SBIR-STTR Award

Optimization of a broad-spectrum Ebolavirus cell entry inhibitor chemical series as a countermeasure for parental and aerosol routes of infection
Award last edited on: 5/29/2023

Sponsored Program
SBIR
Awarding Agency
DOD : CBD
Total Award Amount
$755,162
Award Phase
2
Solicitation Topic Code
CBD192-006
Principal Investigator
Ken J McCormack

Company Information

Arisan Therapeutics Inc

11189 Sorrento Valley Road #104
San Diego, CA 92310
   (919) 559-3653
   kenm@arisanthera.com
   www.arisanthera.com
Location: Single
Congr. District: 50
County: San Bernardino

Phase I

Contract Number: W911QY-20-P-0069
Start Date: 2/3/2020    Completed: 1/3/2021
Phase I year
2020
Phase I Amount
$167,442
Ebolavirus species including Zaire (EBOV), Sudan (SUDV) and Bundibugyo (BDBV) are responsible for severe hemorrhagic fever outbreaks with high case fatalities in Africa. Weaponized pathogens present an additional threat to the health protection of the warfighter and first-generation prophylactic and therapeutic medical countermeasures (MCMs) may prove inadequate in biodefense settings. Ebolaviruses present both potential public health and bioweapons threats and the development of second-generation therapeutics targeting novel mechanisms for antiviral activity may help to provide auxiliary means of protection. We utilized a vesicular stomatitis virus (VSV) based pseudotyped virus platform to identify novel chemical series of Ebola virus cell entry inhibitors and through SAR expansion have identified compounds with submicromolar broad-spectrum ebolavirus antiviral activity. Lead compounds exhibit favorable in vitro and in vivo drug-like properties promoting them as attractive next generation Ebola inhibitors for the development of dual use therapeutics.

Phase II

Contract Number: W911SR-21-C-5049
Start Date: 9/30/2021    Completed: 9/30/2023
Phase II year
2021
Phase II Amount
$587,720
Ebolavirus species including Zaire (EBOV), Sudan (SUDV) and Bundibugyo (BDBV) are responsible for severe hemorrhagic fever outbreaks with high case fatalities in Africa [1,2]. Outbreaks of EBOV in the Democratic Republic of the Congo (DRC) as well as the 2014-2016 outbreak in West Africa highlight the danger that these zoonotic viruses pose through mucosal routes of infection and secondary human to human transmission. Weaponized pathogens present an additional threat to the health protection of the warfighter and first-generation prophylactic and therapeutic medical countermeasures (MCMs) may prove inadequate in biodefense settings. Ebolaviruses present both potential public health and bioweapons threats and the development of second-generation therapeutics targeting novel mechanisms for antiviral activity may help to provide auxiliary means of protection. The objective of this proposal is to demonstrate feasibility of generating a dual use broad-spectrum small molecule ebolavirus therapeutic.