SBIR-STTR Award

Development and cGMP Manufacture of a Vitrified Typhoid Vaccine
Award last edited on: 8/20/15

Sponsored Program
SBIR
Awarding Agency
NIH : NIAID
Total Award Amount
$876,861
Award Phase
2
Solicitation Topic Code
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Principal Investigator
Sims K Kochi

Company Information

Celldex Therapeutics Inc (AKA: T Cell Sciences, Inc.~Virus Research Institute~Avant Immunotherapeutics)

53 Frontage Road Suite 220
Hampton, NJ 08827
   (908) 200-7500
   info@celldextherapeutics.com
   www.celldex.com
Location: Multiple
Congr. District: 07
County: Norfolk

Phase I

Contract Number: 1R43AI053910-01
Start Date: 00/00/00    Completed: 00/00/00
Phase I year
2003
Phase I Amount
$126,861
Ty800 is a live attenuated Salmonella typhi organism intended to be used as a prophylactic single dose oral vaccine for Typhoid fever. Ty800 may have advantages in several respects to current Typhoid fever vaccines, and consequently could be a significant advance when it reaches the market. Ty800 has been given to a limited number of human subjects and immunogenicity has been demonstrated. The goal of this Phase I SBIR grant is to conduct an initial series of experiments to, in part, demonstrate that Ty800 has the necessary basic elements to be a viable marketed human vaccine. Consequently, the specific aims of this proposal during the requested funding period are to 1) determine a protocol for the in vivo Ty800 General Safety Test, suitable to meet the regulations for product release, and to perform an initial GLP General Safety Test using this protocol; 2) perform preliminary evaluations of a Ty800 immunogenicity animal model, with the goal of helping define an animal model for future toxicology studies; 3) develop immunochemistry assays to evaluate the immunogenicity of Ty800 in preclinical animal models and to help define the assays to be used in future clinical trials; 4) evaluate the environmental release survivability of Ty2 and Ty800; 5) determine the antibiotic sensitivity profile of Ty800 using the Kirby-Bauer Method; 6) demonstrate the precise genetic deletion at the phoP/phoQ regulon by sequencing the Ty800 chromosomal DNA.

Thesaurus Terms:
Salmonella typhi, Salmonella vaccine, drug screening /evaluation, oral administration, typhoid, vaccine development active immunization, antigen antibody reaction, gene deletion mutation, nonhuman therapy evaluation guinea pig, immunochemistry, laboratory mouse

Phase II

Contract Number: 2R44AI053910-02
Start Date: 1/1/03    Completed: 8/31/07
Phase II year
2006
Phase II Amount
$750,000
Typhoid fever is an infectious disease that annually afflicts an estimated 16 million people worldwide, resulting in 600,000 deaths. The etiologic agent of typhoid fever, Salmonella typhi (S. typhi), is transmitted to humans by the fecal-oral route through contaminated water or food. The use of antibiotics to treat typhoid fever has transformed an often fatal disease into a readily treatable condition. The recent emergence of multidrug-resistant strains of S. typhi found in regions like Southeast Asia has resulted in an increase in the incidence of severe and fatal typhoid fever as well as heightened medical concerns. These concerns may be partially addressed through the use of an effective typhoid fever vaccine that can control morbidity and mortality and limit the spread of drug resistant strains. There are limitations of commercially available vaccines to typhoid fever, which include inconvenient dosing, parenteral administration frequently associated with local reactogenicity and fever, variable protective efficacy, and unpredictable duration of immunity. AVANT Immunotherapeutics, Inc. is developing live, attenuated S. typhi TySOO as an orally administered, single-dose vaccine against typhoid fever. Freshly prepared TySOO was well tolerated and remarkably immunogenic when administered as a single, oral dose to eleven healthy, adult volunteers. A vigorous mucosal response was also detected within seven days of vaccination. Lyophilized TySOO was recently manufactured for evaluation in a Phase I/I I clinical study sponsored by the Division of Microbiology and Infectious Diseases at the NIAID. Lyophilized TySOO requires storage at -20C, requiring a "cold chain" to maintain vaccine potency. AVANT now has technology to preserve bacterial vaccines using a proprietary preservation process that markedly improves vaccine stability at room temperature. The goals of this proposal are to (1) optimize the production methodology to incorporate this innovative drying technology into the production of a thermostable formulation for TySOO; (2) develop multidose and bulk manufacturing techniques that would significantly reduce cost and manufacturing capacity needed for production of large quantities of doses; and (3) perform scale up and GMP production of preserved TySOO. Meeting these goals will facilitate the advance of TySOO as an oral, single-dose vaccine that can be delivered outside of the storage cold chain.

Thesaurus Terms:
There Are No Thesaurus Terms On File For This Project.