Multicenter Trial Evaluating the Immunogenicity of HPV Vaccination in Girls on Immunosuppressive Therapy.
PRIMAVERA
Multicenter Clinical Trial Evaluating the Immunological Response of Vaccination Against Infection by Human Papillomavirus (HPV) 6, 11, 16, 18 in Girls Receiving Immunosuppressive Therapy.
1 other identifier
interventional
37
1 country
9
Brief Summary
PRIMAVERA is a Phase IIa clinical trial, with the objective to assess the immunologic response to HPV vaccine in a population of immunocompromised girls. The principal hypothesis is that the immunologic response to tetravalent vaccine in girls who received immunosuppressive treatment is comparable to the immunologic response in girls that are not immunosuppressed.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for phase_2
Started Oct 2012
Typical duration for phase_2
9 active sites
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
September 13, 2012
CompletedFirst Posted
Study publicly available on registry
September 18, 2012
CompletedStudy Start
First participant enrolled
October 11, 2012
CompletedPrimary Completion
Last participant's last visit for primary outcome
May 1, 2015
CompletedStudy Completion
Last participant's last visit for all outcomes
October 20, 2016
CompletedJuly 16, 2024
July 1, 2024
2.6 years
September 13, 2012
July 15, 2024
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Seroconversion rate for HPV 16 and 18 at M18
18 months after first dose of vacinne (i.e. Inclusion visit)
Secondary Outcomes (4)
Geometric means of anti-HPV 6, 11, 16 and 18 antibody titers at M7, M18, and M36, respectively.
Samples collected 7, 18 and 36 months after first dose of vaccine
Proportion of patients with a good cell response at M7 and M18
7 and 18 months after first dose of vaccine
Proportion of patients with genital warts or cervical lesions (if relevant)
36 months after first dose of vaccine
Number, type and time of occurrence of adverse events of any grade during 18 months after first dose of vaccine
Assessed at months 2,6,7 and 18 after first dose of vaccine
Study Arms (1)
Girls and young womens receiving immunosuppressive treatment
EXPERIMENTALInterventions
3 injections: at Inclusion visit then 2 and 6 months after.
Eligibility Criteria
You may qualify if:
- Female gender
- Age ≥ 9 years and \< 18 years
- Weight ≥ 25 kg
- Solid organ transplantation: kidney, liver, heart, lung, intestinal or combined transplant; or systemic lupus erythematosus or other systemic immune disease
- Transplantation or diagnosis of lupus or diagnosis of systemic immune disease since more than 6 months
- Immunosuppressant treatment by anti-metabolites or calcineurin inhibitors, with or without associated corticosteroids
- Minimum required period of 3 months considered as stable after transplantation or without relapse of lupus according to physician evaluation
- Written informed consent signed by the investigator and the legal representatives of the patient, and assent by the patient
You may not qualify if:
- Male gender
- Pregnancy
- Age \< 9 years or ≥ 18 years
- Previous HPV vaccination
- Immunosuppressive treatment by anti-TNF (adalimumab, etanercept, infliximab) or monoclonal antibodies (rituximab, anakinra, abatacept) during the last 3 months
- Active malignancy
- Active opportunistic infection
- HIV infection
- Concurrent clinical trial
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (9)
CHU de Bordeaux, HĂ´pital Pellegrin-Enfants
Bordeaux, 33076, France
HCLyon, Hôpital Femme-mère-enfant
Bron, 69677, France
CHU de Lille, HĂ´pital Jeanne de Flandres
Lille, 59037, France
CHU de Montpellier, HĂ´pital Arnaud de Villeneuve
Montpellier, 34295, France
CHU de Nantes, Hôpital Mère-Enfants
Nantes, 44093, France
AP-HP, Hôpital Robert Debré
Paris, 75019, France
AP-HP, HĂ´pital Armand Trousseau
Paris, 75571, France
AP-HP, HĂ´pital Necker-Enfants
Paris, 75743, France
CHU de Toulouse, HĂ´pital des Enfants
Toulouse, 31059, France
Related Publications (34)
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PMID: 8133532BACKGROUNDJoura EA, Kjaer SK, Wheeler CM, Sigurdsson K, Iversen OE, Hernandez-Avila M, Perez G, Brown DR, Koutsky LA, Tay EH, Garcia P, Ault KA, Garland SM, Leodolter S, Olsson SE, Tang GW, Ferris DG, Paavonen J, Lehtinen M, Steben M, Bosch X, Dillner J, Kurman RJ, Majewski S, Munoz N, Myers ER, Villa LL, Taddeo FJ, Roberts C, Tadesse A, Bryan J, Lupinacci LC, Giacoletti KE, Lu S, Vuocolo S, Hesley TM, Haupt RM, Barr E. HPV antibody levels and clinical efficacy following administration of a prophylactic quadrivalent HPV vaccine. Vaccine. 2008 Dec 9;26(52):6844-51. doi: 10.1016/j.vaccine.2008.09.073. Epub 2008 Oct 16.
PMID: 18930097BACKGROUNDGarland SM, Hernandez-Avila M, Wheeler CM, Perez G, Harper DM, Leodolter S, Tang GW, Ferris DG, Steben M, Bryan J, Taddeo FJ, Railkar R, Esser MT, Sings HL, Nelson M, Boslego J, Sattler C, Barr E, Koutsky LA; Females United to Unilaterally Reduce Endo/Ectocervical Disease (FUTURE) I Investigators. Quadrivalent vaccine against human papillomavirus to prevent anogenital diseases. N Engl J Med. 2007 May 10;356(19):1928-43. doi: 10.1056/NEJMoa061760.
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PMID: 16394035BACKGROUNDVilla LL, Costa RL, Petta CA, Andrade RP, Ault KA, Giuliano AR, Wheeler CM, Koutsky LA, Malm C, Lehtinen M, Skjeldestad FE, Olsson SE, Steinwall M, Brown DR, Kurman RJ, Ronnett BM, Stoler MH, Ferenczy A, Harper DM, Tamms GM, Yu J, Lupinacci L, Railkar R, Taddeo FJ, Jansen KU, Esser MT, Sings HL, Saah AJ, Barr E. Prophylactic quadrivalent human papillomavirus (types 6, 11, 16, and 18) L1 virus-like particle vaccine in young women: a randomised double-blind placebo-controlled multicentre phase II efficacy trial. Lancet Oncol. 2005 May;6(5):271-8. doi: 10.1016/S1470-2045(05)70101-7.
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PMID: 16136457BACKGROUND
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- STUDY CHAIR
Geneviève CHENE, MD-PhD
University Hospital, Bordeaux, USMR
- PRINCIPAL INVESTIGATOR
Jerome HARAMBAT, MD
University Hospital, Bordeaux
Study Design
- Study Type
- interventional
- Phase
- phase 2
- Allocation
- NON RANDOMIZED
- Masking
- NONE
- Purpose
- OTHER
- Intervention Model
- SINGLE GROUP
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
September 13, 2012
First Posted
September 18, 2012
Study Start
October 11, 2012
Primary Completion
May 1, 2015
Study Completion
October 20, 2016
Last Updated
July 16, 2024
Record last verified: 2024-07