Larimar Therapeutics Inc To Discuss Initiation of the Phase 2 trial is expected in Q4 2022, with top-line data expected in 2H 2023 Transcript
Greetings, and welcome to the Larimar Therapeutics conference call. (Operator Instructions) As a reminder, this conference is being recorded. I would now like to turn the conference over to your host, Grant Weingarten of LifeSci Advisors.
Thank you. You may begin.
Thank you, operator, and thank you, all, for participating in today's conference call. Before we start, I would like to point out that there is a slide deck that will accompany today's presentation. This slide deck can be viewed using the webcast link provided in the Investors page of Larimar Therapeutics' website.
Also posted on this webpage is a news release issued earlier today, announcing Larimar's planned next steps for the CTI-1601 clinical program following the receipt of FDA clearance to initiate the 25-milligram cohort of a Phase 2 dose exploration trial of CTI-1601 in Friedreich's ataxia patients. In addition, the webpage also includes a separate press release announcing the pricing of a $70 million underwritten offering of
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