Two for FSHD

Facio partners with Evotec to initiate a FSHD drug discovery program

Register for free to listen to this article
Listen with Speechify
HAMBURG, Germany—Evotec AG and Facio Therapies have entered into an agreement aimed at the identification of compounds showing activity as a potential treatment to stop the progression of FSHD (facioscapulohumeral dystrophy), a muscle wasting disease.
Facio Therapies was established in 2014 with a single focus: to find a cure for FSHD, a muscle-wasting disease that generally progresses from the face (“facio”) to the shoulders (“scapulo”) and the upper arms (“humeral”), and sometimes also to the legs. About 20 percent of people with FSHD are eventually confined to a wheelchair.
Worldwide, FSHD devastates the lives of over half a million people and those close to them. The loss of muscle strength has a huge impact on daily life. Living with FSHD means living with pain, fatigue and social isolation. Above all, the future becomes uncertain because the course of the disease is unpredictable. Currently, no therapy for FSHD is available other than forms of temporary symptomatic relief.
“Facio came to Evotec directly based on its reputation as a known expert in the industry in drug discovery,” notes Gabriele Hansen, vice president of corporate communications and investor relations at Evotec. The project with Facio entails the setup and execution of an automated high-throughput screen to identify small molecules having a positive effect on SMCHD1 and DUX4 activity in human FSHD-affected muscle cell lines. The compounds that show promising activity in this screen are expected to be available in the first half of 2016. These compounds will require extensive further testing to produce compounds that are suitable for the development of a therapeutic for the treatment of FSHD, the release announcing the partnership states. All in all, the partners agree that this is a challenging process that may take several years before clinical testing in humans can begin.
“The start of our drug discovery program is a significant step forward in our pursuit to overcome FSHD,” said Facio’s Managing Director David Dasberg. “Evotec is a leader in the field of drug discovery, and their expertise with muscle tissue will allow us to move forward as fast as possible.”
Dr Mario Polywka, chief operating officer of Evotec, commented: “We are very excited about the opportunity to collaborate with Facio on this important disease. With our world-leading expertise in tissue analysis and high-throughput screening, we are confident to add real value to the progression of this program.”
In 2012, Evotec and the Jain Foundation initiated a research project to explore and validate cell-based assay principles useful for high-throughput screening using dysferlin deficient skeletal muscle cells. “The aim of this project is to discover compounds that improve the well-being of these dysferlin- [a muscle protein associated with several forms of muscular dystrophy] deficient skeletal muscle cells,” Hansen explains. “In 2013, Evotec and the Jain Foundation extended and expanded their collaboration to leveraging Evotec’s assay development and screening capabilities.”
In terms of the scope of the project, “The manpower and duration of the project will be led by the science and the needs of the project to drive it to a PDC,” Hansen states. No financial details were disclosed.
Facio Therapies is a Netherlands-based company aiming to overcome FSHD by developing a causal therapy that restores the repression of toxic DUX4. Facio works with leaders in the field to develop an affordable and accessible causal therapy in the most expeditious fashion possible. Being by and for people with FSHD, the business approach is to have a positive impact on lives rather than maximize financial gain. Facio’s founders—Kees van der Graaf (Netherlands), Bill Moss (Australia) and Neil Camarta (Canada)—are business leaders from the FSHD community.
The etiology of the disease is well understood. FSHD is hereditary. If one parent is affected, children have a 50-percent chance of inheriting the same genetic defect. About 95 percent of people with FSHD have a defect on chromosome 4; this is known as FSHD1. The remaining 5 percent have a defect on chromosome 18, which is called FSHD2.
Chromosome 4 contains a series of repeated pieces of DNA, so-called D4Z4 repeat units. People without FSHD have 11-100 D4Z4 repeat units. In people with FSHD1, the D4Z4 array is shortened to 1-10 units. In contrast, people with FSHD2 have a normally sized D4Z4 array. The defect in FSHD2 is a mutation in a gene on chromosome 18 called SMCHD1.
FSHD1 and FSHD2 are clinically indistinguishable. This suggests there is a common factor—and, in fact, there is. Both types of FSHD result in the production of a protein called DUX4. DUX4 plays a normal role in early fetal development, but is highly toxic when produced in muscle tissue. In people without FSHD, the DUX4 gene is repressed. In people with FSHD (whether FSHD1 or FSHD2), the DUX4 gene is “de-repressed” and produces its toxic protein. A causal FSHD therapy needs to take the DUX4 gene back to its normal repressed state.

Subscribe to Newsletter
Subscribe to our eNewsletters

Stay connected with all of the latest from Drug Discovery News.

DDN Magazine May 2024

Latest Issue  

• Volume 20 • Issue 3 • May 2024

May 2024

May 2024 Issue