Evaluate the safety and tolerability of subcutaneous (SC) administration of MAR002 in healthy men
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Number of participants with TEAEs (treatment-emergent adverse events)
Timeframe: From first dose of study drug through final End of Study/Early Termination Visit. End of Study is Day 64 for Cohorts 1 and 2; End of Study is day 169 for Cohorts 3, 4, 5, and 6.