TG Therapeutics, Inc. (NASDAQ:TGTX) Files An 8-K Other Events

TG Therapeutics, Inc. (NASDAQ:TGTX) Files An 8-K Other Events
Item 8.01. Other Events.

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On June 15, 2018, TG Therapeutics, Inc. (the “Company”) issued a press release announcing the presentation of an integrated analysis of long term safety data of umbralisib (TGR-1202), the Company’s PI3K delta inhibitor, as well as the first preclinical data presentation of TG-1701, the Company’s orally available and covalently-bound BTK inhibitor, at the 23rd Congress of European Hematology Association (EHA). On June 15, 2018, the Company also announced updated clinical data from its ongoing Phase I study evaluating umbralisib (TGR-1202), the Company's PI3K delta inhibitor in combination with ruxolitinib, the JAK 1/2 inhibitor, in ruxolitinib experienced patients with myelofibrosis (MF), at the 23rd Congress of EHA. Copies of the press releases are being filed as Exhibits 99.1 and Exhibits 99.2 and incorporated in this Item by reference.

Item 9.01 Financial Statements And Exhibits.

(d) Exhibits.

99.1 Press Release, dated June 15, 2018.

99.2 Press Release, dated June 15, 2018.


TG THERAPEUTICS, INC. Exhibit
EX-99.1 2 v061518_ex991.htm EXHIBIT 99.1 Blueprint Exhibit 99.1   TG Therapeutics,…
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About TG Therapeutics, Inc. (NASDAQ:TGTX)

TG Therapeutics, Inc. (TG) is a biopharmaceutical company focused on the acquisition, development and commercialization of treatments for b-cell malignancies and autoimmune diseases. The Company is developing over two therapies targeting hematological malignancies. TG-1101 (ublituximab) is a glycoengineered monoclonal antibody that targets a specific epitope on the CD20 antigen found on mature B-lymphocytes. The Company is also developing TGR-1202, an orally available Phosphoinositide 3-kinase (PI3K) delta inhibitor. Both TG-1101 and TGR-1202 are in clinical development for patients with hematologic malignancies. The Company also has pre-clinical programs focusing on developing interleukin-1 receptor-associated kinase 4 (IRAK4) inhibitors and anti-PD-L1 and anti-GITR antibodies. The Company also evaluates complementary products, technologies and companies for in-licensing, partnership, acquisition and investment opportunities.

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