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G1 Therapeutics to Present Data on Oral CDK4/6 Inhibitor Lerociclib at European Society for Medical Oncology (ESMO) Virtual 2020 Congress

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G1 Therapeutics (GTHX) announced two presentations featuring data on the investigational oral CDK4/6 inhibitor, lerociclib, at the ESMO Virtual Congress 2020 from September 19-21. These presentations include updated findings from a Phase 2 trial of lerociclib combined with fulvestrant for HR+, HER2- advanced breast cancer. Key details include:

  • Abstract 1407: Updated Phase 2 results.
  • Abstract 1417: cfDNA analysis from Phase 1/2 study.

Lerociclib is a differentiated oral CDK4/6 inhibitor, currently in trials for breast cancer and non-small cell lung cancer.

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RESEARCH TRIANGLE PARK, N.C., Sept. 14, 2020 (GLOBE NEWSWIRE) -- G1 Therapeutics, Inc. (Nasdaq: GTHX), a clinical-stage oncology company, today announced that two presentations highlighting data on the investigational oral CDK4/6 inhibitor lerociclib, including updated findings from a Phase 2 trial of lerociclib in combination with fulvestrant in HR+, HER2- advanced breast cancer patients, will be featured at the ESMO Virtual 2020 Congress being held from September 19-21.

G1 abstract titles are below; more details are available on the ESMO Virtual Congress 2020 website.

Title: Lerociclib (G1T38), a continuously dosed oral CDK4/6 inhibitor, with fulvestrant in HR+/HER2- advanced breast cancer patients: Updated Phase 2 results and dose selection
Abstract Number: 1407
Authors: Iurie Bulat, Arensia Exploratory Medicine Research Unit, Institute of Oncology, Chisinau, Moldova, et al

Title: cfDNA analysis from Phase 1/2 study of lerociclib (G1T38), a continuously dosed oral CDK4/6 inhibitor, with fulvestrant in HR+/HER2- advanced breast cancer patients
Abstract Number: 1417
Presenter: Boris Krastev, MD, MHAT for Women’s Health – Nadezhda, Sofia, Bulgaria

About Lerociclib
Lerociclib is a differentiated oral CDK4/6 inhibitor with potential use in combination with other targeted therapies in certain types of cancer.

At the San Antonio Breast Cancer Symposium (SABCS) in December 2019, G1 reported preliminary Phase 1/2 data on the differentiated safety and tolerability profile of lerociclib, along with preliminary efficacy findings that were consistent with other CDK4/6 inhibitors used in combination with fulvestrant.

Lerociclib is currently being evaluated in two Phase 1/2 clinical trials: a trial in combination with fulvestrant for patients with ER+, HER2- breast cancer (NCT02983071) and in combination with osimertinib in epidermal growth factor receptor mutated (EGFRm) non-small cell lung cancer (NCT03455829).

G1 entered into separate, exclusive agreements with EQRx (rights for U.S., Europe, Japan, and all markets outside Asia-Pacific) and Genor (rights for Asia-Pacific, excluding Japan) for the development and commercialization of lerociclib in all indications. EQRx and Genor are responsible for all costs related to the development and commercialization of lerociclib in their respective territories.

About G1 Therapeutics
G1 Therapeutics, Inc. is a clinical-stage biopharmaceutical company focused on the discovery, development and delivery of next generation therapies that improve the lives of those affected by cancer. The company is developing and advancing two novel therapies: trilaciclib is a first-in-class therapy designed to improve outcomes for patients being treated with chemotherapy; rintodestrant is a potential best-in-class oral selective estrogen receptor degrader (SERD) for the treatment of ER+ breast cancer. In 2020, the company out-licensed global development and commercialization rights to its differentiated oral CDK4/6 inhibitor, lerociclib.

G1 Therapeutics is based in Research Triangle Park, N.C. For additional information, please visit www.g1therapeutics.com and follow us on Twitter @G1Therapeutics.

Contact:
Investors:
Jeff Macdonald
Senior Director, Investor Relations & Corporate Communications
919-907-1944
jmacdonald@g1therapeutics.com

Media:
Christine Rogers
G1 Therapeutics, Inc.
Associate Director, Corporate Communications
984-365-2819
crogers@g1therapeutics.com


FAQ

What are the key findings from GTHX's Phase 2 trial of lerociclib?

The Phase 2 trial of lerociclib in combination with fulvestrant for HR+, HER2- advanced breast cancer presented updated findings at the ESMO Virtual Congress 2020.

When is the ESMO Virtual Congress 2020 where GTHX will present?

The ESMO Virtual Congress 2020 will be held from September 19-21, 2020.

What is the focus of G1 Therapeutics' presentations at the ESMO Congress?

G1 Therapeutics will focus on the investigational oral CDK4/6 inhibitor lerociclib, showcasing its Phase 2 trial results and cfDNA analysis.

What is lerociclib and its significance in cancer treatment?

Lerociclib is an investigational oral CDK4/6 inhibitor being evaluated for use with other therapies in various cancers, particularly in treating HR+, HER2- advanced breast cancer.

What are the abstract numbers for GTHX's presentations at ESMO 2020?

The abstract numbers for G1 Therapeutics' presentations are 1407 for the updated Phase 2 results and 1417 for the cfDNA analysis.

G1 Therapeutics, Inc.

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