MAPP BIOPHARMACEUTICAL, INC. — Department of Health and Human Services SBIR Phase I: NIAID

MAPP BIOPHARMACEUTICAL, INC. — SBIR Phase I award from Department of Health and Human Services.

Phase I SBIR feasibility signal

  • Phase I awards fund proof-of-concept work. For capture teams, they mark early interest from Department of Health and Human Services in a technical approach.
  • Watch for Phase II follow-ons from the same firm/topic family — that conversion path is where budgets and transition pressure rise.
  • Obligated amount $228,758. Cross-check similar awards in the same agency and technology tags for going-rate context.
  • Topic code NIAID links this award to a solicitation family — search the same topic stem for incumbents and recompete timing.

Informational capture context from public federal data — not legal or bid advice.

Amount
$228,758
Agency
Department of Health and Human Services · National Institutes of Health
Program / Phase
SBIR · Phase I
Topic
NIAID
Solicitation
PA14-071
NAICS
Place of performance
CA
Period
2015-01-05 → 2016-12-31

Description

DESCRIPTION provided by applicant Pseudomonas aeruginosa PA an opportunistic Gram negative bacterium is one of the leading nosocomial pathogens worldwide PA is responsible for localized infections of a variety of organ systems including respiratory urinary gastrointestinal skin eye ear and joints and also systemic infections in susceptible individuals Because PA is highly adaptable to survive in common environments mechanical ventilators intravenous lines urinary and dialysis catheters pacemakers and endoscopes can all be potential reservoirs for PA infections Despite the widespread presence and growing significance of PA and the increasing rates of antibiotic treatment failure no efficient and marketable vaccine is currently available Recent advances in the development of anti PA monoclonal antibodies mAbs have offered the possibility that passive immunotherapy may be a viable clinical modality We are examining the treatment effectiveness of a combination of mAbs that can target two common PA LPS serotypes in one formulation using animal models infected with two virulent PA strains The results will provide the basis for pre clinical development of a combination PA therapy with an optimized glycosylation profile The proposed work scope will allow us to determine whether using plant derived manufacturing techniques could enhance manufacturing productivity whether manipulating glycosylation can achieve enhanced potency against bacterial challenge in two mouse models and the effectiveness of using a cocktail of two mAbs to target two common PA serotypes PUBLIC HEALTH RELEVANCE We are developing two IgM monoclonal antibodies for the treatment of Pseudomonas aeruginosa infections The antibody manufacturing system involves plant based production and glycol engineering The goal is to develop a PA therapy using a cocktail of two mAbs to target two common PA serotypes