『Hope in Focus Podcast』のカバーアート

Hope in Focus Podcast

Hope in Focus Podcast

著者: Hope in Focus
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10月19日まで。※適用条件あり
The Hope in Focus Podcast, hosted by Ben Shaberman, brings monthly stories and insights to the Leber congenital amaurosis (LCA) and inherited retinal disease (IRD) community. Together, we discuss personal stories, research and scientific updates—including gene therapy and drug development—tools and resources that support accessibility and independence, and insights to help families better understand early-onset vision loss. Hope in Focus is dedicated to generating awareness, raising funds for research, and providing support, education and outreach to the LCA and IRDs.All rights reserved
エピソード
  • Hope in Focus Podcast | Episode 13 - Inside the LCA10 Clinical Trial: A Conversation with Sepul Bio
    2026/09/02
    In this episode, we speak with Mike, Chief Operating Officer at Sepul Bio, about the company’s promising RNA therapy for LCA10, currently being studied in a Phase 3 clinical trial. Mike shares how he became involved in the inherited retinal disease space and discusses his role at Sepul Bio. We also explore the clinical trial process, how sepofarsen works, the differences between RNA and DNA therapies, and what patients can expect during treatment. Throughout the conversation, Mike emphasizes the importance of patient voices and involvement in the development of new treatments. To learn more about the LCA10 clinical trial, contact Sepul Bio at contact@sepulbio.com or visit their website.
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    35 分
  • Hope in Focus Podcast | Episode 12: Understanding Clinical Trials with Dr. Jason Comander
    2026/07/06
    Dr. Jason Comander is the Ayub Family Chair in Ophthalmology and Director of the Inherited Retinal Disorder Service at Mass Eye and Ear. He has led several groundbreaking clinical trials, including delivering the first commercial dose of LUXTURNA® for LCA2 caused by RPE65 mutations and serving as the lead investigator and surgeon for the first CRISPR-Cas9 gene editing trial for LCA10 caused by CEP290 mutations. In this episode, Dr. Comander explains how gene therapies and gene editing approaches differ, shares insights from his experience leading clinical trials, and discusses what families should know when considering trial participation. He also explores emerging treatment approaches, including optogenetics and cell therapies, and offers an optimistic perspective on the future of inherited retinal disease research.
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    39 分
  • Hope in Focus Podcast | Episode 11 - Finding Her Voice: A Conversation with Sarah Hardwig
    2026/06/03
    In this episode, we sit down with emerging country singer-songwriter Sarah Hardwig, who was diagnosed at just five months old with LCA10 CEP290. Sarah’s vision loss has never stopped her from pursuing her passion for music, showcasing her natural talent, or sharing her voice with others. Sarah opens up about growing up with vision loss, navigating school, and adapting to college life by learning new environments and classroom layouts. She also shares how she discovered her love for singing and songwriting, along with some of the biggest challenges she faced during college. Throughout the conversation, Sarah reflects on the vulnerability that comes with creating and performing music, reminding listeners that “everyone has their own story to tell, and everyone has their own way of telling it.” Stay tuned until the end of the episode for a special sneak peek of a live performance from Sarah.
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    42 分
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