Overview

The Effect of Neu-P11 on Symptoms in Patients With D-IBS

Status:
Completed
Trial end date:
2014-02-01
Target enrollment:
0
Participant gender:
All
Summary
Placebo controlled double-blind study with 40 patients who have an diarrhea-predominant IBS, 20 get Neu-P11, 20 get a placebo. Neu-P11 is a, Melatonin receptor-, Serotonin 5-HT- 1A and 5-HT- 1D - agonist and a serotonin 5-HT- 2B - antagonist.
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Ludwig-Maximilians - University of Munich
Criteria
Inclusion Criteria:

1. Subjects age 18-80 years old

2. Male or female

Women of childbearing potential must have a negative pregnancy test at the screening
visit, on Day 1 of each treatment period, and use a reliable method of contraception
during the entire study duration and for at least 3 months after study drug intake.
Reliable methods of contraception are:

- oral contraception

- Double barrier type devices (e.g., male or female condom, diaphragm,
contraceptive sponge) only in combination with a spermicide.

- Intra-uterine devices in combination with a spermicide. Abstention, rhythm
method, and contraception by the partner alone are not acceptable methods of
contraception. Women not of childbearing potential are defined as postmenopausal
(i.e., amenorrhea for at least 1 year), or surgically or naturally sterile.

3. Subject has IBS confirmed by the Rome III diagnostic criteria

Exclusion Criteria:

1. Subject has current evidence of duodenal ulcer, gastric ulcer, diverticulitis, or
infectious gastroenteritis.

2. Subject has a history of inflammatory bowel disease (e.g. Crohn's disease, ulcerative
colitis, celiac disease), GI malignancy, GI obstruction, gastroparesis, carcinoid
syndrome, pancreatitis, amyloidosis or ileus

3. Subject is a candidate for GI surgery or has a history of GI surgery except
appendectomy and cholecystectomy.

4. Subject has psychiatric disorders which are not controlled (based on the investigator
medical judgment); subject with psychosis are excluded regardless of current therapy.

5. Subject has current or recent history (within 12 months of signing on informed
consent) of drug or alcohol abuse.

6. Subject is pregnant or lactating

7. Subject has history of human immunodeficiency virus (HIV) or hepatitis (B or C)

8. Subject has any condition or circumstance that could cause noncompliance with
treatments or visits

9. Subject has active malignancy within the last 5 years.

10. Subject taking antipsychotic drugs, antispasmodics, antidiarrheals (e.g. loperamide,
lubiprostone and bismuth subsalicylate), narcotics, prokinetic drugs, drugs indicated
for IBS (e.g Alosetron), or warfarin.