SBIR Phase II: Preventing Pneumothorax During Lung Biopsy Using a Novel Hydrogel

Information

  • NSF Award
  • 2208775
Owner
  • Award Id
    2208775
  • Award Effective Date
    8/1/2022 - a year ago
  • Award Expiration Date
    7/31/2024 - 22 days from now
  • Award Amount
    $ 1,000,000.00
  • Award Instrument
    Cooperative Agreement

SBIR Phase II: Preventing Pneumothorax During Lung Biopsy Using a Novel Hydrogel

The broader impact/commercial potential of this Small Business Innovation Research (SBIR) Phase II project is to improve patient outcomes, and reduce the morbidity and costs associated with lung collapse (pneumothorax) during computed tomography (CT)-lung biopsies used for screening lung cancer. Over 400,000 CT-guided lung biopsies are performed in the US, and more than 1.2 million worldwide. Management and treatment of symptomatic pneumothorax often requires multi-day hospital stays and costs on average of $15,000 per patient and $1.3 billion yearly worldwide. Preventing pneumothorax may increase access to lung cancer screenings by de-risking CT-guided lung biopsies and allowing smaller ambulatory surgery centers in remote geographies to perform the screening procedure. Currently, physicians collect limited biopsy samples due to the increased risk of pneumothorax with multiple biopsy passes. Preventing pneumothorax may allow physicians to collect a greater number of biopsy samples and provide sufficient tissue to personalize the cancer treatment and improve patient outcomes. <br/><br/>This Small Business Innovation Research (SBIR) Phase II project is developing a novel biosealant that will reduce or eliminate pneumothorax. Pneumothorax — a collapsed lung - is the most common complication of computed tomography (CT)-guided lung biopsies, occurring in 20-40% of all CT-guided lung biopsies. The focus of the current investigation is to evaluate and demonstrate the possibility of using a biosealant and delivery device to seal needle tracts to prevent pneumothorax before it occurs, thereby filling a large gap in today’s solutions. Phase I data supports an injectable hydrogel formulation that successfully prevented pneumothorax in animal studies. In this Phase II project, the team seeks to refine the formulation for improved surgical performance and validate it with an animal model to demonstrate both efficacy and safety.<br/><br/>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.

  • Program Officer
    Henry Ahnhahn@nsf.gov7032927069
  • Min Amd Letter Date
    8/1/2022 - a year ago
  • Max Amd Letter Date
    8/1/2022 - a year ago
  • ARRA Amount

Institutions

  • Name
    PNEUMONIX MEDICAL INC.
  • City
    BALTIMORE
  • State
    MD
  • Country
    United States
  • Address
    115 W 29TH ST
  • Postal Code
    212184296
  • Phone Number
    2177214841

Investigators

  • First Name
    James
  • Last Name
    Wilkie
  • Email Address
    wilkie@pneumonix.com
  • Start Date
    8/1/2022 12:00:00 AM

Program Element

  • Text
    SBIR Phase II
  • Code
    5373

Program Reference

  • Text
    BIOMEDICAL ENG AND DIAGNOSTICS