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A Phase 1 Multiple Ascending Dose Study to Assess the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of Subcutaneous CTI-1601 Versus Placebo in Subjects With Friedreich's Ataxia

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Trial Profile

A Phase 1 Multiple Ascending Dose Study to Assess the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of Subcutaneous CTI-1601 Versus Placebo in Subjects With Friedreich's Ataxia

Status: Completed
Phase of Trial: Phase I

Latest Information Update: 24 Nov 2024

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At a glance

  • Drugs Nomlabofusp (Primary)
  • Indications Friedreich's ataxia
  • Focus Adverse reactions; Proof of concept
  • Sponsors Larimar Therapeutics

Most Recent Events

  • 18 Nov 2024 According to a Larimar Therapeutics media release, the company presented data from the Company's Phase 1 studies and the Phase 2 dose exploration study of nomlabofusp at the International Congress for Ataxia Research (ICAR) held from Nov 12-15, 2024 in London, U.K. Data from 61 adults, who participated in these studies, evaluating short-term (up to 28 days) SC doses of 25, 50, 75, and 100 mg nomlabofusp were further evaluated and presented in 3 posters.
  • 30 Oct 2024 According to a Larimar Therapeutics media release, the company will present two posters with data from patients participating in our Phase 1 single ascending dose (SAD) and multiple ascending dose (MAD) studies and Phase 2 dose exploration study at the International Congress for Ataxia Research (ICAR) meeting.
  • 19 Oct 2022 According to Larimar Therapeutics media release, the data from phase I clinical program evaluating CTI-1601 for the treatment for Friedreich's Ataxia will be featured in the three presentations at the upcoming International Congress for Ataxia Research. The conference will take place from 1st-4th November 2022 in Dallas, Texas, USA.

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