In a new webcast, Sarepta Therapeutics said it will seek approval for and start a confirmatory trial of eteplirsen in 2014; additional drugs may follow
In parallel with that application, the company is preparing to conduct a large-scale, confirmatory trial of eteplirsen. It plans to open the trial during the first quarter of 2014.
Eteplirsen is an experimental drug designed to treat approximately 13 percent of patients with Duchenne muscular dystrophy (DMD). Its mechanism of action is exon skipping, and its target is exon (section) 51 of the dystrophin gene, which is mutated in DMD.
In September 2013, Sarepta announced that walking distance of trial participants continued to show stabilization 96 weeks (1.8 years) into a phase 2b trial. The stabilized walking distance, measured in a "six-minute walk test," contrasts with the expected decline in walking distance that would be expected in untreated DMD patients over this period of time.
The trial includes 12 participants, although only 10 could be assessed on the six-minute walk test, because two lost the ability to walk early in the study. An additional participant sustained a leg fracture late in the trial and could not be evaluated at all time points. (The two who lost walking ability continue to be treated with eteplirsen and are being evaluated on measures other than walking.)
In an Oct. 17, 2013, webcast, available for replay on the Sarepta site, the DMD community received a comprehensive update about Sarepta's plans for eteplirsen and "follow-on" compounds that target other parts (exons) of the dystrophin gene.
Chris Garabedian, Sarepta's president and CEO, and Ed Kaye, Sarepta's senior vice president and chief medical officer, provided an overview of the company's plans and answered questions from the community.
Representing DMD patients and families on the webcast were: Jane Larkindale, MDA's vice president of research; Sharon Hesterlee and Holly Peay of Parent Project Muscular Dystrophy; Marissa Penrod from Duchenne Alliance; and Debra Miller from Cure Duchenne.
Listeners also were directed to Let's Skip Ahead, Sarepta's new online resource center for families with DMD.
A summary of the Oct. 17 webcast, including a question-and-answer session with representatives from patient organizations, follows.
Sarepta's plans for eteplirsen: FDA application, confirmatory trial
Chris Garabedian and Ed Kaye said:
Sarepta's plans for additional exon-skipping drugs
Chris Garabedian and Ed Kaye said:
Chris Garabedian and Ed Kaye answered questions from representatives of four DMD organizations, including MDA. The questions were based on feedback from the DMD community. Here are some of the questions and answers; they have been lightly edited for clarity and brevity.
Q: What are the repercussions from the recent failure of drisapersen to show efficacy in a phase 3 trial? How do you think this will affect the approval process for eteplirsen or the use of the six-minute walk test?
That study has caused concern about whether the six-minute walk test is appropriate for boys with DMD. We believe it is a good test. In our review of the data, we found it to be a sensitive endpoint.
We focus on patient selection for this endpoint [the six-minute walk test]. We're not trying to improve the six-minute walk distance but to maintain it. We have a cohort [group] expected to deteriorate on the six-minute walk distance, with children who are older than 7 years. By having a homogeneous population that should decline [without treatment] and being able to show that they are stable, we think we have a good study design.
We think these two drugs [drisapersen and eteplirsen] are very different. They are different chemical entities, with very different chemical backbones. We do not think the drisapersen failure is an indictment of exon skipping. Our plans for an NDA submission are intact.
Q: Most of those with DMD develop cardiomyopathy. Has eteplirsen shown any benefit on cardiac measures? What are the expectations on this?
A: Cardiomyopathy is an important part of the disease, but we chose boys for this study who were younger and did not have cardiac problems at the outset of this trial. We have followed them with EKGs and echocardiograms, and we have not seen any changes. However, they were normal to begin with. We will continue to follow these boys long-term. It's too early to tell about the effect.
Q: Do you plan to address patients with duplications in the dystrophin gene or who need to have multiple exons skipped?
A: Currently we do not have a product candidate or effort in place to address duplications or multiple exon skipping. Our current focus is to have every patient with a deletion that could benefit from our technology have a drug available to them. There are some expert scientists and clinicians looking at the possibility of applying exon skipping to other types of mutations such as duplications. This work is at a very early stage, and we will be following it to see how it progresses. We remain committed to exploring the potential of our exon-skipping technology.
Q: Will nonambulatory patients be included in subsequent trials?
A: We are focused on the six-minute walk test [as an outcome measure] for now, as it has been validated for regulatory approval. A lot of outcome measures for the upper extremity have not been validated. Initially we are focusing for our confirmatory study for exon 51 on the six-minute walk test. But as we gain more information about how to look at arm function, we will consider looking at nonambulatory patients. We need more understanding of how to evaluate effectiveness in this patient group, and we need to obtain more safety data.
We have two nonambulatory boys in the current trial who showed dystrophin production at 24 and 48 weeks. They lost ambulation early in the study and could not do the six-minute walk test, but the data suggest stabilization on pulmonary function and on other measures, and safety has been shown.