Other Clinical Trial - An Intravenous Infusion Study of rHIgM22 in

See also
Status	Clinical Trial	Phase
Completed	`NCT04546698` - 5-HT7 Receptor Implication in Inflammatory Mechanisms in Multiple Sclerosis
Completed	`NCT01442233` - Plasma Exchanges in Multiple Sclerosis (MS) Relapses	Phase 3
Temporarily not available	`NCT02606929` - Use of Well Known Drugs for New Destination - MS Improvement (MSNT)	Phase 0
Completed	`NCT02632591` - Use on Human Beings of Mix of Known Drugs for New Destination - MS Treatment	Phase 1

See also

Status

Clinical Trial

Phase

Completed

NCT04546698 - 5-HT7 Receptor Implication in Inflammatory Mechanisms in Multiple Sclerosis

Completed

NCT01442233 - Plasma Exchanges in Multiple Sclerosis (MS) Relapses

Phase 3

Temporarily not available

NCT02606929 - Use of Well Known Drugs for New Destination - MS Improvement (MSNT)

Phase 0

Completed

NCT02632591 - Use on Human Beings of Mix of Known Drugs for New Destination - MS Treatment

Phase 1

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	NCT02398461
Study type	Interventional
Source	Acorda Therapeutics
Contact
Status	Completed
Phase	Phase 1
Start date	April 2015
Completion date	September 21, 2017

An Intravenous Infusion Study of rHIgM22 in Patients With Multiple Sclerosis Immediately Following a Relapse

Clinical Trial Summary

Clinical Trial Description

Study Design

Related Conditions & MeSH terms