Last $1.30 USD
Change Today -0.0001 / -0.01%
Volume 59.5K
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As of 2:43 PM 12/17/14 All times are local (Market data is delayed by at least 15 minutes).

biodel inc (BIOD) Snapshot

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52 Week High
03/6/14 - $3.71
52 Week Low
10/14/14 - $1.20
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biodel inc (BIOD) Details

Biodel Inc., a specialty biopharmaceutical company, focuses on the development and commercialization of treatments for diabetes in the United States. It is involved in developing proprietary insulin formulations for type 1 and type 2 diabetes patients; ultra-rapid-acting insulin analog-based formulations; glucagon formulations and presentations for use as a rescue treatment for diabetes patients experiencing severe hypoglycemia or very low concentrations of blood glucose; and other recombinant human insulin-based formulations. The company was founded in 2003 and is headquartered in Danbury, Connecticut.

35 Employees
Last Reported Date: 12/20/13
Founded in 2003

biodel inc (BIOD) Top Compensated Officers

Chief Executive Officer, President and Direct...
Total Annual Compensation: $677.9K
Chief Medical Officer
Total Annual Compensation: $427.3K
Compensation as of Fiscal Year 2013.

biodel inc (BIOD) Key Developments

Biodel Inc. to Report Q4, 2014 Results on Dec 17, 2014

Biodel Inc. announced that they will report Q4, 2014 results at 5:00 PM, US Eastern Standard Time on Dec 17, 2014

Biodel Inc., Q4 2014 Earnings Call, Dec 17, 2014

Biodel Inc., Q4 2014 Earnings Call, Dec 17, 2014

Biodel Inc. Initiates Clinical Proof of Concept Study in Glucagon Emergency Management Program

Biodel Inc. announced that the company has initiated enrollment of normal human subjects in a Phase 1 clinical trial of its lyophilized glucagon formulation designed for use in a proprietary auto-reconstitution device intended for the rescue of patients with severe hypoglycemia. The combination of the formulation and the auto-reconstitution device constitutes the Glucagon Emergency Management (GEM) system, which is intended to be a more user-friendly glucagon presentation compared to emergency kits currently marketed by Eli Lilly and Novo Nordisk. The Phase 1 proof of concept study is a 6-arm cross over trial in 12 healthy volunteers in which the pharmacokinetics, pharmacodynamics, and safety of 1 mg doses of the GEM glucagon formulation, administered subcutaneously and intramuscularly, will be compared to similar injections of both marketed glucagon products. These data will be help finalize the design and select the comparator to be used in the pivotal bioequivalence study.


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