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Date Title and Summary Additional Formats
Toggle Summary Telaprevir Data Presented at EASL Show Unprecedented SVR Rates in HCV Treatment-Failure Patients in PROVE 3 Study
<i>- Superior SVR rates with telaprevir across all HCV genotype 1 non-responders and relapser patients and patients with cirrhosis - up to 76% in prior relapsers -</i><i>- PROVE 3 showed 51% and 52% SVR rates in telaprevir-based regimens compared to 14% in the 48-week control arm</i><i>-</i><i>- Treatment-failure patient population represents the greatest unmet medical need in HCV -</i>
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Toggle Summary Vertex Pharmaceuticals to Present Data at EASL Suggesting Telaprevir's Potential for Use in a Broad Range of HCV Patients and Highlighting the Company's Expanded STAT-C Portfolio
<i>-PROVE 3 results to be presented at late breaker session on Saturday, April 25, 2009-</i><i>-Interim data from two Phase 2 studies of telaprevir indicate activity across multiple genotypes in treatment-naïve HCV patients-</i><i>-Early data from newly-acquired polymerase inhibitors suggest rapid, powerful antiviral activity with favorable safety and tolerability profile-</i>
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Toggle Summary Vertex Pharmaceuticals Reviews First Quarter Business Progress and Reports First Quarter 2009 Financial Results
<i>- Telaprevir registration program on track; VCH-222 enters multi-dose, 3-day viral kinetic study -</i><i>- VX-770 will start registration program in CF patients with G551D mutation -</i><i>-Vertex ends first quarter with $869 million of cash, cash equivalents and marketable securities-</i>
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Toggle Summary Vertex Pharmaceuticals Announces the Date of its First Quarter 2009 Financial Results Conference Call and Webcast
CAMBRIDGE, Mass., Apr 03, 2009 (BUSINESS WIRE) -- Vertex Pharmaceuticals Incorporated (Nasdaq: VRTX) will announce its first quarter 2009 financial results on Thursday, April 16, 2009 after the financial markets close. The Company will host a conference call at 5:00 p.m. EDT.
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Toggle Summary Vertex Pharmaceuticals Announces Webcast of its Presentation at Two Investor Conferences
CAMBRIDGE, Mass., Mar 30, 2009 (BUSINESS WIRE) -- Vertex Pharmaceuticals Incorporated (Nasdaq: VRTX) today announced that it will webcast its corporate presentation at Citi's 4 th Annual Biotech Day on Wednesday, April 1, 2009 at 2:40 p.m. EDT and at the Canaccord Adams Hepatitis C Conference on
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Toggle Summary Vertex Pharmaceuticals Initiates Phase 2 Development for CFTR Corrector VX-809 in Patients with Cystic Fibrosis
<i><b>- Primary endpoints of safety and tolerability to be evaluated in Phase 2a clinical trial -</b></i><i><b>- Measurements of CFTR function to be assessed as secondary endpoints -</b></i><i><b>- Trial to enroll approximately 90 patients with the F508del CFTR mutation -</b></i>
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Toggle Summary Vertex Pharmaceuticals Announces Acceptance of Telaprevir and VCH-222 Abstracts for Presentation at EASL Annual Meeting
<i><b>- PROVE 3 SVR results accepted as late-breaker oral presentation -</b></i><i><b>- First clinical results for VCH-222 in HCV patients accepted as poster presentation -</b></i>
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Toggle Summary Vertex Pharmaceuticals Announces Webcast of its Presentation at the Cowen & Company 29th Annual Health Care Conference
CAMBRIDGE, Mass., Mar 13, 2009 (BUSINESS WIRE) -- Vertex Pharmaceuticals Incorporated (Nasdaq: VRTX) today announced that it will webcast its corporate presentation at the Cowen &amp; Company 29 th Annual Health Care Conference on Tuesday, March 17, 2009 at 2:25 p.m. EDT.
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Toggle Summary Vertex Pharmaceuticals Closes on Acquisition of ViroChem Pharma
<b>-Purchase Price $100 Million and 10.7 Million Shares-</b><b>-Vertex Acquires Two HCV Polymerase Inhibitors in Deal-</b>
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Toggle Summary Vertex Pharmaceuticals Strengthens HCV Drug Development Portfolio, Adds Novel Polymerase Inhibitors to Shape New Combinations with Telaprevir
<i>- Vertex to acquire privately-held ViroChem Pharma in cash and stock transaction -</i><i>- Two HCV polymerase inhibitors, VCH-222 and VCH-759, have demonstrated significant antiviral activity in early clinical trials -</i><i>- First STAT-C combination trial with telaprevir planned for 2H 2009 start -</i>
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