| Summary of Finite-Lived Intangible Assets |
The following table summarizes our Intangible assets, net: | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | June 30, 2026 | | December 31, 2025 | | (in millions) | | Gross Carrying Amount | | Accumulated Amortization | | Foreign Currency Translation Adjustment | | Net Carrying Amount | | Gross Carrying Amount | | Accumulated Amortization | | Foreign Currency Translation Adjustment | | Net Carrying Amount | | Finite-lived assets: | | | | | | | | | | | | | | | | | | Intangible asset – sofosbuvir | | $ | 10,720 | | | $ | (8,797) | | | $ | — | | | $ | 1,923 | | | $ | 10,720 | | | $ | (8,448) | | | $ | — | | | $ | 2,272 | | Intangible asset – axicabtagene ciloleucel | | 7,110 | | | (3,330) | | | — | | | 3,780 | | | 7,110 | | | (3,127) | | | — | | | 3,983 | | Intangible asset – Trodelvy | | 11,730 | | | (4,704) | | | — | | | 7,026 | | | 11,730 | | | (4,164) | | | — | | | 7,566 | | Intangible asset – Hepcludex(1) | | 1,395 | | | (462) | | | — | | | 933 | | | 845 | | | (415) | | | — | | | 430 | | | Other | | 1,458 | | | (1,087) | | | — | | | 372 | | | 1,483 | | | (1,056) | | | — | | | 428 | | | Total finite-lived assets | | 32,413 | | | (18,382) | | | — | | | 14,032 | | | 31,888 | | | (17,211) | | | — | | | 14,678 | | Indefinite-lived assets – IPR&D(1)(2) | | — | | | — | | | — | | | — | | | 2,300 | | | — | | | — | | | 2,300 | | | Total intangible assets | | $ | 32,413 | | | $ | (18,382) | | | $ | — | | | $ | 14,032 | | | $ | 34,188 | | | $ | (17,211) | | | $ | — | | | $ | 16,978 | |
_______________________________ (1) In May 2026, FDA granted accelerated approval of Hepcludex (bulevirtide) for treatment of adults living with chronic hepatitis delta virus infection. Accordingly, the related IPR&D intangible asset of $550 million was reclassified to finite-lived assets in the second quarter of 2026. (2) During the second quarter of 2026, we recorded an impairment for the remaining $1.75 billion IPR&D intangible asset balance related to sacituzumab govitecan-hziy (“SG”) for NSCLC. See “2026 Impairment” below.
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| Summary of Indefinite-Lived Intangible Assets |
The following table summarizes our Intangible assets, net: | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | June 30, 2026 | | December 31, 2025 | | (in millions) | | Gross Carrying Amount | | Accumulated Amortization | | Foreign Currency Translation Adjustment | | Net Carrying Amount | | Gross Carrying Amount | | Accumulated Amortization | | Foreign Currency Translation Adjustment | | Net Carrying Amount | | Finite-lived assets: | | | | | | | | | | | | | | | | | | Intangible asset – sofosbuvir | | $ | 10,720 | | | $ | (8,797) | | | $ | — | | | $ | 1,923 | | | $ | 10,720 | | | $ | (8,448) | | | $ | — | | | $ | 2,272 | | Intangible asset – axicabtagene ciloleucel | | 7,110 | | | (3,330) | | | — | | | 3,780 | | | 7,110 | | | (3,127) | | | — | | | 3,983 | | Intangible asset – Trodelvy | | 11,730 | | | (4,704) | | | — | | | 7,026 | | | 11,730 | | | (4,164) | | | — | | | 7,566 | | Intangible asset – Hepcludex(1) | | 1,395 | | | (462) | | | — | | | 933 | | | 845 | | | (415) | | | — | | | 430 | | | Other | | 1,458 | | | (1,087) | | | — | | | 372 | | | 1,483 | | | (1,056) | | | — | | | 428 | | | Total finite-lived assets | | 32,413 | | | (18,382) | | | — | | | 14,032 | | | 31,888 | | | (17,211) | | | — | | | 14,678 | | Indefinite-lived assets – IPR&D(1)(2) | | — | | | — | | | — | | | — | | | 2,300 | | | — | | | — | | | 2,300 | | | Total intangible assets | | $ | 32,413 | | | $ | (18,382) | | | $ | — | | | $ | 14,032 | | | $ | 34,188 | | | $ | (17,211) | | | $ | — | | | $ | 16,978 | |
_______________________________ (1) In May 2026, FDA granted accelerated approval of Hepcludex (bulevirtide) for treatment of adults living with chronic hepatitis delta virus infection. Accordingly, the related IPR&D intangible asset of $550 million was reclassified to finite-lived assets in the second quarter of 2026. (2) During the second quarter of 2026, we recorded an impairment for the remaining $1.75 billion IPR&D intangible asset balance related to sacituzumab govitecan-hziy (“SG”) for NSCLC. See “2026 Impairment” below.
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