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News · 26 weeks34+83%
2025-10-262026-04-19
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Latest news
25 items- PRImmutep Announces Abstract Accepted for Presentation at the American Society of Clinical Oncology (ASCO) 2026 Annual MeetingSYDNEY, AUSTRALIA, April 22, 2026 (GLOBE NEWSWIRE) -- Immutep Limited ((ASX: IMM, NASDAQ:IMMP) ("Immutep" or "the Company"), a clinical-stage immunotherapy company targeting cancer and autoimmune diseases, today announces an abstract has been selected for poster presentation at the upcoming 2026 American Society of Clinical Oncology's (ASCO) Annual Meeting, taking place in-person and online from 29 May-2 June 2026 in Chicago, Illinois (United States). The accepted abstract, titled "Impact of eftilagimod alfa, an APC activator via MHC class II, on lymphocyte activation and survival outcomes in metastatic cancer patients," will be presented within the Developmental Therapeutics—Immunotherap
- INSIDERSEC Form 3 filed by new insider Boyce Elisabeth Amanda3 - IMMUTEP Ltd (0001506184) (Issuer)
- SECSEC Form 6-K filed by Immutep Limited6-K - IMMUTEP Ltd (0001506184) (Filer)
- PRImmutep Receives FDA Orphan Drug Designation for Eftilagimod Alfa in Soft Tissue SarcomaSYDNEY, AUSTRALIA, April 15, 2026 (GLOBE NEWSWIRE) -- Immutep Limited ((ASX: IMM, NASDAQ:IMMP) ("Immutep" or "the Company"), a clinical-stage biotechnology company targeting cancer and autoimmune diseases, today announces that the United States Food and Drug Administration (FDA) has granted Orphan Drug Designation (ODD) for eftilagimod alfa ("efti") for the treatment of Soft Tissue Sarcoma (STS), a rare cancer with significant unmet medical need. The FDA's Orphan Drug Designation program is designed to encourage development of therapies for rare diseases affecting fewer than 200,000 people in the United States. Benefits of ODD may include regulatory support, potential tax credits, fee exe
- INSIDERSEC Form 3 filed by new insider Voigt Marc3 - IMMUTEP Ltd (0001506184) (Issuer)
- INSIDERSEC Form 3 filed by new insider Miller Deanne Diem3 - IMMUTEP Ltd (0001506184) (Issuer)
- INSIDERSEC Form 3 filed by new insider Meyers Pete A.3 - IMMUTEP Ltd (0001506184) (Issuer)
- INSIDERSEC Form 3 filed by new insider Winckels Stephan Karel Gerard3 - IMMUTEP Ltd (0001506184) (Issuer)
- INSIDERSEC Form 3 filed by new insider Triebel Frederic Joseph Daniel3 - IMMUTEP Ltd (0001506184) (Issuer)
- INSIDERSEC Form 3 filed by new insider Howard Russell J3 - IMMUTEP Ltd (0001506184) (Issuer)
- INSIDERSEC Form 3 filed by new insider Mueller Christian3 - IMMUTEP Ltd (0001506184) (Issuer)
- PRImmutep Reports Progress from Phase I Study of LAG-3 Agonist for Autoimmune DiseasesImmutep has completed the single ascending dose (SAD) portion of its IMP761 study IMP761 was well tolerated across all dose levels IMP761 data and Phase I results will be presented at the EULAR conference on 4 June 2026 SYDNEY, AUSTRALIA, March 19, 2026 (GLOBE NEWSWIRE) -- Immutep Limited ((ASX: IMM, NASDAQ:IMMP) ("Immutep" or "the Company"), a clinical-stage biotechnology company targeting cancer and autoimmune diseases, today announces a positive update from the placebo-controlled, double-blind first-in-human Phase I study in healthy participants evaluating IMP761, a first-in-class LAG-3 agonist antibody which enhances the physiological inhibitory function of LAG-3 on T-cell receptor s
- SECSEC Form 6-K filed by Immutep Limited6-K - IMMUTEP Ltd (0001506184) (Filer)
- ANALYSTImmutep downgraded by Maxim GroupMaxim Group downgraded Immutep from Buy to Hold
- ANALYSTImmutep downgraded by Robert W. Baird with a new price targetRobert W. Baird downgraded Immutep from Outperform to Neutral and set a new price target of $1.00
- ANALYSTImmutep downgraded by CitizensCitizens downgraded Immutep from Mkt Outperform to Mkt Perform
