ubstantial risks and uncertainties in the process of development,
commercialization, and regulatory review. There is no guarantee
that the products will receive additional regulatory approvals.
There is also no guarantee that the products will continue to be
commercially successful. For further discussion of these and other
risks and uncertainties, see Lilly's filing with the United States
Securities and Exchange Commission. Lilly undertakes no duty to
update forward-looking statements.
(i) American Cancer Society, "Cancer Still a Heavy Burden for
African
Americans,"
http://www.cancer.org/docroot/NWS/content/NWS_1_1x_Cancer_Still_a_Heavy_Burden
_for_African_Americans.asp (April 17, 2007).
(ii) American Cancer Society, "Cancer Facts & Figures for
Hispanics/Latinos 2006-2008," p. 3.
(iii) Obasaju CK, Gonin R, Catalano RB, et al. Subgroup analysis
of African American patients from a randomized Phase 3 trial of
gemcitabine in combination with carboplatin or paclitaxel versus
paclitaxel plus carboplatin in advanced (Stage IIB, IV) non-small
cell lung cancer (Alpha Oncology trial A1-99002L). American Society
of Clinical Oncology (ASCO) Annual Meeting 2007.
(iv) Obasaju CK, Kulkarni P, Wang Y, et al. Effect of race on
the safety and efficacy of pemetrexed therapy in locally advanced
and metastatic non- small cell lung cancer (NSCLC). American
Society of Clinical Oncology (ASCO) Annual Meeting 2007.
CONTACT: Gregory L. Clarke of Eli Lilly and Company,
+1-317-276-5222, ormobile, +1-317-554-7119, or ; or Neil Hochman,
CPRWorldwide, +1-212-453-2067, or mobile, +1-516-784-9089, or
gregory.clarke@lilly.com
n.hochman@cprworldwideusa.com
Ticker Symbol: (:LLY)
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Page: 1 2 3 4 5 6 7 8 9 10 11 Related medicine technology :1.
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