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Concert Pharma (CNCE) Announces Sale of VX-561 Milestones to Vertex (VRTX) for $32 Million
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Concert Pharmaceuticals Announces Sale of VX-561 Milestones to Vertex for $32 Million
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Vertex (VRTX) and CRISPR Therapeutics (CRSP) to Present New Clinical Data on Investigational CRISPR/Cas9 Gene-Editing Therapy CTX001 For Severe Hemoglobinopathies at EHA
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Vertex and CRISPR Therapeutics to Present New Clinical Data on Investigational CRISPR/Cas9 Gene-Editing Therapy CTX001™ For Severe Hemoglobinopathies at the Annual European Hematology Association Vi
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Vertex to Present at the Bank of America Securities 2021 Virtual Health Care Conference on May 13
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Vertex Reports First-Quarter 2021 Financial Results
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Vertex (VRTX) and CRISPR Therapeutics (CRSP) Announce PRIME Designation Granted by EMA to CTX001 for Transfusion-Dependent Beta Thalassemia
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Vertex and CRISPR Therapeutics Announce Priority Medicines (PRIME) Designation Granted by the European Medicines Agency to CTX001™ for Transfusion-Dependent Beta Thalassemia
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Vertex Announces NaV1.8 Inhibitor Advancing to Phase 2 Clinical Development
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Vertex Pharma (VRTX) and Obsidian Therapeutics Establish Collaboration to Discover Novel Therapies That Regulate Gene Editing
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Vertex and Obsidian Therapeutics Establish Collaboration to Discover Novel Therapies That Regulate Gene Editing
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Vertex Pharmaceuticals (VRTX) and CRISPR Therapeutics (CRSP) Amend Collaboration for Development, Manufacturing and Commercialization of CTX001 in Sickle Cell Disease and Beta Thalassemia
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Vertex Pharmaceuticals and CRISPR Therapeutics Amend Collaboration for Development, Manufacturing and Commercialization of CTX001™ in Sickle Cell Disease and Beta Thalassemia
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Vertex to Announce First-Quarter 2021 Financial Results on April 29
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Vertex Pharma (VRTX) Announces FDA Fast Track Designation and Initiation of a Phase 1/2 Clinical Trial for VX-880, a Novel Investigational Cell Therapy for the Treatment of Type 1 Diabetes
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Vertex Announces FDA Fast Track Designation and Initiation of a Phase 1/2 Clinical Trial for VX-880, a Novel Investigational Cell Therapy for the Treatment of Type 1 Diabetes
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Vertex to Present at the Cowen Health Care Conference on March 2
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Vertex Reports Full-Year and Fourth-Quarter 2020 Financial Results
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Vertex Pharma (VRTX) Announces FDA Clearance of IND Application for VX-880
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Vertex Announces FDA Clearance of Investigational New Drug (IND) Application for VX-880, a Novel Cell Therapy for the Treatment of Type 1 Diabetes (T1D)
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Vertex Pharma (VRTX) Announces U.S. FDA Acceptance of sNDA for TRIKAFTA in Children With Cystic Fibrosis Ages 6 through 11 With Certain Mutations
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Vertex Announces U.S. FDA Acceptance of Supplemental New Drug Application for TRIKAFTA® (elexacaftor/tezacaftor/ivacaftor and ivacaftor) in Children With Cystic Fibrosis Ages 6 through 11 With Certai
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Vertex to Announce Fourth-Quarter 2020 Financial Results on February 1
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Vertex Pharma (VRTX) Announces New Drug Submission for TRIKAFTA in Canada to Treat CF
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Vertex Announces New Drug Submission for Investigational Triple Combination Medicine for the Treatment of Cystic Fibrosis Has Been Accepted for Priority Review by Health Canada
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Skyhawk and Vertex Establish a Strategic Collaboration to Discover and Develop Novel Small Molecules that Modulate RNA Splicing for Serious Diseases
