28 Participants Needed

EDK060 for Charcot-Marie-Tooth Disease

Recruiting at 2 trial locations
Age: 18 - 65
Sex: Any
Trial Phase: Phase 1
Sponsor: Novartis Pharmaceuticals

What You Need to Know Before You Apply

What is the purpose of this trial?

This trial explores the safety and metabolism of a treatment called EDK060, a potential new drug for Charcot-Marie-Tooth Disease Type 1A (CMT1A), a condition affecting nerves and muscles. The study includes two groups: one receives EDK060, while the other receives a placebo, a harmless pill resembling the treatment. Individuals with CMT1A confirmed by genetic testing and some nerve function in their arms may qualify for this trial. As a Phase 1 trial, participants will be among the first to receive this new treatment, aiding researchers in understanding its effects in people.

Will I have to stop taking my current medications?

The trial requires that you have not used any drug intended to modify the course of CMT1A within 6 months before screening. Other medications are not specifically mentioned, so it's best to discuss your current medications with the trial team.

Is there any evidence suggesting that EDK060 is likely to be safe for humans?

Research shows that EDK060 is still in the early stages of human testing. Detailed safety information is limited at this point. However, its progression to a Phase 1 trial indicates sufficient promise in lab and animal studies for human testing. Phase 1 trials primarily focus on safety, with participants closely monitored.

Although specific safety data for EDK060 in humans is not yet available, the trial aims to assess how well people tolerate the treatment and its effects in the body. Participants will be carefully observed for any side effects. This early phase is crucial to ensure the treatment's safety for further testing and to identify any potential adverse reactions.

In summary, while EDK060 has not undergone extensive human testing, this trial is designed to gather essential safety information.12345

Why do researchers think this study treatment might be promising?

EDK060 is unique because it targets the underlying causes of Charcot-Marie-Tooth disease, offering a new mechanism of action compared to existing treatments, which mainly focus on managing symptoms. Unlike current options, EDK060 aims to directly modify the disease progression, potentially slowing or halting nerve damage. Researchers are excited about EDK060 because it has the potential to improve long-term outcomes for patients by addressing the root cause of the disease rather than just alleviating symptoms.

What evidence suggests that EDK060 might be an effective treatment for Charcot-Marie-Tooth Disease?

Researchers are investigating EDK060 as a potential treatment for Charcot-Marie-Tooth disease type 1A (CMT1A), a condition that affects nerves and leads to muscle weakness and sensory problems. Although limited data exists on EDK060's effectiveness in improving symptoms, it targets the root causes of nerve damage. Early results from similar treatments have shown promise in addressing these nerve issues. In this trial, participants will receive either EDK060 at various doses or a matching placebo. Current studies are examining how the body processes the drug, which aids in understanding its potential effects on the disease.23456

Are You a Good Fit for This Trial?

Adults aged 18-60 with a clinical diagnosis of Charcot-Marie-Tooth Disease Type 1A (CMT1A) confirmed by genetic testing showing duplication of the PMP22 gene. Participants must be able to provide consent and have detectable nerve conduction velocities in at least one upper extremity.

Inclusion Criteria

I have given my written consent to participate.
My nerve tests in at least one arm show normal signals.
I have been diagnosed with CMT1A and have genetic proof of PMP22 duplication.
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Timeline for a Trial Participant

Screening

Participants are screened for eligibility to participate in the trial

2-4 weeks

Treatment

Participants receive a single ascending dose of EDK060 or placebo to assess safety, tolerability, and pharmacokinetics

1 day

Follow-up

Participants are monitored for safety and effectiveness after treatment, including assessment of adverse events and pharmacokinetic parameters

20 weeks

What Are the Treatments Tested in This Trial?

Interventions

  • EDK060
Trial Overview The trial is evaluating the safety, tolerability, and how the body processes different doses of EDK060 compared to a placebo in adults with CMT1A. Patients will receive either EDK060 at varying doses or a placebo.
How Is the Trial Designed?
2Treatment groups
Experimental Treatment
Placebo Group
Group I: EDK060Experimental Treatment4 Interventions
Group II: PlaceboPlacebo Group1 Intervention

Find a Clinic Near You

Who Is Running the Clinical Trial?

Novartis Pharmaceuticals

Lead Sponsor

Trials
2,963
Recruited
4,275,000+
Founded
1996
Headquarters
Basel, Switzerland
Known For
Precision medicine
Top Products
Gleevec, Cosentyx, Entresto, Kisqali
Dr. Vas Narasimhan profile image

Dr. Vas Narasimhan

Novartis Pharmaceuticals

Chief Executive Officer since 2018

MD from Harvard Medical School

Dr. Shreeram Aradhye profile image

Dr. Shreeram Aradhye

Novartis Pharmaceuticals

Chief Medical Officer since 2021

MD

Citations

A First in Human Study to Assess the Safety, Tolerability ...The purpose of this study is to characterize the safety, tolerability, and pharmacokinetics of EDK060 as compared to placebo in adult patients ...
CMT Clinical Trials - CMT Research FoundationCMT clinical trials are specialized research efforts aimed at developing and testing new treatments for Charcot-Marie-Tooth disease.
EDK060 for Charcot-Marie-Tooth DiseaseTrial Overview The trial is evaluating the safety, tolerability, and how the body processes different doses of EDK060 compared to a placebo in adults with CMT1A ...
4.pubmed.ncbi.nlm.nih.govpubmed.ncbi.nlm.nih.gov/39586049/
Clinical Outcome Assessments and Biomarkers in Charcot ...In this review, we discuss the challenges and successes over the past 2 decades in efforts to design and validate COAs and disease biomarkers of CMT.
EDK-060 - Drug Targets, Indications, PatentsA First-in-human, Multi-center, Randomized, Participant- and Investigator-blinded, Placebo Controlled, Single Ascending Dose Study to Assess the Safety, ...
NCT07140614 | A First in Human Study to Assess the ...The purpose of this study is to characterize the safety, tolerability, and pharmacokinetics of EDK060 as compared to placebo in adult patients with CMT1A.
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