• Live Feeds
    • Press Releases
    • Insider Trading
    • FDA Approvals
    • Analyst Ratings
    • Insider Trading
    • SEC filings
    • Market insights
  • Analyst Ratings
  • Alerts
  • Subscriptions
  • AI SuperconnectorNEW
  • Settings
  • RSS Feeds
Quantisnow Logo
  • Live Feeds
    • Press Releases
    • Insider Trading
    • FDA Approvals
    • Analyst Ratings
    • Insider Trading
    • SEC filings
    • Market insights
  • Analyst Ratings
  • Alerts
  • Subscriptions
  • AI SuperconnectorNEW
  • Settings
  • RSS Feeds
PublishGo to AppAI Superconnector
    Quantisnow Logo

    © 2025 quantisnow.com
    Democratizing insights since 2022

    Services
    Live news feedsRSS FeedsAlertsPublish with Us
    Company
    AboutQuantisnow PlusContactJobsAI superconnector for talent & startupsNEW
    Legal
    Terms of usePrivacy policyCookie policy

    Immutep Appoints Leading Oncologists to its Clinical Advisory Board

    5/18/22 8:00:00 AM ET
    $IMMP
    Biotechnology: Pharmaceutical Preparations
    Health Care
    Get the next $IMMP alert in real time by email

    SYDNEY, AUSTRALIA, May 18, 2022 (GLOBE NEWSWIRE) -- Immutep Limited ((ASX: IMM, NASDAQ:IMMP) ("Immutep" or "the Company"), a biotechnology company developing novel LAG-3-related immunotherapy treatments for cancer and autoimmune diseases, announced today the appointment of four new members to the Company's Clinical Advisory Board (CAB).

    The CAB serves as a strategic resource to Immutep as the Company continues to advance its pipeline of LAG-3 programs, including combination therapy programs for lead product candidate eftilagimod alpha ("efti" or "IMP321").

    Immutep CSO & CMO, Dr. Frederic Triebel, commented: "We are privileged to have a group of leading oncologists on our Clinical Advisory Board and are pleased to welcome several new members. The CAB's experience in the development of ground-breaking new cancer therapies will be invaluable as we look to advance efti into important late-stage development programs. In the coming months, we expect the CAB will particularly focus on our programs addressing metastatic breast and non-small cell lung carcinomas."

    The new appointments to Immutep's CAB are:

    Scott Antonia, M.D., Ph.D. is recognised as a global leader in the development of immunotherapy for lung cancer. He currently serves as the director of the Duke Cancer Institute (DCI) Center for Cancer Immunotherapy and is a member of the Thoracic Oncology disease group as Professor of Medical Oncology. He previously served as the chairman of the Department of Thoracic Oncology at H. Lee Moffitt Cancer Center. He has served as the global principal investigator for the practice-changing Pacific study, which established, as the new global standard of care, anti-PDL1 as consolidative therapy after combined chemo-radiation therapy for locally advanced non-small cell lung cancer. He was also the lead investigator of trials that established the clinical activity of immunotherapy for small cell lung cancer. For the past 27 years, Professor Antonia has directed a translational research program with the overall goal to develop immunotherapeutic strategies for the treatment of cancer patients.

    Leisha A Emens, M.D., Ph.D. is a Professor of Medicine at the UPMC Hillman Cancer Center. She received her MD/PhD in the Medical Scientist Training Program (MSTP) at Baylor College of Medicine, and completed postgraduate training at the National Cancer Institute, the University of Texas at Southwestern, and Johns Hopkins University. She joined the faculty at Johns Hopkins University in 2001, where she rose to the rank of Associate Professor of Oncology before joining the UPMC Hillman Cancer Center. She is a medical oncologist focused on breast cancer and is internationally recognised for her work in breast cancer immunotherapy. She developed and tested a vaccine for breast cancer patients, and more recently has played a key role in the development of the anti-PD-L1 agent

    atezolizumab for triple negative breast cancer and HER2+ breast cancer. Dr. Emens was a member of

    the FDA Advisory Committee on Cellular, Tissue, and Gene Therapies (CTGTC) from 2012 to 2016. She is an active member of ASCO, AACR, and SITC, and is a member of the Cancer Immunology (CIMM) Steering Committee of the AACR. Dr. Emens serves as Vice President of the Society for Immunotherapy of Cancer (SITC) and will ascend to the role of SITC President in 2023. She also serves as section editor for Journal for the Immunotherapy of Cancer (JITC).

