Ireland
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Active, not recruiting Phase 1/2

Open-Label Single Ascending Dose of Adeno-associated Virus Serotype 8 Factor IX Gene Therapy in Adults With Hemophilia B

NCT01687608 · tracked via the Priya Life Science USA tracker
Sponsor
Baxalta now part of Shire
Phase
Phase 1/2
Started
2013-02-11
Last updated
2026-03-20

Condition(s) studied

Hemophilia B

Investigational drug(s) / intervention(s)

AskBio009

AskBio009: Single dose IV injection

Study summary

The purpose of this study is to evaluate the safety of single ascending IV doses of a Factor IX (FIX) Gene Therapy in up to 16 Adults with Hemophilia B.

Eligibility

Sex
MALE
Min age
18 Years
Max age
75 Years
Healthy volunteers
No
Inclusion Criteria: * Males age 18-75 years, inclusive * Established hemophilia B with ≥3 hemorrhages per year requiring treatment with exogenous FIX OR use of FIX prophylaxis because of history of frequent bleeding episodes * Plasma FIX activity ≤2% (\<1% for first cohort; then per protocol) * Negative for active Hepatitis C virus (HCV), defined as Hepatitis C virus antibody negative and negative (undetectable) PCR test for plasma Hepatitis C virus ribonucleic acid (RNA) OR if Hepatitis C virus antibody positive must have ≥2 consecutive negative (undetectable) PCR tests for plasma HCV RNA at least 3 months apart, and negative at screening Exclusion Criteria: * Family history of inhibitor to FIX protein or personal laboratory evidence of having developed inhibitors to FIX protein at any time (\>0.6 Bethesda Units on any single test) * Documented prior allergic reaction to any FIX product * Detectable AAV8 neutralizing antibodies * Markers of hepatic inflammation or overt or occult cirrhosis as evidenced by one or more of the following: * Platelet count \<175,000/μL * Albumin ≤3.5 g/dL * Total bilirubin \>1.5 x ULN and direct bilirubin ≥0.5 mg/dL * Alkaline phosphatase \>2.0 x ULN * ALT or AST \>2.0 x ULN (except for subjects who are HIV infected) * Liver biopsy in the past indicating moderate or severe fibrosis (Metavir staging of 2 or greater) * History of ascites, varices, variceal hemorrhage or hepatic encephalopathy

Primary outcome measure(s)

  • Number of patients experiencing treatment-related adverse events by dose group — Infusion to Week 3 and Infusion to end of study
  • Change from baseline in clinical laboratory evaluations — Change from baseline at week 3 and change from baseline at the end of study

Trial sites (15)

FacilityCityRegionStatus
Orthopaedic Hemophilia Treatment Center Los Angeles California
Children's Hospital Los Angeles Los Angeles California
University of California Davis Medical Center Sacramento California
University of California at San Diego Medical Center San Diego California
U of Colorado School of Medicine, Hemophilia & Thrombosis Treatment Center Aurora Colorado
Emory University Atlanta Georgia
Rush University Medical Center Chicago Illinois
Children's Hospital of Boston Boston Massachusetts
University of Minnesota, Masonic Clinical Research Unit, Clinical and Translational Science Institute Minneapolis Minnesota
Mount Sinai Medical Center New York New York
The Hemophilia Center, Oregon Health and Science University Portland Oregon
Medical University of South Carolina Charleston South Carolina
Gulf States Hemophilia and Thrombosis Center Houston Texas
Bloodworks Northwest Seattle Washington
BloodCenter of Wisconsin Milwaukee Wisconsin

More Baxalta now part of Shire trials in the USA

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT01687608 on ClinicalTrials.gov ↗ ← All trials in the USA