Pipeline — registered trials by phase
A Study of the Effects of Lumacaftor/Ivacaftor (LUM/IVA) on Exercise Tolerance in Subjects With Cystic Fibrosis (CF), Homozygous for the F508del-CFTR Mutation
— · Cystic Fibrosis · Completed · est. 2017-09
Evaluation of Pain Treatment After Total Knee Arthroplasty
— · Pain · Recruiting · est. 2027-01-30
A Phase 1, Open-label Study Evaluating the Pharmacokinetics and Drug-drug Interaction of VX-993 in Healthy Adults
— · Pain · Completed · est. 2024-07-02
A Phase 1 Relative Bioavailability Study of a VX-581 Tablet Formulation
— · Cystic Fibrosis · Not Yet Recruiting · est. 2026-10-27
A Microneurography (MNG) Study of VX-150 in Healthy Participants
— · Pain · Completed · est. 2022-09-14
A Phase 1 Study Evaluating the Safety, Pharmacokinetics, and Pharmacodynamics, of VX-993
— · Pain · Completed · est. 2024-06-12
A Phase 1 Study to Examine the Drug-Drug Interaction of Ciprofloxacin, Itraconazole, and Rifampin on the Combination of Lumacaftor With Ivacaftor in Healthy Adult Subjects
— · Cystic Fibrosis · Completed · est. 2013-09
Absorption, Distribution, Metabolism, and Excretion of 14C-VX-407 After a Single Oral Dose
— · Autosomal Dominant Polycystic Kidney Disease (ADPKD) · Not Yet Recruiting · est. 2026-12-15
Evaluation of the Effects of Omeprazole and Rifampin on the Pharmacokinetics of VX-548 in Healthy Participants
— · Pain · Completed · est. 2023-06-08
A Study Evaluating Safety and Pharmacokinetics of VX-440 in Combination With Tezacaftor/Ivacaftor in Healthy Adult Subjects
— · Cystic Fibrosis · Completed · est. 2016-09-14
An Open-Label, Phase 1 Study in Healthy Adult Subjects to Examine the Effects of Multiple-Dose Ciprofloxacin on Ivacaftor and VX-661 in Combination With Ivacaftor
— · Cystic Fibrosis · Completed · est. 2014-02
Drug-Drug Interaction Study Between Telaprevir and Buprenorphine
— · Hepatitis C, Opioid-Related Disorders · Completed · est. 2011-04
Drug-Drug Interaction Study of VX-809 and VX-770 in Healthy Subjects
— · Cystic Fibrosis · Completed · est. 2009-12
A Study to Assess the Relative Bioavailability Three New Formulations of Telaprevir in Healthy Subjects
— · Chronic Hepatitis C · Completed · est. 2012-06
Study of VX-770 on Desipramine
— · In Development for Cystic Fibrosis · Completed · est. 2010-08
A Study of Vanzacaftor/Tezacaftor/Deutivacaftor (VNZ/TEZ/D-IVA) in Healthy Adult Panelists
— · Cystic Fibrosis · Completed · est. 2024-04-16
A Phase 1 Dose Escalation Study of VX-993 in Healthy Participants
— · Pain · Completed · est. 2023-09-12
A Phase 1 Dose Escalation Study of VX-708 in Healthy Participants
— · Pain · Completed · est. 2023-03-07
A Phase 1, First-in-human Study of VX-634
— · Alpha 1-Antitrypsin Deficiency · Completed · est. 2023-05-24
A Phase 1 Dose Escalation Study to Evaluate Safety and Pharmacokinetics (PK) of VX-840 in Healthy Participants
— · APOL1-mediated Kidney Disease · Completed · est. 2022-11-07
A Study to Examine the Effects of Telaprevir on the Pharmacokinetics of Cyclosporine and Tacrolimus in Healthy Adults
— · Hepatitis C · Completed · est. 2010-04
A Phase 1 Study to Investigate the Food Effect of Lumacaftor in Combination With Ivacaftor
— · Cystic Fibrosis · Completed · est. 2013-08
A Study of Suzetrigine (SUZ) Spray-dried Dispersion (SSD) in Healthy Adult Panelists
— · Pain · Completed · est. 2025-04-24
Drug-Drug Interaction Study of VCH-222 and Telaprevir in Healthy Subjects
