A Thorough QT Study of Telotristat Etiprate

Clinical Trial Description

n/a

Study Design

Allocation: Randomized, Endpoint Classification: Safety Study, Intervention Model: Crossover Assignment, Masking: Double Blind (Subject, Caregiver, Investigator), Primary Purpose: Treatment

Related Conditions & MeSH terms

QT Interval

See also
Status	Clinical Trial	Phase
Enrolling by invitation	`NCT05243537` - QTc Intervals in Former Preterm/Extreme Low Birth Weight Infants: a Pooled Study Proposal
Not yet recruiting	`NCT05225779` - The Effects of Sevoflurane and Desflurane on QT Interval Measured With Cardiac Electrophysiological Balance Index	N/A
Enrolling by invitation	`NCT05822076` - Influence of Thoracic Paravertebral Block on Cardiac Repolarization

See also

Status

Clinical Trial

Phase

Enrolling by invitation

NCT05243537 - QTc Intervals in Former Preterm/Extreme Low Birth Weight Infants: a Pooled Study Proposal

Not yet recruiting

NCT05225779 - The Effects of Sevoflurane and Desflurane on QT Interval Measured With Cardiac Electrophysiological Balance Index

N/A

Enrolling by invitation

NCT05822076 - Influence of Thoracic Paravertebral Block on Cardiac Repolarization

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	NCT02155205
Study type	Interventional
Source	Lexicon Pharmaceuticals
Contact
Status	Completed
Phase	Phase 1
Start date	May 2014

A Thorough QT Study of Telotristat Etiprate

Clinical Trial Summary

Clinical Trial Description

Study Design

Related Conditions & MeSH terms