Ozmosi | Vanzacaftor Drug Profile
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Vanzacaftor

Pronounced as: van-ZA-kaf-tor

Alternative Names: Vanzacaftor, vx-121, vx121, vx 121
Clinical Status: Active
Latest Update: 2026-05-30
Latest Update Note: Clinical Trial Update

Product Description

Vertex is developing VX-121 as a treatment for cystic fibrosis. (Sourced from: https://investors.vrtx.com/news-releases/news-release-details/vertex-initiate-phase-3-development-program-new-once-daily)

Mechanisms of Action: CFTR Modulator

Novel Mechanism: No

Modality: Small Molecule

Route of Administration: Oral

FDA Designation: *

Approval Status: Not Approved

Approved Countries: None

Approved Indications: None

Company: Vertex
Company Location: Eastern America
Company Founding Year: 1989
Additional Commercial Interests: None

Clinical Description

Map of Global Clinical Trials for Vanzacaftor

Countries in Clinic: Australia, Austria, Belgium, Canada, Czech Republic, Denmark, France, Germany, Greece, Hungary, Ireland, Israel, Italy, Netherlands, New Zealand, Norway, Poland, Portugal, Spain, Sweden, Switzerland, United Kingdom, United States

Active Clinical Trial Count: 11

Recent & Upcoming Milestones

  • Clinical Outcomes Reported - Vertex presented P3 Cystic Fibrosis results on 2026-06-05 for Vanzacaftor
  • Clinical Outcomes Reported - Vertex presented P3 Cystic Fibrosis results on 2025-06-04 for Vanzacaftor
  • Clinical Outcomes Reported - Vertex presented P3 Cystic Fibrosis results on 2024-09-27 for Vanzacaftor

Highest Development Phases

Phase 3: Cystic Fibrosis

Trial ID

Trial

Phase

Trial Status

Disease

Primary Completion Date

Probability of Success

Latest Trial Update Date

Data Updated

NCT07349394

VX25-121-014

P1

Completed

Cystic Fibrosis

2026-02-28

50%

2026-04-03

Primary Completion Date|Primary Endpoints|Study Completion Date|Treatments|Trial Status

NCT06299709

VNZ/TEZ/D-IVA

P1

Completed

Cystic Fibrosis

2024-05-23

12%

2024-07-23

Primary Completion Date|Primary Endpoints|Study Completion Date|Treatments|Trial Status

NCT06299696

VX23-121-011

P1

Completed

Cystic Fibrosis

2024-04-16

12%

2024-05-17

Primary Completion Date|Primary Endpoints|Study Completion Date|Treatments|Trial Status

2018-002496-18

2018-002496-18

P2

Active, not recruiting

Cystic Fibrosis

2019-11-02

2022-03-13

Treatments

NCT05422222

VX21-121-105

P3

Active, not recruiting

Cystic Fibrosis

2030-06-30

32%

2026-05-29

NCT05844449

VX22-121-106

P3

Enrolling by invitation

Cystic Fibrosis

2029-07-30

6%

2025-05-08

2024-514173-22-00

VX20-121-104

P3

Active, not recruiting

Cystic Fibrosis

2027-04-16

35%

2025-05-02

2024-513754-29-00

VX21-121-105

P3

Not yet recruiting

Cystic Fibrosis

2027-08-02

32%

2025-05-02

Treatments

NCT05444257

VX20-121-104

P3

Active, not recruiting

Cystic Fibrosis

2026-10-30

35%

2025-09-06

Primary Completion Date|Primary Endpoints|Study Completion Date|Treatments

2022-503081-74-00

VX22-121-106

P3

Recruiting

Cystic Fibrosis

2025-10-31

6%

2025-05-02

Treatments

2021-000712-31

2021-000712-31

P3

Active, not recruiting

Cystic Fibrosis

2024-03-18

2022-03-13