SBIR/STTR Research Award

Targeted therapeutic delivery to diseased lungs using enucleated mesenchymal stem cells

Award identifier ac6e70f385b643fc3a993d4ac7f10ec9ca349228e4ccfb9d2fecc448e9465d02Awarding agency Department of Health and Human Services · National Institutes of Health

Award amount

$297,553

Program and phase

SBIR · Phase I

Award year

2021

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Award details

Awarding agency
Department of Health and Human Services
Branch
National Institutes of Health
Recipient company
CYTONUS THERAPEUTICS INC
Proposal award date
2021-09-20
Contract end date
2022-07-31
UEI
UBM9DERRCXZ9
Solicitation number
PA19-272
Topic code
NHLBI

Research abstract

There is critical need for cell-based therapeutics that can be administered intravenously (IV), and effectively home to and deliver therapeutics to the respiratory system, while maintaining patient safety. Cytonus Therapeutics and UC San Diegoandapos;s Medical Center are co-developing enucleated mesenchymal stem cells with potential to deliver a wide range of biologics to treat respiratory diseases including acute respiratory distress syndrome (ARDS). Our novel platform for therapeutic delivery is to genetically engineer mesenchymal stem cells (MSCs) with inflammation homing proteins and then gently remove the nucleus, thereby providing a highly unique, viable, and safe cell therapeutic (CargocytesTM) with substantial lung homing potential. Enucleation grants the ability to genetically engineer Cargocytes with multiple lung targeting moieties and a wide range of biological payloads, while maintaining a clinically relevant safety profile. Our lung targeting strategy is built on the key potential of Cargocyte therapeutics to perform active-targeted delivery to the lungs via an intravenous route (i.v.). Nucleated MSCs will first be extensively engineered with established chemoattractant receptors CXCR4/CCR2 and inflamed endothelial adhesion molecule PSGL-1 and then enucleated prior to i.v. administration. Proof-of-concept preclinical studies will then be performed to determine whether Cargocytes engineered with lung trophic molecules home to inflamed lungs in a clinically relevant murine model of ARDS. Therefore, Aim 1 studies will determine if Cargocytes engineered with CCXCR4/CCR2 and PSGL-1 home to inflamed lung tissues and Aim 2 studies will determine if Cargocytes exit the vasculature and move into the inflamed/damaged lung parenchyma. If Cargocytes home to inflamed lung tissues and exit the vasculature, it could provide an effective means to treat a wide range of respiratory diseases.There is critical need for cell-based therapeutics that can be administered intravenously (IV), effectively home to and deliver therapeutic to damaged and inflamed lungs, while maintaining patient safety. The objective of this Phase I application is to first develop a clinical prototype of an enucleated mesenchymal stem therapeutic (Cargocyte) and demonstrate its ability to home to lungs using a clinically relevant mouse model of acute lung injury.

Technology keywords

Not reported

Other awards by this recipient

Verified by the same UEI. These are other public SBIR/STTR award pages, not a merged company record.

Awards with the same topic code

Verified by an exact topic code match. This is not a text-similarity match.

Research funding history

6 SBIR/STTR records share this UEI (2020–2023). Reported award amounts total $3,905,661. Reported amounts are not federal obligations.

Phases: Phase I, Phase II

Agencies: Department of Health and Human Services

Agency intelligence

Department of Health and Human Services

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