New Data to be Presented from EFTISARC-NEO Phase II Evaluating Novel Triple Combination including Immutep’s Efti in Soft Tissue Sarcoma
18 Septembre 2024 - 2:00PM
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 new data from EFTISARC-NEO, a Phase II
investigator-initiated trial of eftilagimod alpha (efti) in
combination with radiotherapy plus KEYTRUDA® (pembrolizumab) for
patients with soft tissue sarcoma (STS), will be
presented at the Connective Tissue Oncology Society (CTOS) 2024
Annual Meeting taking place 13-16 November 2024, in San Diego,
California.
Presentation Details |
Title: |
Preliminary Results from a Phase 2 EFTISARC-NEO Trial of
Neoadjuvant Soluble LAG-3 Protein Eftilagimod Alpha, Pembrolizumab,
and Concurrent Radiotherapy in Patients with Resectable Soft Tissue
Sarcoma |
Presenter: |
Pawel Sobczuk, M.D., Ph.D., Department of Soft Tissue/Bone
Sarcoma and Melanoma, Maria Sklodowska-Curie National Research
Institute of Oncology, Warsaw, Poland |
Date: |
Thursday, 14 November
2024 |
Format: |
Poster Presentation |
|
|
EFTISARC-NEO is the first to evaluate efti in a
neoadjuvant setting, which importantly provides access to tumour
tissue before and after treatment to assess efti’s impact on the
tumour microenvironment. Initial efficacy data from this novel
triple combination reported in May 2024 showed very encouraging
results in the first six patients with the majority having deep
responses rarely seen in STS patients with standard therapeutic
approaches.
STS is an orphan disease with high unmet medical
need and a poor prognosis for patients. The incidence of STS varies
in different regions across Europe, with ~23,400 cases annually
according to the RARECARE project. In the United States, the number
of new STS cases in 2024 is estimated to be ~13,590 with ~5,200
deaths, according to the American Cancer Society.
The open-label EFTISARC-NEO Phase II study will
treat up to 40 patients and is being conducted by the Maria
Skłodowska-Curie National Research Institute of Oncology in Warsaw.
The trial is primarily funded with an approved grant from the
Polish government awarded by the Polish Medical Research Agency
program. For more information, visit clinicaltrials.gov
(NCT06128863).
Immutep will announce the data to the ASX and
make the poster presentation available on the Posters &
Publications section of Immutep’s website, after the presentation
at CTOS 2024.
About ImmutepImmutep 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:Catherine Strong, Sodali & Co.+61
(0)406 759 268; catherine.strong@sodali.com
U.S. Media:Chris Basta, VP,
Investor Relations and Corporate Communications+1 (631) 318 4000;
chris.basta@immutep.com
Immutep (NASDAQ:IMMP)
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