SBIR/STTR Research Award

A BIOMATERIAL FOR ESOPHAGEAL REPAIR

Award identifier 2dc38816ae3bc344e876a2043a2caa80018045c6f8736234ff4590359a4bcb13Awarding agency Department of Health and Human Services · National Institutes of Health

Award amount

$0

Program and phase

SBIR · Phase I

Award year

2002

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Award details

Awarding agency
Department of Health and Human Services
Branch
National Institutes of Health
Recipient company
ACELL, INC.
Proposal award date
Not reported
Contract end date
Not reported
UEI
Not reported
Solicitation number
Not reported
Topic code
Not reported

Research abstract

DESCRIPTION (provided by applicant): ACell is a tissue engineering company and its core technology is based upon a porcine derived extracellular matrix (ECM) harvested from the urinary bladder (UBM) that serves as a constructive scaffold for tissue reconstruction. Successful completion of Phase I studies showed that the UBM-ECM can be configured into a tube shaped device with mechanical and material properties suitable for the repair of esophageal tissue. These studies also showed that primary canine esophageal epithelial cells could attach, proliferate and differentiate in vitro upon the UBM scaffold. Finally, a preliminary study in a dog model demonstrated the ability of the resorbable UBM scaffold to replace native esophageal tissue with host derived tissues that included an intact squamous epithelium, submucosal vascularized collagenous tissue and subjacent bundles of skeletal muscle appropriate for the resected segment of cervical esophagus. The present Phase II SBIR proposal seeks support to pursue the development of the UBM bioscaffold as a device for the repair or replacement of damaged or missing esophageal tissue; a surgical application that currently has very limited options. There are three studies described, each of which addresses a clearly defined specific aim: (1) to determine the fate and mode of degradation of the porcine derived UBM scaffold when used as an esophageal repair device in a dog model; (2) to complete ISO-9001 testing as a prerequisite to regulatory submission of an Investigational Device Exemption (DE); and (3) to examine the safety and efficacy of the UBM device in a definitive chronic study using an animal model. The work will be conducted by an experienced interdisciplinary group of investigators and will combine the expertise of ACell's professional staff, the certified laboratories of the North America Science Associates (NamSA), and a university partner. A timeline for completion of the studies, clearly defined criteria for success, and plans for subsequent Phase III work are included in this Phase II proposal.

Technology keywords

Not reported

Agency intelligence

Department of Health and Human Services

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