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VZV Vaccine for Hematopoietic Stem Cell Transplantation (VZIDST)

Primary Purpose

Varicella Zoster Infection

Status
Completed
Phase
Phase 2
Locations
Hong Kong
Study Type
Interventional
Intervention
Zostavax
Normal Saline
Sponsored by
The University of Hong Kong
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Varicella Zoster Infection focused on measuring double-blind, randomized, intradermal, VZVv, HSCT

Eligibility Criteria

18 Years - 60 Years (Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • patients undergoing allogeneic hemopoietic stem cell transplant
  • HLA identical sibling donors
  • participants willing to provide written informed consents

Exclusion Criteria:

  • history of zoster in the 12 months prior to transplantation
  • exposure to VZV within 4 weeks of transplantation
  • neomycin sensitivity
  • sensitivity to any components of the zoster vaccine

Sites / Locations

  • Ivan Hung

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm Type

Experimental

Active Comparator

Placebo Comparator

Placebo Comparator

Arm Label

ID varicella zoster vaccine (VZVv) group

SC VZVv group

ID NS Group

SC NS Group

Arm Description

intradermal 0.65 mL Zostavax

subcutaneous 0.65 mL Zostavax

intradermal 0.65 mL normal saline

subcutaneous 0.65 mL normal saline

Outcomes

Primary Outcome Measures

Herpes Zoster Reactivation
Incidence of herpes zoster in stem-cell transplant recipients

Secondary Outcome Measures

Immunological response in recipients
Geometric mean concentration of anti-VZV antibody (IU/mL)
Immunological response in donors
Geometric mean concentration of anti-VZV antibody (IU/mL)
Adverse reaction
Rate of adverse reaction in donors after vaccination

Full Information

First Posted
December 29, 2014
Last Updated
October 21, 2019
Sponsor
The University of Hong Kong
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1. Study Identification

Unique Protocol Identification Number
NCT02329457
Brief Title
VZV Vaccine for Hematopoietic Stem Cell Transplantation
Acronym
VZIDST
Official Title
Efficacy and Safety of a Novel Intradermal Live-attenuated Varicella Zoster Vaccine in Hematopoietic Stem Cell Transplantation Donors: a Randomized Double Blind Placebo-controlled Trial
Study Type
Interventional

2. Study Status

Record Verification Date
October 2019
Overall Recruitment Status
Completed
Study Start Date
December 2014 (Actual)
Primary Completion Date
September 2019 (Actual)
Study Completion Date
October 2019 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
The University of Hong Kong

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Hematopoietic stem cell transplantation (HSCT) is well-established therapy for patients with malignant hematological diseases. Varicella zoster virus (VZV) reactivation, clinically manifested as herpes zoster (HZ), is a major complication that affects up to 50% of patients. Most patients will require hospitalization. Despite treatment with high dose acyclovir, patients may develop severe complications including the disabling postherpetic neuralgia, corneal ulceration, viral dissemination and secondary bacterial infection. The median onset of infection is the fifth month following transplantation, with 91% of cases occurring within the first year. Direct vaccination of transplants recipients with subcutaneous live-attenuated VZVv before transplantation and up to one year after transplantation is contraindicated. A small prospective non-randomized study has demonstrated that subcutaneous vaccination for donors before HSCT may offer some protection against VZV reactivation in the recipients. Recently, dose-sparing influenza vaccine delivered via a novel intradermal microneedle has been shown to elicit a good immunogenic response in both healthy and elderly subjects. We sought to assess the efficacy and safety of the novel intradermal live-attenuated VZVv in sibling donors undergoing HSCT.
Detailed Description
Hematopoietic stem cell transplantation (HSCT) is well-established therapy for patients with malignant hematological diseases. Varicella zoster virus (VZV) reactivation, clinically manifested as herpes zoster (HZ), is a major complication that affects up to 50% of patients. Most patients will require hospitalization. Despite treatment with high dose acyclovir, patients may develop severe complications including the disabling postherpetic neuralgia, corneal ulceration, viral dissemination and secondary bacterial infection. The median onset of infection is the fifth month following transplantation, with 91% of cases occurring within the first year. Direct vaccination of transplants recipients with subcutaneous live-attenuated VZVv before transplantation and up to one year after transplantation is contraindicated. A small prospective non-randomized study has demonstrated that subcutaneous vaccination for donors before HSCT may offer some protection against VZV reactivation in the recipients. Recently, dose-sparing influenza vaccine delivered via a novel intradermal microneedle has been shown to elicit a good immunogenic response in both healthy and elderly subjects. We sought to assess the efficacy and safety of the novel intradermal live-attenuated VZVv in sibling donors undergoing HSCT. We plan to enroll 160 pairs of adult donors and patients who undergo allogeneic HLA matched sibling HSCT in this prospective randomized double-blind placebo-controlled trial over a period of 3 years. Enrolled donors and patients will be randomized into 4 groups: Group 1: intradermal full dose live-attenuated VZVv; Group 2: subcutaneous full dose live-attenuated VZVv; Group 3: intradermal 0.9% normal saline as control; Group 4: subcutaneous 0.9% normal saline as the second control All vaccines will be given to the donors within 28 days before HSCT. All intradermal vaccines will be given via a microneedle syringe. Both the investigators and participants will be blinded to the randomization process. The primary end point is the occurrence of HZ in the patients within 12 months of transplantation. The secondary end points are the safety and immunological response in the patients and donors.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Varicella Zoster Infection
Keywords
double-blind, randomized, intradermal, VZVv, HSCT