— · Hepatitis C · Completed · est. 2010-01
A Study to Evaluate the Relative Bioavailability of a Fixed-dose Combination Tablet of VX-121/Tezacaftor/Deutivacaftor
— · Cystic Fibrosis · Completed · est. 2022-11-09
A Phase 1 Study Evaluating Safety, Tolerability, and Pharmacokinetics of VX-407 in Healthy Participants
— · Autosomal Dominant Polycystic Kidney Disease (ADPKD) · Completed · est. 2026-02-24
Evaluation of Efficacy and Safety of VX-993 for Pain Associated With Diabetic Peripheral Neuropathy
— · Diabetic Peripheral Neuropathic Pain · Recruiting · est. 2027-03-25
A Study to Evaluate the Effect of VX-661 in Combination With Ivacaftor on Chest Imaging Endpoints in Subjects With Cystic Fibrosis, Homozygous for the F508del CFTR Mutation
— · Cystic Fibrosis · Completed · est. 2018-07
Phase 2a Study of VX-407 in Participants With ADPKD Who Have a Subset of PKD1 Gene Variants (AGLOW)
— · Autosomal Dominant Polycystic Kidney Disease (ADPKD) · Active Not Recruiting · est. 2027-07-22
A 12-week Study of 4 Doses of VX-509 in Subjects With Active Rheumatoid Arthritis
— · Rheumatoid Arthritis · Completed · est. 2011-07
A Phase 1/2 Study of VX-522 in Participants With Cystic Fibrosis (CF)
— · Cystic Fibrosis · Completed · est. 2026-04-21
A Study to Evaluate Efficacy and Safety of VX-150 in Subjects With Acute Pain Following Bunionectomy
— · Acute Pain · Completed · est. 2017-12-01
Phase 2 Study of VX-950, Pegasys® With and Without Copegus® in Hepatitis C
— · Chronic Hepatitis C · Completed · est. 2008-05
Safety Study of Ivacaftor in Subjects With Cystic Fibrosis
— · Cystic Fibrosis · Completed · est. 2008-08
Evaluation of the Efficacy and Safety of VX-864 in Subjects With the PiZZ Genotype
— · Alpha1-Antitrypsin Deficiency · Completed · est. 2021-05-04
A Safety, Tolerability, and Efficacy Study of VX-264 in Participants With Type 1 Diabetes
— · Type 1 Diabetes · Active Not Recruiting · est. 2027-03-12
A Study to Investigate VX-787 Given to Adult Volunteers Inoculated With Live Influenza Virus
— · Influenza Virus · Completed · est. 2012-10
Study of VX-121 in Healthy Subjects and in Subjects With Cystic Fibrosis
— · Cystic Fibrosis · Completed · est. 2019-05-03
A Proof-of-concept Study of VCH-759 for the Treatment of Hepatitis C-infection.
— · Hepatitis C, Chronic · Completed
A Study Evaluating Efficacy and Safety of VX-548 for Acute Pain After an Abdominoplasty
— · Acute Pain · Completed · est. 2021-12-05
A Phase 2 Study to Evaluate Effects of VX-661/Ivacaftor on Lung and Extrapulmonary Systems in Subjects With Cystic Fibrosis, Homozygous for the F508del-CFTR Mutation
— · Cystic Fibrosis · Completed · est. 2017-06
A Study to Evaluate the Safety and Efficacy of VX-121 Combination Therapy in Subjects With Cystic Fibrosis
— · Cystic Fibrosis · Completed · est. 2019-12-10
Inaxaplin in Participants With Proteinuric APOL1 Mediated Kidney Disease With or Without Comorbidities
— · Proteinuric Kidney Disease · Completed · est. 2026-07-20
Phase 2a Study of VX-147 in Adults With APOL1-mediated Focal Segmental Glomerulosclerosis
— · Glomerulosclerosis, Focal Segmental · Completed · est. 2021-11-11
A Study to Evaluate the Efficacy and Safety of Quadruple Therapy (VX-222, Telaprevir,Peginterferon-Alfa-2a, Ribavirin) in Subjects With Chronic Hepatitis C With Compensated Cirrhosis
— · Chronic Hepatitis C Virus · Completed · est. 2013-09
A Study of the Efficacy and Safety of VX-150 in Subjects With Osteoarthritis of the Knee
