Country for PR: China
Contributor: PR Newswire Asia (China)
Thursday, August 13 2020 - 08:00
AsiaNet
Australian Therapeutic Goods Administration Approves the First Phase I Trial of ATG-017 for the Treatment of Patients with Advanced Solid Tumors and Hematological Malignancies
SHANGHAI and MELBOURNE, Australia, Aug. 13, 2020 /PRNewswire-AsiaNet/ --

Antengene Corporation, a leading innovative hematology and oncology-focused 
biopharmaceutical company, announced today the authorization of the 
first-in-human trial of ATG-017 (ERASER trial) by the Australian Therapeutic 
Goods Administration (TGA). ATG-017 is a potent and selective small molecule 
extracellular signal--regulated kinases 1 and 2 (ERK1/2) inhibitor. The study 
will enroll patients with advanced solid tumors and hematological malignancies. 
Today's milestone marks the first TGA trial authorization for Antengene and is 
the first clinical trial for ATG-017 globally.

ATG-017 is an oral, potent and highly selective inhibitor of ERK1/2, which are 
related protein-serine/ threonine kinases that function as the terminal kinases 
in the RAS-RAF-MEK-ERK signal transduction cascade. This pathway participates 
in the control of numerous processes which include apoptosis, cell 
proliferation, and cellular immune response. In preclinical studies, ATG-017 
has proven to regulate a large variety of cellular processes by targeting 
ERK1/2 and has shown to be effective in inhibiting the viability of tumor cell 
lines in vitro as well as the tumor growth in vivo. 

"This first human trial for ATG-017 in Australia is a significant step for our 
company's global clinical strategy and we will initiate overseas trials 
continuously for a number of novel drugs in our pipeline in the near future," 
said Dr. Jay Mei, M.D., Ph.D., Founder, Chairman and CEO of Antengene. "Our 
vision is to treat patients beyond borders. For Australian patients with 
life-threatening diseases and patients around the world, we are passionately 
working to continue to develop and commercialize more novel therapies to make a 
difference in patient 
lives."                                                           

"Aberrations in the MAPK pathway are amongst the most common in malignant 
cancer, so developing effective drugs targeting this pathway remains a high 
priority. We are excited to begin this trial with the ERK-targeting agent 
ATG-017, and bring together our group of highly experienced Australian 
investigators and sites to begin this collaboration with Antengene," said 
Associate Professor Jayesh Desai, Head of the Phase I/ Early Drug Development 
Program at the Peter MacCallum Cancer Centre.

"The RAS-MAPK pathway is a major player in a range of largely incurable 
hematological malignancies, so the potential to effectively target it with 
ATG-017 represents an exciting opportunity for Australian cancer patients. We 
very much look forward to collaborating with Antengene on this new trial," said 
Professor Andrew Spencer, Head of the Malignant Haematology and Stem Cell 
Transplantation Service at the Alfred Hospital, Melbourne.   

In November 2019, Antengene entered into a licensing agreement with AstraZeneca 
(LSE/STO/NYSE: AZN) under which Antengene has been granted the exclusive global 
rights to further develop, manufacture and commercialize AZD0364 (ATG-017). 
ATG-017 is currently being studied in clinical trials for the treatment of 
various solid tumors and hematological malignancies.

About ATG-017

ATG-017 is a potent and selective small molecule extracellular signal–regulated 
kinases 1 and 2 (ERK1/2) inhibitor in clinical development for the treatment of 
various solid tumors, non-Hodgkin's lymphoma, acute myeloid leukemia (AML) and 
multiple myeloma.

About Antengene

Antengene is a biopharmaceutical company with integrated drug discovery, 
clinical development, manufacturing and commercialization anchored in the Asia 
Pacific region and with a global layout, aiming to provide the most advanced 
first-in-class/best-in-class anti-cancer drugs and other treatments for 
patients in China, the rest of Asia and around the world. In April 2017, 
Celgene (now Bristol-Myers Squibb), a global leading innovative 
biopharmaceutical company became a founding partner and obtained an equity 
position as an investor in Antengene. Antengene has built a product pipeline of 
12 clinical and pre-clinical stage programs, obtained 9 IND approvals with 12 
ongoing cross-regional clinical trials in the Asia Pacific region. The vision 
of Antengene, "Treating Patients Beyond Borders", is to meet the unmet medical 
needs of patients in the Asia Pacific region and around the world through our 
research & development and commercialization of first-in-class/best-in-class 
cancer medicines. For more information, please visit www.antengene.com.

Forward-looking Statement

The forward-looking statements made in this article relate only to the events 
or information as of the date on which the statements are made in this article. 
Except as required by law, we undertake no obligation to update or revise 
publicly any forward-looking statements, whether as a result of new 
information, future events or otherwise, after the date on which the statements 
are made or to reflect the occurrence of unanticipated events. You should read 
this article completely and with the understanding that our actual future 
results or performance may be materially different from what we expect. In this 
article, statements of, or references to, our intentions or those of any of our 
Directors or our Company are made as of the date of this article. Any of these 
intentions may alter in light of future development.

SOURCE  Antengene Corporation