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Exelixis Inc (OQ:EXEL)

Business Focus: Bio Therapeutic Drugs

INK Edge Outlook

Insider Chart - Past 6 Months

Insider Filings

Latest 10 SEC Form 4 filings for EXEL*US within the last 6 months
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Company News

Apr 16, 2024 16:05 ET
Exelixis to Release First Quarter 2024 Financial Results on Tuesday, April 30, 2024
Exelixis, Inc. (Nasdaq: EXEL) announced today that its first quarter 2024 financial results will be released on Tuesday, April 30, 2024 after the markets close. At 5:00 p.m. ET / 2:00 p.m. PT, Exelixis management will host a conference call and webcast to discuss the results and provide a general business update. Access to the event is available via the
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Feb 27, 2024 16:05 ET
Exelixis to Webcast Fireside Chats as Part of Investor Conferences in March
Exelixis, Inc. (Nasdaq: EXEL) today announced that members of the company’s management team will participate in fireside chats at the following investor conferences in March:
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Valuation Ratios

Industry
Sector
Beta
0.58
--
--
Price to Sales - TTM
3.73
5.48
2.99
Price to Book - most recent quarter
3.01
2.18
2.06
Price to Cash Flow per share - TTM
29.20
17.27
13.35
Price to Free Cash Flow per share - TTM
23.28
16.77
23.10
See all valuations

Business Summary

Sector:  Healthcare Industry:  Biotechnology & Medical Research

Exelixis, Inc. is an oncology company. The Company is engaged in developing medicines and combination regimens at the forefront of cancer care. It has produced four marketed pharmaceutical products, two of which are formulations of its flagship molecule, cabozantinib. Cabozantinib is an inhibitor of multiple tyrosine kinases, including MET, AXL, VEGF receptors and RET and has been also approved as CABOMETYX tablets for advanced renal cell carcinoma (RCC), for previously treated hepatocellular carcinoma (HCC) and for previously treated, radioactive iodine (RAI)-refractory differentiated thyroid cancer (DTC), and as COMETRIQ capsules for progressive, metastatic medullary thyroid cancer (MTC). The Company's other two products are COTELLIC, an inhibitor of MEK approved as part of multiple combination regimens to treat specific forms of advanced melanoma and MINNEBRO an oral, non-steroidal, selective blocker of the mineralocorticoid receptor (MR) approved the treatment of hypertension.

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