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Goodwill and Intangible Assets (Tables)
12 Months Ended
Dec. 31, 2021
Goodwill and Intangible Assets Disclosure [Abstract]  
Goodwill
The following table summarizes the changes in the carrying amount of Goodwill:
December 31,
(in millions)20212020
Beginning balance$8,108 $4,117 
Goodwill resulting from acquisitions226 3,991 
Measurement period adjustments(2)— 
Ending balance$8,332 $8,108 
Indefinite-Lived Intangible Assets
The following table summarizes our Intangible assets, net:
 December 31, 2021December 31, 2020
(in millions)Gross 
Carrying
Amount
Accumulated
Amortization
Foreign Currency Translation AdjustmentNet Carrying AmountGross 
Carrying
Amount
Accumulated
Amortization
Foreign Currency Translation AdjustmentNet Carrying Amount
Finite-lived assets
Intangible asset - sofosbuvir$10,720 $(5,651)$— $5,069 $10,720 $(4,952)$— $5,768 
Intangible asset - axicabtagene ciloleucel(1)
7,110 (1,501)— 5,609 6,200 (1,105)— 5,095 
Intangible asset - Trodelvy(2)
5,630 (507)— 5,123 4,600 (63)— 4,537 
Intangible asset - Hepcludex845 (72)— 773 — — — — 
Other(3)
1,610 (650)961 1,377 (540)(1)836 
Total finite-lived assets25,915 (8,381)17,535 22,897 (6,660)(1)16,236 
Indefinite-lived assets - IPR&D(4)
15,920 — — 15,920 16,890 — — 16,890 
Total intangible assets$41,835 $(8,381)$$33,455 $39,787 $(6,660)$(1)$33,126 
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(1)     Gross carrying amount as of December 31, 2021 includes $910 million reclassified in the first quarter of 2021 from indefinite-lived assets - IPR&D following the March 2021 FDA approval of Yescarta for the treatment of adult patients with relapsed or refractory follicular lymphoma.
(2)     Gross carrying amount as of December 31, 2021 includes Trodelvy for metastatic TNBC and Trodelvy for use in adult patients with locally advanced or metastatic UC. The amount related to UC of $1.0 billion was reclassified to finite-lived assets from indefinite-lived assets - IPR&D upon the accelerated approval by FDA in April 2021.
(3)     In October 2021, FDA granted approval of Tecartus for the treatment of adult patients with relapsed or refractory B-cell precursor acute lymphoblastic leukemia. Accordingly, the related amount of $200 million was reclassified to finite-lived assets in the fourth quarter of 2021.
(4)    Gross carrying amount as of December 31, 2021 includes IPR&D from our 2021 acquisition of MYR and remaining IPR&D from our 2020 acquisition of Immunomedics. Gross carrying amount as of December 31, 2020 includes IPR&D from our 2020 acquisition of Immunomedics and remaining IPR&D from our 2017 acquisition of Kite.
Finite-Lived Intangible Assets
The following table summarizes our Intangible assets, net:
 December 31, 2021December 31, 2020
(in millions)Gross 
Carrying
Amount
Accumulated
Amortization
Foreign Currency Translation AdjustmentNet Carrying AmountGross 
Carrying
Amount
Accumulated
Amortization
Foreign Currency Translation AdjustmentNet Carrying Amount
Finite-lived assets
Intangible asset - sofosbuvir$10,720 $(5,651)$— $5,069 $10,720 $(4,952)$— $5,768 
Intangible asset - axicabtagene ciloleucel(1)
7,110 (1,501)— 5,609 6,200 (1,105)— 5,095 
Intangible asset - Trodelvy(2)
5,630 (507)— 5,123 4,600 (63)— 4,537 
Intangible asset - Hepcludex845 (72)— 773 — — — — 
Other(3)
1,610 (650)961 1,377 (540)(1)836 
Total finite-lived assets25,915 (8,381)17,535 22,897 (6,660)(1)16,236 
Indefinite-lived assets - IPR&D(4)
15,920 — — 15,920 16,890 — — 16,890 
Total intangible assets$41,835 $(8,381)$$33,455 $39,787 $(6,660)$(1)$33,126 
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(1)     Gross carrying amount as of December 31, 2021 includes $910 million reclassified in the first quarter of 2021 from indefinite-lived assets - IPR&D following the March 2021 FDA approval of Yescarta for the treatment of adult patients with relapsed or refractory follicular lymphoma.
(2)     Gross carrying amount as of December 31, 2021 includes Trodelvy for metastatic TNBC and Trodelvy for use in adult patients with locally advanced or metastatic UC. The amount related to UC of $1.0 billion was reclassified to finite-lived assets from indefinite-lived assets - IPR&D upon the accelerated approval by FDA in April 2021.
(3)     In October 2021, FDA granted approval of Tecartus for the treatment of adult patients with relapsed or refractory B-cell precursor acute lymphoblastic leukemia. Accordingly, the related amount of $200 million was reclassified to finite-lived assets in the fourth quarter of 2021.
(4)    Gross carrying amount as of December 31, 2021 includes IPR&D from our 2021 acquisition of MYR and remaining IPR&D from our 2020 acquisition of Immunomedics. Gross carrying amount as of December 31, 2020 includes IPR&D from our 2020 acquisition of Immunomedics and remaining IPR&D from our 2017 acquisition of Kite.
Estimated Future Amortization Expense of Finite-Lived Intangible Assets
The following table summarizes the estimated future amortization expense associated with our finite-lived intangible assets as of December 31, 2021:
(in millions)Amount
2022$1,778 
20231,778 
20241,778 
20251,773 
20261,765 
Thereafter8,663 
Total$17,535