A Single Escalating Dose and Multiple Dose Study of BAY 1093884 in Subjects With Severe Hemophilia Types A or B, With or Without Inhibitors

PHASE1CompletedINTERVENTIONAL
Enrollment

32

Participants

Timeline

Start Date

October 28, 2015

Primary Completion Date

July 9, 2018

Study Completion Date

October 11, 2018

Conditions
Hemophilia AHemophilia B
Interventions
DRUG

BAY1093884

Single escalating dose with a starting dose of 0.3 mg/kg for the first cohort. Drug will be administered via IV infusion over 1 hour and SC injection. Based on safety, PK and PD results the doses for the other cohorts will be determined.

DRUG

BAY1093884

Multiple dose cohort with a single 150-mg SC injection once a week for 6 weeks.

Trial Locations (10)

1756

Sofia

4002

Plovdiv

9010

Varna

10249

Berlin

35392

Giessen

79044

Lviv

167-0035

Suginami

Unknown

Kiev

NW3 2QG

London

M13 9WL

Manchester

Sponsors

Lead Sponsor

All Listed Sponsors
lead

Bayer

INDUSTRY