TRxA BRIDGe Awards: Stage 1 Grant
Funding Amount
Up to US $250,000
Deadline
Deadline not published
Grant Type
Foundation
Can we apply?
Check your organization against each line. Taken from the listing; confirm with the funder's guidelines.
Not eligible / not funded
- Not eligible: Biologics, including natural peptides or antibodies, cell and gene therapy applications, and diagnostic and medical devices are not eligible at this time; nor are drug repurposing initiatives.
Overview
The TRxA BRIDGe Awards: Stage 1 aims to support academic researchers in early drug lead optimization, facilitating the translation of novel therapeutics into Investigational New Drug (IND) supporting data packages. This initiative, led by the Critical Path Institute, provides essential resources, strategic guidance, and access to contract research organizations to enhance drug development efforts. Eligible projects include those demonstrating strong structure-activity relationships and established pharmacology assays, fostering innovation in drug discovery.
NOTE:
The deadline for submitting a pre-proposal through the portal is by midnight in the time zone in which you are located. It is recommended that you set up your username and password at least one week prior to this submission deadline to allow sufficient time for troubleshooting in the event you experience any technical difficulties.Prior to submission of an application, you can schedule a time to speak with the TRxA team to gain consensus on the appropriate funding level.
Translational Therapeutics Accelerator (TRxA)
The Critical Path Institute’s (C-Path) Translational Therapeutics Accelerator (TRxA) is a global drug discovery and development program focused on supporting academic scientists in defining optimal strategies for advancing new, cutting-edge therapeutics from the lab to patients.
TRxA operates as a not-for-profit drug accelerator providing the following for academic researchers who have applied for and received a grant award:
Resources and hands-on guidance, working closely with academic researchers to develop comprehensive data packages for potential drug candidates, a key to garnering interest from biotechnology and pharmaceutical companies to invest in clinical trials.Tactical and strategic drug discovery and development leadership, including regulatory science considerations, bringing diverse expertise to pivotal early-stage academic study designs and implementation.Engagement of contract research organizations (CRO) to perform critical discovery phase experiments (e.g., key toxicology and other specialized studies) and/or validate academic studies to develop the type of comprehensive data package pharmaceutical companies require when licensing drug products.
TRxA’s focus is translating early-stage novel therapeutics into Investigational New Drug (IND) supporting data packages that garner interest for licensing opportunities; we are helping “BRIDGe” (Breakthrough Research and Innovation in Drug Development Grants) the drug development valley of death. Projects eligible for TRxA BRIDGe funding and support include early lead optimization through IND-enabling studies of small molecule therapeutics. Biologics, including natural peptides or antibodies, cell and gene therapy applications, and diagnostic and medical devices are not eligible at this time; nor are drug repurposing initiatives.
TRxA funding and support is reserved for faculty at universities and non-profit institutions, anywhere around the world. Awards are not limited to specific therapeutic indications. TRxA offers funding and support for three (3) types of translational projects, ranging from early lead optimization to IND enabling studies.
Stage 1Early lead optimization to late lead seriesStage 2Late lead series to selection of clinical candidate Stage 3Candidate selection through IND enabling studies
Entry criteriaProject is in early drug lead optimizationTractable drug leads from multiple chemical series have been identified (demonstration of optimizable structure-activity-relationships [SAR])Established in vitro pharmacology assays (biochemical and cell-based potency and selectivity)Access to an available or conceived in vivo pharmacodynamic modelSuccess criteriaWell defined compound progression pathway with established criteriaOptimized leads from multiple series (demonstration of optimizable SAR)Characterized in vitro pharmacology properties including cell-based activityCharacterized absorption, distribution, metabolism, and excretion (ADME) properties (in vitro and rodent in vivo)Demonstrated in vivo pharmacology in pharmacodynamic modelAccess to an available or conceived in vivo efficacy model
What Critical Path Institute actually gave
Source: IRS Form 990, 2025
- Grants in 2025
- 17
- Total given
- $3.76M
- Median grant
- $127K
- Range
- $23K–$1.32M
- By dollars: Massachusetts 35%, California 12%, Illinois 10%. Top recipient cities: Quincy, MA; Evanston, IL; San Francisco, CA.
- 0% of grants with a stated purpose were for general or operating support.
- 71% of recipients were new grantees, not repeat recipients.
Example grants
National Organization for Rare Disorders · Quincy, MA
Subaward
$1.32M
Northwestern University · Evanston, IL
Subaward
$382K
University of California · San Francisco, CA
Subaward
$348K
Seattle Children's Hospital · Seattle, WA
Subaward
$235K
Wake Forest University · Charlotte, NC
Subaward
$216K
Focus Areas & Funding Uses
Fields of Work
- Science research
Categories
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