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CompletedNCT00258947Updated Feb 1, 2012

Evaluation of Take and Safety of a Smallpox Vaccine in Healthy Young Adults

A Phase 2 interventional study of Smallpox vaccine, LISTER strain, from chick embryo cells in Smallpox and Poxvirus Infection, sponsored by Sanofi. Completed at 6 sites in France. Open to participants aged 18 Years to 25 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2012-02-01.

Sponsored by Sanofi · Phase 2, Interventional, and Prevention

Phase
Phase 2
Study type
Interventional
Enrollment
230
Allocation
Randomized
Ages
18 Years to 25 Years
Sex
All
01

Study summary

Primary Objective:

To estimate the smallpox vaccination take rate in healthy young adults not previously vaccinated with a smallpox vaccine.

Secondary Objectives:

To describe antibody response to vaccination and evaluate the take for each subject at various timepoints for each batch and pooled batches and to evaluate local signs, symptoms, and overall safety in healthy young adults not previously vaccinated with a smallpox vaccine.

02

Conditions studied

  • Smallpox
  • Poxvirus Infection

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Keywords

  • Smallpox
  • Orthopoxvirus
  • Poxvirus
  • Vaccina Virus
  • LISTER Strain
  • Bioterrorism
03

In context

Smallpox

73 studies on the registry are indexed under Smallpox; 5 are open to participants now.

This study's enrollment of 230 is above the median of 148 across 62 interventional studies indexed under Smallpox.

Browse Smallpox studies →

Lead sponsor

Sanofi is the lead sponsor of 1,508 studies on the registry; 90 are open to participants now.

Of its 198 completed or terminated interventional studies of FDA-regulated products, 118 (60%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 25 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Inclusion criteria

  • Aged 18 to 25 years on the day of screening
  • Informed consent form signed
  • Able to attend all scheduled visits and to comply with all trial procedures
  • For a woman, inability to bear a child or negative serum pregnancy test performed at screening (Visit 01)
  • Subject entitled to national social security
  • Subject registered in the French file of healthy volunteers in clinical trials
  • For a woman of child-bearing potential: use of an effective method of contraception (hormonal or barrier method) from at least 3 months prior to screening to 3 months following trial vaccination
  • For a woman, inability to bear a child or negative urine pregnancy test.

Exclusion criteria

Exclusion Criteria:

  • Previous smallpox vaccination confirmed by vaccination record or typical scar
  • Participation in another trial in the 3 months before or during the trial period
  • Acute intercurrent or chronic illness during the trial
  • Breast-feeding
  • Allergy or sensitivity to any known components of vaccinia immune globulin or previous reaction to immunoglobulins or trial vaccine
  • Congenital or acquired immunodeficiency or immunosuppressive therapy or any treatment including corticosteroids
  • Treatment with antiviral drugs within 1 month before vaccination
  • History of organ or bone marrow transplant or skin disorders
  • Personal or family history of autoimmune disease or cardiac disease, including cardiac risk factors
  • History or current central nervous system disease
  • Ongoing acute infectious disease
  • Blood or blood-derived products received in the past 6 months
  • Any vaccination with a live-attenuated vaccine within the 60 days or other vaccines within 40 days preceding the trial vaccination
  • Vaccination planned in the 8 weeks following the trial vaccination
  • Planned or foreseeable close contact after vaccination with infants less than 12 months, or with immuno-suppressed persons, pregnant and/or lactating woman, or practice of contact or water sports after vaccination before the crust separates
  • Skin wound near the vaccination site
  • Apparent lack of personal hygiene
  • Subject deprived of freedom by an administrative or court order, or in an emergency setting, or hospitalized without his/her consent
  • HIV, hepatitis B or hepatitis C seropositivity (screening tests)
  • Abnormal lab values for hematological parameters or cardiac enzyme (screening tests)
  • Feverish illness (oral temperature >=37.5°C, rectal equivalent temperature >=38.0°C) on the day of vaccination.
05

Study design

Phase
Phase 2
Primary purpose
Prevention
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Quadruple (Participant, Care provider, Investigator, Outcomes assessor)
Enrollment
230 participants (actual)

Interventions

  • BiologicalSmallpox vaccine, LISTER strain, from chick embryo cells
06

Study locations

6 sites
  • Gieres, France
  • Lagord, France
  • Montpellier, France
  • Paris, France
  • Poitiers, France
  • Rouen, France
07

References and documents

Related links

08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Feb 1, 2012, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT00258947
Lead sponsor
Sanofi
Responsible party
Sponsor
First posted
Nov 28, 2005
Start date
Sep 2005
Primary completion
Dec 2006
Completion
Jan 2007
Last update
Feb 1, 2012

Study contacts

Medical Director
study director · Sanofi Pasteur Inc

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in Jan 2012. You cannot join it, but the record below documents what was studied.

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