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Persistence of Immune Response After Vaccination With MCC

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Novartis

Status and phase

Completed
Phase 4

Conditions

Prevention of Meningococcal Infection

Treatments

Procedure: BLOOD DRAW

Study type

Interventional

Funder types

Industry

Identifiers

NCT00310687
M14P2E1
Impact N° 919

Details and patient eligibility

About

Persistence of Immune response after vaccination with MCC

Sex

All

Ages

11 to 20 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • healthy adolescents vaccinated with Meningococcal C Conjugate vaccine

Exclusion criteria

  • ascertained or suspected disease caused by N. meningitidis
  • household contact with individuals with proven N. meningitidis serogroup C infection
  • significant acute or chronic infections
  • any other serious disease

Trial design

Primary purpose

Prevention

Allocation

Non-Randomized

Interventional model

Single Group Assignment

Masking

None (Open label)

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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