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Vertex (VRTX) Announces FDA Approvals of TRIKAFTA, SYMDEKO, and KALYDECO for Use in People With CF With Certain Rare Mutations
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Vertex Announces FDA Approvals of TRIKAFTA® (elexacaftor/tezacaftor/ivacaftor and ivacaftor), SYMDEKO® (tezacaftor/ivacaftor and ivacaftor) and KALYDECO® (ivacaftor) for Use in People With CF With
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CRISPR Therapeutics and Vertex Present New Data for Investigational CRISPR/Cas9 Gene-Editing Therapy, CTX001™ at American Society of Hematology Annual Meeting and Exposition, Together With Publicati
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CRISPR Therapeutics and Vertex to Host Investor Webcast to Review Data Presented at the 62nd American Society of Hematology Annual (ASH) Meeting and Exposition for Investigational CRISPR/Cas9 Gene-Edi
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Vertex (VRTX) Announces European Commission Approval for SYMKEVI With KALYDECO for Eligible Children With Cystic Fibrosis Ages 6-11 Years
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Vertex Announces European Commission Approval for SYMKEVI® (tezacaftor/ivacaftor) With KALYDECO® (ivacaftor) for Eligible Children With Cystic Fibrosis Ages 6-11 Years
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Vertex Recommends Rejection of ‘Mini-Tender’ Offer From TRC Capital Investment Corporation
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Vertex to Present at the Jefferies Virtual London Health Care Conference on November 19
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Vertex Pharma (VRTX) Reports European Commission Approval of Label Extension for KALYDECO (ivacaftor)
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Vertex Announces European Commission Approval for KALYDECO® (ivacaftor) as First and Only CFTR Modulator to Treat Eligible Infants With Cystic Fibrosis as Early as Four Months of Age
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CRISPR/Cas9 Gene-Editing Therapy CTX001™ for Severe Hemoglobinopathies Accepted for Plenary Presentation at the 62nd American Society of Hematology (ASH) Meeting and Exposition
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Vertex Reports Third-Quarter 2020 Financial Results
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Vertex to Announce Third-Quarter 2020 Financial Results on October 29
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Vertex Pharma (VRTX) has decided to stop dosing in trial and will discontinue development of VX-814
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Vertex Provides Update on its Clinical Programs Targeting Alpha-1 Antitrypsin Deficiency
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Vertex Pharma (VRTX) Announces FDA Approves KALYDECO as First and Only CFTR Modulator to Treat Eligible Infants With CF as Early as Four Months of Age
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FDA Approves KALYDECO® (ivacaftor) as First and Only CFTR Modulator to Treat Eligible Infants With CF as Early as Four Months of Age
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Vertex to Present New Data at European and North American Virtual Cystic Fibrosis Conferences Highlighting Long-Term Use of CFTR Modulators
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CRISPR Therapeutics (CRSP), Vertex Pharmaceuticals (VRTX) Announce PRIME Designation Granted by EMA to CTX001 for Treatment of Sickle Cell Disease
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CRISPR Therapeutics and Vertex Pharmaceuticals Announce Priority Medicines (PRIME) Designation Granted by the European Medicines Agency (EMA) to CTX001™ for the Treatment of Sickle Cell Disease
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Vertex Pharma (VRTX) Announces Positive Phase 3 Study for TRIKAFTA in Children Ages 6-11 Years With CF to Support Submissions for Global Regulatory Approvals
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Vertex Announces Positive Phase 3 Study for TRIKAFTA® (elexacaftor/tezacaftor/ivacaftor and ivacaftor) in Children Ages 6-11 Years With Cystic Fibrosis to Support Submissions for Global Regulatory Ap
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The Vertex Foundation Announces €1 Million Donation to Ronald McDonald House Charities at the New Children’s Hospital in Ireland
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Vertex Pharma (VRTX) Announces FDA Accepts its sNDA for TRIKAFTA, SYMDEKO and KALYDECO for Additional CFTR Mutations

