About this trial
The purpose of the study is to evaluate the safety, tolerability, pharmacokinetics, and pharmacodynamics of VX-670 at different single and multiple doses in participants with DM1.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
None
Disqualifiers
None
Trial design
Sequential
Treatments tested in this trial
VX-670
DrugSolution for intravenous administration.
Placebo
DrugSolution for intravenous administration.
Treatment groups
Trial outcomes
Primary outcomes
Parts A and B: Safety and Tolerability as Assessed by Number of Participants With Adverse Events (AEs)
Secondary outcomes
Part A: Maximum Observed Concentration (Cmax) of VX-670 and its Active Component in Plasma
Part A: Area Under the Concentration Versus Time Curve (AUC) of VX-670 and its Active Component in Plasma
Part B: Maximum Observed Concentration (Cmax) of VX-670 and its Active Component in Plasma After Each Dose
Part B: Area Under the Concentration Versus Time Curve (AUC) of VX-670 and its Active Component in Plasma After Each Dose
Sponsors and contacts
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