Inflammatory Bowel Disease (IBD) is a collective name for Crohn?s Disease and Ulcerative Colitis (UC). Bothconditions manifest with a pathological inflammation of the bowel that causes breaks in mucosal integrity, frankulceration and the risk of more severe complications. While the etiology of IBD is complex and not fullyunderstood, the two distinguishing hallmarks of IBD are dysregulation of normal immune function and impairedepithelial repair. None of the currently available treatment modalities have a specific targeted effect to retainmucosal integrity or to heal breaches in the gut mucosa. Moreover, most drugs in development are focused onmodifying the local inflammatory response and not on protection and repair of the intestinal epithelium.It is highly attractive if a treatment modality could indeed target the damaged gut mucosa, as this wouldcomplement approaches directed to the abnormal inflammatory response. Such a treatment paradigm wouldretain mucosal integrity and prevent or ameliorate a local breach, thereby reducing the impact infiltratingexternal (intra-luminal) factors may have on the pathophysiological process. Additionally, it could facilitatehealing of breaches in the mucosa and restore integrity.Avexegen Therapeutics, Inc. in collaboration with Mark Frey?s group at Children?s Hospital, Los Angeles(CHLA), has identified Neuregulin-4 (NRG?4), a naturally occurring constituent of human breast milk, as anovel mucosal healing peptide. NRG-4 leverages physiological mechanisms to both directly protect theintestinal epithelium and to attenuate the inflammatory cascade. These actions have been shown to promotemucosal healing and the restoration of the damaged gut barrier in multiple experimental animal models ofintestinal inflammation The NRG-4 product platform offers a wide range of product forms for the treatment ofIBD. Based on the evidence gathered thus far, NRG-4 has a high potential for being a stand-alone treatmentfor these disorders or a complement to other treatment approaches.In this SBIR Phase I project, Avexegen aims to establish: (a) independent confirmation of pre-clinical findingsfrom the Frey lab on the therapeutic potential of NRG-4 as a mucosal healing factor. This will be done by a 4week in vitro potency determination study followed by an 8 week dose response study in a DSS mouse model.(b) Proof of concept of efficacy of oral administration in an IBD disease model. This will be done by firstconducting a 4 week signaling study to demonstrate luminal ErbB4 receptor activation upon oral NRG-4administration, and in vitro assessment of metabolic stability in a pancreatic digestive enzyme mix. Next, a 3month analytical method and formulation development study will be conducted, and then followed with an 8week dose-response study in a DSS mouse model using an oral NRG-4 formulation. These studies will add tothe pre-clinical data package for filing the IND, and help transform IBD treatment and potentially other gastrointestinaldisorders where the repair and retention of intestinal mucosal integrity are key treatment objectives.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Small Business Innovation Research Grants (SBIR) - Phase I (R43)
Project #
1R43DK112435-01
Application #
9337922
Study Section
Special Emphasis Panel (ZRG1-BCMB-G (10)B)
Program Officer
Densmore, Christine L
Project Start
2016-09-20
Project End
2017-08-31
Budget Start
2016-09-01
Budget End
2017-08-31
Support Year
1
Fiscal Year
2016
Total Cost
$110,620
Indirect Cost
Name
Avexegen Therapeutics, Inc.
Department
Type
DUNS #
076813979
City
Oakland
State
CA
Country
United States
Zip Code
94611