investigator: Jeffrey D Wayne, MD
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Los Angeles, California
Phone: 213-413-2500
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Marrero, Louisiana 70072
Principal Investigator: Gary Reiss
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Miami, Florida 33136
Principal Investigator: Mark E Kutner
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Omaha, Nebraska
Principal Investigator: Ronald Anderson
Phone: 402-934-0044
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Orlando, Florida 32804
Principal Investigator: Judith L White, MD
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Oxon Hill, Maryland 20745
Principal Investigator: Stephen Ong
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Panorama City, California
Principal Investigator: Juan Frias
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Pompano Beach, Florida 33060
Principal Investigator: Daniel Lindenberg
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Raleigh, North Carolina 27607
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San Antonio, Texas 78224
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San Diego, California
Principal Investigator: Taddese T Desta, MD
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Walnut Creek, California 94598
Principal Investigator: Helen Stacey
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Waxahachie, Texas 75165
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Wyoming, Michigan 45519
Principal Investigator: Allan Coates
Phone: 616-328-5344
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