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OpenTrials
Completed

NCT Number: NCT01016548

Evaluation of Influenza H1N1 Vaccine in Adults With Lymphoid Malignancies on Chemotherapy

The purpose of this study is to determine whether adults with hematologic malignancies on active systemic therapy or shortly after bone marrow transplantation need one or two doses of adjuvanted vaccine to achieve best possible rates of protection. An additional research question is whether baseline biomarkers of the cellular and humoral immune systems are associated with an antibody response to vaccination.

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Key information

About this study

The novel influenza H1N1 virus responsible for a world-wide pandemic throughout 2009 (H1N1(2009)) is expected to cause a second wave of infection during the 2009/10 winter season. Vaccines against H1N1(2009) will be available in early November, 2009. Adults with hematologic disorders are at high risk of influenza-related complications, including death. Given that the vaccination dosing for the pandemic vaccine has been developed on healthy individuals, it is unknown whether this subgroup of patients will respond similarly. We will evaluate the safety and efficacy of the pandemic vaccine in patients with lymphoid malignancies receiving active systemic treatment, or who have recently undergone stem cell transplantation. Patients will be randomized to one or two doses of the approved adjuvanted vaccine; immune responses will be measured to identify the optimal regimen. Also, we will look for an association between biomarkers of the immune system and a response to the vaccine; this will be done by measuring baseline CD3, 4, 8, 19, and 56 cells by flow cytometry.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Male or female, ages 20-65
  • Diagnosis of lymphoproliferative disorder
  • One of the following types of systemic treatment: active chemo/immunotherapy at enrollment or completed within the last 3 months, OR auto/allo stem cell transplant recipient within the past 12 months
  • Able to provide consent and comply with trial requirements

Exclusion criteria

  • Systemic hypersensitivity to hen's eggs, thimerosal, gentamicin
  • History of life-threatening reaction to prior influenza vaccination
  • Thrombocytopenia or bleeding disorder contraindicating IM injection
  • Pregnancy
  • Laboratory-confirmed infection with H1N1(2009)
  • IVIG infusion within the last three months

Treatment and study plan

AS03-adjuvanted H1N1 pandemic influenza vaccine

Biological

One dose constitutes 0.5mL of suspended vaccine via the intramuscular route.

Other names: Arepanrix(R), ATC Code J07BB02

Primary outcomes

  1. Seroconversion rates.

    Time frame: Day 0, 21, 42

Secondary outcomes

  1. Adverse events to vaccination.

    Time frame: Day 7, 21, 28.

Sponsors and collaborators

Lead sponsor

University Health Network, Toronto

Other

Collaborators

  • Princess Margaret Hospital, Canada

Registry information

Official study title

Evaluation of Pandemic H1N1(2009) Influenza Vaccine in Adults With Lymphoid Malignancies on Active Systemic Treatment or Post Stem Cell Transplantation

Important dates

Study start
2009
Primary completion
2010
Study completion
2010
First posted
Nov 19, 2009
Registry last updated
Jun 4, 2010

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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