A Phase 1, Randomized, Double-blind, Placebo-controlled, Single- and Multiple-dose Escalation Study Evaluating the Safety, Pharmacokinetics, and Pharmacodynamics of VX-973 in Healthy Adults
Overview
- Phase
- Phase 1
- Intervention
- VX-973
- Conditions
- Pain
- Sponsor
- Vertex Pharmaceuticals Incorporated
- Enrollment
- 30
- Locations
- 1
- Primary Endpoint
- Part A: Safety and Tolerability as Assessed by Number of Participants With Adverse Events (AEs) and Serious Adverse Events (SAEs)
- Status
- Completed
- Last Updated
- 8 months ago
Overview
Brief Summary
The purpose of the study is to evaluate the safety, tolerability, pharmacokinetics, and pharmacodynamics of single and multiple doses of VX-973 in healthy participants.
Detailed Description
This clinical trial information was submitted voluntarily under the applicable law and, therefore, certain submission deadlines may not apply. (That is, clinical trial information for this applicable clinical trial was submitted under section 402(j)(4)(A) of the Public Health Service Act and 42 CFR 11.60 and is not subject to the deadlines established by sections 402(j)(2) and (3) of the Public Health Service Act or 42 CFR 11.24 and 11.44.).
Investigators
Eligibility Criteria
Inclusion Criteria
- •Body mass index (BMI) of 18.0 to 32.0 kilogram per meter square (kg/m\^2)
- •A total body weight of more than (\>) 50 kg
- •Participants of non-childbearing potential
- •Nonsmoker or ex-smoker for at least 3 months before screening
Exclusion Criteria
- •History of febrile illness or other acute illness that has not fully resolved within 14 days before the first dose of study drug
- •Any condition possibly affecting drug absorption, distribution, metabolism, or excretion
- •Other protocol defined Inclusion/Exclusion criteria may apply.
Arms & Interventions
Part A: Single Ascending Dose
Participants will be randomized to receive a single dose of VX-973 under fasted conditions.
Intervention: VX-973
Part B: Multiple Ascending Dose
Participants will be randomized to receive multiple doses of VX-973 under fasted conditions.
Intervention: VX-973
Placebo Part A
Participants will be randomized to receive placebo matched to VX-973.
Intervention: Placebo
Placebo Part B
Participants will be randomized to receive placebo matched to VX-973.
Intervention: Placebo
Outcomes
Primary Outcomes
Part A: Safety and Tolerability as Assessed by Number of Participants With Adverse Events (AEs) and Serious Adverse Events (SAEs)
Time Frame: From Day -1 up to Day 30
Part B: Safety and Tolerability as Assessed by Number of Participants With Adverse Events (AEs) and Serious Adverse Events (SAEs)
Time Frame: From Day -1 up to Day 85
Secondary Outcomes
- Part A: Maximum Observed Plasma Concentration (Cmax) of VX-973(From Day 1 up to Day 30)
- Part B: Maximum Observed Plasma Concentration (Cmax) of VX-973(From Day 1 up to Day 85)
- Part A: Area Under the Concentration Versus Time Curve (AUC) of VX-973(From Day 1 up to Day 30)
- Part B: Area Under the Concentration Versus Time Curve (AUC) of VX-973(From Day 1 up to Day 85)
- Part A: Time Taken for VX-973 to Reach Maximum Concentration (tmax)(From Day 1 up to Day 30)
- Part B: Time Taken for VX-973 to Reach Maximum Concentration (tmax)(From Day 1 up to Day 85)
- Part B: Pain Tolerance Threshold (PTT) for the Cold Pressor Test(From Day 1 up to Day 53)