Welcome to our dedicated page for Immutep news (Ticker: IMMP), a resource for investors and traders seeking the latest updates and insights on Immutep stock.
Immutep Limited (IMMP) news covers a late-stage biotechnology company focused on Lymphocyte Activation Gene-3 (LAG-3)–related immunotherapies for cancer and autoimmune disease. The company regularly reports clinical, regulatory and corporate developments across its diversified LAG-3 portfolio, led by the MHC Class II agonist eftilagimod alfa (efti) and the LAG-3 agonist antibody IMP761.
On this page, readers can follow updates on Immutep’s major oncology programs, including the global TACTI-004 (KEYNOTE-F91) Phase III trial in first-line non-small cell lung cancer, as well as Phase II and investigator-initiated studies in head and neck squamous cell carcinoma, soft tissue sarcoma and metastatic breast cancer. News items highlight trial milestones such as patient enrolment progress, primary endpoint readouts, translational biomarker data and presentations at international conferences like the European Society for Medical Oncology (ESMO), the World Conference on Lung Cancer and the San Antonio Breast Cancer Symposium.
For autoimmune disease, Immutep publishes updates on the Phase I program for IMP761, a first-in-class LAG-3 agonist antibody designed to silence dysregulated self-antigen-specific memory T cells. News coverage includes safety, pharmacodynamic findings and proof-of-concept data from the ongoing first-in-human study.
Investors can also track regulatory interactions, such as Fast Track designations, FDA feedback on late-stage development strategies and completion of Project Optimus requirements, alongside business developments like the strategic collaboration and exclusive licensing agreement with Dr. Reddy’s Laboratories for efti in selected global markets. Corporate news, including R&D tax incentives from French and Australian government programs and quarterly activity reports, provides additional context on funding and operational progress.
Bookmark this page to monitor Immutep’s latest announcements, clinical data disclosures and SEC Form 6-K filings that shape the outlook for IMMP and its LAG-3–focused pipeline.
Immutep Limited (NASDAQ: IMMP) announced a collaboration with Merck KGaA for a Phase I/IIa clinical trial named INSIGHT-005, focusing on eftilagimod alpha in combination with bintrafusp alfa in previously treated patients with solid tumours. This new trial builds on previous encouraging data from the INSIGHT trial. The first patient is set to be enrolled in mid-2021, with initial data expected by early 2022. The study aims to investigate the safety and efficacy of this combination therapy, enhancing Immutep's ongoing relationship with Merck.
Immutep Limited (ASX: IMM; NASDAQ: IMMP) has announced the grant of a new patent by the Chinese Patent Office for its combination therapy involving eftilagimod alpha and chemotherapy agents like oxaliplatin. This adds to existing patents in Europe, Australia, Japan, and the U.S., enhancing Immutep's intellectual property rights in China until December 19, 2034. EOC Pharma, Immutep's partner in China, will develop this therapy, highlighting increasing collaboration in the oncology sector.
Immutep Limited (NASDAQ: IMMP) announced that CEO Marc Voigt will present at the Jefferies Virtual Healthcare Conference from June 1-4, 2021. The corporate presentation, alongside Chief Scientific and Medical Officer Dr. Frederic Triebel, is scheduled for June 4 at 12:30 PM ET. A live webcast will be available for the event. Immutep is focused on developing immunotherapy treatments for cancer and autoimmune diseases, with its lead product candidate being eftilagimod alpha (IMP321), which activates antigen presenting cells.
Immutep Limited (NASDAQ: IMMP) announced new data from its TACTI-002 and INSIGHT-004 studies presented at the 2021 ASCO Annual Meeting. The TACTI-002 study focused on eftilagimod alpha's efficacy as an immunotherapy for metastatic non-small cell lung cancer and squamous head and neck carcinoma. Meanwhile, the INSIGHT-004 trial evaluated the safety of eftilagimod alpha with avelumab in advanced solid tumors. These studies represent significant advancements in Immutep's ongoing research into LAG-3 related cancer treatments, potentially enhancing investor interest.
Immutep Limited (ASX: IMM; NASDAQ: IMMP) provided a significant update on its clinical trials, notably AIPAC and TACTI-002, reporting that AIPAC has reached 72% of events and TACTI-002 is progressing well with 54 patients enrolled. New data from these studies is expected to be presented at ASCO in June 2021. The TACTI-003 trial, evaluating efti with pembrolizumab, aims to start mid-2021, while the company maintains a robust financial position with a cash runway extending into 2023.
Immutep Limited (NASDAQ: IMMP) announced new data from its TACTI-002 and INSIGHT-004 studies, to be presented during the American Society of Clinical Oncology (ASCO) 2021 Annual Meeting from June 4-8. This includes three poster presentations focused on the efficacy of eftilagimod alpha in combination with pembrolizumab and avelumab across various cancers. The abstracts will be available on May 19, with further data shared in a subsequent webcast. These studies are pivotal in advancing LAG-3 immunotherapy treatments for cancer.
Immutep Limited (ASX: IMM; NASDAQ: IMMP) has made significant strides in its clinical trials, successfully dosing the final HNSCC patient in Stage 2 of Part C of the TACTI-002 study. Recruitment has begun for both first and second line NSCLC patients in the trial. The Phase II EAT COVID trial has also advanced into its randomized segment. As of March 31, 2021, the company reported a strong cash position of $51.7 million, providing a runway beyond 2022. The company has bolstered intellectual property protections for its lead candidate, eftilagimod alpha, with a new patent granted.
Immutep Limited (ASX: IMM; NASDAQ: IMMP) announced a cash rebate of A$1,155,055 from the Australian Federal Government’s R&D tax incentive program. This rebate pertains to expenses from eligible R&D activities during the 2020 fiscal year, primarily focusing on the TACTI-mel and TACTI-002 clinical studies involving eftilagimod alpha (efti). With approval from AusIndustry, Immutep’s Australian and overseas activities related to TACTI-002 are eligible for this tax incentive for three years, using the funds to further its clinical trials.
Immutep Limited (NASDAQ: IMMP) announced that its lead candidate, eftilagimod alpha (efti), has received FDA Fast Track designation for first-line recurrent or metastatic head and neck squamous cell carcinoma (HNSCC). This designation is based on promising data from its Phase II TACTI-002 trial, showing a 36% overall response rate. Additionally, preparations for the new Phase IIb TACTI-003 trial are advancing. Fast Track designation allows Immutep expedited development and review processes with the FDA, potentially leading to quicker patient access.
Immutep Limited (ASX: IMM; NASDAQ: IMMP) announced the grant of patent number EP3317301 by the European Patent Office, covering combination therapies involving its LAG525 antibody and spartalizumab for cancer treatment. This patent, co-owned with Novartis AG, extends until July 28, 2036. LAG525 is evaluated in several clinical trials by Novartis, and Immutep stands to receive milestone and royalty payments from its development.