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Alternatives to Benzathine Penicillin for Treatment of Syphilis

ID: NIH/NIAID 134 • Type: SBIR / STTR Topic • Match:  100%
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Description

Fast-Track proposals will be accepted Direct-to-Phase II proposals will be accepted Number of anticipated awards: 2-3 Budget (total costs): Phase I: $300,000 for up to one year; Phase II: $1,500,000 for up to 3 years Background Injectable benzathine penicillin (BPG) is currently the only CDC-recommended first line therapy for treatment of infection with Treponema pallidum (syphilis) in all populations, including pregnant persons and infants. There are several barriers that limit use of BPG: BPG is not available orally. Only a limited number of facilities in a single country currently manufacture the raw active pharmaceutical ingredient which means the supply chain can easily be disrupted and shortages of BPG are common in the US and globally. Page 119 BPG may sometimes not be administered at lower-level facilities or by non-physician medical staff out of fear of anaphylactic reactions that might require referral to a tertiary care center. Alternative therapies to BPG that address some of these barriers are urgently needed, as acquired and congenital syphilis rates are increasing rapidly. WHO estimates over six million persons per year are infected with syphilis, and many more are treated presumptively for syphilis. Clinicians and health systems are eager for BPG alternatives. Recent advances in the ability to culture T. pallidum mean that identification of alternatives to BPG is now more feasible than has been possible in the past.

Overview

Response Deadline
Nov. 14, 2023 Past Due
Posted
Aug. 25, 2023
Open
Aug. 25, 2023
Set Aside
Small Business (SBA)
Place of Performance
Not Provided
Source
Alt Source

Program
SBIR Phase I / II
Structure
Contract or Grant
Phase Detail
Phase I: Establish the technical merit, feasibility, and commercial potential of the proposed R/R&D efforts and determine the quality of performance of the small business awardee organization.
Phase II: Continue the R/R&D efforts initiated in Phase I. Funding is based on the results achieved in Phase I and the scientific and technical merit and commercial potential of the project proposed in Phase II. Typically, only Phase I awardees are eligible for a Phase II award
Duration
6 Months - 1 Year
Size Limit
500 Employees
On 8/25/23 National Institutes of Health issued SBIR / STTR Topic NIH/NIAID 134 for Alternatives to Benzathine Penicillin for Treatment of Syphilis due 11/14/23.

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