A Study of Recombinant AAV2/6 Human Factor 8 Gene Therapy SB-525 (PF-07055480) in Subjects With Severe Hemophilia A
Launched by PFIZER · Feb 17, 2017
Trial Information
Current as of June 04, 2025
Completed
Keywords
ClinConnect Summary
The proposed clinical study uses a recombinant adeno-associated virus 2/6 (AAV2/6) vector encoding the cDNA for the B-domain deleted human F8 (hF8). The secreted FVIII has the same amino acid sequence as approved recombinant anti hemophilic factors (Refacto® and Xyntha®). The SB-525 (PF-07055480) vector encodes a liver-specific promotor module and AAV2/6 exhibits liver tropism, thus providing the potential for long-term hepatic production of FVIII in hemophilia A subjects.
The constant production of FVIII after a single SB-525 (PF-07055480) administration may provide potential benefit in d...
Gender
MALE
Eligibility criteria
- Inclusion Criteria:
- • Male ≥18 years of age
- • Severe hemophilia A (past evidence of circulating FVIII activity of \< 1% normal)
- • Treated or exposed to FVIII concentrates or cryoprecipitate for at least 150 exposure days
- • ≥12 bleeding episodes if receiving on-demand therapy over the preceding 12 months
- • Agree to use double barrier contraceptive until at least 3 consecutive semen samples are negative for AAV 2/6 after SB-525 infusion
- Exclusion Criteria:
- • Presence of neutralizing antibodies
- • Current inhibitor, or history of FVIII inhibitor (except for transient low titer inhibitor detected in childhood)
- • History of hypersensitivity response to FVIII
- • History of Hepatitis B or HIV-1/2 infection
- • History of Hepatitis C, unless viral assays in two samples, collected at least 6 months apart, are negative
- • Evidence of any bleeding disorder in addition to hemophilia A
- • Markers of hepatic inflammation or overt or occult cirrhosis
- • History of chronic renal disease or creatinine ≥ 1.5 mg/dL
- • Presence of liver mass on magnetic resonance imaging (MRI), or, positive alpha fetoprotein
- • Presence of \> grade 2 liver fibrosis on elastography for subjects with history of treated Hepatitis C or suspicion of chronic liver disease
About Pfizer
Pfizer Inc. is a global leader in biopharmaceutical innovation, dedicated to discovering, developing, and delivering advanced therapies that enhance patient outcomes across a wide range of medical conditions. With a rich history of scientific research and a commitment to quality, Pfizer focuses on areas such as oncology, immunology, cardiology, and rare diseases. The company leverages cutting-edge technology and collaborates with healthcare professionals, regulatory bodies, and academic institutions to conduct rigorous clinical trials that ensure the safety and efficacy of its products. Pfizer's mission is to bring breakthroughs that change patients' lives, exemplifying its commitment to health and wellness worldwide.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Atlanta, Georgia, United States
Duarte, California, United States
Sacramento, California, United States
Sacramento, California, United States
Little Rock, Arkansas, United States
Pittsburgh, Pennsylvania, United States
Miami, Florida, United States
Tampa, Florida, United States
Sacramento, California, United States
Nashville, Tennessee, United States
Sacramento, California, United States
Sacramento, California, United States
Sacramento, California, United States
Sacramento, California, United States
San Francisco, California, United States
San Francisco, California, United States
San Francisco, California, United States
Pittsburgh, Pennsylvania, United States
Pittsburgh, Pennsylvania, United States
Seattle, Washington, United States
Nashville, Tennessee, United States
Nashville, Tennessee, United States
Patients applied
Trial Officials
Pfizer CT.gov Call Center
Study Director
Pfizer
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported
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