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NCT07349394CompletedPhase 1

Effect of Vanzacaftor/Tezacaftor/Deutivacaftor (VNZ/TEZ/D-IVA) on the PK of Rosuvastatin in Healthy Participants

A Phase 1, Open-label, Drug-Drug Interaction Study to Evaluate the Effect of Multiple Doses of Vanzacaftor/Tezacaftor/Deutivacaftor on the Pharmacokinetics of Rosuvastatin in Healthy Subjects

Source: ClinicalTrials.gov · Last updated 2 Apr 2026

Brief summary (registry, in English)

The purpose of this study is to evaluate the effect of multiple doses of vanzacaftor/tezacaftor/deutivacaftor (VNZ/TEZ/D-IVA) on the PK of rosuvastatin and the safety and tolerability of coadministration of VNZ/TEZ/D-IVA with rosuvastatin.

Status (registry)
Completed
Phase (registry)
Phase 1
Study type
Interventional
Enrollment
18 (actual)
First submitted
8 Jan 2026
Start date
Jan 2026
Primary completion date
Feb 2026
Lead sponsor
Vertex Pharmaceuticals Incorporated
NCT number
NCT07349394

What you commit to

  • Study type: Interventional · Phase 1
  • Participants enrolled: 18
  • From Jan 2026 to the primary completion date, Feb 2026
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • History of febrile illness within 5 days before the first dose of study drug
  • Female participants who are pregnant, nursing, or planning to become pregnant during the study or within 90 days after the last dose of the study drug
  • Male participants with a female partner who is pregnant, nursing, or planning to become pregnant during the study or within 90 days after the last dose of the study drug
    • Other protocol defined Inclusion/Exclusion criteria may apply.

Other illness

  • Any condition possibly affecting drug absorption

Who the study is looking for

  • Body mass index (BMI) of 18.0 to 32.0 kilogram per meter square (Kg/m\^2), both inclusive
  • A total body weight greater than (\>)50 kg

Age in the registry: 18 years to 55 years · Sex: All · Accepts healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Altasciences - Kansas City
Coordinator of this site? Confirm its status
Overland ParkUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.