Full Press Release Details
Enrolment Target for INSIGHT-003 Trial in 1st Line NSCLC
SYDNEY, AUSTRALIA 6 February 2023 Immutep Limited (ASX: IMM; NASDAQ: IMMP)
( Immutep or the Company ), a clinical-stage biotechnology company developing novel LAG-3 immunotherapies for cancer and autoimmune diseases, today announces the investigator-initiated INSIGHT-003 trial has reached its enrolment target of 20 patients with 1L NSCLC. INSIGHT-003 is the first trial evaluating Immutep s lead product candidate, eftilagimod
alpha ( efti or IMP321 ) as part of a triple combination therapy with standard-of-care anti-PD-1 therapy and chemotherapy.
Immutep s CSO & CMO Dr Frederic Triebel said, The
promising initial efficacy and favourable safety results reported in November 2022 from this first triple combination approach instils more confidence in the flexibility of our novel immunotherapy, efti, to be combined with various therapeutics and
safely drive superior patient outcomes. We are pleased to have reached our enrolment target and look forward to reporting as the results mature further. Additional data from INSIGHT-003 will help further
inform our next steps in 1st line NSCLC.
In a poster presented at the Society for
Immunotherapy of Cancer (SITC) Annual Meeting 2022, initial results in 1L NSCLC patients show the triple combination therapy is well-tolerated and provides promising early signals of therapeutic activity with an Objective Response Rate (ORR) of
72.7% (8/11) and a Disease Control Rate (DCR) of 90.9% (10/11). Nine patients had a PD-L1 Tumour Proportion Score (TPS) of <50% and this group reported an encouraging ORR of 66.7% and DCR of 88.9%. Patients
with a PD-L1 of <50% represent approximately two-thirds of the 1L NSCLC patient population and are less responsive to anti-PD-1 therapy compared to patients with a PD-L1 TPS of 50%.
Additional data from INSIGHT-003 is expected to be presented throughout calendar year 2023. For more information on
the study, please see the poster titled Feasibility of eftilagimod alpha (soluble LAG-3 protein) combined with
standard-of-care-therapy in advanced non-small-cell lung cancer (NSCLC). Initial results from INSIGHT 003 in the
Posters & Publications section of Immutep s website.
INSIGHT-003 is an investigator-initiated study conducted by the Institute of Clinical Cancer Research IKF at
Krankenhaus Nordwest in Frankfurt. It is being run as the third arm (Stratum C) of the ongoing Phase I INSIGHT trial with Prof. Dr. Salah-Eddin Al-Batran as lead investigator. The study is evaluating a triple combination therapy in front line non-small cell lung cancer patients consisting of efti administered subcutaneously in conjunction with an existing approved
standard-of-care combination of anti-PD-1 therapy (pembrolizumab) and chemotherapy
(carboplatin and pemetrexed) delivered intravenously. The trial will assess the safety, tolerability, and initial efficacy of the combination.
Immutep is a clinical stage biotechnology company developing novel LAG-3 immunotherapy for cancer and
autoimmune disease. We are pioneers in the understanding and advancement of therapeutics related to Lymphocyte Activation Gene-3 (LAG-3), and our diversified product
portfolio harnesses its unique ability to stimulate or suppress the immune response. Immutep is dedicated to leveraging its expertise to bring innovative treatment options to market for patients in need and to maximise value for shareholders. For
more information, please visit www.immutep.com.
Australian Investors/Media:
Catherine Strong, Citadel-MAGNUS
U.S. Investors/Media:
Chris Basta, VP, Investor Relations and Corporate Communications
+1 (631) 318 4000; chris.basta@immutep.com
announcement was authorised for release by the Board of Immutep Limited.
Immutep Limited, Level 33, Australia Square, 264
George Street, Sydney NSW 2000, Australia