NCT05347394

A Phase 1 Dose Escalation Study of Oral VX-708 in Healthy Participants

A Phase 1, Randomized, Double-blind, Placebo-controlled, Single- and Multiple-dose Escalation Study Evaluating the Safety, Pharmacokinetics, and Pharmacodynamics of Oral VX-708 in Healthy Subjects

• Status: Completed
• Phase: Phase 1
• Study type: Interventional
• Enrollment: 100 (actual)
• Sponsor: Vertex Pharmaceuticals Incorporated · Industry
• Sex: All
• Age: 18 Years – 55 Years
• Healthy volunteers: Accepted

Summary

The purpose of this study is to evaluate the safety, tolerability, pharmacokinetics, and pharmacodynamics of single and multiple ascending doses of VX-708 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.).

Conditions

• Acute Pain

Interventions

Type	Name	Description
DRUG	VX-708	Solution or suspension for oral administration.
DRUG	Placebo	Placebo matched to VX-708 for oral administration.

Timeline

• Start date: 2022-04-08
• Primary completion: 2023-04-14
• Completion: 2023-04-14
• First posted: 2022-04-26
• Last updated: 2023-05-15

Locations

1 site across 1 country: United Kingdom

Regulatory

• FDA-regulated drug study