- PRTACTI-004 Phase III Study in First Line NSCLC to be discontinued following Futility AnalysisIndependent Data Monitoring Committee Recommends Discontinuation of Phase III Trial Following Futility Analysis SYDNEY, AUSTRALIA, March 13, 2026 (GLOBE NEWSWIRE) -- Immutep Limited ((ASX: IMM, NASDAQ:IMMP) ("Immutep" or "the Company"), today announced that the Independent Data Monitoring Committee (IDMC) for the TACTI-004 Phase III study evaluating eftilagimod alfa ("efti") in patients in 1st line non-small cell lung cancer has recommended the discontinuation of the trial following a planned interim futility analysis in accordance with the study protocol. Based on its review of the available safety and efficacy data, the IDMC recommended that the trial be discontinued for futility. In
- SECSEC Form 6-K filed by Immutep Limited6-K - IMMUTEP Ltd (0001506184) (Filer)
- ANALYSTCitizens initiated coverage on Immutep with a new price targetCitizens initiated coverage of Immutep with a rating of Mkt Outperform and set a new price target of $6.00
- PRImmutep Achieves 50% Enrolment in Global TACTI-004 (KEYNOTE-F91) Phase III Trial in 1L NSCLCThe registrational TACTI-004 trial in first line non-small cell lung cancer (1L NSCLC) has enrolled 378 patients globally, 50% of the trial's targeted enrolment Futility analysis and completion of patient enrolment remain on track for the first quarter and the third quarter of CY2026, respectively SYDNEY, AUSTRALIA, Feb. 06, 2026 (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 achieved 50% of the patient enrolment target in the TACTI-004 (KEYNOTE-F91) Phase III trial evaluating eftilagimod alfa (efti) in combination with MSD's (Merck & Co., Inc.,
- SECSEC Form 6-K filed by Immutep Limited6-K - IMMUTEP Ltd (0001506184) (Filer)
- PRImmutep Quarterly Activities Report Q2 FY26Media Release Entered into strategic collaboration with Dr. Reddy's for commercialisation of eftilagimod alfa (efti) in all countries outside North America, Europe, Japan, and Greater ChinaIn January 2026, Immutep received ~A$30 million upfront payment from Dr. Reddy's and is eligible to receive up to ~A$528 million in potential milestones, plus royalties on commercial sales of eftiStrong operational progress reported for TACTI-004 (KEYNOTE-F91) Phase III trial evaluating efti in first line non-small cell lung cancer (1L NSCLC), with completion of the futility analysis on track for the first quarter of CY2026Data from INSIGHT-003 at ESMO Congress 2025 show combination of efti with KEYTRUDA®
- SECSEC Form 6-K filed by Immutep Limited6-K - IMMUTEP Ltd (0001506184) (Filer)
- PRImmutep Announces Positive Update on IMP761, a First-in-Class LAG-3 Agonist Antibody for Autoimmune Diseases, from Phase I StudySingle-ascending dose portion of study has successfully completed 2.5 and 7 mg / kg levelsDose dependent immunosuppressive effect against a strong foreign antigen observed with continued favourable safety profileSubstantial reduction in T cell activity highlights the potential efficacy of IMP761 in treating autoimmune diseasesGiven encouraging efficacy and safety, the trial will continue as planned and further updates are anticipated in 1H CY2026 including presentation of data at a major medical conference SYDNEY, AUSTRALIA, Dec. 22, 2025 (GLOBE NEWSWIRE) -- Immutep Limited ((ASX: IMM, NASDAQ:IMMP) ("Immutep" or "the Company"), a late-stage immunotherapy company targeting cancer and auto
- PRImmutep Announces Strong Operational Progress in Global TACTI-004 (KEYNOTE-F91) Phase III and Enrolment Continues at Robust PaceThe registrational TACTI-004 Phase III has enrolled 289 patients globally, over 38% of the trial's targeted enrolmentStrong operational progress continues globally with over 120 activated clinical sites and 27 countries having received full regulatory approvals including the United States Futility analysis remains on track for the first quarter of CY2026 and completion of patient enrolment in the third quarter of CY2026 SYDNEY, AUSTRALIA, Dec. 16, 2025 (GLOBE NEWSWIRE) -- Immutep Limited ((ASX: IMM, NASDAQ:IMMP) ("Immutep" or "the Company"), a late-stage immunotherapy company targeting cancer and autoimmune diseases, today reports strong operational progress in the TACTI-004 (KEYNOTE-F91