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Home/NVCR/Filing changes

NVCR — what changed in the latest 10-Q

A section-by-section comparison of NVCR's newest periodic SEC filing (10-K/10-Q) against the prior same-form filing: paragraphs added and removed per section, with verbatim excerpts. Purely a deterministic text diff — no similarity scores, no directional read, not investment advice.

Comparing 10-Q · 2026-10-29 vs the prior 10-Q · 2026-07-23

SectionOutcomeAddedRemovedMinorUnchanged
MD&AText added/removed+39−26~1532
Market risk (Item 3)No paragraph-level changes0001
Controls & proceduresText added/removed+2−1~10
Legal proceedingsNo paragraph-level changes0001
Risk factorsNo material changes reported (points to the 10-K)————
Other informationText added/removed+3−102

Counts are paragraphs; added/removed means text added or removed vs the prior filing — no direction or judgement implied.

Representative excerpts

Up to 5 excerpts of about 300 characters per section, quoted verbatim from the two SEC filings.

MD&A

Text added vs the prior filing · source: 10-Q · 2026-10-29

  • approved in Japan for the treatment of adult patients with unresectable locally advanced pancreatic cancer concurrent with gem/nab-pac.
  • In June, we announced that we received a CE certificate to market Optune Pax for the first-line treatment of locally advanced pancreatic cancer of exocrine origin, concomitant with gem/nab-pac in accordance with guideline recommendations. The CE Mark is supported by data from the Phase 3 PANOVA-3 tr…
  • In October, we announced that we received approval from Japan's Ministry of Health, Labour, and Welfare (MHLW) for Optune Pax for the treatment of adult patients diagnosed with unresectable locally advanced pancreatic cancer, concomitant with gem/nab-pac. The approval is supported by data from PANOV…
  • In October, we entered into a Collaboration Agreement with Verastem Oncology ("Verastem") to explore the concomitant use of TTFields therapy together with VS-7375, an oral KRAS G12D inhibitor, and chemotherapy in
  • locally advanced pancreatic cancer. We plan to initiate a clinical trial to evaluate safety and tolerability in approximately 25 patients.

Text removed vs the prior filing · source: 10-Q · 2026-07-23

  • concomitant with gemcitabine and nab-paclitaxel in accordance with guideline recommendations. We have submitted the regulatory application required to market Optune Pax in Japan.
  • In June, we announced topline results from the Phase 3 TRIDENT trial ("TRIDENT"), evaluating the initiation of TTFields therapy at the start of chemoradiation ("Early Start Arm") compared to initiation of TTFields therapy during the maintenance phase of treatment ("Maintenance Start Arm"), following…
  • In June, we announced that we received a CE certificate to market Optune Pax for the first-line treatment of locally advanced pancreatic cancer of exocrine origin, concomitant with gemcitabine and nab-paclitaxel (gem/nab-pac) in accordance with guideline recommendations. The CE Mark is supported by …
  • As a result of FDA approval of Optune Pax during the first quarter, we incurred a non-cash general and administrative expense of approximately $43,406 related to 901,284 PSUs granted in March 2020 to an executive officer that were expensed for U.S. GAAP purposes, but not actually converted to Ordina…
  • Net revenues. Net revenues increased 16% to $183.6 million for the three months ending June 30, 2026 from $158.8 million for the same period in 2025. For the three months ended June 30, 2026 the net revenue increase primarily resulted from $16.1 million in growth from international markets and $8.7 …

Controls & procedures

Text added vs the prior filing · source: 10-Q · 2026-10-29

  • appropriate, to allow timely decisions regarding required disclosure. Management recognizes that any controls and procedures, no matter how well designed and operated, can provide only reasonable assurance of achieving their objectives and management necessarily applies its judgment in evaluating th…
  • There has been no change in our internal control over financial reporting during the quarter ended September 30, 2026 that has materially affected, or is reasonably likely to materially affect, our internal control over financial reporting.

Text removed vs the prior filing · source: 10-Q · 2026-07-23

  • There has been no change in our internal control over financial reporting during the quarter ended June 30, 2026 that has materially affected, or is reasonably likely to materially affect, our internal control over financial reporting.

Other information

Text added vs the prior filing · source: 10-Q · 2026-10-29

  • The following table describes contracts, instructions or written plans for the purchase or sale of our securities that are intended to satisfy the affirmative defense conditions of Rule 10b5–1(c) promulgated under the Securities Exchange Act of 1934, as amended (each a "Rule 10b5-1 Plan") adopted by…
  • Name and TitleTitleDate of AdoptionDuration of Rule 10b5-1 PlanAggregate Number of Securities to be Purchased Pursuant to the Rule 10b5-1 PlanAggregate Number of Securities to be Sold Pursuant to the Rule 10b5-1 Plan
  • This plan amends and replaces the plan adopted by Mr. Leung on August 29, 2025. During the three-month period ending September 30, 2026, none of our other executive officers or directors terminated a Rule 10b5-1 trading plan or adopted or terminated a non-Rule 10b5-1 trading arrangement (as defined …

Text removed vs the prior filing · source: 10-Q · 2026-07-23

  • During the three-month period ending June 30, 2026, neither we nor any of our executive officers or directors adopted or terminated any contract, instruction or written plan for the purchase or sale of our securities that are intended to satisfy the affirmative defense conditions of Rule 10b5–1(c) p…

How to read Risk Factors (Item 1A) in a 10-Q

A 10-Q risk-factor section usually takes one of three forms; this page classifies it as one of:

  • Pointer — the filer states there have been no material changes and points back to the annual 10-K risk factors; there is no own risk text to compare this quarter.
  • Partial update — the filer carves out specific updated risks ("except as set forth below"); the excerpts show exactly what is new this quarter.
  • Restated in full — the quarter carries the complete risk-factor text. When the prior quarter was only a pointer there is no prior full text to diff against, so the page flags the section as restated instead.

This describes the filing structure only — it is never a judgement on whether risk went up or down.

Source: text-level diff of the two SEC EDGAR filings · deterministic (no AI-generated content) · for reference only · not investment advice

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