SBIR-STTR Award

Development of Antisense Oligonucleotides to Regulate Gamma' Fibrinogen Levels
Award last edited on: 2/5/2024

Sponsored Program
SBIR
Awarding Agency
NIH : NHLBI
Total Award Amount
$277,710
Award Phase
1
Solicitation Topic Code
839
Principal Investigator
David H Farrell

Company Information

Gamma Therapeutics Inc

2611 SW Third Avenue Suite 280n
Portland, OR 97201
   (503) 222-2313
   info@gamma-therapeutics.com
   www.gamma-therapeutics.com
Location: Single
Congr. District: 03
County: Multnomah

Phase I

Contract Number: 1R41HL170874-01
Start Date: 8/24/2023    Completed: 7/31/2024
Phase I year
2023
Phase I Amount
$277,710
g' (pronounced "gamma prime") fibrinogen (GPF) is an alternative splice isoform of the blood coagulation factorfibrinogen. This fibrinogen variant contains a high affinity binding site for the coagulation factor thrombin thatlocalizes thrombin on the growing blood clot. Thrombin binds to GPF via thrombin's heparin binding site. Thisallows thrombin to continue forming the blood clot even in the presence of its inhibitor protein, antithrombin III,with the cofactor heparin. In addition, GPF forms clots that are resistant to breakdown by fibrinolytic enzymes,such that the clots persist in the blood vessel. Because of these activities, GPF is a risk factor forcardiovascular disease, including heart attacks and stroke. We have recently found that COVID-19 patientscan develop extraordinarily high levels of GPF, which likely contributes to the thrombotic events that are seenin COVID-19 patients. In support of this hypothesis, critically ill COVID-19 patients are heparin resistant and donot benefit from heparin treatment. High GPF levels like these sequester thrombin in an active form that cannotbe inhibited by antithrombin III/heparin. If the GPF levels could be lowered, many of these thrombotic eventscould likely be prevented. The Specific Aims of this application are therefore to:1) Develop antisense morpholino oligos that bind their target g gene sequences and are taken up bythe HepG2 human liver cell line.This will be accomplished using electrophoretic mobility shift assays to ensure that the antisense oligos bind totheir target sequences. Cellular uptake into liver cells will be assayed using fluorescein-labeled oligos in a well-established tissue culture model of fibrinogen synthesis, the human HepG2 liver cell line. This cell lineexpresses both the gA and g' isoforms of the human g chain.2) Optimize the morpholino oligomers for effectiveness in vivo using HepG2 cells.This will be accomplished by assaying the lead compounds developed in Aim 1 in HepG2 cells. The absolutelevels and the relative expression ratios of the gA and g' mRNAs will be quantitated using RT-PCR. Totalfibrinogen and GPF will be measured by ELISA.Milestones - The criteria for progress to animal studies in primates in Phase II are:1. Development of antisense morpholino oligomers that bind their target g gene sequences.2. Demonstration that the antisense morpholino oligomers modulate GPF levels in HepG2 liver cells.

Public Health Relevance Statement:
PROJECT NARRATIVE The blood clotting factor g' fibrinogen (GPF) can reach extreme levels in COVID-19 patients. However, there are currently no drugs available that specifically modulate the levels of GPF. The goal of this project is therefore to develop antisense agents that modulate levels of GPF.

Project Terms:

Phase II

Contract Number: ----------
Start Date: 00/00/00    Completed: 00/00/00
Phase II year
----
Phase II Amount
----
© Copyright 1983-2024  |  Innovation Development Institute, LLC   |  Swampscott, MA  |  All Rights Reserved.