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Multiple Ascending Dose Study of CTI-1601 Versus Placebo in Subjects With Friedreich's Ataxia

Friedreich Ataxia Clinical Trial

Official title:
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

Clinical Trial Summary

To evaluate the safety and tolerability of multiple ascending doses of CTI-1601 in participants with Friedreich's ataxia

Clinical Trial Description

Multiple Ascending Dose (MAD), Double-Blind, Placebo Controlled Study. To evaluate the safety and tolerability of multiple ascending doses of CTI-1601 in subjects with Friedreich's ataxia. Secondary Objectives: 1. To evaluate the pharmacokinetics (PK) of CTI-1601 following, multiple, increasing, doses of subcutaneously (SC) administered CTI-1601. 2. To evaluate the pharmacodynamics (PD) of CTI-1601 following, multiple, increasing, doses of SC administered CTI-1601. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04519567
Study type Interventional
Source Larimar Therapeutics, Inc.
Contact
Status Completed
Phase Phase 1
Start date July 31, 2020
Completion date March 16, 2021
View Details
See also
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