TG Therapeutics Highlights Data Selected for Presentation at the 63rd American Society of Hematology (ASH) Annual Meeting

NEW YORK, Nov. 04, 2021 (GLOBE NEWSWIRE) -- TG Therapeutics, Inc. (NASDAQ: TGTX), today announced the release of six abstracts that will be presented at the upcoming 63^rd American Society of Hematology (ASH) annual meeting and exposition, to be held December 11 – 14, 2021, virtually and also live at the Georgia World Congress Center in Atlanta, Georgia. Abstracts are now publicly available online via the ASH meeting website at .

Michael S. Weiss, Chairman and Chief Executive Officer, stated, “We are looking forward to a live ASH annual meeting this year where we will be sharing six presentations, including three oral presentations. Specifically, we are pleased to share new data from the UNITY-NHL Phase 2b trial showing the U2 combination in patients with relapsed or refractory marginal zone lymphoma and diffuse large b-cell lymphoma. We are also excited to share two novel analyses from the UNITY-CLL Phase 3 trial. One highlighting the outcomes of U2 treated patients who had comorbidities or required certain concomitant medications, both of which represent areas of high unmet need as these patients may be poor candidates for BTK therapy. The other presentation sharing the efficacy and safety of U2 by CLL pre-treatment status, that is, comparing the treatment naïve cohort with the previously treated cohort. Finally, we will also share two presentations from studies evaluating U2 triplet regimens with a BTK, namely TG-1701 and ibrutinib. We believe these presentations showcase the strength of our combination B-cell platform, which has the potential to produce multiple product opportunities in the future.”

ASH Presentation Details:

Oral Presentations:

Oral Presentation Title: 

• Session Date/Time: Saturday, December 11, 2021 / 10:00 AM ET
• Session Name: 623. Mantle Cell, Follicular, and Other B-Cell Lymphomas: Clinical and Epidemiological: Targeted Therapy in Low Grade Lymphoma
• Room: Georgia World Congress Center, A411-A412
• Lead Author: Julio Chavez, MD, MS, Moffitt Cancer Center, Tampa, FL
  
  

Oral Presentation Title: 

• Session Date/Time: Sunday, December 12, 2021 / 5:30 PM ET       
• Session Name: 626. Aggressive Lymphomas Prospective Therapeutic Trials: Novel Agents and Combinations
• Room: Georgia World Congress Center, Thomas Murphy Ballroom 1-2
• Lead Author: John Burke, MD, Rocky Mountain Cancer Centers / US Oncology Research, Aurora, CO

Oral Presentation Title: 

• Session Date/Time: Sunday, December 12, 2021 / 10:30 AM ET
• Session Name: 642. Chronic Lymphocytic Leukemia: Clinical and Epidemiological I
• Room: Georgia World Congress Center, B401-B402
• Lead Author: Lindsey E. Roeker, MD, CLL Program, Leukemia Service, Division of Hematologic Oncology, Memorial Sloan-Kettering Cancer Center, New York, NY

Poster Presentations:

Poster Presentation Title: 

• Date/Time: Saturday, December 11, 2021 / 5:30 PM - 7:30 PM ET
• Session Name: 642. Chronic Lymphocytic Leukemia: Clinical and Epidemiological: Poster I
• Location: Georgia World Congress Center, Hall B5
• Lead Author: Chan Y. Cheah, MBBS, DMSc, Linear Clinical Research, Nedlands, Australia; Medical School, University of Western Australia, Perth, Australia; and Department of Haematology, Sir Charles Gairdner Hospital, Perth, Australia

Poster Presentation Title: 

• Date: Monday, December 13, 2021 / 6:00 PM - 8:00 PM
• Session Name: 642. Chronic Lymphocytic Leukemia: Clinical and Epidemiological: Poster III
  
  Location: Georgia World Congress Center, Hall B5
• Lead Author: Javier Pinilla-Ibarz, MD, Lymphoma Section Head, Director of Immunotherapy, Malignant Hematology Division at the H. Lee Moffitt Cancer Center in Tampa, Florida
  
  

Poster Presentation Title: 

• Date/Time: Monday, December 13, 2021 / 6:00 PM - 8:00 PM
• Session Name: 642. Chronic Lymphocytic Leukemia: Clinical and Epidemiological: Poster III
• Location: Georgia World Congress Center, Hall B5
• Lead Author: Ryan Jacobs, MD, Department of Hematology, Lymphoma Division, Assistant Professor of Medicine, Levine Cancer Institute/Atrium Health, Charlotte, NC

Abstracts are now publicly available via the ASH meeting website at . Final presentations will be accessible at the above dates/times via the publications page of TG corporate website at .

ABOUT TG THERAPEUTICS, INC.

TG Therapeutics is a fully-integrated, commercial stage biopharmaceutical company focused on the acquisition, development and commercialization of novel treatments for B-cell malignancies and autoimmune diseases. In addition to an active research pipeline including five investigational medicines across these therapeutic areas, TG has received accelerated approval from the U.S. FDA for UKONIQ^® (umbralisib), for the treatment of adult patients with relapsed/refractory marginal zone lymphoma who have received at least one prior anti-CD20-based regimen and relapsed/refractory follicular lymphoma who have received at least three prior lines of systemic therapies. Currently, the Company has three programs in Phase 3 development for the treatment of patients with relapsing forms of multiple sclerosis (RMS) and patients with chronic lymphocytic leukemia (CLL) and several investigational medicines in Phase 1 clinical development. For more information, visit , and follow us on Twitter  and .

UKONIQ^® is a registered trademark of TG Therapeutics, Inc.

Cautionary Statement

This press release contains forward-looking statements that involve a number of risks and uncertainties. For those statements, we claim the protection of the safe harbor for forward-looking statements contained in the Private Securities Litigation Reform Act of 1995. In addition to the risk factors identified from time to time in our reports filed with the Securities and Exchange Commission, factors that could cause our actual results to differ materially include the following: the risk that interim, top-line, or other early clinical trial results, that may have supported the acceptance of our data for presentation or influenced our decision to proceed with additional clinical trials, will not be reproduced in final data sets or in future studies; the risk that the safety profile observed with umbralisib, ublituximab or TG-1701, or combinations thereof, may change as additional patients are exposed for longer durations; the risk that the U2 combination will not prove to be a safe and efficacious combination, or backbone for triple therapy combinations; the risk that we will not be able to meet the regulatory submission or clinical trial timelines that we project or achieve other anticipated milestones, including the risk that the evolving and unpredictable COVID-19 pandemic delays achievement of those milestones; and the risk that our compounds will not receive regulatory approval or become commercially successful products. Further discussion about these and other risks and uncertainties can be found in our Annual Report on Form 10-K for the fiscal year ended December 31, 2020, our most recent Quarterly Report filed on Form 10-Q, and our other filings with the U.S. Securities and Exchange Commission.

Any forward-looking statements set forth in this press release speak only as of the date of this press release. We do not undertake to update any of these forward-looking statements to reflect events or circumstances that occur after the date hereof. This press release and prior releases are available at . The information found on our website is not incorporated by reference into this press release and is included for reference purposes only.

CONTACT:

Investor Relations

Email:

Telephone: 1.877.575.TGTX (8489), Option 4

Media Relations:

Email:

Telephone: 1.877.575.TGTX (8489), Option 6