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VERTEX PHARMACEUTICALS INC / MA

For the period ended Jun 30, 2026. Filed Aug 4, 2026.

View on SEC.gov

About this filing

A company's report for each of its first three quarters. The financial statements are not audited. It shows how the business has moved since the last annual report, and what management says changed.

Jun 30, 2026 · Filed Aug 4, 2026

VRTX$547.09+0.8%Stored close · as of Nov 6, 2026

What changed in Risk Factors?

Read the current filing

Previous report: 10-Q

Period ended 2026-03-31; filed 2026-05-05.

0000875320-26-000173

Item 1A. Risk Factors

Current report: 10-Q

Period ended 2026-06-30; filed 2026-08-04.

0000875320-26-000259

Item 1A. Risk Factors

The baseline is this issuer’s latest earlier reporting period of the same form that was filed before the current report. A previous 10-Q is a different quarter, not a year-over-year comparison. Amendments are excluded.

Compared 57 previous paragraphs and 76 current paragraphs.

49 unchanged; 6 reworded; 21 added; 2 removed; 0 previous and 0 current paragraphs rearranged.

Tables are not compared: 0 previous and 0 current tables excluded. Dates, whitespace, punctuation and numbering changes are ignored; changes to financial figures remain significant.

A changed paragraph is not evidence that risk increased or decreased. An unchanged paragraph does not establish that risk stayed the same.

Added paragraphs (21)

Current report

We may be unable to complete the Crinetics Acquisition, successfully integrate Crinetics’ business, or realize the

Current report

potential commercial benefits of the strategic acquisition, which could adversely affect our business and financial

Current report

Our inability to complete the Crinetics Acquisition or to successfully integrate the Crinetics business could havea

Current report

material adverse effect on our business. The Crinetics Acquisition may not be completed for a number of reasons, including

Current report

the need to satisfy customary closing conditions, the need for antitrust and/or other regulatory approvals, as well as potential

Current report

disputes or litigation that may arise. We provide no assurance that the Crinetics Acquisition will occur or that the closing

Current report

conditions to the Crinetics Acquisition will be satisfied in a timely manner or at all. Our realization of the value from the

Current report

Crinetics Acquisition relies on successful integration of its operations. We may not be able to integrate Crinetics’ business

Current report

successfully into our existing business, make Crinetics’ business profitable, retain key employees or realize anticipated cost

Current report

savings or synergies, if any, from the acquisition, which could adversely affect our business and financial condition. Further,

Current report

our ongoing business may be disrupted, and our management's attention may be diverted by integration activities. In addition,

Current report

the anticipated benefits of the Crinetics Acquisition depend on revenues from PALSONIFY and the commercial potential of

Current report

atumelnant. If PALSONIFY does not achieve the sales, market acceptance, or other commercial performance we expect, if

Current report

development ofatumelnant is delayed or terminated, or if we fail to obtain approval or fail to successfully commercialize

Current report

atumelnant, we may not realize the expected revenue growth or income contribution from these assets on the anticipated

Current report

timeline, or at all, which could adversely affect our business and financial condition.

Current report

povetacicept;

Current report

•our expectations, plans and anticipated timeline for the pending Crinetics Acquisition, including regarding Crinetics’

Current report

business and operations, the commercial potential of PALSONIFY, and the anticipated potential of atumelnant and

Current report

Crinetics’ other pipeline assets;
Removed paragraphs (2)

Previous report

have been no material changes from the risk factors previously disclosed in the Annual Report on Form 10-K.

Previous report

expedited basis of six months from the date of FDA acceptance of the BLA;
Reworded paragraphs (6)

Previous wording

Report on Form 10-K for the year ended December 31, 2025, which was filed with the SEC on February 13, 2026. There

Current wording

Report on Form 10-K for the year ended December 31, 2025, which was filed with the SEC on February 13, 2026.

Previous wording

•our ability to continue to launch, commercialize and market our products and our ability to obtain label expansions

Current wording

•our ability to continue to launch, commercialize and market our products, including the anticipated launch of

Previous wording

for existing therapies, including the anticipated launch of povetacicept for the treatment of IgAN;

Current wording

povetacicept for the treatment of IgAN, and our ability to obtain label expansions for existing therapies;

Previous wording

regulatory approval, including our expectations regarding the FDA’s review of the BLA for povetacicept on an

Current wording

regulatory approval, including our expectations regarding the FDA’s review of our BLA for accelerated approval of

Previous wording

•our plans to build and maintain our global supply chains and manufacturing infrastructure and capabilities, including

Current wording

•our plans to maintain and expand our global supply chains and manufacturing infrastructure and capabilities,

Previous wording

for biologics, cell and gene therapies;

Current wording

including for biologics, cell and gene therapies;