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GOODWILL AND INTANGIBLE ASSETS (Tables)
9 Months Ended
Sep. 30, 2021
Goodwill and Intangible Assets Disclosure [Abstract]  
Schedule of Goodwill
The following table summarizes the changes in the carrying amount of goodwill:
(in millions)Amount
Balance at December 31, 2020$8,108 
Goodwill resulting from the acquisition of MYR226 
Measurement period adjustments(2)
Balance at September 30, 2021$8,332 
Schedule of Finite-Lived Intangible Assets
The following table summarizes our Intangible assets, net:
 September 30, 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 $(5,477)$— $5,243 $10,720 $(4,952)$— $5,768 
Intangible asset - axicabtagene ciloleucel(1)
7,110 (1,400)— 5,710 6,200 (1,105)— 5,095 
Intangible asset - Trodelvy(2)
5,630 (390)— 5,240 4,600 (63)— 4,537 
Intangible asset - Hepcludex
845 (50)— 795 — — — — 
Other1,410 (619)792 1,377 (540)(1)836 
Total finite-lived assets25,715 (7,936)17,780 22,897 (6,660)(1)16,236 
Indefinite-lived assets - IPR&D(1)(2)(3)(4)
16,120 — — 16,120 16,890 — — 16,890 
Total intangible assets$41,835 $(7,936)$$33,900 $39,787 $(6,660)$(1)$33,126 
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(1)     Gross carrying amount as of September 30, 2021 includes $910 million reclassified 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 September 30, 2021 includes Trodelvy for metastatic triple-negative breast cancer which was granted approval by FDA in April 2021 and Trodelvy for use in adult patients with locally advanced or metastatic urothelial cancer (“UC”) which was granted accelerated approval by FDA in April 2021. The amount related to UC of $1.0 billion was reclassified to finite-lived assets from indefinite-lived assets - IPR&D.
(3)     Gross carrying amount as of September 30, 2021 includes $1.2 billion recognized from the first quarter 2021 acquisition of MYR. See Note 6. Acquisitions for additional information.
(4)     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 will be reclassified to finite-lived assets in the fourth quarter of 2021.
Schedule of Indefinite-Lived Intangible Assets
The following table summarizes our Intangible assets, net:
 September 30, 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 $(5,477)$— $5,243 $10,720 $(4,952)$— $5,768 
Intangible asset - axicabtagene ciloleucel(1)
7,110 (1,400)— 5,710 6,200 (1,105)— 5,095 
Intangible asset - Trodelvy(2)
5,630 (390)— 5,240 4,600 (63)— 4,537 
Intangible asset - Hepcludex
845 (50)— 795 — — — — 
Other1,410 (619)792 1,377 (540)(1)836 
Total finite-lived assets25,715 (7,936)17,780 22,897 (6,660)(1)16,236 
Indefinite-lived assets - IPR&D(1)(2)(3)(4)
16,120 — — 16,120 16,890 — — 16,890 
Total intangible assets$41,835 $(7,936)$$33,900 $39,787 $(6,660)$(1)$33,126 
_______________________________
(1)     Gross carrying amount as of September 30, 2021 includes $910 million reclassified 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 September 30, 2021 includes Trodelvy for metastatic triple-negative breast cancer which was granted approval by FDA in April 2021 and Trodelvy for use in adult patients with locally advanced or metastatic urothelial cancer (“UC”) which was granted accelerated approval by FDA in April 2021. The amount related to UC of $1.0 billion was reclassified to finite-lived assets from indefinite-lived assets - IPR&D.
(3)     Gross carrying amount as of September 30, 2021 includes $1.2 billion recognized from the first quarter 2021 acquisition of MYR. See Note 6. Acquisitions for additional information.
(4)     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 will be reclassified to finite-lived assets in the fourth quarter of 2021.
Schedule of Estimated Future Amortization Expense
The following table summarizes the estimated future amortization expense associated with our finite-lived intangible assets as of September 30, 2021:
(in millions)Amount
2021 (remaining three months)$441 
20221,764 
20231,764 
20241,764 
20251,759 
Thereafter10,288 
Total$17,780