The purpose of this study is to assess the safety and biological activity of ATYR1940 in participants with LGMD2B and FSHD.
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Number of Participants With Treatment Emergent Adverse Events (TEAEs) and Serious Adverse Events (SAEs)
Timeframe: Up to End of Study (up to Week 25)
Number of Participants With a Clinically Significant Electrocardiogram (ECG) Abnormality Leading to a TEAE
Timeframe: Up to End of Study (up to Week 25)
Number of Participants With a Clinically Significant Pulmonary Function Event Resulting in a TEAE
Timeframe: Up to End of Study (up to Week 25)
Number of Participants With a Clinical Laboratory Abnormality Leading to an AE
Timeframe: Up to End of Study (up to Week 25)
Number of Participants With Vital Sign Abnormality Resulting in a TEAE
Timeframe: Up to End of Study (Up to Week 25)