A Single-arm Study to Evaluate Safety and Effectiveness of VX-548 for Acute Pain

Vertex Pharmaceuticals

Status and phase

Completed

Phase 3

Conditions

Pain

Treatments

Drug: VX-548

Study type

Interventional

Funder types

Industry

Identifiers

VX22-548-107

Details and patient eligibility

About

The purpose of this study is to evaluate the safety and effectiveness of VX-548 in treating acute pain.

Enrollment

258 patients

Sex

All

Ages

18 to 80 years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

Key Inclusion Criteria:

Body mass index (BMI) of greater than or equal to (≥) 18.0 to less than (<) 40.0 kilogram per meter square (kg/m^2)
Non-surgical participants with pain of new origin (not related to a prior known condition) that is moderate or severe on the verbal categorical rating scale (VRS) and ≥4 on the numeric pain rating scale (NPRS)
Surgical participants reporting pain at the surgical site that is moderate or severe on the VRS and ≥4 on the NPRS

Key Exclusion Criteria:

Surgical participants:
- History of previous surgery due to the same condition, except for procedures for which a previous surgery on the contra-lateral limb or organ is allowed
- History of a prior surgical procedure in the same region of the body that resulted in any perioperative complications or that, in the opinion of the investigator or medical monitor, would preclude participation in the study
History of any illness or any clinical condition that, in the opinion of the investigator, might confound the results of the study or pose an additional risk in administering study drug to the participant

Other protocol defined Inclusion/Exclusion criteria may apply.