The purpose of this study is to evaluate the efficacy, safety and tolerability of oral omadacycline as compared to placebo in the treatment of adults with Nontuberculous Mycobacterial (NTM) pulmonary disease caused by Mycobacterium abscessus complex (MABc)
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Percentage of Participants With Clinical Response on NTM Symptom Assessment Scale at Day 84
Timeframe: Day 1 to Day 84
Percentage of Participants With Clinical Response on NTM Symptom Assessment Scale at Day 84 With no Deterioration in Severity of Symptoms That Were Present at Baseline.
Timeframe: Day 1 to Day 84
Number of Participants With Treatment-emergent Adverse Events (TEAEs) and Serious Adverse Events (SAEs)
Timeframe: From screening period (up to 8 weeks prior to randomization) through Day 114 (at any study timepoint)
Change From Baseline in Laboratory Test Parameters - Hepatic and Enzymatic Biomarkers
Timeframe: Day 1 (Baseline) to Day 84/EOT
Number of Participants With Potentially Clinically Significant (PCS) Laboratory Parameter
Timeframe: Day 1 through Day 84 (at any study timepoint)
Change From Baseline in Systolic and Diastolic Blood Pressure
Timeframe: Day 1 (Baseline) to Day 84/EOT
Change From Baseline in Heart Rate
Timeframe: Day 1 (Baseline) to Day 84/EOT
Number of Participants With PCS Threshold Vital Signs Measurement
Timeframe: Day 1 through Day 84 (at any study timepoint)
Change From Baseline in ECG PR Interval, QRS Duration, QT Interval, and QTcF Interval
Timeframe: Day 1 (Baseline) to Day 84/EOT
Number of Participants With PCS QTcF Value
Timeframe: Day 1 through Day 84/EOT (at any study timepoint)