SBIR/STTR Research Award

PancreasCHIP - A diagnostic tool for Inheritable Pancreatic Disease

Award identifier 494a96f0b1d019bddf3cd07a64d51144243fde41447a2234e9d08f9f9ee96e4fAwarding agency Department of Health and Human Services · National Institutes of Health

Award amount

$266,046

Program and phase

SBIR · Phase I

Award year

2015

Explore This Research Award in CaptureIQ

Research the technology, evaluate the recipient and agency, identify related opportunities, and explore potential follow-on work with CaptureIQ.

Award details

Awarding agency
Department of Health and Human Services
Branch
National Institutes of Health
Recipient company
P2D, INC
Proposal award date
2015-03-01
Contract end date
2017-02-28
UEI
KX3EAX2JEMV8
Solicitation number
PA14-071
Topic code
300

Research abstract

DESCRIPTION provided by applicant Pancreatitis is a painful condition that may become recurrent or chronic in genetically susceptible individuals Patients with pancreatitis suffer multiple hospital admissions pain episodes addiction to pain medications and psychosocial stressors by missing school by the child and work by family members As an important underlying etiology of pancreatitis genetic factors are becoming an integral component of diagnostic algorithms In order to translate recent advances into opportunities to improve clinical care we propose to develop a high throughput gene chip that identifies mutations in the genes that cause the most common forms of inherited syndromes of pancreatitis In this Phase I application we will test the technical merit of a gene sequencing platform that is customized to patients with pancreatitis which we call the PancreasCHIP Our Specific Aim in this Phase I application is to determine the accuracy of the PancreasCHIP to sequence the target genes We will pursue this aim by testing two hypotheses First we hypothesize that the PancreasCHIP sequences the target genes at andgt accuracy In preliminary studies we analyzed the nucleotide composition of the target genes and designed a one step TruSeq multiplex platform to generate amplicons for all exons and target intron exon boundaries with andgt coverage We will generate amplicons in healthy subjects serving as controls and compare chip readouts with known sequences Second we hypothesize that the PancreasCHIP identifies mutations in patients with pancreatitis To this end we will examine whether the sequence output produced by the PancreasCHIP detects insertions deletions or indels in DNA of patients with chronic familial pancreatitis Collectively these experiments will validate the technical merits of PancreasCHIP and will position us for future experiments to further bench test the assay and develop an automated detection algorithm in a future Phase II application Ultimately our goal is to bring the customized sequencing platform to full use in the clinic to readily facilitate diagnostics and personalized care of patients with pancreatic diseases PUBLIC HEALTH RELEVANCE Pancreatic disease is common in children and adults Pancreatitis is an inflammation of the pancreas that leads to either a one time attack or in a subset of cases to recurrent attacks that lead to multiple hospital admissions and painful episodes Pancreatitis is a burden on patients families as well as the society with health care expenses ongoing pain issues and lost time from school or work We propose to design a gene chip for the evaluation of the genetic cause of pancreatitis This grant application will develop and determine the technical merit of the andquot PancreasCHIPandquot as a mutation screening tool that will look for mutations in the six genes known to cause this disease simultaneously When fully validated the chip will cut the cost and decrease the wait time for genetic testing results

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

52 SBIR/STTR records share this UEI (2001–2021). Reported award amounts total $21,593,440. Reported amounts are not federal obligations.

Phases: Phase I, Phase II, Phase II – Direct to Phase II

Agencies: Department of Health and Human Services

Agency intelligence

Department of Health and Human Services

Back to SBIR/STTR Research Awards

Don't take our word for it. Ask AI about RFPCapture.

See what leading AI assistants have to say about RFPCapture and CaptureIQ.

Gemini opens without a prefilled question. The question is copied to your clipboard when the button works. You can also copy it here:

What is RFPCapture.com and its CaptureIQ platform from Smart Logic AI? How does it help federal contractors discover opportunities, evaluate bid/no-bid decisions, research government contracts, and prepare proposals? How does it compare with other federal capture platforms? Use independent sources where available.