Positive Initial Clinical Data Reported from Immutep’s Efti Combined with Radiotherapy and Checkpoint Inhibitor from Phase II Trial in Soft Tissue Sarcoma

On May 2, 2024 Immutep reported initial encouraging data from EFTISARC-NEO, a Phase II investigator-initiated trial of eftilagimod alpha (efti) in combination with radiotherapy, a standard-of-care treatment, plus KEYTRUDA (pembrolizumab) for patients with soft tissue sarcoma (STS) (Press release, Immutep, MAY 2, 2024, View Source [SID1234642534]).

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The EFTISARC-NEO study is the first to evaluate efti in a neoadjuvant setting, which takes place before intended surgery, and the first to combine efti with radiotherapy. Importantly, the neoadjuvant setting allows for the impact of this novel combination to be assessed in the tumour microenvironment (TME).

The triple combination has revealed no new safety findings and has been well tolerated in the first six patients who have completed the 10 weeks of treatment followed by surgery 2-3 weeks later. Initial efficacy data is very encouraging with 4 of 6 patients (67%) having near-complete responses according to EORTC-STBSDG, which measures responses via tissue pathology after surgery. These deep responses are rarely seen in STS patients with standard therapeutic approaches including
radiotherapy.

Katarzyna Kozak, M.D., Ph.D., and Paweł Sobczuk, M.D., Ph.D., medical oncologists at the Department of Soft Tissue/Bone Sarcoma and Melanoma at MSCNRIO (Warsaw), and the trial’s principal investigators stated: "The initial pathologic responses from this novel combination are very encouraging and supportive of the potential synergistic effects of this new therapeutic approach. Indeed we have seen a high degree of hyalinization/fibrosis in the surgical samples which we rarely see with standard treatments. We look forward to continuing this study."

Frédéric Triebel, M.D., Ph.D, Immutep’s Chief Scientific Officer, added: "We are pleased to see these early results from EFTISARC-NEO, which has allowed efti for the first time to be clinically evaluated in a non-metastatic cancer setting. The ability to evaluate tumour specimens is helping elucidate the significant anti-cancer immune response efti drives through its direct maturation and activation of antigen-presenting cells as an MHC Class II agonist. If the positive trend of strong pathological responses continues in this rare orphan disease, we will pursue all available avenues to bring this innovative therapy to soft tissue sarcoma patients in need of new, effective therapies in an expeditious manner."

Efti’s targeting and unique activation of dendritic cells, the most potent professional antigenpresenting cells, as a MHC Class II agonist leads to broad adaptive and innate immunity to fight cancer, including proliferation of CD8+ cytotoxic T cells that can be armed with radiotherapy-induced tumour antigens. The combination of efti with radiotherapy and anti-PD-1 therapy has the potential to generate a robust anti-tumour immune response in the immunosuppressed tumour microenvironment of soft tissue sarcoma.

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 (MSCNRIO) in Warsaw. The trial is primarily funded with an approved grant from the Polish government awarded by the Polish Medical Research Agency program. The study’s primary endpoint is the pathologic response rate (defined as percentage of tumor hyalinization/fibrosis) to the treatment assessed at the time of surgical resection. The lower the number of viable tumor cells and the higher the extent of hyalinization/fibrosis observed in patients’ tumor specimens will determine the therapy’s effectiveness. For more information, visit clinicaltrials.gov (NCT06128863).

The trial is ongoing with 14 patients now enrolled and additional clinical data is planned to be presented at a medical conference in H2 CY2024.

About Soft Tissue Sarcoma
Soft tissue sarcoma (STS), an orphan disease, represents a high unmet medical need with a poor prognosis. The incidence of STS varies in different regions, with approximately 23,400 cases annually and a crude incidence of 4.7 per 100,000 in Europe, according to the RARECARE project. In the United States, the number of new cases is estimated to be 13,400 annually with 5,140 deaths, according to the American Cancer Society.

About The Maria Skłodowska-Curie National Research Institute of Oncology
The Maria Skłodowska Curie National Research Institute of Oncology is the leading Polish comprehensive cancer centre, as well as the primary government research institution devoted solely to oncology. Founded in 1932 by Maria Sklodowska-Curie, it is currently divided into 28 specialised clinical departments responsible for the diagnostics and therapy of different tumour types such as: Breast Cancer Clinic, Head and Neck Cancer Clinic, General and Visceral Surgery, Thoracic Surgery, Urology, Gynaecology, Haematology, Soft Tissue/Bone Sarcoma and Melanoma Clinic, Radiation Oncology, Brachytherapy and Diagnostic Radiology, Pathology and Molecular Medicine and Cell Research, Oncology, Gastroenterology, Cancer Epidemiology and Prevention Division and others.

