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Clinical Trials in France / NCT06430385
Recruiting Phase 1/2

ATTUNE: A Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of Intrathecally-Administered ION440 in Participants With Methyl CpG Binding Protein 2 (MECP2) Duplication Syndrome (MDS)

NCT06430385 · tracked via the Priya Life Science France tracker
Phase
Phase 1/2
Started
2024-10-21
Last updated
2026-03-24

Condition(s) studied

Methyl CpG Binding Protein 2 (MECP2) Duplication Syndrome

Investigational drug(s) / intervention(s)

ION440Sham procedure

ION440: ION440 will be administered by intrathecal bolus (ITB) injection.

Sham procedure: An LP will be performed with CSF collection but will not be followed by the administration of study treatment by ITB injection.

Study summary

The primary purpose of this study is to evaluate the safety and tolerability of ION440.

Eligibility

Sex
MALE
Min age
2 Years
Max age
65 Years
Healthy volunteers
No
Key Inclusion criteria for Part 1: 1. Males aged ≥ 2 to ≤ 65 years, depending on specific cohort and group, at the time of informed consent. 1. Group A: ≥ 8 to ≤ 65 years old 2. Group B: 2 to 7 years old, inclusive 2. Participant has at least one parent or caregiver ≥ 18 years old capable of providing informed consent and able to comply with all study requirements and activities. 3. Participant has a documented diagnosis of MDS with genetic confirmation of MECP2 duplication. 4. Is currently receiving stable doses of concomitant medications for at least 1 month prior to screening. 5. Able to complete all study procedures, measurements and visits to support primary and secondary endpoints, in the opinion of the Investigator. Key Exclusion criteria for Part 1: 1. Documented diagnosis of severe MECP2 duplications including terminal duplication and/or translocation or MECP2 triplication OR clinical features associated with severe variant structure including (a) onset of seizures prior to age 5 (for those aged 5 and above at signing of ICF), (b) oxygen dependence, (c) microcephaly, IF MECP2 genetic structure information is unavailable. 2. Clinically significant vital sign or ECG abnormality at Screening 3. Known brain or spinal disease that would interfere with the LP procedure, or CSF circulation or presence of other factors would affect the safety of the LP procedure. 4. Has any concomitant disease or condition or circumstance, or any finding at Screening that, in the opinion of the Investigator, makes the participant unsuitable for enrollment or that could interfere with the conduct of the study or that would pose an unacceptable risk to the participant in this study. 5. Treatment with an investigational drug, biological agent, or device within 30 days of Screening, or 5 half-lives of investigational agent, whichever is longer. 6. Previous treatment with an oligonucleotide (including siRNA) within 4 months of Screening if single dose received, or within 12 months of Screening if multiple doses received (this exclusion does not apply to vaccines - both mRNA and viral vector vaccines are allowed including COVID-19). For centrally administered ASOs, a minimum of 12 months washout is required irrespective of the number of doses received. 7. Currently enrolled in a clinical trial of an investigational agent or device or has used any investigational agent or device within 5 half-lives of investigational agent, whichever is longer. 8. Has a history of gene therapy or cell transplantation or any other experimental brain surgery. 9. Active infection requiring systemic antiviral or antimicrobial therapy that will not be completed prior to Baseline (Day 1). 10. Has experienced Status Epilepticus in the past 6 months. Key Inclusion criteria for Part 2: 1. Participants in ION440-CS1, Part 1/MAD who received at least one dose of Study Drug /Sham in Part 1/MAD, missed no more than 1 study visit, and attended the Follow Up visit (Visit 6). 2. All inclusion criteria in Part 1/MAD apply (participants will not be required to undergo new Screening bloodwork). Key Exclusion criteria for Part 2: 1\. Has developed any concomitant disease (e.g., gastrointestinal, renal, hepatic, endocrine, respiratory, or cardiovascular system disease) or condition or circumstance, or any finding during Part 1/MAD that, in the opinion of the Investigator, makes the participant unsuitable for continued treatment (e.g., could interfere with the conduct of the study or that would pose an unacceptable risk to the participant in this study).

Primary outcome measure(s)

Trial sites (11)

FacilityCityRegionStatus
Rady Children's Hospital San Diego California Recruiting
University of Colorado Hopsital - Anschutz Medical Campus Aurora Colorado Recruiting
Kennedy Krieger Baltimore Maryland Recruiting
Boston Children's Hospital Boston Massachusetts Recruiting
Gillette Children's Specialty Healthcare Saint Paul Minnesota Recruiting
Children's Hospital of Philadelphia Philadelphia Pennsylvania Recruiting
Vanderbilt University Medical Center Nashville Tennessee Recruiting
Baylor College of Medicine Houston Texas Recruiting
Kepler University Hospital Linz Austria Recruiting
CHU Dijon Bourgogne Dijon France Recruiting
Hospital Saint Joan de Deu Barcelona Spain Recruiting

More Ionis Pharmaceuticals, Inc. trials in France

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06430385 on ClinicalTrials.gov ↗ ← All trials in France