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2304222

Project Grant

Overview

Grant Description
SBIR Phase I: Drug Discovery Using Stem Cell Derived Organoids - The broader impact/commercial potential of this Small Business Innovation Research (SBIR) Phase I project is to enable the development of new therapies for rare diseases in children. An estimated 350 million people worldwide - half of which are children - suffer from an estimated 7,000+ known rare diseases annually, yet 95% of rare diseases still lack treatment.

Even though >80% of rare diseases are genetic in origin, there have been relatively few actual drug discoveries. This is an enormous problem as 30% of children with rare diseases will not live to see their 5th birthdays. To address this, drug development can be accelerated by screening investigational drugs against micro-organs (?organoids?) that resemble young organs and have the same gene mutations as the patients.

In a simple petri dish, organoids enable the direct study of the relationship between a patient's genes and his/her disease. Such organoids present an opportunity to rapidly identify new disease mechanisms and targeted therapies. The team is scaling organoid technology into an automated drug development platform that is high throughput, robust, and applicable to multiple genetic diseases in children.

This project advances drug development for pediatric rare diseases by accomplishing two primary objectives: (1) automated heart, liver, and brain organoid derivation from human stem cells, and (2) automated machine learning (ML) detection of disease in organoids derived from patients with genetic diseases affecting any of these three organs. To do this, a combination of robotics and specific protocols will differentiate tissue- and disease-specific organoids under standardized conditions. The organoids are monitored with microscopy as they transition between tissue state. The ML model learns what healthy organoids look like and uses that information to identify when an organoid exhibits a disease phenotype.

These objectives are important for reducing batch-to-batch organoid variability and human error that can confound drug discovery efforts. In these same organoid models, drug screening and development will be performed to try to reverse or retard the disease phenotype unique to each disease. The result of this research will be the production of organoids with high accuracy and precision, as well as an automated means for detecting changes in heart, liver, and neural organoids that will be essential for finding new therapies.

This award reflects NSF's statutory mission and has been deemed worthy of support through evaluation using the Foundation's intellectual merit and broader impacts review criteria.
Awarding / Funding Agency
Place of Performance
San Carlos, California 94070-4002 United States
Geographic Scope
Single Zip Code
Related Opportunity
None
Rosebud Biosciences was awarded Project Grant 2304222 worth $274,829 from National Science Foundation in August 2023 with work to be completed primarily in San Carlos California United States. The grant has a duration of 1 year and was awarded through assistance program 47.084 NSF Technology, Innovation, and Partnerships.

SBIR Details

Research Type
SBIR Phase I
Title
SBIR Phase I:Drug discovery using stem cell derived organoids
Abstract
The broader impact/commercial potential of this Small Business Innovation Research (SBIR) Phase I project is to enable the development of new therapies for rare diseases in children.An estimated 350 million people worldwide - half of which are children - suffer from an estimated 7,000+ known rare diseases annually, yet 95% of rare diseases still lack treatment. Even though greater than80% of rare diseases are genetic in origin, there have been relatively few actual drug discoveries. This is an enormous problem as 30% of children with rare diseases will not live to see their 5th birthdays. To address this, drug development can be accelerated by screening investigational drugs against micro-organs (“organoids”) that resemble young organs and have the same gene mutations as the patients. In a simple petri dish, organoids enable the direct study of the relationship between a patient’s genes and his/her disease.Such organoids present an opportunity to rapidly identify new disease mechanisms and targeted therapies. The team is scaling organoid technology into an automated drug development platform that is high throughput, robust, and applicable to multiple genetic diseases in children. _x000D_ _x000D_ This project advances drug development for pediatric rare diseases by accomplishing two primary objectives: (1) automated heart, liver, and brain organoid derivation from human stem cells, and (2) automated machine learning (ML) detection of disease in organoids derived from patients with genetic diseases affecting any of these three organs. To do this, a combination of robotics and specific protocols will differentiate tissue- and disease-specific organoids under standardized conditions. The organoids are monitored with microscopy as they transition between tissue state. The ML model learns what healthy organoids look like and uses that information to identify when an organoid exhibits a disease phenotype. These objectives are important for reducing batch-to-batch organoid variability and human error that can confound drug discovery efforts. In these same organoid models, drug screening and development will be performed to try to reverse or retard the disease phenotype unique to each disease. The result of this research will be the production of organoids with high accuracy and precision, as well as an automated means for detecting changes in heart, liver, and neural organoids that will be essential for finding new therapies._x000D_ _x000D_ This award reflects NSF's statutory mission and has been deemed worthy of support through evaluation using the Foundation's intellectual merit and broader impacts review criteria.
Topic Code
PT
Solicitation Number
NSF 22-551

Status
(Complete)

Last Modified 8/17/23

Period of Performance
8/15/23
Start Date
7/31/24
End Date
100% Complete

Funding Split
$274.8K
Federal Obligation
$0.0
Non-Federal Obligation
$274.8K
Total Obligated
100.0% Federal Funding
0.0% Non-Federal Funding

Activity Timeline

Interactive chart of timeline of amendments to 2304222

Additional Detail

Award ID FAIN
2304222
SAI Number
None
Award ID URI
SAI EXEMPT
Awardee Classifications
For-Profit Organization (Other Than Small Business)
Awarding Office
491503 TRANSLATIONAL IMPACTS
Funding Office
491503 TRANSLATIONAL IMPACTS
Awardee UEI
WV8CZB3JHU21
Awardee CAGE
None
Performance District
CA-15
Senators
Dianne Feinstein
Alejandro Padilla

Budget Funding

Federal Account Budget Subfunction Object Class Total Percentage
Research and Related Activities, National Science Foundation (049-0100) General science and basic research Grants, subsidies, and contributions (41.0) $274,829 100%
Modified: 8/17/23