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GOODWILL AND OTHER INTANGIBLE ASSETS
12 Months Ended
Dec. 31, 2016
Goodwill and Intangible Assets Disclosure [Abstract]  
Goodwill and Intangible Assets Disclosure [Text Block]
GOODWILL AND OTHER INTANGIBLE ASSETS

 
 
 
 
December 31,
Dollars in Millions
 
Estimated
Useful Lives
 
2016
 
2015
Goodwill
 
 
 
$
6,875

 
$
6,881

 
 
 
 
 
 
 
Other intangible assets:
 
 
 
 
 
 
Licenses
 
5 – 15 years
 
$
564

 
$
574

Developed technology rights
 
9 – 15 years
 
2,357

 
2,357

Capitalized software
 
3 – 10 years
 
1,441

 
1,302

IPRD
 
 
 
107

 
120

Gross other intangible assets
 
 
 
4,469

 
4,353

Less accumulated amortization
 
 
 
(3,084
)
 
(2,934
)
Total other intangible assets
 
 
 
$
1,385

 
$
1,419


Amortization expense of other intangible assets was $178 million in 2016, $183 million in 2015 and $286 million in 2014. Future annual amortization expense of other intangible assets is expected to be approximately $220 million in 2017, $200 million in 2018, $170 million in 2019, $130 million in 2020, and $100 million in 2021. Other intangible asset impairment charges were $33 million in 2016, $181 million in 2015 and $380 million in 2014.

A $160 million IPRD impairment charge was recognized in 2015 for BMS-986020 (LPA1 Antagonist) which was in Phase II development for treatment of IPF. The full write-off was required after considering the occurrence of certain adverse events, voluntary suspension of the study and an internal assessment indicating a significantly lower likelihood of regulatory and commercial success. BMS acquired BMS-986020 with its acquisition of Amira Pharmaceuticals, Inc. in 2011. In addition, a contingent consideration liability of $8 million related to the acquisition was also reversed because of the lower likelihood of success.

A $310 million IPRD impairment charge was recognized in 2014 for peginterferon lambda which was in Phase III development for treatment of HCV. The full write-off was required after assessing the potential commercial viability of the asset and estimating its fair value. The assessment considered the lower likelihood of filing for registration in certain markets after completing revised projections of revenues and expenses. A significant decline from prior projected revenues resulted from the global introduction of oral non-interferon products being used to treat patients with HCV and no other alternative uses for the product.