    Martin Forster, M.D., Ph.D., is an associate professor at University College London (UCL) and consultant medical oncologist at University College Hospital. He specialises in lung cancer, thoracic and head and neck cancers and has a particular interest in drug development and in using the increasing understanding of cancer biology to design studies that distinguish patient populations most likely to gain benefit from new drugs and new drug combinations. Professor Forster is a core member of the lung and head and neck cancer teams and runs a research-based practice, being principal investigator or chief investigator for over 50 early and late-phase clinical trials, from first-in-human to registration Phase III trials. Professor Forster is the current clinical lead for the UCL Experimental Cancer Medicine Centre (ECMC) and clinical lead for cancer research at the University College London Hospitals (UCLH).

    Hans Wildiers, M.D., Ph.D., is a dedicated breast cancer researcher and medical oncologist. He has been a staff member at the Department of Medical Oncology at the University Hospital Leuven, Belgium, since 2004. In addition, he coordinates the Leuven Multidisciplinary Breast Centre since 2015. Professor Wildiers has coordinated several academic studies in the field of breast cancer and geriatric oncology and authored more than 300 peer reviewed papers. He has also been active on the board the International Society of Geriatric Oncology (SIOG), for many years, including serving as its president from November 2018 to October 2020. In addition, from 2009 to 2015, Professor Wildiers chaired the European Organisation for the Research and Treatment of Cancer's (EORTC) task force on cancer in the elderly.

    Further information on Immutep's CAB may be found here: https://www.immutep.com/about-us/leadership-team.html

    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 and infectious disease. 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 www.immutep.com or by contacting:

    Australian Investors/Media:

    Catherine Strong, Citadel-MAGNUS

    +61 (0)406 759 268; [email protected]

    U.S. Media:

    Tim McCarthy, LifeSci Advisors

    +1 (212) 915.2564; [email protected]



    Primary Logo

    Get the next $IMMP alert in real time by email

    Crush Q3 2025 with the Best AI Superconnector

    Stay ahead of the competition with Standout.work - your AI-powered talent-to-startup matching platform.

    AI-Powered Inbox
    Context-aware email replies
    Strategic Decision Support
    Get Started with Standout.work

    Recent Analyst Ratings for
    $IMMP

    DatePrice TargetRatingAnalyst
    5/17/2024$10.00Overweight
    CapitalOne
    8/3/2023$7.00Outperform
    Robert W. Baird
    8/3/2021$8.30Buy
    Ladenburg Thalmann
    7/16/2021$8.00Buy
    Maxim Group
    More analyst ratings

    $IMMP
    Analyst Ratings

    Analyst ratings in real time. Analyst ratings have a very high impact on the underlying stock. See them live in this feed.

    View All

    CapitalOne initiated coverage on Immutep with a new price target

    CapitalOne initiated coverage of Immutep with a rating of Overweight and set a new price target of $10.00

    5/17/24 7:43:01 AM ET
    $IMMP
    Biotechnology: Pharmaceutical Preparations
    Health Care

    Robert W. Baird initiated coverage on Immutep with a new price target

    Robert W. Baird initiated coverage of Immutep with a rating of Outperform and set a new price target of $7.00

    8/3/23 6:20:48 AM ET
    $IMMP
    Biotechnology: Pharmaceutical Preparations
    Health Care

    Ladenburg Thalmann initiated coverage on Immutep with a new price target

    Ladenburg Thalmann initiated coverage of Immutep with a rating of Buy and set a new price target of $8.30

    8/3/21 8:13:45 AM ET
    $IMMP
    Biotechnology: Pharmaceutical Preparations
    Health Care

    $IMMP
    Press Releases

    Fastest customizable press release news feed in the world

    View All

    $IMMP
    SEC Filings

    View All

    Immutep Receives Positive Feedback from FDA on Late-Stage Clinical Development of Eftilagimod Alfa in Head and Neck Cancer with CPS <1

