SBIR-STTR Award

Topical Therapeutic to Promote Healing of Chronic Wounds
Award last edited on: 2/17/22

Sponsored Program
STTR
Awarding Agency
NIH : NIGMS
Total Award Amount
$219,306
Award Phase
1
Solicitation Topic Code
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Principal Investigator
Susan P Perrine

Company Information

Phoenicia BioSciences Inc (AKA: Gene Regulation Laboratories)

45 Beaver Road
Weston, MA 02493
   (617) 335-7002
   sperrine@bu.edu
   www.phoeniciabiosciences.com

Research Institution

Boston University

Phase I

Contract Number: 1R41GM101869-01A1
Start Date: 8/1/13    Completed: 7/31/14
Phase I year
2013
Phase I Amount
$219,306
Chronic refractory, or non-healing, wounds or ulcerations of the extremities represent a major medical condition affecting millions of patients. A chronic wound is defined as a wound that does not show signs of significant healing, or progresses, after use of topical/surgical treatment measures for six months. Non-healing wounds affect 6.5 million patients, affecting nearly 2% of the U.S. population, with an annual cost to the healthcare system of $25 billion. These numbers are rising with the aging population and the increasing incidence of diabetes, a leading cause of refractory leg ulcers. Other common causes of chronic wounds include venous stasis ulcers, and decubitus ulcers which develop in immobilized patients. Current treatments for extremity (diabetic, venous stasis) or decubitus ulcers often do not produce sustained or complete healing. Among diabetics, over half of ulcers recur within three years, and 15% ultimately require amputations, with significant consequent disability. New therapeutic agents that promote complete wound closure are needed for this enormous health burden. The Principal Investigators have identified a drug (Arginine Butyrate, AB) which, when given parenterally, dramatically accelerates healing, including complete healing in a highly-refractory chronic wound population, sickle cell leg ulcers, [which heal 10-20 times more slowly than comparable decubitus or diabetic ulcers]. The parenterally-delivered drug had a benign safety profile. Although parenteral (IV) delivery via indwelling port devices was acceptable for the extremely severe population studied in the prior clinical trial, a topical delivery system would offer many feasibility advantages for broader application and not require delivery primarily in clinical facilities. Phoenicia Biosciences has developed an innovative prototype topical spray delivery system of the same drug. This first-in-class therapeutic should provide a highly significant impact on the suffering and economic burden imposed by the growing health care problem of chronic wounds. The Aims of this Phase I application are: (I) Develop a new topical dendrimer hydrogel spray preparation of AB, and test the activity of the new topical preparation in two animal models of wound healing (a chronic wound healing model and diabetic chronic wound healing model); (II.) Perform CMC studies required for a new IND of the novel topical formulation of Arginine Butyrate. These IND enabling studies will allow this new therapeutic to be tested in clinical trials.

Public Health Relevance Statement:


Public Health Relevance:
Chronic wounds or ulcerations of the extremities represent a major medical condition affecting 6.5 million patients (nearly 2% of the U.S. population), with an annual cost of $25 billion in the USA alone. Current treatments for extremity (diabetic, venous stasis) ulcers or decubitus ulcers generally fail to yield satisfactory results. Phoenicia Biosciences has identified a drug which, when given parenterally, dramatically accelerates healing, including complete healing in a very- refractory chronic wound setting, and proposes in this Phase I application to refine development of a topical preparation of the same agent, to allow broader application to the refractory wound market.

Project Terms:
Affect; aging population; Amputation; Animal Model; Arginine Butyrate; arm; base; Benign; Blood Vessels; Chronic; Clinical; Clinical Trials; cost; Decubitus ulcer; Dendrimers; Development; Devices; Diabetes Mellitus; diabetic; Diabetic ulcer; disability; Drug Formulations; Economic Burden; Employee Strikes; Healed; healing; Health; Health Care Costs; Healthcare; Healthcare Systems; Histologic; Home environment; Hydrogels; Incidence; Infusion procedures; innovation; Intravenous; Leg Ulcer; Limb structure; Marketing; Measures; Medical; Modeling; novel; novel therapeutics; Operative Surgical Procedures; Outcome; Patients; Pharmaceutical Preparations; Pharmacologic Substance; Phase; Phase II Clinical Trials; Pilot Projects; Population; Population Study; Preparation; pressure; Principal Investigator; prototype; public health relevance; Randomized; Recurrence; Refractory; Safety; Sickle Cell; Sickle Cell Anemia; Small Business Technology Transfer Research; Stasis Ulcer; System; Technology; Testing; Therapeutic; Therapeutic Agents; Time; Topical application; Topical Preparation; Ulcer; validation studies; Venous; wound; Wound Healing

Phase II

Contract Number: ----------
Start Date: 00/00/00    Completed: 00/00/00
Phase II year
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Phase II Amount
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