A First in Human Study to Assess the Safety, Tolerability, and Pharmacokinetics of EDK060 in Adults With CMT1A.

Novartis

Status and phase: Enrolling; Phase 1

Conditions: Charcot-Marie-Tooth Disease, Type 1A

Treatments: Drug: EDK060, dose D; Other: Placebo; Drug: EDK060, dose C; Drug: EDK060, dose B; Drug: EDK060, dose A

Study type: Interventional

Funder types: Industry

Identifiers

NCT07140614

CEDK060A12101

Details and patient eligibility

About

The purpose of this study is to characterize the safety, tolerability, and pharmacokinetics of EDK060 as compared to placebo in adult patients with CMT1A.

Enrollment: 28 estimated patients

Sex: All

Ages: 18 to 60 years old

Volunteers: No Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria:

• Provide written informed consent before any assessment is performed.
• Be male or female and 18 to 60 (inclusive) years of age at the time of screening.
• Participant must have a clinical diagnosis of Charcot-Marie-Tooth Disease Type 1A (CMT1A) including verified documentation of genetic testing showing duplication of the PMP22 gene by an accredited/certified laboratory (according to local regulations)
• Have detectable upper extremity nerve conduction velocities (sensory and motor) in at least one extremity at screening.

Exclusion Criteria

• Unable to communicate well with the investigator, to understand and comply with the visits and procedures of the study.
• History of cardiac, renal, liver, hematological, immune system disorders.
• Pregnant/nursing female participants. Women of child-bearing potential, defined as all women physiologically capable of becoming pregnant, unless they are using highly effective methods of contraception during dosing and for the duration of the follow-up period. Sexually active males unless they use a condom during intercourse.
• Inability or unwillingness to provide serial skin biopsy samples.
• Inability or unwillingness to undergo repeated venipuncture or in the opinion of the investigator, participant would be at an increased risk for adverse events related to these procedures.
• Use of any drug intended to modify the course of CMT1A within 6 months from screening, including but not limited to: PTX-3003 (baclofen, sorbitol, and naltrexone in combination).
• History of compression neuropathy within the last 6 months from screening and/or other conditions that can cause peripheral neuropathy, including but not limited to diabetes, chronic alcoholism, exposure to neurotoxic medications, exposure to environmental neurotoxins, traumatic nerve injury, thyroid disease, or infections.

Other protocol-defined inclusion/exclusion criteria may apply

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Triple Blind

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28 participants in 2 patient groups, including a placebo group

EDK060

Experimental group

Description:

Doses A; B; C; D

Treatment:

Drug: EDK060, dose B

Drug: EDK060, dose A

Drug: EDK060, dose C

Drug: EDK060, dose D

Placebo

Placebo Comparator group

Description:

Matching placebo

Treatment:

Other: Placebo