Avidity Biosciences, Inc.
11
2
4
4
Key Highlights
Risk & Performance
Pipeline Risk Assessment
Pipeline Risk Assessment
Based on historical performance
Moderate Risk
Score: 35/100
0.0%
0 terminated/withdrawn out of 11 trials
100.0%
+13.5% vs industry average
27%
3 trials in Phase 3/4
0%
0 of 4 completed trials have results
Key Signals
Enrollment Performance
Analytics
Activity Timeline
Global Presence
Clinical Trials (11)
Motor Outcomes to Validate Evaluations in FSHD (MOVE FSHD)
Role: collaborator
Managed Access Program for Del-zota in Participants With DMD Mutations Amenable to Exon 44 Skipping
Role: lead
Phase 1/2 Study of AOC 1020 in Participants With Facioscapulohumeral Muscular Dystrophy (FSHD)
Role: lead
Global Open-Label Extension Study of Del-desiran for the Treatment of DM1
Role: lead
Study of AOC 1001 in Adult Myotonic Dystrophy Type 1 (DM1) Patients
Role: lead
Global Study of Del-desiran for the Treatment of DM1
Role: lead
A Study to Evaluate Del-brax (Also Referred to as AOC 1020) in Participants With FSHD
Role: lead
Extension of AOC 1001-CS1 (MARINA) Study in Adult Myotonic Dystrophy Type 1 (DM1) Patients
Role: lead
Study of AOC 1044 in Healthy Adult Volunteers and Participants With Duchenne Muscular Dystrophy (DMD) Mutations Amenable to Exon 44 Skipping
Role: lead
Ph2 Open-label Study of AOC 1044 in Duchenne Muscular Dystrophy Participants With Mutations Amenable to Exon44 Skipping
Role: lead
Phase 2 Open-label Extension Study of AOC 1020 in Participants with Facioscapulohumeral Muscular Dystrophy (FSHD)
Role: lead
All 11 trials loaded