NCT01687192

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

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
37

participants targeted

Target at P25-P50 for phase_2

Timeline
Completed

Started Oct 2012

Typical duration for phase_2

Geographic Reach
1 country

9 active sites

Status
completed

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

Completed
5 days until next milestone

First Posted

Study publicly available on registry

September 18, 2012

Completed
23 days until next milestone

Study Start

First participant enrolled

October 11, 2012

Completed
2.6 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

May 1, 2015

Completed
1.5 years until next milestone

Study Completion

Last participant's last visit for all outcomes

October 20, 2016

Completed
Last Updated

July 16, 2024

Status Verified

July 1, 2024

Enrollment Period

2.6 years

First QC Date

September 13, 2012

Last Update Submit

July 15, 2024

Conditions

Keywords

SeroconversionImmunosuppressed treatmentHPV vaccinationImmunogenicity

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

EXPERIMENTAL
Biological: HPV prophylactic vaccine Gardasil

Interventions

3 injections: at Inclusion visit then 2 and 6 months after.

Girls and young womens receiving immunosuppressive treatment

Eligibility Criteria

Age9 Years - 18 Years
Sexfemale
Healthy VolunteersNo
Age GroupsChild (0-17), Adult (18-64)

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

Location

HCLyon, Hôpital Femme-mère-enfant

Bron, 69677, France

Location

CHU de Lille, HĂ´pital Jeanne de Flandres

Lille, 59037, France

Location

CHU de Montpellier, HĂ´pital Arnaud de Villeneuve

Montpellier, 34295, France

Location

CHU de Nantes, Hôpital Mère-Enfants

Nantes, 44093, France

Location

AP-HP, Hôpital Robert Debré

Paris, 75019, France

Location

AP-HP, HĂ´pital Armand Trousseau

Paris, 75571, France

Location

AP-HP, HĂ´pital Necker-Enfants

Paris, 75743, France

Location

CHU de Toulouse, HĂ´pital des Enfants

Toulouse, 31059, France

Location

Related Publications (34)

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    PMID: 17471531BACKGROUND
  • Tam LS, Chan PK, Ho SC, Yu MM, Yim SF, Cheung TH, Wong MC, Li EK. Natural history of cervical papilloma virus infection in systemic lupus erythematosus - a prospective cohort study. J Rheumatol. 2010 Feb;37(2):330-40. doi: 10.3899/jrheum.090644. Epub 2009 Dec 23.

    PMID: 20032093BACKGROUND
  • Kirnbauer R, Hubbert NL, Wheeler CM, Becker TM, Lowy DR, Schiller JT. A virus-like particle enzyme-linked immunosorbent assay detects serum antibodies in a majority of women infected with human papillomavirus type 16. J Natl Cancer Inst. 1994 Apr 6;86(7):494-9. doi: 10.1093/jnci/86.7.494.

    PMID: 8133532BACKGROUND
  • Joura 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: 18930097BACKGROUND
  • Garland 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.

    PMID: 17494926BACKGROUND
  • FUTURE II Study Group. Quadrivalent vaccine against human papillomavirus to prevent high-grade cervical lesions. N Engl J Med. 2007 May 10;356(19):1915-27. doi: 10.1056/NEJMoa061741.

    PMID: 17494925BACKGROUND
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    PMID: 16394035BACKGROUND
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    PMID: 15863374BACKGROUND
  • Ault KA; Future II Study Group. Effect of prophylactic human papillomavirus L1 virus-like-particle vaccine on risk of cervical intraepithelial neoplasia grade 2, grade 3, and adenocarcinoma in situ: a combined analysis of four randomised clinical trials. Lancet. 2007 Jun 2;369(9576):1861-1868. doi: 10.1016/S0140-6736(07)60852-6.

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MeSH Terms

Conditions

Lupus Erythematosus, SystemicHIV Seropositivity

Condition Hierarchy (Ancestors)

Connective Tissue DiseasesSkin and Connective Tissue DiseasesAutoimmune DiseasesImmune System DiseasesHIV InfectionsBlood-Borne InfectionsCommunicable DiseasesInfectionsSexually Transmitted Diseases, ViralSexually Transmitted DiseasesLentivirus InfectionsRetroviridae InfectionsRNA Virus InfectionsVirus DiseasesGenital DiseasesUrogenital DiseasesImmunologic Deficiency Syndromes

Study Officials

  • Geneviève CHENE, MD-PhD

    University Hospital, Bordeaux, USMR

    STUDY CHAIR
  • Jerome HARAMBAT, MD

    University Hospital, Bordeaux

    PRINCIPAL INVESTIGATOR

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

Locations