"Won't Somebody Help Us Please....
Find a Cure for This Disease?"

Finding the Cure for DM Foundation

A 501(c)3 Non Profit Organization

Research Update:  12/31/2019

Just a quick and simple update on the research we are sponsoring through your generous contributions:

Regarding Project New Hope - our latest efforts have been on the development of an IV form of the therapy to replace the need to inject it intrathecally (into the cerebrospinal fluid) - we have developed and manufactured the test agent and we will be starting clinical testing in the new year.

The clinical trial funded by Morris Animal Foundation is ongoing and going well. This trial was made possible by the work we have performed in Project New Hope.

Best wishes for a happy, healthy, and productive New Year, filled with hope for treatment or cure for DM!!

Update on the New Hope Phase 2 Study: 8/2019

With the generous funding and continued support from the Finding a Cure for DM Foundation, the Phase 2 study of the New Hope project allowed us to make further progress in demonstrating the use of the U1 Adaptor Oligonucleotide (U1AO) gene silencing technology for the therapeutic application to DM. The U1AO design is notable for its efficiency in uptake, potency, and specific and long-lasting target effect, without any induction of immune response and it represents an ideal candidate for DM.

The aim of the study was to show that a U1AO formulation able to silence canine SOD1, called U1cSOD1, administered intrathecally (into the CSF) to both normal and endstage DM-affected dogs would be well-tolerated with no adverse effects and would achieve silencing of the canine SOD1 gene. We have demonstrated that U1cSOD1 achieves therapeutically relevant SOD1 gene-silencing in dogs with and without DM. Our work has allowed to conclude the following:

• Treatment with U1cSOD1 does not cause any side effects in dogs.

• U1cSOD1 does silence the mutated SOD1 gene in dogs.

This work resulted in the identification of U1cSOD1 as a promising treatment for DM due to the following successful results:

• U1cSOD1 maintains its high efficacy and stability in dogs.

• U1cSOD1 is safe in dogs.

• U1cSOD1 effectively silences expression of the SOD1 gene in dogs with DM.

Thanks to this phase of work funded by the Finding a Cure for DM Foundation we were able to obtain a grant from the Morris Animal Foundation to treat dogs with DM. In this clinical trial we are evaluating the safety and clinical effects of monthly U1cSOD1 treatment in DM dogs. We are glad to report that the Morris study is going very well and that we now feel very confident about the safety of our therapy.

In view of this and to gather data that would be required to fund an extensive DM clinical trial, which is our long-term goal, we have initiated work to look at the route, dose and dosing frequency needed to achieve the best results by measuring levels of U1cSOD1 and SOD1 in the blood, urine and CSF of dogs undergoing treatment. The ultimate goal is to find the efficacious dose and dosing frequency with the least invasive delivery method for the dogs to minimize the number of treatments needed.

12/10/2018: MORRIS ANIMAL FOUNDATION AWARDS GRANT!                                                

WE ARE PLEASED AND EXTREMELY GRATEFUL TO ANNOUNCE that the MORRIS ANIMAL FOUNDATION has awarded our 

PROJECT NEW HOPE research team a grant to continue research along the same lines as our own sponsored study!!!

This is exciting news for the potential beneficial treatment for our DM babies!
We are immensely thankful and very Blessed for each and every one of you that have and continue to support FCDMF in our quest to help our DM pups and families.
It is with data that was collected through Project New Hope that you have supported and sponsored, that our team was able to be awarded this grant.
We are hopeful of a very positive outcome as a result!
We wish you all a very MERRY CHRISTMAS, and HAPPY 2019!
Here is a brief summary of the clinical trial that could be starting as soon as next week!


“The scope of this grant is to investigate the safety of the U1 Adaptor technology in dogs with DM. In this safety trial in 4 dogs diagnosed with degenerative myelopathy, we will deliver a U1 Adaptor-technology-based treatment that silences the SOD1 gene into the cerebrospinal fluid around the spinal cord to prevent production of SOD1 protein within neurons. The treatments will be repeated every month up to 12 months, perhaps even longer, and the treated dogs will be monitored for side effects and for a change in progression of their clinical signs. Demonstration of safety of this treatment will allow us to perform a much larger clinical trial to determine whether U1 Adaptor targeting of SOD1 is an effective treatment for a disease that is currently fatal.”

UPDATE ON PHASE TWO OF  PROJECT "NEW HOPE!" : STAGE ONE!    1/24/2018

*** We are very pleased to provide an update on Phase Two, stage one (of 3) of Project "New Hope". We are very optimistic and remain very hopeful for more positive outcome in the future! We could never have gotten this far without your support. We are very thankful to you all for your generous donations and continued support! Here is an update, as provided by the esteemed Doctors involved in this research: "Dear friends, We would like to update you on our New Hope Phase 2 project. We are very happy to report that the first stage of the study is complete with very exciting preliminary results. The first dogs were treated achieving good gene silencing and no adverse conditions! The initial expectations were successfully met and we hope for further great results. Thanks to your support, we are now able to start the second phase in which we will confirm our preliminary results and we anticipate we will have enough data to design our first clinical trial for dogs with DM. As you know this study is very important as it will establish a foundation towards a therapy for DM.

Thank you again for your support and we look forward to providing an update at the end of this work."

Drs. Natasha Olby and Sam Gunderson.

