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ASX/Media Release Immutep Announces Publication of Abstracts for ASCO 2023 Annual Meeting New data published from Part C of TACTI-002 Phase II Trial evaluating eftilagimod alpha plus pembrolizumab in metastatic 2nd line

Key Takeaway: Immutep Limited announced the publication of abstracts for the ASCO 2023 Annual Meeting, highlighting data from Part C of its TACTI-002 Phase II trial involving eftilagimod alpha in metastatic cancer patients. The presentation will feature final results in head and neck squamous cell carcinoma, while another abstract for the AIPAC-003 Phase III trial was also shared. Eftilagimod alpha is under evaluation for multiple solid tumors and shows promise due to its favorable safety profile and innovative mechanism of action.

Market Sentiment Analysis

POSITIVE FACTORS

  • New data from the TACTI-002 trial has been published, enhancing knowledge of eftilagimod alpha's efficacy.
  • The upcoming poster presentation at ASCO promises to share more mature data which could validate the trial's outcomes.
  • Eftilagimod alpha has received Fast Track Designation from the FDA in crucial cancer indications.

Full Press Release Details

Immutep Announces Publication of Abstracts for ASCO 2023 Annual Meeting
SYDNEY, AUSTRALIA 26 May 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 disease, today announces data from Part C of its
TACTI-002 Phase II trial has been published in an abstract available on the 2023 American Society of Clinical Oncology s (ASCO) Annual Meeting s official website. A Trial
in Progress abstract for the Phase II/III AIPAC-003 trial has also been published.
The TACTI-002 poster will contain more mature (longer follow up) and final data that is not part of the abstract and will be available on the Posters & Publication section of Immutep s website after
its presentation at ASCO. Abstracts are available at ASCO.org.
Title: Final results from TACTI-002 Part C: A Phase II study of eftilagimod alpha (soluble LAG-3 protein) and pembrolizumab in patients with metastatic 2nd line head and neck squamous cell carcinoma unselected for PD-L1
Poster Session: Head and Neck Cancer
Date and Time: 5 June
2023, 2:15PM-5:15PM EDT
Presenter: Dr. Bernard Doger, START
Madrid-FJD, Fundaci n Jim nez D az University Hospital, Madrid, Spain
Title: AIPAC-003: A randomized, double-blind, placebo-controlled phase 3 trial
testing eftilagimod alpha (soluble LAG-3) in HER2-neg/low metastatic breast cancer patients receiving paclitaxel, following an
open-label dose optimization.
Poster Session: Breast Cancer Local/Regional/Adjuvant
Date and Time: 4 June 2023, 9:00AM-12:00PM EDT
Presenter: Dr. Nuhad K. Ibrahim, Professor, Department of Breast Medical Oncology, Division of Cancer Medicine, The University of Texas MD Anderson
Cancer Center, Houston, TX
About Eftilagimod Alpha (Efti)
Efti is Immutep s proprietary soluble LAG-3 protein and MHC Class II agonist that stimulates both innate and
adaptive immunity for the treatment of cancer. As a first-in-class antigen presenting cell (APC) activator, efti binds to MHC (major histocompatibility complex)
Class II molecules on APC leading to activation and proliferation of CD8+ cytotoxic T cells, CD4+ helper T cells, dendritic cells, NK cells, and monocytes. It also upregulates the expression of key biological molecules like IFN- and CXCL10 that further boost the immune system s ability to fight cancer.
Efti is under evaluation for a variety of solid tumours including non-small cell lung cancer (NSCLC), head and neck
squamous cell carcinoma (HNSCC), and metastatic breast cancer. Its favourable safety profile enables various combinations, including with anti-PD-[L]1 immunotherapy
and/or chemotherapy. Efti has received Fast Track Designation in 1st line HNSCC and in 1st line NSCLC from the United States Food and Drug Administration (FDA).
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 patients in need and to maximise value for shareholders. For more information, please visit www.immutep.com.
Australian Investors/Media:
+61 (0)406 759 268; cstrong@citadelmagnus.com
Chris Basta, VP, Investor Relations and
Corporate Communications
+1 (631) 318 4000; chris.basta@immutep.com
This announcement was authorised for release by the CEO of Immutep Limited.
Immutep Limited, Level 33, Australia Square, 264 George Street, Sydney NSW 2000, Australia

Frequently Asked Questions

What is the TACTI-002 trial about?

The TACTI-002 trial evaluates eftilagimod alpha with pembrolizumab in metastatic head and neck cancer.

When will the ASCO 2023 presentations take place?

The TACTI-002 presentation is on June 5, and AIPAC-003 on June 4, 2023.

What is Eftilagimod Alpha used for?

Eftilagimod Alpha treats various solid tumors and boosts the immune response.

Who will present the TACTI-002 trial results?

Dr. Bernard Doger will present the TACTI-002 trial results.

What designation has Efti received from the FDA?

Efti has received Fast Track Designation for first-line HNSCC and NSCLC.

Last updated: May 26, 2023