Clinical Trials in the USA / NCT01687608
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
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
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)
| Facility | City | Region | Status |
|---|---|---|---|
| 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
A Long-term Study of ADYNOVI/ADYNOVATE in Participants With Haemophilia A
Active, not recruiting
Other trials for the same condition
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