The 10-K against last year's
1217 changes: 826 added, 345 removed, 46 reworded
10-K 0000875320-26-000056 (2026-02-13) vs 10-K 0000875320-25-000053 (2025-02-13) Not compared: Legal Proceedings, Accounting Policies.
The redline
The paragraph that changed most in each section
Marked against last year's 10-K:
cut words struck through, new words highlighted and underlined.
MD&A 217 words changed in this paragraph; it is 37% similar to last year's version.
Source: Item 7, 10-K 0000875320-26-000056 vs Item 7, 10-K 0000875320-25-000053
Risk Factors 96 words changed in this paragraph; it is 31% similar to last year's version.
Source: Item 1A, 10-K 0000875320-26-000056 vs Item 1A, 10-K 0000875320-25-000053
Every change, by type
Sentences and paragraphs added, removed or reworded
Sentences and paragraphs of VRTX's Risk Factors and MD&A, 10-K 2026-02-13 against 10-K 2025-02-13. Each links to the text at sec.gov.
AddedRisk Factors
Investing in our common stock involves a high degree of risk, and you should carefully consider the risks and
AddedRisk Factors
uncertainties described below in addition to the other information included or incorporated by reference in this Annual
AddedRisk Factors
Report on Form 10-K. If any of the following risks or uncertainties occur, our business, financial condition or results of
AddedRisk Factors
Our success depends on our ability to develop and commercialize additional medicines.
AddedRisk Factors
We invest significant resources in research and development to discover and develop transformative medicines for
AddedRisk Factors
people with serious diseases. Product development is highly uncertain and expensive. Product candidates may appear
AddedRisk Factors
promising in research and development but may fail to reach commercial success for many reasons, including:
AddedRisk Factors
•competition based on, among other factors, safety, efficacy, patient convenience, pricing and reimbursement.
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AddedRisk Factors
Substantially all our net product revenues have been derived from the sale of our CF medicines. We may be unable to
AddedRisk Factors
sustain or increase revenues from sales of our CF medicines in the future for any number of reasons, including the potential
AddedRisk Factors
introduction of competitive products or the inability to successfully develop and commercialize next-generation medications
AddedRisk Factors
or medicines to treat people with CF who cannot benefit from our current CF medicines. Our concentrated source of revenue
AddedMD&A
We are a global biotechnology company that invests in scientific innovation to create transformative medicines for
AddedMD&A
people with serious diseases, with a focus on specialty markets. We have approved medicines for cystic fibrosis (“CF”),
AddedMD&A
sickle cell disease (“SCD”), transfusion dependent beta thalassemia (“TDT”), and acute pain, and we continue to serially
AddedMD&A
innovate and advance next-generation clinical and research programs in these areas. Our mid- and late-stage clinical pipeline
AddedMD&A
includes programs across a range of modalities in additional serious diseases, including IgA nephropathy, APOL1-mediated
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kidney disease, neuropathic pain, type 1 diabetes, primary membranous nephropathy, autosomal dominant polycystic kidney
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Collectively, our five CF medicines, led by TRIKAFTA/KAFTRIO, are being used to treat nearly three quarters of the
AddedMD&A
people with CF in the U.S., Europe, Australia, and Canada. ALYFTREK, our newest CF medicine, is approved in the United
AddedMD&A
States (the “U.S.”), the United Kingdom (the “U.K.”), the European Union (the “E.U.”), Canada, New Zealand, Switzerland,
AddedMD&A
CASGEVY, our ex-vivo, non-viral CRISPR/Cas9 gene-edited cell therapy, is approved in the U.S., the E.U., the U.K.,
AddedMD&A
the Kingdom of Saudi Arabia (“Saudi Arabia”), the Kingdom of Bahrain (“Bahrain”), Qatar, the United Arab Emirates (the
AddedMD&A
JOURNAVX, our selective non-opioid NaV1.8 pain signal inhibitor, is approved in the U.S. for the treatment of people