 *********  NEW!!  2017 DM CLINICAL TRIAL BEGINS !!  ********* 

We at Finding the Cure for DM, are constantly striving to locate Research Projects or Clinical Trials whose priority is to find a treatment or a cure for Canine Degenerative Myelopathy. FCDMF is committed to donating or Sponsoring these types of programs at minimum, 

on an annual basis.

Under the AWA, research institutions are required to provide an Institutional Animal Care and Use Committee (IACUC) protocol to FCDMF before consideration for grant awards.

If you or your Institution would like to be considered for a grant of this nature, 

please contact us HERE.  

(Please note that due to our small stature, FCDMF does not permit overhead charges to be included in financial awards)

 

FCDMF has been sponsoring project "New Hope", a new, initial research project with the ultimate goal of silencing the gene(s) that contribute to DM symptoms. If successful, we anticipate it will stop further progression of symptoms in its tracks.

Currently, the ONLY funding has been by your donations through Finding the Cure for DM Foundation. We hope you will find it in your heart to continue your generosity, bringing us one step closer to a Cure! Thank you for all you have done to help us initiate this promising research!

4/29/2016 Update :

***** 4/29/2016While the initiation of Project New Hope was aimed at evaluating the possibility of silencing the SOD1 gene, which by many is perceived to be a contributing factor to DM, we have now evaluated a different gene.
Due to the positive preliminary progress report for silencing the cSOD1 gene, we have extended this study to include another gene reputed to have some significance in DM symptoms. The Canine DRB1 gene, also reputed to contribute to the symptoms of Degenerative Myelopathy. WE HAVE VERY POSITIVE RESULTS! Our science team at Silagene has concluded that in vitro, using their U1 Adaptor technology, they have indeed been able to silence the Canine DRB1 gene! This is terrific news, and is a direct reflection of our supporters pulling together for a great cause, so close to all of our hearts! Thank you..one and all, for believing in and continuing to help support this research! However, it does not end here. Project "New Hope" is only in it's infancy stage. We will now be taking steps into finding a Clinical Veterinarian to participate and continue reaching further into this study, in the hopes of eventually leading us into Canine Clinical Trials!
Contrary to the ALS comparison, investigating DRB1 has led scientists to believe that GSDM may be a different “type” of DM, inherently more like PPMS (Primary Progressive MS.)
Targeting this second gene will enhance the ability to bring in DM-expert veterinarians for moving the project forward. Furthermore, being able to target two genes, either alone or together, should greatly broaden the interest to those who want to do clinical trials.
Please see the newest update below, and please consider FCDMF for your charitable contributions to continue to help move these studies forward. 
FDCMF, through your donations, is currently the ONLY funding source for project New Hope. 
We are more than grateful to have you fighting DM beside us! Thank You!!
2/13/2016*****ADDENDUM TO PROJECT "NEW HOPE." 
This addendum for the SOD1 silencing consists of the evaluation of the DLA-DRB1 gene that we would like to extend into project "New Hope."
While the initiation of Project New Hope was aimed at evaluating the possibility of silencing the SOD1 gene, which by many is perceived to be a contributing factor to DM, we would now like to begin evaluating a different gene.
Due to the positive preliminary progress report for silencing the cSOD1 gene, we would like to extend this study to include another gene reputed to have some significance in DM symptoms.
This next portion of the study would revolve around the silencing of the DLA-DRB1 gene. In past studies, related research indicated that DRB1 housed the 1101 allele, also thought to contribute primarily to GSDM.
Contrary to the ALS comparison, investigating DRB1 has led scientists to believe that GSDM may be a different “type” of DM, inherently more like PPMS (Primary Progressive MS.)
Targeting a second gene will enhance the ability to bring in DM-expert veterinarians for moving the project forward. Furthermore, being able to target two genes, either alone or together, should greatly broaden the interest to those who want to do clinical trials.
While the initial study into the feasibility of silencing the SOD1 gene has been funded by previous donations and fundraising events, future studies in this direction will require additional funding.
As well, to initiate research and silencing of the DLA-DRB1 gene, funding will be also required.
To date, the ONLY funding of this project has been with your donations through the Finding the Cure for DM Foundation. We hope you will find it in your heart to continue your generous contributions to this much needed research.
If you would like your donation to go to only the DRB1 portion of this study, please make a note with your contribution, and it will be allocated to DRB1. The same applies to the SOD1 portion of this study.
If there is no preference as to which portion of research your donations go to, no note is required.
We at FCDMF wish to thank all who have contributed to initiate this program, and those who continue to help see it continue.
Please review the attached proposal for the possibility of extending DM research into silencing of the DRB1 gene.
02/13/2016:   RESEARCH UPDATE!! 
We would like to share the preliminary progress of Project New Hope, SOD1 gene silencing.
In this initial in vitro study, Silagene has had very good success in silencing up to 75% of the SOD1 gene, with their patented U1 Adaptor Technology.
This is wonderful news, and offers great potential for continuing this line of research!
It is our hope that with continual funding, it may be possible to continue research and be into canine clinical trials of this procedure within a year.
The attached document outlines the progress of Project New Hope up to this point in time.
We anticipate it will fill your heart with “New Hope,” as it has ours!
Furthermore, due to the positive preliminary results with the SOD1 gene, in a time and money saving opportunity, we would like to move forward with an extension of the current study to another gene reputed to be a possible link to canine DM.
This next portion of the study would revolve around the silencing of the DLA-DRB1 gene, which houses the 1101 allele.
Please anticipate the next announcement which clarifies the purpose of the intended work on the DLA-DRB1 gene.