Other Clinical Trial - An Open-label Study of KW-3357

Clinical Trial Summary

The purpose of this study is to evaluate the efficacy and safety of KW-3357 compared to plasma-derived antithrombin using multi-center, open-label, parallel-group, comparative method in patients with Disseminated Intravascular Coagulation (DIC) associated with infection.

See also
	Status	Clinical Trial	Phase
	Terminated	`NCT01384409` - A Phase 3 Clinical Study of KW-3357 in Patients With DIC	Phase 3
	Completed	`NCT01384396` - A Clinical Study of KW-3357 in Patients With DIC	Phase 3

See also

Status

Clinical Trial

Phase

Terminated

NCT01384409 - A Phase 3 Clinical Study of KW-3357 in Patients With DIC

Phase 3

Completed

NCT01384396 - A Clinical Study of KW-3357 in Patients With DIC

Phase 3

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	NCT01384903
Study type	Interventional
Source	Kyowa Hakko Kirin Co., Ltd
Contact
Status	Completed
Phase	Phase 3
Start date	June 2011
Completion date	May 2013

An Open-label Study of KW-3357 — 3357-004

Clinical Trial Summary

Clinical Trial Description

Study Design

Related Conditions & MeSH terms