Overview

This trial is active, not recruiting.

Condition infectious disease
Treatments nu300, acthib, prevnar 13
Phase phase 2
Sponsor Nuron Biotech Inc.
Start date March 2013
End date January 2014
Trial size 220 participants
Trial identifier NCT01732198, CP-NU300-02

Summary

Evaluate the safety and tolerability of a single booster dose of NU300, co-administered with Prevnar 13® over a 28 day period following the injection compared to a single booster of ACTHIB co-administered with Prevnar 13® over a 28 day period following the injection.

Evaluate the immunogenicity, as determined by anti-PRP polysaccharide response, of a single booster dose of NU300 co-administered with Prevnar 13® compared to a single booster dose of ActHIB® co-administered with Prevnar 13®.

Evaluate the individual IgG antibody quantitative response to the 13 antigens in Prevnar 13® following NU300 co-administration with Prevnar 13® compared to the IgG antibody response to the pneumococcal polysaccharides following ActHIB® co-administration with Prevnar 13® 28 days following injection.

United States No locations recruiting
Other Countries No locations recruiting

Study Design

Allocation randomized
Endpoint classification safety/efficacy study
Intervention model parallel assignment
Masking double blind (subject, caregiver, investigator, outcomes assessor)
Primary purpose prevention
Arm
(Experimental)
NU300 at a single dose of 0.5 mL IM
nu300
prevnar 13
(Active Comparator)
ActHIB at a dose of 0.5 ml IM
acthib
prevnar 13

Primary Outcomes

Measure
safety and efficacy
time frame: one month

Secondary Outcomes

Measure
Evaluate the individual IgG antibody quantitative response to the 13 antigens in Prevnar 13®
time frame: one month

Eligibility Criteria

Male or female participants from 12 months up to 15 months old.

Inclusion Criteria: 1. Written informed consent obtained from the parent or guardian of the subject 2. Male or female subjects 12-15 months of age at the time of booster vaccination, who had previously received complete primary vaccination series with a licensed Hib product and Prevnar 13® in accordance with the FDA approved labels. 3. Subjects for whom the investigator believes that the parent/guardian can and will comply with the requirements of the protocol 4. Subjects free of obvious health problems as established by medical history and clinical examination before entering the study Exclusion Criteria: 1. Previous booster vaccination against Hib and/or Prevnar 13® 2. Any confirmed or suspected Haemophilus influenzae or pneumococcal illness. 3. Administration of a vaccine not foreseen by the study protocol during the period starting from 30 days before and ending 28 days after administration of study vaccines (before the blood draw at Visit 2). 4. Chronic administration of immunosuppressants or other immune-modifying drugs within 30 days prior to dosing in the study. 5. Any confirmed or suspected immunosuppressive or immunodeficient condition based on medical history and/or clinical examination. 6. Early pre-term birth (delivery before 32 weeks). 7. Major congenital defects or serious chronic diseases, or serious conditions including history of seizures, apnea, etc. 8. Concurrent participation in another clinical study at any time during the study period or within the previous 6 months in which the subject has been or will be exposed to an investigational or non-investigational product (pharmaceutical product, formula, or device) 9. Presence of a moderate or severe illness with or without fever at the time of vaccination (fever is defined as a temperature of ≥ 38.0C [100.4F]). 10. Known history of thrombocytopenia or any coagulation disorder. 11. Known hypersensitivity to any of the components of the vaccines. 12. Known hypersensitivity to latex. 13. The subject is unable to provide an adequate blood draw for immunogenicity assays, and safety panels at Visit 1

Additional Information

Official title A Phase 2, Multicenter, Randomized, Double-Blind, Immunogenicity, Reactogenicity, and Safety Study of NU300 Booster Dose Compared to ActHIB®, Both Co-administered With Prevnar 13® at 12-15 Months of Age, in Healthy Toddlers Who Have Received a Primary Series of a Licensed Hib Vaccine and Prevnar 13®
Trial information was received from ClinicalTrials.gov and was last updated in September 2013.
Information provided to ClinicalTrials.gov by Nuron Biotech Inc..