Study to Evaluate the Effects of RM-131 in Patients With Chronic Constipation

Phase 1

Completed

• Conditions: Chronic Constipation
• Interventions: Drug: RM-131; Drug: Placebo

• Registration Number: NCT02137642
• Lead Sponsor: Motus Therapeutics, Inc.

Brief Summary

The purpose of this study is to evaluate safety and tolerability as well as the effects of RM-131 on colonic motor and sensory effects in patients with chronic constipation.

Detailed Description

Not available

Study Timeline

• Study First Submitted: 2014-05-12
• Study First Submitted QC: 2014-05-13
• Study First Posted: 2014-05-14
• Study Start: 2014-08
• Primary Completion: 2014-11
• Study Completion: 2014-11
• Status Verified: 2016-09
• Last Update Submitted: 2016-09-21
• Last Update Posted: 2016-09-22

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 18

Inclusion Criteria

1. Able to provide written informed consent prior to any study procedures, and be willing and able to comply with study procedures.
2. Subjects with chronic IDIOPATHIC constipation, including experiencing constipation for 12 or more weeks in the preceding 12 months. Chronic constipation is to be defined by the Rome III criteria for Functional Constipation
3. Stable concomitant medications defined as no changes in regimen for at least 2 weeks prior to the study period.
4. Body mass index of 18-40 kg/m2
5. Female patients must have negative urine pregnancy tests and must not be lactating. For females able to bear children, a hormonal (i.e., oral, implantable, or injectable) and single-barrier method, or a double-barrier method of birth control must be used throughout the study. Female patients unable to bear children must have this documented in their medical history. (i.e., tubal ligation, hysterectomy, or post-menopausal [defined as a minimum of one year since the last menstrual period]).

Exclusion Criteria

1. Unable or unwilling to provide informed consent or to comply with study procedures

2. Diagnosis of secondary constipation e.g. underlying general neurological disease such as Parkinsonism, multiple sclerosis, diseases associated with peripheral neuropathy, iatrogenic constipation

3. Structural or metabolic diseases that affect the GI system NOTE: Patients with clinical suspicion of upper or lower GI obstruction must have been evaluated per standard of care and obstruction ruled out before screening

4. Unable to withdraw the following medications 48 hours prior to the colon study day and throughout the study:

   • Medications that alter GI transit including laxatives, magnesium and aluminum containing antacids, prokinetics, erythromycin, narcotics, aspirin, anti-cholinergics, tricyclic antidepressants, SNRI and newer antidepressants. With the exception of GoLYTELY which will be taken the evening prior to colon study day. 4- Selective serotonin reuptake inhibitor (SSRI) antidepressants are permissible at low, stable doses. All medications shall be reviewed and dis/approved by the principal investigator on a case by case basis.
   • Analgesic drugs including opiates, NSAIDs and COX-2 inhibitors
   • GABAnergic agents
   • Benzodiazepines NOTE: stable doses of thyroid replacement, estrogen replacement and birth control (but with adequate backup contraception as drug-interactions with birth control have not been conducted) are permissible.
   • Drugs with a low therapeutic index, such as warfarin, digoxin, anti-seizure medications

5. History of recent surgery (within 60 days of screening)

6. Acute or chronic illness or history of illness, which in the opinion of the Investigator, could pose a threat or harm to the patient or obscure interpretation of laboratory test results or interpretation of study data such as frequent angina, Class III or IV congestive heart failure, moderate impairment of renal or hepatic function, poorly controlled diabetes, etc.

7. Any clinically significant abnormalities on physical examination or laboratory abnormalities identified in the medical record, as determined by the Investigator

8. Acute GI illness within 48 hours of initiation of the colonic study day

9. Females who are pregnant or breastfeeding

10. History of alcohol or substance abuse; Alcohol use 2 days before colonic study day

11. Participation in a clinical study involving an investigational medication within the 30 days prior to dosing in the present study

12. Any other reason, which in the opinion of the Investigator, would confound proper interpretation of the study

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
RM-131	RM-131	-
Placebo	Placebo	-

Primary Outcome Measures

Name	Time	Method
Effect of RM-131 on postprandial high amplitude propagated contractions (HAPC) per hour	Measured during the 2 hour study procedure	Change from baseline HAPC

Trial Locations

Locations (1)

Mayo Clinic - Rochester; 🇺🇸 Rochester, Minnesota, United States