AOC 1044
DrugAOC 1044 will be administered via intravenous (IV) infusion
NCT Number: NCT05670730
AOC 1044-CS1 (EXPLORE44) is a Phase 1/2 study to evaluate the safety, tolerability, pharmacokinetics, and pharmacodynamic effects of single and multiple ascending doses of AOC 1044 in healthy adult volunteers and participants with DMD mutations amenable to exon 44 skipping.
Part A is a single dose design with multiple cohorts (dose levels) in healthy adult volunteers.
Part B is a multiple-ascending dose design with 3 cohorts (dose levels) in participants with Duchenne.
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Notify Me7 year–55 year
Male
Interventional
Phase 1 / Phase 2
Arkansas Children's, Little Rock, Arkansas, United States
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Part A:
Key Inclusion Criteria:
Key Exclusion Criteria:
Part B:
Key Inclusion Criteria:
Key Exclusion Criteria:
AOC 1044 will be administered via intravenous (IV) infusion
Placebo will be administered via intravenous (IV) infusion.
Other names: Saline
Time frame: Through study completion, up to Day 85 (Part A) or Day 169 (Part B)
Time frame: Through Week 8 (Part A); Through Week 12 (Part B)
Maximum plasma concentration (Cmax) of AOC 1044
Time frame: Through Week 8 (Part A); Through Week 12 (Part B)
Terminal half-life (T1/2) of AOC 1044
Time frame: Through Week 8 (Part A); Through Week 12 (Part B)
Area under the concentration-time curve (AUC) of AOC 1044
Time frame: Through Week 4 (Part A); Through Week 16 (Part B)
Time frame: Day 1-2 (0-24 hours after first dose) (Part A); Day 1-2 (0-24 hours after first dose) (Part B)
Fraction of PMO44 excreted in urine
Time frame: Baseline, Week 16
Time frame: Baseline, Week 16
Time frame: Baseline, Week 16
Avidity Biosciences, Inc.
Industry
A Phase 1/2, Randomized, Placebo-controlled, Double-blind, Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamic Effects of Single and Multiple Ascending Doses of AOC 1044 Administered Intravenously to Healthy Adult Volunteers and Participants With DMD Mutations Amenable to Exon 44 Skipping
Acronym: EXPLORE44
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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