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Toggle Summary Vertex Announces Plans to Enroll Additional Treatment Arm in Ongoing Phase 2 Combination Study of Telaprevir and VX-222 for the Treatment of People with Hepatitis C
-New treatment arm to evaluate all oral, triple combination regimen of telaprevir, VX-222, and ribavirin- CAMBRIDGE, Mass., Nov 10, 2010 (BUSINESS WIRE)-- Vertex Pharmaceuticals Incorporated (Nasdaq: VRTX) today announced plans to enroll an additional treatment arm as part of its ongoing Phase 2
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Toggle Summary New Data From Phase 3 Studies Showed Superior SVR (Viral Cure) Rates Achieved with Telaprevir-Based Combination Therapy in People with Hepatitis C, Regardless of Race or Stage of Liver Disease
<i>-75% of people treated in the Phase 3 ADVANCE study achieved a viral cure with telaprevir; majority of people treated for a total of 24 weeks-</i> <br /> <i>-62% of African Americans/Blacks in the ADVANCE study achieved a viral cure with telaprevir-</i> <br /> <i>-Low discontinuation rates of all drugs due to adverse events-</i> <br />
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Toggle Summary Vertex Pharmaceuticals Announces Start of a Phase 3b Study of Twice-Daily Telaprevir in People Not Treated Previously for Hepatitis C
<i>- First Phase 3 study to evaluate twice-daily (BID) dosing of a protease inhibitor for hepatitis C -</i> <br /> <i>- All patients will receive telaprevir-based combination therapy -</i> <br />
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Toggle Summary Vertex Pharmaceuticals Reports Third Quarter 2010 Financial Results and Highlights Progress in Hepatitis C and Cystic Fibrosis Development Programs
<i>-Hepatitis C:</i> <i>New Drug Application submission for telaprevir on track for fourth quarter 2010-</i> <br /> <i>-Cystic Fibrosis:</i> <i>Phase 3 registration program ongoing for VX-770-</i> <br /> <i>-Pipeline:</i> <i>Ongoing proof-of-concept clinical trials in hepatitis C, cystic fibrosis, epilepsy and rheumatoid arthritis-</i> <br /> <i>-Financial:</i> <i>Company ends third quarter with a cash position of $1.2 billion-</i> <br />
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Toggle Summary Vertex Pharmaceuticals Initiates Clinical Trial to Evaluate Combination Regimens of VX-770 and VX-809 Targeting the Defective Protein Responsible for Cystic Fibrosis
<i><b>-Primary endpoints of safety, tolerability and effect on CFTR function as measured by sweat chloride-</b></i> <br /> <i><b>-Phase 2a proof of mechanism clinical trial to enroll people with the most common mutation of cystic fibrosis, known as F508del-</b></i> <br />
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Toggle Summary Vertex Pharmaceuticals Announces Exercise of Underwriter's Option to Purchase Additional Convertible Senior Subordinated Notes
CAMBRIDGE, Mass., Sep 24, 2010 (BUSINESS WIRE) -- Vertex Pharmaceuticals Incorporated (Nasdaq: VRTX) today announced that the underwriter for its offering of 3.35% convertible senior subordinated notes due 2015 has exercised in full its option to purchase an additional $25 million aggregate
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Toggle Summary Vertex Pharmaceuticals Announces Pricing of its Public Offering of Convertible Senior Subordinated Notes
CAMBRIDGE, Mass., Sep 23, 2010 (BUSINESS WIRE) -- Vertex Pharmaceuticals Incorporated (Nasdaq: VRTX) today announced that it has entered into an agreement to sell $375.0 million aggregate principal amount of 3.35% convertible senior subordinated notes due 2015.
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Toggle Summary Vertex Pharmaceuticals Announces Proposed Public Offering of Convertible Senior Subordinated Notes
CAMBRIDGE, Mass., Sep 22, 2010 (BUSINESS WIRE) -- Vertex Pharmaceuticals Incorporated (Nasdaq: VRTX) today announced that intends to offer, subject to market and other conditions, $375.0 million aggregate principal amount of convertible senior subordinated notes due 2015 in an underwritten public
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Toggle Summary 65% of People Whose Prior Treatment for Hepatitis C Was Unsuccessful Achieved SVR (Viral Cure) with Telaprevir-Based Therapy in Phase 3 REALIZE Study
<i>-17% of people achieved SVR with pegylated-interferon and ribavirin alone in the control arm-</i> <br /> <i>-Safety and tolerability results were consistent with prior Phase 3 studies-</i> <br /> <i>-Completion of rolling New Drug Application submission on track for the fourth quarter 2010-</i> <br />
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Toggle Summary Phase 3 ILLUMINATE Study Supports 24-Week Telaprevir-Based Therapy Within a Response-Guided Regimen for People with Hepatitis C Who Had Not Received Prior Treatment
<i>-Viral cure rates of 92% and 88% with 24 and 48-week regimens, respectively, in people who met certain response criteria-</i> <br /> <i>-Safety and tolerability results were similar to those seen in the Phase 3 ADVANCE study</i>- <br />
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