First Humans Dosed in New CMT Drug Trial

by | Jul 14, 2025 | 0 comments

A New CMT Treatment Is One Step Closer

Augustine Therapeutics Begins Phase I Trial of AGT‑100216

Exciting news for the CMT community! TRIAD partner, Augustine Therapeutics has officially dosed the first human participant in their Phase I clinical trial of AGT‑100216—a potential disease-modifying therapy for Charcot-Marie-Tooth disease.

This trial is the first-ever clinical study of a peripherally restricted, selective HDAC6 inhibitor for CMT. AGT‑100216 is designed to target the root causes of nerve damage with fewer side effects, giving hope for safer, long-term treatment options.

What’s happening now?

The Phase I trial focuses on healthy volunteers to test:

  • Safety & tolerability
  • How the drug behaves in the body (pharmacokinetics)
  • Early signs of effectiveness (pharmacodynamics)

Why it matters:

CMT affects 1 in 2,500 people, and there are currently no approved treatments that slow or stop the disease. This milestone is a huge step forward in bringing a targeted therapy closer to those who need it most.

Next steps?

Pending results, Augustine plans to move into patient-centric trials. With strong backing from global investors and scientific leaders, this program is gaining momentum—and fast.

Learn more about the trial here

Thank you for being part of the movement to cure CMT. Every step forward starts with YOU.

Don’t forget to JOIN GRIN!

Learn more on this topic

Related Blog Posts

Global Registry For Inherited Neuropathies: Your Questions Answered

Global Registry For Inherited Neuropathies: Your Questions Answered

Why are we asking you to join our registry? It’s simple. Without you, researchers won’t have the essential patient information to develop the drugs, gene therapy, and clinical trials for Charcot-Marie-Tooth and other inherited neuropathies.
This is why the Hereditary Neuropathy Foundation (HNF) created the Global Registry for Inherited Neuropathies (GRIN). The registry collects the historical, clinical, and genetic information on patients diagnosed with the various forms of inherited neuropathies to help advance therapy development for these debilitating disorders. We understand there may be some hesitation joining our registry. To help mitigate any concerns, we’ve have the answers to your most common questions.

Join the conversation

Leave a Comment

0 Comments

Submit a Comment

Your email address will not be published. Required fields are marked *

Newsletter

Join for notifications on events, campaigns, & news