SBIR-STTR Award

Megakaryocyte Reagents Specific for Their Maturation
Award last edited on: 3/5/2007

Sponsored Program
SBIR
Awarding Agency
NIH : NIDDK
Total Award Amount
$1,042,616
Award Phase
2
Solicitation Topic Code
847
Principal Investigator
Ronald L Brown

Company Information

Quality Biological Inc (AKA: QBI)

7581 Lindbergh Drive
Gaithersburg, MD 20879
Location: Multiple
Congr. District: 06
County: Montgomery

Phase I

Contract Number: 1R43DK055395-01
Start Date: 9/1/1999    Completed: 8/31/2000
Phase I year
1999
Phase I Amount
$100,000
Description: (Adapted from Applicant's ) The goal of this project is to develop clinical grade serum-free reagents for megakaryocyte proliferation and differentiation. This will permit novel hematopoietic rescue techniques for disorders such as thrombocytopenias. Preliminary data indicate that culture of CD34+ cells in the investigators' serum-free medium outperformed currently available alternatives. The proposed reagents will be optimized with regard to cytokines, culture times and other parameters. In addition to clinical applications, the reagents will enable the standardization of ex vivo protocols in laboratories. PROPOSED COMMERCIAL APPLICATION: Develop a clinical grade serum-free medium that will support the proliferation/differentiation of megakaryocytes/platelets for reinfusion into patients. Such a technology will be invaluable in fighting diseases/ infections and in coagulation.

Public Health Relevance Statement:


Project Terms:
megakaryocyte; thrombocytopenia; cell differentiation; reagent /indicator; tissue /cell culture; technology /technique development; CD34 molecule; cell proliferation

Phase II

Contract Number: 2R44DK055395-02
Start Date: 9/1/1999    Completed: 6/30/2003
Phase II year
2001
(last award dollars: 2002)
Phase II Amount
$942,616

The overall objective of this proposal is to develop a clinical-grade Megakaryocyte Development Medium (MDM) that supports the ex vivo development of human megakaryocytes. Use of this unique medium will provide information on several critical gap-areas concerning these elusive yet critically important cells; lipid metabolism, regulation of maturation, and clinical utility. The innovative aspects are the studies on enhancing lipid metabolism, the use of cytokine/matrix molecule combinations, and an in vivo megakaryocyte-transplantation model. MDM will have clinical use in developing therapies for thrombocytopenia and other platelet disorders, in that it allows generation of large numbers of megakaryocytes (> 10/9) that are not possible via routine bone marrow aspiration. MDM also allows for the standardization of megakaryocyte culture conditions between laboratories. Building on the successful results of our Phase I studies, we have designed relevant and highly critical experiments in our Phase II proposal to investigate the following goals. Specific Aim 1 addresses the further optimization of MDM, with a particular focus on enhancing megakaryocyte lipid metabolism. Specific Aim 2 examines the effects of specific cytokines and matrix molecules as complex regulatory signals. Specific Aim 3 is to test and/or long-term engraftment. This aim also provides a pre-clinical animal model for cellular-based therapies of platelet disorders. Specific Aim 4 is to scale these cultures up to levels producing 1-5 x 10/9 megakaryocytes per culture. Successful completion of this Phase II proposal will result in a widely used commercial product, a clinically relevant animal model, and much needed information to further our studies on the development of these biologically important cells. PROPOSED COMMERCIAL APPLICATION: The development of clinical grade reagents that will support megakaryocyte proliferation and differentiation will be valuable in developing novel approaches for the treatment of hematopoietic disorders such as thrombocytopenia.

Public Health Relevance Statement:


Project Terms:
biotechnology; megakaryocyte; thrombocytopenia; cell differentiation; growth media; reagent /indicator; lipid metabolism; tissue /cell culture; technology /technique development; CD34 molecule; cell proliferation