— · Osteoarthritis · Completed · est. 2016-08
24-week Study With Open Label Extension of VX-509, an Oral JAK3 Inhibitor, in Subjects Taking Methotrexate
— · Rheumatoid Arthritis · Completed · est. 2014-07
A Phase 3 Study of Tezacaftor (VX-661) in Combination With Ivacaftor (VX-770) in Subjects Aged 12 Years and Older With Cystic Fibrosis (CF), Who Have One F508del-CFTR Mutation and a Second Mutation That Has Been Demonstrated to be Clinically Responsive to Ivacaftor
— · Cystic Fibrosis · Completed · est. 2017-09
Safety and Pharmacokinetic Study of Lumacaftor/Ivacaftor in Participants 1 to Less Than 2 Years of Age With Cystic Fibrosis, Homozygous for F508del
— · Cystic Fibrosis · Completed · est. 2021-10-29
Safety and Pharmacokinetic Study of Lumacaftor/Ivacaftor in Subjects Aged 2 Through 5 Years With Cystic Fibrosis, Homozygous for F508del
— · Cystic Fibrosis · Completed · est. 2017-09
Study of Ivacaftor in Subjects With Cystic Fibrosis (CF) Who Have the R117H-CF Transmembrane Conductance Regulator (CFTR) Mutation (KONDUCT)
— · Cystic Fibrosis · Completed · est. 2013-10
A Study to Evaluate Efficacy of Ivacaftor in Subjects With Cystic Fibrosis Who Have a 3849 + 10KB C→T or D1152H CFTR Mutation
— · Cystic Fibrosis · Completed · est. 2018-12-18
A Study Evaluating the Long-term Safety of VX-445 Combination Therapy
— · Cystic Fibrosis · Completed · est. 2022-12-14
Evaluation of Efficacy, Safety, and Tolerability of Povetacicept in Participants With Primary Membranous Nephropathy (pMN)
— · Primary Membranous Nephropathy · Recruiting · est. 2028-12-29
Evaluation of Efficacy and Safety of VX-548 for Acute Pain After a Bunionectomy
— · Acute Pain · Completed · est. 2023-12-15
A Study to Evaluate the Safety and Efficacy of Long-term Treatment With TEZ/IVA in CF Participants With an F508del CFTR Mutation
— · Cystic Fibrosis · Completed · est. 2020-10-28
A Rollover Safety Study of Lumacaftor/Ivacaftor in Subjects Aged 2 Years and Older With Cystic Fibrosis, Homozygous for the F508del-CFTR Mutation
— · Cystic Fibrosis · Completed · est. 2019-07-17
Evaluation of Long-term Safety and Efficacy of ELX/TEZ/IVA TC Combination Therapy in Participants With Cystic Fibrosis Who Are 6 Years of Age and Older
— · Cystic Fibrosis · Completed · est. 2024-02-24
Evaluation of Long-term Safety and Efficacy of ELX/TEZ/IVA in Cystic Fibrosis (CF) Participants 2 Years and Older
— · Cystic Fibrosis · Completed · est. 2026-01-29
A Phase 2/3 Open-label Extension Study to Evaluate Long-Term Safety and Efficacy With VX-509 in Subjects With Rheumatoid Arthritis
— · Rheumatoid Arthritis · Completed · est. 2014-07
Roll-Over Study of Ivacaftor in Cystic Fibrosis Pediatric Subjects With a CF Transmembrane Conductance Regulator Gene (CFTR) Gating Mutation
— · Cystic Fibrosis · Completed · est. 2015-12
A Phase 3 Rollover Study of Lumacaftor in Combination With Ivacaftor in Subjects 12 Years and Older With Cystic Fibrosis
— · Cystic Fibrosis, Homozygous or Heterozygous for the F508del-CFTR Mutation · Completed · est. 2016-04
A Randomized, Double-Blind, Placebo-Controlled, Parallel-Group Study to Evaluate the Efficacy and Safety of VX-661 in Combination With Ivacaftor
— · Cystic Fibrosis · Completed · est. 2017-01-20
Evaluation of Efficacy and Safety of Elexacaftor/Tezacaftor/Ivacaftor (ELX/TEZ/IVA) in Cystic Fibrosis Subjects Without an F508del Mutation
— · Cystic Fibrosis · Completed · est. 2023-07-05
