CYTOMX THERAPEUTICS, INC. (NASDAQ:CTMX) Files An 8-K Regulation FD Disclosure
Item 7.01
Regulation FD Disclosure
On February 26, 2019, CytomX Therapeutics, Inc. (“CytomX” or the “Company”) issued a press release announcing that it will hold a Research and Development Day (“R&D Day”) conference at 8:00 AM ET on Tuesday, February 26, 2019.The event will be webcast live under the “Investors & News” section of the CytomX website.A copy of the Press Release is furnished as Exhibit 99.1 to this Current Report and is incorporated herein by reference.
The information in this Item 7.01, including Exhibit 99.1, shall not be deemed “filed” for purposes of Section 18 of the Security Exchange Act of 1934, as amended (the “Exchange Act”) or otherwise subject to the liabilities of that section, nor shall it be deemed incorporated by reference in any filing under the Securities Act of 1933, as amended, or the Exchange Act, except as expressly set forth by specific reference in such filing.
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Item 9.01. |
Financial Information and Exhibits |
(d) Exhibits
CytomX Therapeutics, Inc. Exhibit
EX-99.1 2 ctmx-ex991_23.htm EX-99.1 ctmx-ex991_23.htm Exhibit 99.1 CytomX Therapeutics 2019 Research and Development Day Highlights Clinical Data from Lead Programs and the Broad Potential of Probody™ Therapeutic Platform – CX-2009,…
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About CYTOMX THERAPEUTICS, INC. (NASDAQ:CTMX)
CytomX Therapeutics, Inc. is an oncology-focused biopharmaceutical company. The Company is engaged in the development of a class of antibody therapeutics based on its Probody technology platform. It uses its platform to create cancer immunotherapies against clinically validated targets, as well as to develop cancer therapeutics against a range of targets. A Probody therapeutic consists of three components produced as a single protein by standard antibody production methodology: an active anti-cancer antibody, a mask for the antibody and a protease-cleavable linker. Its Probody product candidate, CX-072, is directed against programmed death-ligand 1 (PD-L1). CX-072 is based on a monoclonal antibody targeting PD-L1. Its product candidate, CX-2009, is directed against the target CD-166. It is developing a programmed cell death protein 1 (PD-1) Probody therapeutic as an additional approach to block the PD-L1/PD-1 pathway. It is also conducting Integrin alpha-3 PDC program.
