Phase 1
N=119
HEPLISAV-B® in Adults With End-Stage Renal Disease (ESRD) Undergoing Hemodialysis
End Stage Renal Disease on Hemodialysis (Diagnosis)
Bottom Line
View on ClinicalTrials.gov: NCT03934736 ↗Enrolled (actual)
119
Serious AEs
48.7%
Results posted
Aug 2024
Primary outcome: Primary: Percentage of Subjects Reporting Clinically Significant Adverse Events - Medically-attended Adverse Events, Serious Adverse Events, and Immune-mediated Adverse Events of Special Interest — 0.8; 66.4; 48.7 percentage of participants
Study Design & Population
- Study type
- Interventional
- Phase
- Phase 1
- Interventions
- HEPLISAV-B® (Drug)
- Age
- Adult, Older Adult · 18+ yrs
- Sex
- All
- Sponsor
- Dynavax Technologies Corporation
- Primary completion
- Oct 2020
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Percentage of Subjects Reporting Clinically Significant Adverse Events - Medically-attended Adverse Events, Serious Adverse Events, and Immune-mediated Adverse Events of Special Interest |
0.8; 66.4; 48.7 | — |
| PRIMARY Seroprotection Rate (SPR) = Percentage of Participants Who Have a Seroprotective Immune Response |
20.3; 56.8; 78.7; 89.3 | — |
| SECONDARY Percentage of Subjects With Anti-HBs Concentration ≥100 mIU/mL |
5.4; 33.8; 57.3; 81.3 | — |
| SECONDARY Serum Anti-HBsAg Geometric Mean Concentration (GMC) |
4.4; 33.5; 155.3; 1061.8 | — |
| SECONDARY Seroprotection Rate (SPR) = Percentage of Participants Who Have a Seroprotective Immune Response |
20.3; 56.8; 78.7; 89.3 | — |
Summary
This is an open-label, single arm study design to evaluate HEPLISAV-B® in adults with ESRD who are initiating or undergoing hemodialysis.
Eligibility Criteria
Inclusion Criteria
- Male and female subjects at least 18 years of age
- Laboratory confirmed negative serology result to hepatitis B virus (HBV) surface antigen (HBsAg), antibody to hepatitis B surface antigen (anti-HBs), and antibody to hepatitis B core antigen (anti-HBc) prior to first study injection
- Must be clinically stable and in the opinion of the investigator able to comply with all study procedures
- Must be able and willing to provide informed consent
- Receiving hemodialysis or will initiate hemodialysis within 4 weeks of first study injection
- Women of childbearing potential (WOCBP) must consistently use an acceptable method of contraception or confirm in writing she will abstain from sexual activity from the Screening visit through 4 weeks after the last dose of study injection. Acceptable birth control methods include but are not limited to oral contraceptive medication, an intrauterine device (IUD), an injectable contraceptive (such as medroxyprogesterone acetate or Depo-Provera®), a birth control patch, or a barrier method (such as condom or diaphragm with spermicide).
Exclusion Criteria
- Previous receipt of any hepatitis B vaccine
- History of human immunodeficiency virus (HIV) or hepatitis C virus (HCV) infection or antibody to HIV or HCV
- History of sensitivity to any component of study vaccine
- Substance or alcohol abuse that in the opinion of the investigator would interfere with compliance or with interpretation of the study results
- Recent or ongoing history of febrile illness (within 7 days of the first study injection)
- Has received any of the following prior to the first study injection:
- Within 14 days:
a. Any inactivated vaccine
- Within 28 days:
- Systemic corticosteroids (more than 3 consecutive days) or other immunomodulatory or immune suppressive medication with the exception of inhaled steroids
- Any live virus vaccine
- Granulocyte colony-stimulating factor (G-CSF) or granulocyte-macrophage colony-stimulating factor (GM-CSF)
- Any other investigational medicinal agent
- Within 90 days:
- Blood products or immunoglobulin
- If female and pregnant, nursing, or planning to become pregnant during the study
- Undergoing chemotherapy or expected to receive chemotherapy during the study period
- Has a medical condition considered by the investigator likely to interfere with the subject's compliance or the interpretation of study assessments, including the following laboratory abnormalities which the investigator may consider if severe:
- Anemia
- Thrombocytopenia
- Leukocytosis
- Neutropenia
- Metabolic acidosis
- Increased alanine aminotransferase (ALT) or aspartate aminotransferase (AST)
- Hyperkalemia
- Hypokalemia
- Is scheduled to undergo a kidney transplant within 6 months of the first study injection
Data sourced from ClinicalTrials.gov (NCT03934736). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.