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

A Clinical Study of KW-3357 in Patients Diagnosed as Disseminated Intravascular Coagulation (DIC) by Japanese Association for Acute Medicine-defined DIC Criteria

Status
Terminated
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01384409
Acronym
3357-006
Enrollment
5
Registered
2011-06-29
Start date
2012-02-29
Completion date
2012-10-31
Last updated
2017-03-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Disseminated Intravascular Coagulation (DIC)

Brief summary

To evaluate the efficacy and safety of KW-3357 with concomitant use of heparin using multi-center, non-comparative, open-label method in patients diagnosed as disseminated intravascular coagulation (DIC) by Japanese Association for Acute Medicine-defined DIC criteria.

Interventions

Intravenous infusion once a day

Sponsors

Kyowa Kirin Co., Ltd.
Lead SponsorINDUSTRY

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
20 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Japanese Association for Acute Medicine-defined DIC criteria score \>= 4 * Antithrombin activity \<= 70% * Written informed consent from patient or guardian

Exclusion criteria

* Anamnesis or complication of serious drug allergy * Serious liver disorder, such as fulminant hepatitis and decompensated cirrhosis * Pregnant, nursing, or possibly pregnant woman * Possibility for the promotion of bleeding by concomitant use of heparin

Design outcomes

Primary

MeasureTime frameDescription
Mortality28 days
Organ symptomsScreening, 4, 6 days (or discontinuation)Sepsis related organ failure assessment score
SeverityScreening, 4, 6 days (or discontinuation)The Acute Physiology and Chronic Health Evaluation II score
Plasma antithrombin activityScreening, 2, 3, 4, 5, 6 days (or discontinuation)
Safetyup to 6 days (or discontinuation)Number of patients with adverse events
DIC resolution6 days (or discontinuation)Japanese Association for Acute Medicine-defined DIC criteria score \< 4
DIC scoreScreening, 2, 3, 4, 5, 6 days (or discontinuation)Based on the Japanese Association for Acute Medicine-defined DIC criteria

Countries

Japan

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026