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 2, Phase 3
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
100 (Actual)

8. Arms, Groups, and Interventions

Arm Title
ID varicella zoster vaccine (VZVv) group
Arm Type
Experimental
Arm Description
intradermal 0.65 mL Zostavax
Arm Title
SC VZVv group
Arm Type
Active Comparator
Arm Description
subcutaneous 0.65 mL Zostavax
Arm Title
ID NS Group
Arm Type
Placebo Comparator
Arm Description
intradermal 0.65 mL normal saline
Arm Title
SC NS Group
Arm Type
Placebo Comparator
Arm Description
subcutaneous 0.65 mL normal saline
Intervention Type
Biological
Intervention Name(s)
Zostavax
Intervention Description
varicella zoster vaccine
Intervention Type
Biological
Intervention Name(s)
Normal Saline
Intervention Description
normal saline placebo vaccine
Primary Outcome Measure Information:
Title
Herpes Zoster Reactivation
Description
Incidence of herpes zoster in stem-cell transplant recipients
Time Frame
12 months post transplantation
Secondary Outcome Measure Information:
Title
Immunological response in recipients
Description
Geometric mean concentration of anti-VZV antibody (IU/mL)
Time Frame
30, 90, 180 and 360 days post transplantation
Title
Immunological response in donors
Description
Geometric mean concentration of anti-VZV antibody (IU/mL)
Time Frame
30, 90, 180 and 360 days post transplantation
Title
Adverse reaction
Description
Rate of adverse reaction in donors after vaccination
Time Frame
21 days after vaccination

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
60 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: patients undergoing allogeneic hemopoietic stem cell transplant HLA identical sibling donors participants willing to provide written informed consents Exclusion Criteria: history of zoster in the 12 months prior to transplantation exposure to VZV within 4 weeks of transplantation neomycin sensitivity sensitivity to any components of the zoster vaccine
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Ivan FN Hung, MD FRCP
Organizational Affiliation
The University of Hong Kong
Official's Role
Principal Investigator
Facility Information:
Facility Name
Ivan Hung
City
Hong Kong
Country
Hong Kong

12. IPD Sharing Statement

Citations:
PubMed Identifier
12097537
Citation
Hata A, Asanuma H, Rinki M, Sharp M, Wong RM, Blume K, Arvin AM. Use of an inactivated varicella vaccine in recipients of hematopoietic-cell transplants. N Engl J Med. 2002 Jul 4;347(1):26-34. doi: 10.1056/NEJMoa013441.
Results Reference
result
PubMed Identifier
17417658
Citation
Leung AY, Chow HC, Kwok JS, Lui CK, Cheng VC, Yuen KY, Lie AK, Liang R. Safety of vaccinating sibling donors with live-attenuated varicella zoster vaccine before hematopoietic stem cell transplantation. Bone Marrow Transplant. 2007 Jun;39(11):661-5. doi: 10.1038/sj.bmt.1705673. Epub 2007 Apr 9.
Results Reference
result

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VZV Vaccine for Hematopoietic Stem Cell Transplantation

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