• SKIP TO CONTENT
  • SKIP NAVIGATION
  • Patient Resources
    • COVID-19 Patient Resource Center
    • Clinical Trial Listings
    • What is Clinical Research?
    • Volunteering for a Clinical Trial
    • Understanding Informed Consent
    • Useful Resources
    • FDA Approved Drugs
  • Professional Resources
    • Research Center Profiles
    • Market Research
    • FDA Approved Drugs
    • Training Guides
    • Books
    • eLearning
    • Events
    • Newsletters
    • White Papers
    • SOPs
    • eCFR and Guidances
  • White Papers
  • Clinical Trial Listings
  • Advertise
  • COVID-19
  • Sign In
  • Create Account
  • Sign Out
  • My Account
Home » BioAdvance commits $2.9M to 15 life sciences companies

BioAdvance commits $2.9M to 15 life sciences companies

August 1, 2016
CenterWatch Staff

BioAdvance announced that during the past 12 months it added nine new companies and technologies to its portfolio and made follow-on investments in six of its existing companies. Overall, these investments represent a $2.9 million commitment to the success and growth of life science companies and to this region.

“We continue to see significant demand for BioAdvance’s early stage funding, and these commitments reflect the diversity of innovation in the life sciences pipeline throughout our region,” said Barbara Schilberg, CEO of BioAdvance. “What these entrepreneurs and scientists have in common is a passion to improve patient health, and we are delighted to be in a position to continue supporting these and other entrepreneurial efforts in the future.”

Commitments to new companies or technologies include:

  • Bainbridge Health, Philadelphia, PA, $54,000—to develop, in partnership with CHOP, technology solutions to reduce medication errors and enhance patient safety.
  • Cohero Health, New York, NY, $283,000—to develop and commercialize products to track how patients are using their respiratory medication and their response to that medication.
  • Genome Profiling, Newark, DE, $100,000—to discover novel epigenetic biomarkers based on its proprietary, genome-wide methylation profiling platform to revolutionize the way to treat, diagnose, and predict chronic and life-threatening disease.
  • Mebias Discovery, Philadelphia, PA, $800,000—to launch its platform for identifying biased ligands for next generation GPCR drugs that provide improved efficacy and/or safety over current therapies.
  • Noble MD, Bryn Mawr, PA, $400,000—to commercialize its lead product Theo, a “digital healthcare advisor” for risk identification, coding, and management by physician practices.
  • Olive Devices, Philadelphia, PA, $50,000—to develop smart glasses to improve communication and personalize education for the hearing impaired.
  • Oncora Medical, Philadelphia, PA, $100,000—to develop a SaaS-based product that integrates all patient EMR/genetic/imaging information to create a personalized radiation treatment plan.
  • Penn State/Hershey, Dr. Zissis Chroneos, $50,000—to support a proof-of-concept study to assess the potential of a novel monoclonal antibody therapeutic for treating post-influenza pulmonary complications.
  • The OneHealth Company, Philadelphia, PA, $500,000—to launch a new contract research organization that de-risks new drugs and treatments through efficacy testing in pets suffering the natural counterpart of a human disease.

Follow-on investments during the last twelve months include:

  • CarePartners Plus, Horsham, PA, $30,000—to commercialize its patient engagement platform Wellby.
  • Enzium, Philadelphia, PA, $140,000—to develop its proprietary protease assay technology for use in measuring drug levels of the new Direct Oral Anticoagulants in patients.
  •  Hsiri Therapeutics, King of Prussia, PA, $70,000—to develop novel siderophore-based antibiotics for hard to treat, resistant bacteria.
  • Jenrin Discovery, Chadds Ford, PA, $10,000—to continue preclinical development of its lead program addressing diabetes, obesity and NASH.
  • RiboNova, Wynnewood, PA, $175,000—to develop small molecules against novel defective transfer RNA anti-cancer targets and to pursue a clinical trial in mitochondrial diseases.
  • WellTrackONE, New York, NY, $162,000—to continue to expand its risk management strategies by utilizing wellness screenings and services.

The highlight of BioAdvance’s fiscal year ending June 30, 2016 was the acquisition of Novira Therapeutics by Johnson & Johnson, following the completion of a phase Ib clinical trial of Novira’s lead compound that is being developed to treat hepatitis B. Novira, founded by two ex-Merck scientific executives, received an initial investment from BioAdvance in the fall of 2008 and over the years and multiple financings became BioAdvance’s largest investment. Novira raised a $23 million Series A financing in 2012 from 5AM Ventures, Versant and Canaan Partners.

In July 2016, HealthQx (King of Prussia, PA) was acquired by McKesson to expand its ability to help customers rapidly and cost-effectively transition to value-based care by automating and scaling complex payment models, such as retrospective and prospective bundled payment. HealthQX has been developing and commercializing a data analytics platform using pharmacy, medical, eligibility and provider data to analyze how well a provider is managing costs, quality and outcomes across an episode of care. HealthQX aligns payment incentives around quality. BioAdvance made its first investment in HealthQx in 2014.

Upcoming Events

  • 12Apr

    The Participant Playbook Webinar Series, Part 3 — Rethinking the Development of Participant-Centric Clinical Trial Technology

  • 25Apr

    Effective Root Cause Analysis and CAPA Investigations for Drugs, Devices and Clinical Trials

  • 26Apr

    FDA’s New Laws and Regulations: What Drug and Biologics Manufacturers Need to Know

  • 27Apr

    Califf’s FDA, 2023 and Beyond: Key Developments, Insights and Analysis

  • 17May

    2023 WCG Avoca Quality Consortium Summit

  • 21May

    WCG MAGI Clinical Research Conference – 2023 East

Featured Products

  • Spreadsheet Validation: Tools and Techniques to Make Data in Excel Compliant

    Spreadsheet Validation: Tools and Techniques to Make Data in Excel Compliant

  • Surviving an FDA GCP Inspection

    Surviving an FDA GCP Inspection: Resources for Investigators, Sponsors, CROs and IRBs

Featured Stories

  • Five Ws

    Consider the Five ‘W’s to Understand Potential Participants

  • QandA-360x240.png

    Perspectives from Smaller-Sized CROs: Q&A with Cheryle Evans

  • White House

    Trial Stakeholders Advise White House on Emergency Research Infrastructure

  • SurveywBlueBackground-360x240.png

    Stress Levels Continue to Climb in Healthcare Workforce, Survey Finds

Standard Operating Procedures for Risk-Based Monitoring of Clinical Trials

The information you need to adapt your monitoring plan to changing times.

Learn More Here
  • About Us
  • Contact Us
  • Privacy Policy
  • Do Not Sell or Share My Data

Footer Logo

300 N. Washington St., Suite 200, Falls Church, VA 22046, USA

Phone 617.948.5100 – Toll free 866.219.3440

Copyright © 2023. All Rights Reserved. Design, CMS, Hosting & Web Development :: ePublishing