    SYDNEY, AUSTRALIA, Aug. 05, 2025 (GLOBE NEWSWIRE) -- Immutep Limited ((ASX: IMM, NASDAQ:IMMP) ("Immutep" or "the Company"), a late-stage immunotherapy company targeting cancer and autoimmune diseases, today announces it has received positive and constructive feedback from the US Food and Drug Administration (FDA), regarding future clinical development of its first-in-class MHC Class II agonist, eftilagimod alfa ("efti"), for first line treatment of recurrent/metastatic head and neck squamous cell carcinoma (1L HNSCC) patients who have PD-L1 expression below 1 (Combined Positive Score [CPS] <1). Based on its review of the encouraging data in 1L HNSCC with CPS <1 from the TACTI-003 (KEYNOTE

    8/5/25 8:00:00 AM ET
    $IMMP
    Biotechnology: Pharmaceutical Preparations
    Health Care

    Immutep Quarterly Activities Report Q4 FY25

    Media Release The pivotal TACTI-004 Phase III trial in first line non-small cell lung cancer (1L NSCLC) 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 2025 American Society for Clinical Oncology (ASCO) Annual MeetingNovel combination of efti with KEYTRUDA® (pembrolizumab) and chemotherapy in INSIGHT-003 trial achieves high response rate of 60.8% and 90.2% disease control rate (N=51) in 1L NSCLC In high unmet need patients with TPS <50% (N=47), who represent over two-thirds of 1L NSCLC population, the triple combination with efti achieved a 59.6% response rate as comp

    7/30/25 8:00:00 AM ET
    $IMMP
    Biotechnology: Pharmaceutical Preparations
    Health Care

    Immutep to Present Pivotal TACTI-004 Trial in Progress Poster at the 2025 World Conference on Lung Cancer

    SYDNEY, AUSTRALIA, July 29, 2025 (GLOBE NEWSWIRE) -- Immutep Limited ((ASX: IMM, NASDAQ:IMMP) ("Immutep" or "the Company"), a late-stage immunotherapy company targeting cancer and autoimmune diseases, today announces an upcoming poster presentation for the pivotal TACTI-004 (KEYNOTE-F91) Phase III trial at the IASLC 2025 World Conference on Lung Cancer (WCLC), taking place in Barcelona, Spain, from 6-9 September 2025. The Trial in Progress poster includes an overview and study design of the TACTI-004 Phase III evaluating the Company's antigen presenting cell (APC) activator, eftilagimod alfa (efti) in combination with MSD's (Merck & Co., Inc., Rahway, NJ, USA) anti-PD-1 KEYTRUDA® (pembrol

    7/29/25 8:00:00 AM ET
    $IMMP
    Biotechnology: Pharmaceutical Preparations
    Health Care

    SEC Form 6-K filed by Immutep Limited

    6-K - IMMUTEP Ltd (0001506184) (Filer)

    8/6/25 7:14:15 PM ET
    $IMMP
    Biotechnology: Pharmaceutical Preparations
    Health Care

    SEC Form 6-K filed by Immutep Limited

    6-K - IMMUTEP Ltd (0001506184) (Filer)

    7/30/25 8:39:56 PM ET
    $IMMP
    Biotechnology: Pharmaceutical Preparations
    Health Care

    SEC Form 6-K filed by Immutep Limited

    6-K - IMMUTEP Ltd (0001506184) (Filer)

    6/23/25 8:42:02 PM ET
    $IMMP
    Biotechnology: Pharmaceutical Preparations
    Health Care

    $IMMP
    Large Ownership Changes

    This live feed shows all institutional transactions in real time.

    View All

    SEC Form SC 13G/A filed by Immutep Limited (Amendment)

    SC 13G/A - IMMUTEP Ltd (0001506184) (Subject)

    2/9/24 7:59:50 AM ET
    $IMMP
    Biotechnology: Pharmaceutical Preparations
    Health Care

    SEC Form SC 13G/A filed by Immutep Limited (Amendment)

    SC 13G/A - IMMUTEP Ltd (0001506184) (Subject)

    2/9/23 7:57:21 AM ET
    $IMMP
    Biotechnology: Pharmaceutical Preparations
    Health Care

    SEC Form SC 13G filed by Immutep Limited

    SC 13G - IMMUTEP Ltd (0001506184) (Subject)

    2/9/22 8:58:14 AM ET
    $IMMP
    Biotechnology: Pharmaceutical Preparations
    Health Care

    $IMMP
    Leadership Updates

    Live Leadership Updates

    View All

    Immutep Appoints Leading Research Institute to Conduct First-in-Human Phase I Study of IMP761

