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Last $0.05 USD
Change Today -0.017 / -24.29%
Volume 156.0K
As of 3:44 PM 11/24/15 All times are local (Market data is delayed by at least 15 minutes).

omni bio pharmaceutical inc (OMBP) Snapshot

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52 Week High
12/19/14 - $0.45
52 Week Low
06/15/15 - $0.01
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omni bio pharmaceutical inc (OMBP) Details

Omni Bio Pharmaceutical, Inc. operates as a biopharmaceutical company in the United States. It holds a license to use patent for the treatment of diabetes using plasma-derived alpha-1 antitrypsin (p-AAT), a protein that is purified from human blood. The company also holds licenses for the use of patents and patent applications covering the use of p-AAT in the treatment of cellular transplantation and graft rejection, radiation protection, bacterial and viral diseases, myocardial remodeling, and inflammatory bowel disease indications. In addition, it holds licenses for patent applications covering compositions of various Fc-AAT constructs. Omni Bio Pharmaceutical, Inc. was founded in 2006 and is headquartered in Fort Collins, Colorado.

1 Employees
Last Reported Date: 06/16/14
Founded in 2006

omni bio pharmaceutical inc (OMBP) Top Compensated Officers

Chairman and Chief Executive Officer
Total Annual Compensation: $180.0K
Chief Scientific Officer and Member of Scient...
Total Annual Compensation: $90.0K
Compensation as of Fiscal Year 2014.

omni bio pharmaceutical inc (OMBP) Key Developments

Omni Bio Pharmaceutical, Inc. Announces Clinical Data for Use of Alpha-1 Antitrypsin in Steroid-Resistant Graft Versus Host Disease

Omni Bio Pharmaceutical, Inc. announced the presentation of interim clinical data demonstrating the ability of plasma-derived alpha-1 antitrypsin (AAT) to reduce inflammation and promote healing of damaged tissues in patients with graft-versus-host disease (GvHD), a common and potentially life-threatening complication following bone marrow transplantation. The positive interim results support continued clinical studies of this novel approach to treating GvHD and also highlight the potential value of Omni Bio's novel, recombinant AAT candidate, AAT-Fc, currently in preclinical development. Data from the first seven patients to complete the Phase 1/2 study were presented at the 56th annual meeting of the American Society of Hematology in San Francisco by Omni Bio's academic collaborators from the University of Washington and the Fred Hutchinson Cancer Research Center. Following allogeneic stem cell transplants to treat leukemic malignancies, the patients in the study all developed severe acute GvHD symptoms (severe diarrhea, loss of mucosal lining in the gut) but did not respond satisfactorily to standard of treatment including high dose steroids. The patients then received intravenous doses of plasma-derived AAT every other day for a total of 8 doses (15 days) in an attempt to alleviate their GvHD symptoms. The investigators concluded that the administration of AAT as a safe salvage therapy for gut GvHD is feasible without clinically relevant toxicity. Stool sampling showed a decrease in intestinal AAT clearance and endoscopic evaluation confirmed healing of the bowel mucosa. The overall findings suggest that further evaluation of AAT as treatment for steroid refractory GvHD, or as first line therapy, is warranted.

Omni Bio Pharmaceutical, Inc. Presents at 7th annual Biotech Showcase Conference 2015, Jan-13-2015 03:30 PM

Omni Bio Pharmaceutical, Inc. Presents at 7th annual Biotech Showcase Conference 2015, Jan-13-2015 03:30 PM. Venue: Parc 55 Wyndham San, Francisco - Union Square, San Francisco, CA 94102, United States. Speakers: Bruce E. Schneider, Chairman and Chief Executive Officer.

Omni Bio Pharmaceutical, Inc. Announces Presentation of Phase 1/2 Clinical Data for AAT at American Heart Association Scientific Sessions

Omni Bio Pharmaceutical, Inc. announced the presentation of Phase 1/2 clinical data for plasma-derived alpha-1 antitrypsin ("p-AAT"), demonstrating its ability to inhibit the inflammatory response in patients with acute ST-elevation myocardial infarction ("STEMI"), the most severe type of heart attack. The data were presented in a poster at the American Heart Association Scientific Sessions 2014, in Chicago. Importantly, these latest clinical findings further highlight the potential value of Omni Bio's first-in-class recombinant AAT candidate, AAT-Fc. STEMI patients are at particularly high risk for developing heart failure due to tissue damage caused by the intense inflammatory response that occurs following acute myocardial infarction. It is well-known that the degree of inflammation at the time of a heart attack is predictive of adverse outcomes including unfavorable cardiac remodeling, heart failure and cardiac death. In the current study, principal investigator Antonio Abbate, M.D., Ph.D., and colleagues at The Virginia Commonwealth University concluded that a single administration of p-AAT significantly inhibited the acute inflammatory response following STEMI, and was associated with a decreased incidence of heart failure over a 12-week follow up period.


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