Effect of Relamorelin on Satiation, Gastric Volume, Gastric Accommodation

Clinical Trial Description

n/a

Study Design

Allocation: Randomized, Endpoint Classification: Pharmacodynamics Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Basic Science

Related Conditions & MeSH terms

Gastric Motility

See also
	Status	Clinical Trial	Phase
	Terminated	`NCT04066231` - ANTERO-4: VIPUN Gastric Monitoring System in an Erythromycin Model	N/A
	Recruiting	`NCT04200144` - Endoscopic Sleeve Gastroplasty for Obesity and Microbiota Randomized Trial	N/A

See also

Status

Clinical Trial

Phase

Terminated

NCT04066231 - ANTERO-4: VIPUN Gastric Monitoring System in an Erythromycin Model

N/A

Recruiting

NCT04200144 - Endoscopic Sleeve Gastroplasty for Obesity and Microbiota Randomized Trial

N/A

Interventional studies are often prospective and are specifically tailored to evaluate direct impacts of treatment or preventive measures on disease.

Observational studies are often retrospective and are used to assess potential causation in exposure-outcome relationships and therefore influence preventive methods.

Expanded access is a means by which manufacturers make investigational new drugs available, under certain circumstances, to treat a patient(s) with a serious disease or condition who cannot participate in a controlled clinical trial.

Clinical trials are conducted in a series of steps, called phases - each phase is designed to answer a separate research question.

Phase 1: Researchers test a new drug or treatment in a small group of people for the first time to evaluate its safety, determine a safe dosage range, and identify side effects.
Phase 2: The drug or treatment is given to a larger group of people to see if it is effective and to further evaluate its safety.
Phase 3: The drug or treatment is given to large groups of people to confirm its effectiveness, monitor side effects, compare it to commonly used treatments, and collect information that will allow the drug or treatment to be used safely.
Phase 4: Studies are done after the drug or treatment has been marketed to gather information on the drug's effect in various populations and any side effects associated with long-term use.

NCT number	NCT02466711
Study type	Interventional
Source	Motus Therapeutics, Inc.
Contact
Status	Completed
Phase	Phase 1
Start date	June 2015
Completion date	September 2015

Effect of Relamorelin on Satiation, Gastric Volume, Gastric Accommodation and Distal Gastric Function in Healthy Volunteers

Clinical Trial Summary

Clinical Trial Description

Study Design

Related Conditions & MeSH terms