SBIR-STTR Award

Development of PEG Hemoglobin blood substitute to treat hemorrhagic shock
Award last edited on: 2/7/14

Sponsored Program
SBIR
Awarding Agency
NIH : NHLBI
Total Award Amount
$949,717
Award Phase
2
Solicitation Topic Code
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Principal Investigator
Abraham Abuchowski

Company Information

Prolong Pharmaceuticals Inc

300 Corporate Court Suite 8
South Plainfield, NJ 07080
   (908) 444-4660
   info@prolongpharma.com
   www.prolongpharma.com
Location: Single
Congr. District: 06
County: Middlesx

Phase I

Contract Number: 268200800010C-0-0-1
Start Date: 8/1/13    Completed: 7/31/14
Phase I year
2008
Phase I Amount
$101,339
Hemorrhage is a leading cause of death from severe trauma. Hemoglobin blood substitutes(HBOC) have a number of advantages in treating hemorrhage including improved availabilty with decreased storage demands. Prolong Pharmaceuticals has developed a PEGylated bovine hemoglobin (PEG-Hb) that is designed to enhance the delivery of oxygen to tissues. In the Phase l component of this Fast-Track SBIR contract we will begin to optimize the production of this material as a starting point for large scale production of PEG-Hb in the Phase II SBIR contract. In this phase II component of the Fast-Track SBIR contract, we will develop and implement the scale-up production of PEG-Hb developed in the phase I SBIR. This wil involve three parallel tasks including the large scale purification of bovine hemoglobin and synthesis of PEG-Hb in itsappropriate formulation

Phase II

Contract Number: 4R44HL093959-02
Start Date: 00/00/00    Completed: 00/00/00
Phase II year
2009
Phase II Amount
$848,378
Hemorrhage is the leading cause of death from combat trauma and the second leading cause of civilian death. Trauma is mainly treated with intravenous liquids, such as isotonic crystalloid solutions. Although volume expa nsion is desirable, none of these solutions is capable of overcoming tissue oxygen deficits (ischemia). Proper use of transfused blood can assist in resuscitation; however there are significant problems with its use, including storage restraints, availabil ity, typing, risk of disease transmission and immune suppression. These issues make the routine use of stored human blood for use outside the hospital impractical. In an attempt to overcome many of these issues, efforts have been made to develop hemoglobin based oxygen carrier (HBOCs) blood substitutes which have advantages such as decreased chance of disease transmission, lack of a need for typing, and most importantly improved availability with decreased storage demands. Prolong Pharmaceuticals has develo ped a unique HBOC product for the treatment of severe hemorrhagic shock consisting of a combination of PEGylated bovine hemoglobin (PEG-Hb) and hypertonic saline (HS). It is specifically designed to increase the oxygen carrying capacity of blood as well as to enhance the delivery of oxygen to tissues by keeping the vasculature open through its hypertonic-oncotic actions. We have found this product to be capable of rapidly restoring tissue oxygenation and repaying oxygen debt in an animal model of severe tra umatic shock. In this Fast- Track SBIR grant, we will conduct the preclinical studies needed to support an IND to conduct clinical testing of the product. In the phase I component, we will conduct pharmacokinetic analysis of PEG-Hb/HS to define optimal dos ing for follow up efficacy and toxicology assessment and to establish dosing parameters for future clinical studies. In the phase II SBIR component we will conduct additional efficacy studies to determine the extent of survival that PEG-Hb/HS induces in ou r animal model of trauma and will also perform toxicology assessment to support the future use of this product in the treatment of trauma.