Larimar Therapeutics Inc at Guggenheim Healthcare Talks: Genomic Medicines and Rare Disease Days (Virtual) Transcript
Good afternoon, everyone. My name is Yatin Suneja. I'm one of the biotech analysts here at Guggenheim. It is my pleasure to welcome our next presenting company. We have here with us Larimar Therapeutics, and from the company, we have the Chief Executive Officer, Carole Ben-Maimon.
Carole, we'll use the next 20, 25 minutes in a fireside chat format. But why don't you maybe take five minutes, make some opening comments, tell us what Larimar is all about, what are some of the key upcoming milestones, and then we'll go into the Q&A.
Sure, happy to. Thanks for having us today. It's nice to talk to everybody.
So Larimar is a clinical-stage company. We have our lead program, CTI-1601. It is a replacement therapy for frataxin, which is the protein that's missing in patients with Friedreich's ataxia. These patients are born looking healthy, become clumsy, and then ultimately end up in wheelchairs and die from cardiac disease,
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