A Study Evaluating the Long-term Safety and Efficacy of VX-121 Combination Therapy
— · Cystic Fibrosis · Active Not Recruiting · est. 2026-10-30
Evaluation of Efficacy and Safety of Suzetrigine for Acute Pain After an Abdominoplasty
— · Acute Pain · Completed · est. 2023-08-25
Evaluation of Efficacy and Safety of Suzetrigine for Pain Associated With Diabetic Peripheral Neuropathy
— · Diabetic Peripheral Neuropathic Pain · Recruiting · est. 2027-05-31
A Study Evaluating the Long-term Safety and Efficacy of VX-445 Combination Therapy
— · Cystic Fibrosis · Completed · est. 2023-01-09
Long-term Safety of Lumacaftor/Ivacaftor in Participants With Cystic Fibrosis Who Are Homozygous for F508del and 12 to <24 Months of Age at Treatment Initiation
— · Cystic Fibrosis · Completed · est. 2023-08-22
A Study to Evaluate the Efficacy and Safety of Lumacaftor in Combination With Ivacaftor in Subjects With CF, Homozygous for the F508del-CFTR Mutation
— · Cystic Fibrosis · Completed · est. 2016-09
A Study to Evaluate the Safety of Long-term Ivacaftor Treatment in Participants With Cystic Fibrosis Who Are Less Than 24 Months of Age at Treatment Initiation and Have an Approved Ivacaftor-Responsive Mutation
— · Cystic Fibrosis · Completed · est. 2023-10-02
A Phase 3 Study of VX-445 Combination Therapy in Cystic Fibrosis (CF) Subjects Heterozygous for F508del and a Gating or Residual Function Mutation (F/G and F/RF Genotypes)
— · Cystic Fibrosis · Completed · est. 2020-06-12
No approved products listed under this sponsor in Drugs@FDA (partnered or subsidiary products may be listed elsewhere).
Source: ClinicalTrials.gov (trials where Vertex is lead sponsor; 82 active or completed) and Drugs@FDA (0 approved products). Registry data can include older or partnered programs; the company's own pipeline page is the official list.
SEC filings — insider trading forms excluded
- 8-K2026-09-01Current report (material event)
- 10-Q2026-08-04Quarterly report
- 8-K2026-08-03Current report (material event)
- 8-K2026-07-07Current report (material event)
- SCHEDULE 13G/A2026-05-14SCHEDULE 13G/A
- SCHEDULE 13G/A2026-05-14SCHEDULE 13G/A
- S-8 POS2026-05-13S-8 POS
- S-8 POS2026-05-13S-8 POS
- S-8 POS2026-05-13S-8 POS
- S-8 POS2026-05-13S-8 POS
- S-8 POS2026-05-13S-8 POS
- S-8 POS2026-05-13S-8 POS
- S-8 POS2026-05-13S-8 POS
- S-82026-05-13Employee stock plan
- 8-K2026-05-13Current report (material event)
- 10-Q2026-05-05Quarterly report
- 8-K2026-05-04Current report (material event)
- SCHEDULE 13G2026-04-30SCHEDULE 13G
- DEFA14A2026-04-29DEFA14A
- 8-K2026-04-29Current report (material event)
- UPLOAD2026-04-14UPLOAD
- ARS2026-04-02Annual report to holders
- DEFA14A2026-04-02DEFA14A
- DEF 14A2026-04-02Proxy statement
- CORRESP2026-04-01CORRESP
- 8-K2026-03-31Current report (material event)
- SCHEDULE 13G/A2026-03-27SCHEDULE 13G/A
- UPLOAD2026-03-18UPLOAD
- 10-K2026-02-13Annual report
- 8-K2026-02-12Current report (material event)
- SCHEDULE 13G/A2026-02-12SCHEDULE 13G/A
- 10-Q2025-11-04Quarterly report
- 8-K2025-11-03Current report (material event)
- 10-Q2025-08-05Quarterly report
- 8-K2025-08-04Current report (material event)
- 8-K2025-05-19Current report (material event)
- 8-K2025-05-14Current report (material event)
- SCHEDULE 13G2025-05-13SCHEDULE 13G
- UPLOAD2025-05-07UPLOAD
- 10-Q2025-05-06Quarterly report
Source: SEC EDGAR. Forms 3/4/5 and 144 (insider transactions) are intentionally left out.