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Vertex Pharma (VRTX) Reports New Data from VX-880 Phase 1/2 Trial
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Vertex Presents New Data from VX-880 Phase 1/2 Clinical Trial at the American Diabetes Association 82nd Scientific Sessions
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Vertex Pharma (VRTX), CRISPR Therapeutics (CRSP) Announce Acceptance of Late-Breaking Abstract for CTX001 at EHA
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Vertex and CRISPR Therapeutics Announce Acceptance of Late-Breaking Abstract for CTX001™ at the 2022 Annual European Hematology Association (EHA) Congress
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Vertex to Present New Data on VX-880 Clinical Trial at 82nd American Diabetes Association Annual Conference
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Vertex Pharma (VRTX) Appoints Suketu Upadhyay to its Board
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Suketu Upadhyay Elected to Vertex Board of Directors
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Vertex Announces Further Expansion in the Boston Seaport at Dedication of the Jeffrey Leiden Center for Cell and Genetic Therapies
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Vertex Announces $50 Million Commitment to Health Equity With Three Initial Grants
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Vertex Reports First Quarter 2022 Financial Results
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Vertex Pharma (VRTX) Issues Update on Phase 1/2 Clinical Trial of VX-880
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Vertex Provides Updates on Phase 1/2 Clinical Trial of VX-880 for the Treatment of Type 1 Diabetes
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Vertex to Announce First Quarter 2022 Financial Results on May 5
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Health Canada Grants Marketing Authorization for TRIKAFTA® (elexacaftor/tezacaftor/ivacaftor and ivacaftor) in Children With Cystic Fibrosis Ages 6 Through 11 years With At Least One F508del Mutation
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Vertex Announces Statistically Significant and Clinically Meaningful Results From Two Phase 2 Proof-of-Concept Studies of VX-548 for the Treatment of Acute Pain
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Vertex Announces Reimbursement Agreement in Australia for TRIKAFTA® (elexacaftor/tezacaftor/ivacaftor and ivacaftor) for Patients With Cystic Fibrosis Ages 12 Years and Older With at Least One F508de
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Vertex Pharma (VRTX) Advances VX-147 Into Pivotal Clinical Development for People With APOL1-Mediated Kidney Disease
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Vertex Advances VX-147 Into Pivotal Clinical Development for People With APOL1-Mediated Kidney Disease
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Vertex to Present at Cowen’s 42nd Annual Health Care Conference on March 8
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Vertex Reports Fourth Quarter 2021 and Full Year Financial Results
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Vertex to Announce Fourth Quarter 2021 Financial Results on January 26
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Vertex Pharma (VRTX) Announces EU Approval of KAFTRIO in Combination With Ivacaftor to Treat Children With Cystic Fibrosis Ages 6 to 11 Years
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European Commission Approves KAFTRIO® (ivacaftor/tezacaftor/elexacaftor) in Combination With Ivacaftor to Treat Children With Cystic Fibrosis Ages 6 to 11 Years
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Vertex to Present at the 40th Annual J.P. Morgan Healthcare Conference on January 10
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Vertex Pharma (VRTX) Announces Positive Results From Phase 2 Study of VX-147 in APOL1-Mediated Focal Segmental Glomerulosclerosis
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Vertex Announces Positive Results From Phase 2 Study of VX-147 in APOL1-Mediated Focal Segmental Glomerulosclerosis
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Vertex Pharma (VRTX) Enters Reimbursement Agreement in Spain for KAFTRIO in Combination With Ivacaftor
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Vertex Announces Reimbursement Agreement in Spain for KAFTRIO® (ivacaftor/tezacaftor/elexacaftor) in Combination With Ivacaftor to Treat People With Cystic Fibrosis 12 Years and Older With At Least O
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Vertex Pharma (VRTX) Announces Positive CHMP Opinion for KAFTRIO in Combination With Ivacaftor in Children With Cystic Fibrosis Ages 6 Through 11
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Vertex Receives CHMP Positive Opinion for KAFTRIO® (ivacaftor/tezacaftor/elexacaftor) in Combination With Ivacaftor in Children With Cystic Fibrosis Ages 6 Through 11
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Vertex Reports Third-Quarter 2021 Financial Results
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Vertex and Mammoth Biosciences Announce Collaboration to Develop In Vivo Gene-Editing Therapies for Serious Diseases
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Vertex to Announce Third-Quarter 2021 Financial Results on November 2
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Vertex Pharma (VRTX) to Present Long-Term Data Demonstrating Significant Benefits of Treatment With CFTR Modulators at North American Cystic Fibrosis Conference
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Vertex to Present Long-Term Data Demonstrating Significant Benefits of Treatment With CFTR Modulators at North American Cystic Fibrosis Conference (NACFC)
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Vertex Pharma (VRTX) Reports Positive Day 90 Data for the First Patient in the Phase 1/2 Clinical Trial Dosed With VX-880
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Vertex Announces Positive Day 90 Data for the First Patient in the Phase 1/2 Clinical Trial Dosed With VX-880, a Novel Investigational Stem Cell-Derived Therapy for the Treatment of Type 1 Diabetes
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Vertex to Present at the Morgan Stanley Virtual 19th Annual Global Healthcare Conference on September 15th
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Vertex Announces Publication in The New England Journal of Medicine of Phase 3 Results for TRIKAFTA® (elexacaftor/tezacaftor/ivacaftor and ivacaftor) in People With Cystic Fibrosis
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Vertex and Arbor Biotechnologies Establish New Partnership to Develop Novel ex vivo Engineered Cell Therapies
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Vertex Pharma (VRTX) Appoints Stuart A. Arbuckle as Chief Operating Officer
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Vertex Appoints Stuart A. Arbuckle as Chief Operating Officer
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Vertex Reports Second-Quarter 2021 Financial Results
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Vertex to Initiate Phase 3 Development Program for New Once-Daily Triple Combination Regimen in People With Cystic Fibrosis
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Vertex Initiates Phase 2 Clinical Trial Program for VX-548 for the Treatment of Acute Pain
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Vertex to Announce Second-Quarter 2021 Financial Results on July 29
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Vertex and CRISPR Therapeutics Present New Data in 22 Patients With Greater Than 3 Months Follow-Up Post-Treatment With Investigational CRISPR/Cas9 Gene-Editing Therapy, CTX001™ at European Hematolo
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Vertex Pharma (VRTX) Announces U.S. FDA Approval for TRIKAFTA in Children With Cystic Fibrosis Ages 6 through 11 With Certain Mutations
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Vertex Announces U.S. FDA Approval for TRIKAFTA® (elexacaftor/tezacaftor/ivacaftor and ivacaftor) in Children With Cystic Fibrosis Ages 6 through 11 With Certain Mutations
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CORRECTING and REPLACING Vertex Announces U.S. FDA Approval for TRIKAFTA® (elexacaftor/tezacaftor/ivacaftor and ivacaftor) in Children With Cystic Fibrosis Ages 6 through 11 With Certain Mutations

