ENTR-601-45 Exon 45 Skipping Therapy for Duchenne Muscular Dystrophy: ELEVATE-45 Clinical Trial

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• Assigned male at birth with clinical signs compatible with Duchenne muscular dystrophy as determined by the investigator.
• Part A: 4-20 years of age, inclusive.
• Ambulatory Status Part A: ambulatory with a Performance of the Upper Limb v2.0 (PUL 2.0) Entry as per protocol at Screening.
• Adequate muscle for obtaining tissue biopsy as assessed by the investigator.
• Other protocol-defined criteria apply.

• Any significant concomitant medical condition that might interfere with the ability to comply with protocol requirements.
• Has an acute illness within 4 weeks prior to the first dose of study drug which may interfere with study measurements or jeopardize participant's safety.
• Use of the following medications :
• Prior or current treatment with any exon skipping therapy within the previous 12 months
• Prior or current treatment with any gene therapy
• Use of anti-coagulants, anti-thrombotics, or anti-platelet agents from 30 days prior to screening and until the end of the study
• Use of an immunosuppressant (other than systemic or oral corticosteroid for DMD condition) from 30 days prior to screening until the end of the study.
• Treatment with a histone deacetylase (HDAC) inhibitor, including (but not limited to) givinostat from 30 days prior to screening until the end of the study
• Laboratory abnormalities.
• Daytime ventilator dependence or any use of invasive mechanical ventilation via tracheostomy.
• Has an abnormal electrocardiogram (ECG) reading assessed as clinically significant by the investigator, and/or a QT interval with Fridericia correction method (QTcF) >450 msec at Screening or prior to the first dose of study drug on Day 1.
• Received any experimental or investigational drug, etc. within 3 months prior to first dose or within 5 half-lives (whichever is longer).
• Other protocol-defined criteria apply.

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