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Phase 2 N=354 Randomized Triple-blind Prevention

A Study to Evaluate the Safety and Immunogenicity of Inactivated Varicella Zoster Virus (VZV) Vaccine in Adults With Autoimmune Disease (V212-009)

Herpes Zoster

Enrolled (actual)
354
Serious AEs
2.9%
Results posted
Jan 2019
Primary outcome: Primary: Geometric Mean Fold Rise (GMFR) in Varicella-Zoster (VZV) Antibody Responses Measured by Glycoprotein Enzyme-linked Immunosorbent Assay (gpELISA) — 1.57 Ratio — p=<0.0001

Study Design & Population

Study type
Interventional
Phase
Phase 2
Interventions
V212 (Biological); Placebo (Biological)
Age
Adult, Older Adult · 18+ yrs
Sex
All
Sponsor
Merck Sharp & Dohme LLC
Primary completion
Feb 2013

Outcome Measures

OutcomeResultp-value
PRIMARY
Geometric Mean Fold Rise (GMFR) in Varicella-Zoster (VZV) Antibody Responses Measured by Glycoprotein Enzyme-linked Immunosorbent Assay (gpELISA)
1.57 <0.0001 sig
PRIMARY
GMFR in VZV Antibody Response Measured by VZV Interferon-gamma (IFN-g) Enzyme-linked Immunospot (ELISPOT) Assay
2.01 <0.0001 sig
PRIMARY
Percentage of Participants With a Serious Adverse Event
2.8; 1.6
SECONDARY
Percentage of Participants With an Injection-site Adverse Event Prompted on the Vaccination Report Card
46.0; 1.6; 42.2; 14.5; 40.1; 4.8
SECONDARY
Percentage of Participants With a Systemic Adverse Event Prompted on the Vaccination Report Card
51.6; 46.8
SECONDARY
Percentage of Participants With Elevated Temperature Prompted on the Vaccination Report Card
7.0; 4.9

Summary

This is a study to evaluate the safety and immunogenicity of V212 vaccine in adults with autoimmune disease, including participants with rheumatoid arthritis, psoriatic arthritis, psoriasis, inflammatory bowel disease, systemic lupus erythematosus, multiple sclerosis, and other similar diseases. The primary hypothesis is that vaccination with V212 vaccine will elicit significant VZV-specific immune responses at approximately 28 days after vaccination 4. The statistical criterion for significance requires that the lower bound of the 2-sided 95% confidence interval of the geometric mean fold rise in vaccine recipients is >1.0.

Eligibility Criteria

Inclusion Criteria

  • Diagnosed with an autoimmune disease
  • Clinically stable disease for at least 30 days before enrollment
  • Not likely to undergo hematopoietic stem cell transplantation during the study period
  • Receiving at least one parenteral or oral biologic agent, such as a Tumor Necrosis factor (TNF) alpha inhibitor, or a parenteral or oral non-biologic therapy, at a stable dose for at least 3 months, with no planned or anticipated changes
  • History of varicella, antibodies to VZV, or residence for at least 30 years in a country with endemic VZV infection, or if participant is less than 30 years old, attended primary or secondary school in a country with endemic VZV infection

Exclusion Criteria

  • Prior history of Herpes Zoster (shingles) within 1 year before enrollment
  • Prior varicella or zoster vaccine
  • Active central nervous system lupus erythematosus requiring therapeutic intervention within 90 days of enrollment
  • Prior or planned therapy containing rituximab or other anti-Cluster of Differentiation (CD) 20 monoclonal antibodies from 3 months before enrollment through 28 days postdose 4
  • Systemic corticosteroid therapy, prednisone, or equivalent over 40 mg daily at the time of enrollment
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT01527383). 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.

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