IMMP Immutep

Immutep Appoints LAG-3 Pioneer, Frédéric Triebel to Board

Immutep Appoints LAG-3 Pioneer, Frédéric Triebel to Board

SYDNEY, AUSTRALIA, Sept. 13, 2022 (GLOBE NEWSWIRE) -- (ASX: IMM; NASDAQ: IMMP) (“Immutep” or “the Company”), a biotechnology company developing novel LAG-3-related immunotherapy treatments for cancer and autoimmune disease, is pleased to announce the appointment of its Chief Scientific Officer and Chief Medical Officer, Professor Frédéric Triebel, M.D. Ph.D. as Executive Director. Prof. Triebel will join the Immutep Board with immediate effect.

Prof. Triebel pioneered the recently validated LAG-3 field of immuno-oncology, having discovered the LAG-3 gene, its functions and medical usefulness while working at Institut Gustave Roussy (IGR), a large cancer centre in Paris. He founded Immutep S.A. in 2001 to develop LAG-3 product candidates as human medicines and became Chief Medical Officer and Chief Scientific Officer of Immutep following the Company’s acquisition of Immutep S.A in December 2014. While working at IGR as an oncologist, he was also a Professor in Immunology at Paris University and a Director of an INSERM Unit from 1991 to 1996.        

Immutep Chair, Russell Howard said: “It is a privilege to welcome Frédéric to Immutep’s Board. His discovery of the LAG-3 gene led to the emergence of LAG-3 as the 3rd immune checkpoint, after CTLA-4 and PD-1, earning him global industry recognition and respect. His ongoing work has positioned Immutep to lead this exciting space, with the greatest number of unique LAG-3 candidates currently in clinical development. Given Immutep’s growing industry profile as we commence our commercialisation journey, it is more important than ever that Frédéric is directly involved in setting our strategy.”

Prof. Triebel holds an M.D. and a Ph.D. in immunology (Paris University) and successfully developed several research programs in immunogenetics and immunotherapy, leading to 153 publications and 31 patents.

Prof. Triebel said: “I am very excited about the potential of our four LAG-3 product candidates, particularly efti which has reported strong clinical results over the last couple of years. Efti stands out for many reasons including its unique mechanism of action as an APC activator, a consistently favourable safety profile, and very good efficacy results across multiple tumour types, including patients with high unmet need. These factors are opening up multiple collaboration opportunities and commercialisation pathways for efti. I look forward to working as part of the Board to realise the value of this promising product candidate.”

About Immutep

Immutep is a globally active biotechnology company that is a leader in the development of LAG-3-related immunotherapeutic products for the treatment of cancer and autoimmune disease. Immutep is dedicated to leveraging its technology and expertise to bring innovative treatment options to market for patients and to maximize value to shareholders. Immutep is listed on the Australian Securities Exchange (IMM), and on the NASDAQ (IMMP) in the United States.

Immutep’s current lead product candidate is eftilagimod alpha (“efti” or “IMP321”), a soluble LAG-3 fusion protein (LAG-3Ig), which is a first-in-class antigen presenting cell (APC) activator being explored in cancer. Immutep is also developing an agonist of LAG-3 (IMP761) for autoimmune disease.

Additional LAG-3 products, including antibodies for immune response modulation, are being developed by Immutep’s large pharmaceutical partners.

Further information can be found on the Company’s website or by contacting:

Australian Investors/Media:

Catherine Strong, Citadel-MAGNUS

+61 (0)406 759 268;

U.S. Media:

Tim McCarthy, LifeSci Advisors

+1 (917) 679 9282; 



EN
13/09/2022

Underlying

To request access to management, click here to engage with our
partner Phoenix-IR's CorporateAccessNetwork.com

Reports on Immutep

 PRESS RELEASE

Immutep Receives A$4.6 million R&D Tax Incentive from French Governmen...

Immutep Receives A$4.6 million R&D Tax Incentive from French Government Media Release SYDNEY, AUSTRALIA, Nov. 03, 2025 (GLOBE NEWSWIRE) -- (ASX: IMM; NASDAQ: IMMP) ("Immutep“ or “the Company”), a late-stage immunotherapy company targeting cancer and autoimmune diseases, is pleased to announce it has received a €2,588,954 (~ A$4,567,769 ) research and development (R&D) tax incentive payment in cash from the French Government under its Crédit d’Impôt Recherche scheme (CIR). The “Crédit d’Impôt Recherche” (CIR), meaning “Research Tax Credit”, is a French government tax incentive by which ...

 PRESS RELEASE

Immutep Quarterly Activities Report Q1 FY26

Immutep Quarterly Activities Report Q1 FY26 Media Release Pivotal TACTI-004 (KEYNOTE-F91) Phase III trial evaluating eftilagimod alfa (efti) in first line non-small cell lung cancer continues to build momentum and is recruiting patients at a growing number of activated clinical sites and countriesTrial in Progress poster for TACTI-004 presented at the World Conference on Lung Cancer (WCLC) 2025, where physician feedback continued to be encouragingPositive feedback received from the FDA regarding future late-stage clinical development of efti in first line head and neck cancer patients with...

 PRESS RELEASE

Primary Endpoint Met in EFTISARC-NEO Phase II Evaluating Neoadjuvant E...

Primary Endpoint Met in EFTISARC-NEO Phase II Evaluating Neoadjuvant Efti in Soft Tissue Sarcoma and Data Presented at ESMO Congress 2025 Novel combination including eftilagimod alfa (efti) in neoadjuvant setting drives 51.5% tumour hyalinization/fibrosis in patients with soft tissue sarcoma (p

 PRESS RELEASE

Two Posters at ESMO Congress 2025 Highlight Immutep’s Focus on Changin...

Two Posters at ESMO Congress 2025 Highlight Immutep’s Focus on Changing Treatment Landscape in First Line Non-Small Cell Lung Cancer Novel combination of efti with KEYTRUDA® and chemotherapy generates strong response rates across all PD-L1 expression levels in first line non-small cell lung cancer (1L NSCLC) including 61.7% ORR in low & no PD-L1 (TPS

 PRESS RELEASE

Immutep Announces Successful Completion of FDA Project Optimus Require...

Immutep Announces Successful Completion of FDA Project Optimus Requirements Confirmation of 30mg efti as optimal biological dose relevant for Immutep’s oncology pipeline and potential future Biological License Applications (BLA)Registrational TACTI-004 (KEYNOTE-F91) Phase III trial in first line non-small cell lung cancer now in process of opening clinical sites in the United States SYDNEY, AUSTRALIA, Oct. 13, 2025 (GLOBE NEWSWIRE) -- (ASX: IMM; NASDAQ: IMMP) (“Immutep” or “the Company”), a late-stage immunotherapy company targeting cancer and autoimmune diseases, today announces that p...

ResearchPool Subscriptions

Get the most out of your insights

Get in touch