KURA ONCOLOGY TO REPORT FIRST QUARTER 2024 FINANCIAL RESULTS

On May 1, 2024 Kura Oncology, Inc. (Nasdaq: KURA), a clinical-stage biopharmaceutical company committed to realizing the promise of precision medicines for the treatment of cancer, reported that it will report first quarter 2024 financial results after the close of U.S. financial markets on Thursday, May 2, 2024. Kura’s management will host a webcast and conference call at 4:30 p.m. ET / 1:30 p.m. PT that day to discuss the financial results and provide a corporate update (Press release, Kura Oncology, MAY 2, 2024, View Source [SID1234642522]).

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The live call may be accessed by dialing (888) 886-7786 for domestic callers and (416) 764-8658 for international callers. A live webcast and archived replay of the event will be available here or online from the investor relations section of the company website at www.kuraoncology.com.

Quarterly report which provides a continuing view of a company’s financial position

On May 01, 2024 Corcept Therapeutics Incorporated (NASDAQ: CORT), a commercial-stage company engaged in the discovery and development of medications to treat severe endocrinologic, oncologic, metabolic and neurologic disorders by modulating the effects of the hormone cortisol, reported its results for the quarter ended March 31, 202 (Press release, Corcept Therapeutics, MAY 2, 2024, https://ir.corcept.com/node/15751/html [SID1234642508]).

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Immetas Therapeutics and GC Biopharma Announce Research Collaboration to Discover and Develop mRNA Therapeutics to Treat Autoimmune Diseases

On May 1, 2024 Immetas Therapeutics and GC Biopharma reported that they have entered into a research collaboration to discover and develop novel mRNA therapeutics for the treatment of a broad range of autoimmune diseases (Press release, Immetas Therapeutics, MAY 1, 2024, View Source [SID1234642588]). The collaboration combines Immetas’ proprietary platform for modulating innate immune pathways with GC Biopharma’s messenger RNA (mRNA) therapeutic and lipid nanoparticle (LNP) delivery platforms.

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"Immetas is pursuing an innovative approach to treating autoimmune diseases based on recent scientific advances in inflammation research and emerging technologies to target critical components in chronic inflammation pathways," said Jae Uk Jeong, PhD, Executive Vice President and head of R&D at GC Biopharma. "With our expertise in mRNA and nanoparticle delivery, this agreement allows us to jointly explore multiple projects with potential to make substantial improvements in the treatments offered to patients with autoimmune disorders."

J. Gene Wang, MD, PhD, co-founder and CEO of Immetas Therapeutics, commented, "As a leading global pharmaceutical company focused on hematologic and rare diseases, GC Biopharma has built a powerful mRNA/LNP platform that is well suited for accessing innate immune pathways to treat chronic inflammation-mediated disorders. Immetas has generated a comprehensive toolbox to modulate inflammasome activity by targeting multiple pathway mediators with various modalities. Our combined efforts offer the potential to generate a new class of therapeutics for chronic inflammation-mediated disorders with a high level of specificity and precision."

Under the collaboration agreement, Immetas will be responsible for identifying therapeutic targets, generating and characterizing payload molecules, defining disease indications and creating translational and clinical development strategies. GC Biopharma will be responsible for the design and manufacture mRNA constructs for payload expression, selection of LNP and delivery formulations, and characterization of the combination product candidates. Both companies will jointly conduct subsequent development activities. Additional terms were not disclosed.

Immetas’ approach is based on selective modulation of inflammasomes, key sensors and mediators of the innate immune pathway. Inflammasomes have been well characterized in chronic disorders involving multiple body systems, however, current inflammasome inhibitors to date have shown poor selectivity and presented safety challenges. Immetas has established a comprehensive platform that has generated novel therapeutic molecules targeting various components in the pathway with a high level of selectivity compared with traditional inhibitors to this structurally conserved family. The selection of modality, expression and delivery to optimize treatment outcome are determined by spatial and temporal requirement to effectively disrupt distinct disease biology in each condition. GC Biopharma’s mRNA/LNP approach is one of two delivery platforms Immetas is leveraging.

GC Biopharma has selected mRNA as the new development platform and has been conducting related research since 2017.

GSK makes a strong start to 2024 with improving outlook for the year

On May 1, 2024 GlaxoSmithKline reported a strong start to 2024 with improving outlook for the year (Press release, GlaxoSmithKline, MAY 1, 2024, View Source [SID1234642545]).

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