Suzetrigine
DrugTablets for oral administration.
Other names: VX-548, SUZ, Journavx
NCT Number: NCT06887959
The purpose of this study is to evaluate the effectiveness, safety, and tolerability of SUZ for acute pain after laparoscopic procedures of the intraperitoneal or retroperitoneal cavities or arthroscopic orthopedic procedures.
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Notify Me18 year and older
All sexes
Interventional
Phase 4
Scottsdale Clinical Trials, Scottsdale, Arizona, United States
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Key Inclusion Criteria:
Key Exclusion Criteria:
-Participated in previous study with Suzetrigine or received Journavx
Other protocol defined Inclusion/Exclusion criteria will apply.
Tablets for oral administration.
Other names: VX-548, SUZ, Journavx
Time frame: From Day 3 up to Day 14
Vertex Pharmaceuticals Incorporated
Industry
A Phase 4, Open-label, Single-arm Study Evaluating the Effectiveness and Safety of Suzetrigine As Part of Multimodal Therapy for Acute Pain After Laparoscopic Procedures of the Intraperitoneal or Retroperitoneal Cavities or Arthroscopic Orthopedic Procedures
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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