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Study identifier: NCT04460235 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Clinical Trial Assessing the Immunogenicity of an Anti-pneumococcal Vaccination Strategy (PCV13+PPV23 Versus PREVENAR20) in Adult Patients Treated for a Lymphoma

Condition: Vaccine · Streptococcus Pneumoniae · Lymphoma, Non-Hodgkin  ·  Sponsor: Poitiers University Hospital

PhasePhase 4
Planned participants160
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

The French Public Health Council recommended pneumococcal vaccination combined strategy for all immunocompromised patients in 2012. This strategy consisted in conjugated 13-valent pneumococcal (PCV13) injection followed 2 months later by polysaccharide 23-valent (PPV23) vaccine injection. In 2024, Health authorities changed guidelines to recommend one injection of PREVENAR20 instead of the 2-vaccine scheme general practitioners are usually in charge of this vaccination. Conjugated pneumococcal vaccine enhances the immunogenicity of the polysaccharide vaccine. Acute leukemia and lymphoma are treated with multiple courses of chemotherapy, impairing the immune system and potentially the response to vaccination. These patients are more at risk for developing pneumococcal invasive diseases than the general population. However, efficacy of pneumococcal vaccination is poorly documented in this setting. We assume that 65% of the patients are non-responders to double compared to 45% for PCV20PREVENAR20 vaccination, according to their anti-pneumococcal immunoglobulin G (Ig) titers and the opsonophagocytic activity (OPA). To assess the immunogenicity of the pneumococcal vaccination combined strategy in adult population of acute leukemia and lymphoma, we will measure anti-pneumococcal serotype-specific IgG titers and OPA at different time-points after completion of the combined vaccine strategy. The primary objective is to assess the immunogenicity of pneumococcal vaccination combined st…

This description comes directly from the study's public registry record.

Talk to the study team

Mathieu Puyade, MD, PhD  ·  0033 5 49 44 32 76  ·  mathieu.puyade@chu-poitiers.fr

Always discuss trial participation with your own doctor first.

Locations (7)

Chu AngersAngers, FranceRecruiting
CHU BordeauxBordeaux, FranceTerminated
CHU LimogesLimoges, FranceRecruiting
Chu NantesNantes, FranceTerminated
Ch PerigueuxPérigueux, FranceRecruiting
CHU PoitiersPoitiers, FranceRecruiting
CHU ToursTours, FranceRecruiting

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Source record: clinicaltrials.gov/study/NCT04460235