    Media Release Centre for Human Drug Research (CHDR) will conduct Phase I trial to evaluate IMP761, a first-in-class LAG-3 agonist antibody designed to restore balance to the immune system and address the underlying cause of autoimmune diseasesCHDR will utilize its unique challenge model that enables insights into IMP761's pharmacological activity early in clinical developmentTrial expected to begin mid-CY2024 SYDNEY, AUSTRALIA, April 18, 2024 (GLOBE NEWSWIRE) -- 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 it has entered into an agreem

    4/18/24 8:00:00 AM ET
    $IMMP
    Biotechnology: Pharmaceutical Preparations
    Health Care

    Immutep Selects Charles River Laboratories for IMP761's GLP Toxicology Study

    Media Release Appointment of Charles River Laboratories ("Charles River") to run Immutep's preclinical toxicology study evaluating the safety and toxicity of IMP761Forms a key step prior to first-in-human trials for this first-in-class LAG-3 agonist antibody designed to treat the underlying cause of multiple autoimmune diseasesCharles River is a highly respected, global provider of drug discovery and non-clinical development solutions operating more than 110 sites across more than 20 countries SYDNEY, AUSTRALIA, May 29, 2023 (GLOBE NEWSWIRE) -- Immutep Limited ((ASX: IMM, NASDAQ:IMMP) ("Immutep" or "the Company"), a clinical-stage biotechnology company developing novel LA

    5/29/23 8:00:00 AM ET
    $IMMP
    Biotechnology: Pharmaceutical Preparations
    Health Care

    Immutep Quarterly Activities Report

    Media Release Initiation of integrated Phase II/III AIPAC-003 trial evaluating eftilagimod alpha (efti) and paclitaxel in HER2-neg/low metastatic breast cancer and triple-negative breast cancerPositive final data reported from patients with 2nd line non-small cell lung cancer refractory to anti-PD-(L)1 therapies, including Overall Survival rate of 39% at 21 monthsRandomised TACTI-003 Phase IIb trial has reached 75% enrolment subsequent to quarter end and top line results anticipated in H2 of CY2023Expansion of INSIGHT-003 evaluating triple combination of efti, pembrolizumab and chemotherapy post encouraging initial safety and efficacy in 1st line non-small cell lung cancerSolid cash pos

    4/27/23 8:00:00 AM ET
    $IMMP
    Biotechnology: Pharmaceutical Preparations
    Health Care

    $IMMP
    Financials

    Live finance-specific insights

    View All

    Immutep's Efti in Combination with KEYTRUDA® Generates Excellent Overall Survival Benefit in Patients with Metastatic Non-Small Cell Lung Cancer

    Media Release Median Overall Survival reaches 35.5 months in first-line treatment of metastatic non-small cell lung cancer patients expressing PD-L1 (TPS >1%), 23.4 months in patients with low PD-L1 expression (TPS 1-49%), and has not been reached in patients with high PD-L1 expression (TPS >50%), exceeding expectationsPromising Overall Survival, Overall Response Rate, Progression Free Survival, and Duration of Response visible across all PD-L1 subgroups (TPS <1%, ≥1%, 1-49%, and ≥50%), differentiates efti in combination with KEYTRUDA® from other chemotherapy-free immuno-oncology combinations in non-small cell lung cancerExceptional durability and quality of responses exhibited through ove

    10/23/23 8:00:00 AM ET
    $IMMP
    Biotechnology: Pharmaceutical Preparations
    Health Care

    Immutep Announces Publication of Abstracts at ESMO Congress 2023

    Media Release New updated data from TACTI-002, including more mature Overall Survival data, will be presented during the Mini Oral session on Saturday, October 21st, at 9:05 CESTImmutep to host webcast to discuss ESMO 2023 clinical data on Monday, October 23rd, at 8AM AEDT (Sunday, October 22nd, at 5PM ET) SYDNEY, AUSTRALIA, Oct. 16, 2023 (GLOBE NEWSWIRE) -- 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 the publication of abstracts with data from the TACTI-002 and INSIGHT-003 trials in 1st line non-small cell lung cancer (1L NSCLC) at t

    10/16/23 8:00:00 AM ET
    $IMMP
    Biotechnology: Pharmaceutical Preparations
    Health Care