A Study of Fitusiran (ALN-AT3SC) in Severe Hemophilia A and B Patients Without Inhibitors



Status:Recruiting
Conditions:Anemia, Hematology
Therapuetic Areas:Hematology
Healthy:No
Age Range:12 - Any
Updated:1/25/2019
Start Date:July 2, 2018
End Date:October 9, 2020
Contact:Trial Transparency email recommended (Toll free number for US & Canada)
Email:Contact-US@sanofi.com
Phone:800-633-1610

Use our guide to learn which trials are right for you!

ATLAS-A/B: A Phase 3 Study to Evaluate the Efficacy and Safety of Fitusiran in Patients With Hemophilia A or B, Without Inhibitory Antibodies to Factor VIII or IX

The purpose of this study is to determine the frequency of bleeding episodes in patients
receiving fitusiran as prophylactic treatment of hemophilia compared with patients who are
assigned to continue with their regular medication. In addition, the study will assess
safety, quality of life, pharmacodynamics (PD), and pharmacokinetics (PK).


Inclusion Criteria:

- Males, ≥12 years of age

- Severe hemophilia A or B without inhibitors

- (Severity confirmed by a central laboratory where FVIII level is <1% or FIX level
is ≤2% at Screening; Inhibitors defined as Nijmegen modified Bethesda assay
inhibitor titer of <0.6 BU/mL at Screening)

- A minimum of 6 bleeding episodes requiring factor concentrate treatment within the
last 6 months prior to Screening.

- Willing and able to comply with the study requirements and to provide written informed
consent and assent

Exclusion Criteria:

- Known co-existing bleeding disorders other than hemophilia A or B

- Antithrombin (AT) activity <60% at Screening

- Co-existing thrombophilic disorder

- Clinically significant liver disease

- Active HCV infection

- HIV positive with a CD4 count of <200 cells/μL

- History of arterial or venous thromboembolism

- Inadequate renal function

- History of multiple drug allergies or history of allergic reaction to an
oligonucleotide or N-Acetylgalactosamine (GalNAc)

- History of intolerance to SC injection(s)

- Any other conditions or comorbidities that would make the patient unsuitable for
enrollment or could interfere with participation in or completion of the study, per
Investigator judgment
We found this trial at
11
sites
Phoenix, Arizona 85016
343
mi
from 91732
Phoenix, AZ
Click here to add this to my saved trials
530 South Main Street
Akron, Ohio 44311
2039
mi
from 91732
Akron, OH
Click here to add this to my saved trials
Ann Arbor, Michigan 48109
1932
mi
from 91732
Ann Arbor, MI
Click here to add this to my saved trials
Boston, Massachusetts 02114
2578
mi
from 91732
Boston, MA
Click here to add this to my saved trials
6330 Quadrangle Drive
Chapel Hill, North Carolina 27517
2198
mi
from 91732
Chapel Hill, NC
Click here to add this to my saved trials
Cleveland, Ohio 44195
2033
mi
from 91732
Cleveland, OH
Click here to add this to my saved trials
Las Vegas, Nevada 89109
217
mi
from 91732
Las Vegas, NV
Click here to add this to my saved trials
89 Commercial Road
Melbourne, 3004
7949
mi
from 91732
Melbourne,
Click here to add this to my saved trials
Orange, California
21
mi
from 91732
Orange, CA
Click here to add this to my saved trials
San Diego, California
106
mi
from 91732
San Diego, CA
Click here to add this to my saved trials
Tampa, Florida
2136
mi
from 91732
Tampa, FL
Click here to add this to my saved trials