Welcome to our dedicated page for Vertex Pharmaceuticals news (Ticker: VRTX), a resource for investors and traders seeking the latest updates and insights on Vertex Pharmaceuticals stock.
Vertex Pharmaceuticals Incorporated (Nasdaq: VRTX) is a global biotechnology company with approved medicines in cystic fibrosis, sickle cell disease, transfusion-dependent beta thalassemia and acute pain, and a broad pipeline across kidney disease, neuropathic pain, type 1 diabetes and other serious conditions. The VRTX news feed on Stock Titan brings together company press releases and other coverage that highlight how its commercial portfolio and research programs are evolving over time.
News about Vertex often focuses on clinical data readouts, regulatory milestones and commercial updates. Recent announcements have covered progress in cystic fibrosis, including data on ALYFTREK and other CFTR modulators presented at scientific conferences, and updates on next-generation CFTR correctors and CFTR mRNA therapies. Vertex also regularly reports on CASGEVY, its CRISPR/Cas9 gene-edited cell therapy for severe sickle cell disease and transfusion-dependent beta thalassemia, including longer-term outcomes data and plans for regulatory submissions in additional age groups.
Investors and followers of VRTX news can also expect updates on JOURNAVX, the company’s oral non-opioid NaV1.8 inhibitor for moderate-to-severe acute pain in adults, including information on prescription trends, payer coverage and hospital formulary adoption. In kidney diseases, Vertex issues news on povetacicept and inaxaplin, including Phase 1/2 and Phase 3 trial data in IgA nephropathy, primary membranous nephropathy and APOL1-mediated kidney disease, as well as regulatory designations such as Breakthrough Therapy and Fast Track.
Additional news items may include financial results, participation in major healthcare investor conferences, and updates on programs in type 1 diabetes, autosomal dominant polycystic kidney disease and myotonic dystrophy type 1. For anyone tracking VRTX stock, this news page offers a centralized view of how Vertex’s marketed products and pipeline advance through clinical development, regulatory review and commercialization.
Vertex Pharmaceuticals (Nasdaq: VRTX) has received FDA Fast Track Designation for VX-880, an investigational islet cell therapy aimed at treating type 1 diabetes (T1D) with severe hypoglycemia and impaired awareness. A Phase 1/2 clinical trial has begun, enrolling approximately 17 patients, focusing on the safety and efficacy of VX-880. The therapy aims to restore insulin-secreting pancreatic islet function, marking a significant step for T1D treatments. Clinical trial sites have opened at several major institutions, indicating a commitment to advancing diabetes therapy.
Vertex Pharmaceuticals (Nasdaq: VRTX) will present at the Cowen Health Care Conference on March 2, 2021, at 9:50 a.m. ET. The live audio of the presentation can be accessed via Vertex's website in the 'Investors' section. Vertex is a biotechnology company focused on scientific innovation, offering approved medicines for cystic fibrosis and developing treatments for other serious diseases like pain and genetic disorders. Founded in 1989, it operates globally and is recognized as a top employer.
Vertex Pharmaceuticals reported strong financial results for FY 2020, with GAAP product revenues of $6.2 billion, up 49% year-over-year. The company achieved a net income of $2.7 billion, a 130% increase compared to the previous year. Key drug sales, particularly TRIKAFTA, contributed significantly to growth, with U.S. revenues at $4.8 billion. For FY 2021, Vertex projects product revenues between $6.7 billion and $6.9 billion, anticipating continued momentum from TRIKAFTA and ongoing pipeline advancements in various disease areas.
Vertex Pharmaceuticals (Nasdaq: VRTX) has received FDA clearance to initiate a Phase 1/2 clinical trial for VX-880, a new stem cell-derived pancreatic islet cell therapy aimed at treating type 1 diabetes (T1D). The trial will focus on patients with impaired hypoglycemic awareness and severe hypoglycemia, with around 17 participants expected. VX-880 is designed to restore the body’s insulin production capability. Vertex highlights the potential impact of this therapy, coinciding with the centenary of insulin's discovery.
Vertex Pharmaceuticals announced the FDA's acceptance of their supplemental New Drug Application (sNDA) for TRIKAFTA to treat cystic fibrosis in children aged 6-11 with certain gene mutations. The FDA granted Priority Review, with a target action date of June 8, 2021. The application is supported by data from a Phase 3 study involving approximately 1,500 additional children who may benefit from the treatment. Vertex also plans to file a Marketing Authorization Application in the EU within the first half of 2021.
Vertex Pharmaceuticals (Nasdaq: VRTX) plans to announce its fourth-quarter 2020 financial results on February 1, 2021, after market close. A conference call will follow at 4:30 p.m. ET, accessible via dial-in or live webcast on Vertex's website. Vertex focuses on innovative treatments for serious diseases, primarily cystic fibrosis, and is expanding its pipeline to include therapies for conditions like sickle cell disease and Duchenne muscular dystrophy. The company consistently ranks as a top employer in the biotech industry.
Vertex Pharmaceuticals (Nasdaq: VRTX) will present at the J.P. Morgan Healthcare Conference on January 11, 2021, at 9:10 a.m. ET. Interested parties can access the live audio through the company's website at www.vrtx.com. Vertex is a global biotech firm focused on creating medicines for serious diseases, particularly cystic fibrosis. The company has a robust pipeline in various conditions, including genetic and cell therapies for sickle cell disease, beta thalassemia, and more. Vertex is recognized for its workplace environment and commitment to innovation.
Vertex Pharmaceuticals (Nasdaq: VRTX) announced that Health Canada has accepted its New Drug Submission for TRIKAFTA®, an investigational triple combination medicine for cystic fibrosis (CF) in patients aged 12 and older, under Priority Review. This designation shortens the review period from 300 to 180 days, with an expected approval in the first half of 2021. CF affects approximately 75,000 people globally and is caused by mutations in the CFTR gene, leading to severe lung damage. Vertex is committed to providing innovative treatments to improve patient outcomes.
Vertex Pharmaceuticals (NASDAQ: VRTX) has entered a strategic collaboration with Skyhawk Therapeutics to develop small molecules that target RNA splicing for serious diseases. Vertex will pay Skyhawk $40 million upfront and has the option to exclusively license any candidates developed. The deal includes potential milestone payments of up to $2.2 billion and royalties on future sales. This partnership aims to leverage Skyhawk's innovative technology and Vertex's R&D expertise to transform treatment options for patients.
Vertex Pharmaceuticals has received FDA approval for the expanded eligibility of its cystic fibrosis drugs TRIKAFTA, SYMDEKO, and KALYDECO. The approval allows individuals aged 12 and older with specific CFTR gene mutations, along with those aged 6 and 4 months, to access these treatments. This change potentially benefits over 600 new patients who previously lacked treatment options, increasing the number of eligible mutations for TRIKAFTA to 177, SYMDEKO to 154, and KALYDECO to 97.
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