Double Blinded Healthy Volunteer study evaluating D-2570 against placebo in various doses.
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Incidence of adverse events
Timeframe: From Informed Consent through study completion, an average of 48 days
Result of Pharmacokinetic endpoint
Timeframe: From Randomization through study completion, an average of 20 days
Result of Pharmacokinetic endpoint
Timeframe: From Randomization through study completion, an average of 20 days
Result of Pharmacokinetic endpoint
Timeframe: From Randomization through study completion, an average of 20 days
Result of Pharmacokinetic endpoint
Timeframe: From Randomization through study completion, an average of 20 days
Result of Pharmacokinetic endpoint
Timeframe: From Randomization through study completion, an average of 20 days.
Result of Pharmacokinetic endpoint
Timeframe: From Randomization through study completion, an average of 20 days
Result of Pharmacokinetic endpoint
Timeframe: From Randomization through study completion, an average of 20 days
Result of Pharmacokinetic endpoint
Timeframe: From Randomization through study completion, an average of 20 days