Immutep Receives FDA Fast Track Designation for LAG-3 Therapeutic Eftilagimod Alpha for First Line Non-Small Cell Lung Cancer

October 4, 2022

https://www.globenewswire.com/news-release/2022/10/04/2527727/0/en/Immutep-Receives-FDA-Fast-Track-Designation-for-LAG-3-Therapeutic-Eftilagimod-Alpha-for-First-Line-Non-Small-Cell-Lung-Cancer.html

SYDNEY, AUSTRALIA, Oct. 04, 2022 (GLOBE NEWSWIRE) — Immutep Limited (ASX:IMM; NASDAQ:IMMP) (“Immutep” or “the Company”), a clinical-stage biotechnology company developing novel immunotherapies for cancer and autoimmune disease, today announced the United States Food and Drug Administration (FDA) has granted Fast Track designation to eftilagimod alpha (“efti” or “IMP321”) in combination with pembrolizumab for the treatment of 1st line non-small cell lung cancer (NSCLC). Efti is the Company’s first-in-class soluble LAG-3 clinical stage candidate which activates antigen presenting cells (APC) to engage both the innate and adaptive immune system to target solid tumors.

Read more at globenewswire.com

Related news for (IMMP)

NASDAQ and NYSE quotes and data are delayed 15 minutes unless indicated otherwise. Market data and exchange information are provided for informational purposes only and is not intended for trading purposes. Neither 24/7 Market News Editors, 247 Market News, or data and content providers shall be liable for any errors or omissions, delays, misquotes or other market information relayed in any press materials. You should Use Realtime data to conduct due diligence before investing or trading, and trading in any stock is risky you could lose all your money.