Geneva, Sept. 21 -- International Clinical Trials Registry received information related to the study (NCT07813039) titled 'A Phase 1 Relative Bioavailability Study of a VX-581 Tablet Formulation' on Sept. 4.
Study Type: Interventional
Study Design:
Allocation: Randomized. Intervention model: Crossover Assignment. Primary purpose: Treatment. Masking: None (Open Label).
Primary Sponsor: Vertex Pharmaceuticals Incorporated
Condition:
Cystic Fibrosis
Intervention:
Drug: VX-581
Recruitment Status: Not recruiting
Phase: Phase 1
Date of First Enrollment: September 7, 2026
Target Sample Size: 16
To know more, visit https://clinicaltrials.gov/study/NCT07813039
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