Other Clinical Trial - Intravenous Iloprost in Subjects With Symptomatic

See also
Status	Clinical Trial	Phase
Completed	`NCT02260557` - Effects of Selexipag in Adults With Raynaud's Phenomenon Secondary to Systemic Sclerosis	Phase 2
Terminated	`NCT04915950` - A Study to Assess the Effect of Oral Temanogrel on Digital Blood Flow in Adult Participants With Raynaud's Phenomenon Secondary to Systemic Sclerosis	Phase 2
Completed	`NCT02228850` - Study of Acute Peripheral Vascular Effects, Safety and Tolerability in Subjects With Raynaud's Phenomenon Secondary to Systemic Sclerosis	Phase 2

See also

Status

Clinical Trial

Phase

Completed

NCT02260557 - Effects of Selexipag in Adults With Raynaud's Phenomenon Secondary to Systemic Sclerosis

Phase 2

Terminated

NCT04915950 - A Study to Assess the Effect of Oral Temanogrel on Digital Blood Flow in Adult Participants With Raynaud's Phenomenon Secondary to Systemic Sclerosis

Phase 2

Completed

NCT02228850 - Study of Acute Peripheral Vascular Effects, Safety and Tolerability in Subjects With Raynaud's Phenomenon Secondary to Systemic Sclerosis

Phase 2

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	NCT04040322
Study type	Interventional
Source	Eicos Sciences, Inc.
Contact
Status	Completed
Phase	Phase 3
Start date	October 14, 2019
Completion date	June 9, 2021

Intravenous Iloprost in Subjects With Symptomatic Raynaud's Phenomenon Secondary to Systemic Sclerosis (Phase 3)

Clinical Trial Summary

Clinical Trial Description

Study Design

Related Conditions & MeSH terms