ZYMERON CORPORATION — Department of Defense SBIR Phase I: DHA211-008

ZYMERON CORPORATION — SBIR Phase I award from Department of Defense.

Phase I SBIR feasibility signal

  • Phase I awards fund proof-of-concept work. For capture teams, they mark early interest from Department of Defense 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 $249,999. Cross-check similar awards in the same agency and technology tags for going-rate context.
  • Topic code DHA211-008 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
$249,999
Agency
Department of Defense · Defense Health Program
Program / Phase
SBIR · Phase I
Topic
DHA211-008
Solicitation
21.1
NAICS
Place of performance
NC
Period
2021-07-26 → 2022-02-25

Description

The rapid development and spread of microbial antibiotic resistance have rendered many previously potent antibiotics useless. P. aeruginosa is one of the most common gram-negative bacteria implicated in nosocomial infection and the second most common pathogen implicated in ventilator-associated pneumonia. The excessive use of antibiotics during treatment further accelerates development of multidrug-resistant (MDR) P. aeruginosa strains, leading to the ineffectiveness of the empirical antibiotic therapy against this microorganism. Zymeron is developing a new generation of host defensing peptide (HDP) mimetics as antibiotic candidates for the treatment of MDR P. aeruginosa infections. Our preliminary results indicate that synthetic mimetics of core pharmacophore pattern offer the advantages of protease resistance, reduced cytotoxicity, and good chemical stability over natural HDP. With further structural optimization, the Phase I results will demonstrate the efficacy of promising lead compounds against clinical isolates of MDR P. aeruginosa strains and the minimal toxicity in cell-based assays for the further preclinical development of peptidomimetics as antibiotic drug candidates for the treatment of P. aeruginosa Infections.