Lilly To Release Early-Stage Pipeline Data Targeting Key Cancer Pathways At AACR 2014
"Harnessing Breakthroughs - Targeting Cures" is the theme of this year's AACR meeting and one that is mirrored throughout Lilly's early-stage oncology research. Lilly's oncology pipeline is among the most robust across the pharmaceutical industry and includes a broad range of large and small molecules being investigated to treat a wide range of cancers including lung, breast, colorectal, gastric, liver and hematologic malignancies. Lilly research presented at AACR will represent early findings from several of those early-stage clinical agents.
Data from bemaciclib, Lilly's CDK4/6 inhibitor LY2835219 as a potential treatment for metastatic breast cancer, has been accepted as a late-breaking presentation that will be included at AACR's Clinical Trials Symposium and will be featured in an official AACR-sponsored press conference.
"The CDK4/6 pathway is one of the most commonly implicated pathways in all cancers, making it an important area for research," said
Lilly's B-Raf inhibitor LY3009120 will be highlighted at AACR's New Drugs on the Horizon special session where first data disclosures of promising, new anti-cancer compounds that target key pathways will occur. There will also be an oral presentation on Lilly's c-MET kinase inhibitor, LY2801653.
"As we gain a better understanding about the distinct tumor biologies and other individual characteristics that make one tumor different than another, we are able to apply this knowledge to our development of potential new cancer treatments, such as those we are presenting at AACR," said Dr. Gaynor. "Each step we take during early-stage research - both in the lab and on clinical trials - leads us toward the same overall goal: to increase the number of treatment options available to patients."
Select Lilly early-stage pipeline studies, along with the times and locations of their data sessions, are highlighted below.
- Abstract #CT232: Clinical Trials Symposium:
Monday, April 7, 2014 1:30 pm- 1:50 pm
- Clinical activity of LY2835219, a novel cell cycle inhibitor selective for CDK4 and CDK6, in patients with metastatic breast cancer
Amita Patnaik, M.D., FRCP(C)
- Note: Abstract #CT232 to be presented at AACR press conference on
April 6at 7:30 am
B-Raf Inhibitor (LY3009120)
- Abstract #7135: New Drugs on the Horizon Special Session:
Sunday, April 6, 2014 3:45 pm to 4:10 pm
- Identification of LY3009120 as a pan inhibitor of Raf isoforms and dimer with activity against BRaf or Ras mutant tumor cells and minimal paradoxical activation
Sheng-Bin Peng, Ph.D.
c-MET Inhibitor (LY2801653)
- Abstract #CT237: Clinical Trials Minisymposium:
Monday, April 7, 2014 3:20 pm- 3:35 pm
- Interim results of a first-in-human Phase I study of the oral MET kinase inhibitor, LY2801653, in patients with advanced cancer
Jimmy Hwang, M.D.
- Abstract #4403: Poster Presentation:
Tuesday April 8, 2014 1:00 pm to 5:00 pm
- Preclinical evaluation of LY2801653, an orally bioavailable small molecule oncokinase inhibitor, in cholangiocarcinoma models
S. Betty Yan, Ph.D.
- Location: Hall A-E, Section 24
FGFR Inhibitor (LY2874455)
- Abstract #CT215: Poster Presentation:
Monday, April 7, 2014 8:00 am to 12:00 pm
- A Phase 1 Study of LY2874455, a Fibroblast Growth Factor Receptor Inhibitor, in Patients with Advanced Cancer
- Author/Speaker: Dr. Jeanne Tie
- Location: Hall A-E, Section 38
This press release contains forward-looking statements about the potential of LY2835219, LY2801653, LY3009120 and LY2874455 as treatments for various cancers and reflects Lilly's current beliefs. However, as with any pharmaceutical product, there are substantial risks and uncertainties in the process of development and commercialization. There is no guarantee that future study results for these products will be consistent with study findings to date, that these products will receive regulatory approvals, or will prove to be commercially successful. For further discussion of these and other risks and uncertainties, see Lilly's filings with the
212-453-2067 (office) / 516-784-9089 (mobile)
News Provided by Acquire Media