CI

At a glance

ClinicalIndex Comparison Record
Phase 2Completed· 375 enrolled
Drug / intervention
Non-adjuvanted study formulation NmCV-5 +2 morebiological
Likely dose
Non-adjuvanted study formulation NmCV-5 5 microgramsfrom record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT03295318
NCT03295318Phase 2Completed

A Phase 2, Observer-blind, Randomized, Controlled Study to Evaluate the Safety and Immunogenicity of Two Formulations of Investigational Meningococcal Groups ACYWX Conjugate Vaccine, Administered to Healthy Malian Children 12-16 Months of Age

Serum Institute of India Pvt. Ltd.·interventional·Posted Sep 27, 2017·Updated May 25, 2025

In Brief

A Phase 2 clinical trial evaluating Non-adjuvanted study formulation NmCV-5, Adjuvanted study formulation NmCV-5, and 1 other intervention for Meningitis, Meningococcal. Completed, enrolled 375 participants across 1 site.

Detailed Summary

Out of the 13 identified serogroups of Neisseria meningitidis (Nm) the six serogroups (A, B, C, W, Y and X) are responsible for majority of infections. Presently available vaccines effectively protect against A, B, C, W and Y serogroups; but no vaccine that is protective against serogroup X is available yet. Serum Institute of India Private Limited (SIIPL) has developed a conjugate vaccine against serogroups A, C, Y, W and X (NmCV-5). The first-in-human Phase 1 study was among 60 healthy adults in USA did not show no any safety issues. This phase 2 study is designed to evaluate safety and immunogenicity of the non-adjuvanted and adjuvanted formulations of NmCV-5 in healthy children 12-16 months of age, in comparison with the licensed quadrivalent meningococcal conjugate vaccine (Menactra®). Both vaccines will be administered in two dose schedule 3 months apart. among vaccine-naïve healthy subjects in Mali. Safety will be assessed by collecting solicited reactions till day 7 post each dose whereas adverse events will be collected throughout the study. Each subject will be followed up for 84 days post each vaccine dose. The vaccine immunogenicity will measured using a rabbit complement serum bactericidal activity assay (rSBA).

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesMali
CollaboratorsPATH

Timeline

Phase 2CompletedFinished
201820192020202120222023202420252026
First PostedSep 27, 2017
Enrollment StartNov 15, 2017
Primary CompletionAug 31, 2018
TodayJul 2, 2026
Enrollment to primary: 10 monthsPosted 8.8 years ago

Interventions

Non-adjuvanted study formulation NmCV-5biological

Non-adjuvanted formulation of polyvalent conjugate meningococcal vaccine against serogroups A,C,Y,W\&X (NmCV-5) is available as lyophilised powder of polysacchride antigens A\&X conjugated to tetanus toxoid and C,Y\&W conjugated to CRM protein. The diluent contains Normal Saline. Each antigen content is 5 micrograms per 0.5 mL dose of vaccine.

Adjuvanted study formulation NmCV-5biological

Adjuvanted formulation of polyvalent conjugate meningococcal vaccine against serogroups A,C,Y,W\&X (NmCV-5) is available as lyophilised powder of polysacchride antigens A\&X conjugated to tetanus toxoid and C,Y\&W conjugated to CRM protein. The diluent contains Alum as adjuvant with Normal Saline. Each antigen content is 5 micrograms per 0.5 mL dose of vaccine

Menactrabiological

Menactra is available as ready to used solution containing polysacchride antigens A,C,Y\&WX conjugated to diphtheria toxoid. Each antigen content is 4 micrograms per 0.5 mL dose of vaccine.