Actuate Therapeutics Announces Nature Medicine Publication of Clinical Trial Results Showing Doubling of the Rate of Survival with Elraglusib Plus Chemotherapy in Previously Untreated Metastatic Pancreatic Ductal Adenocarcinoma

On April 14, 2026 Actuate Therapeutics, Inc. (NASDAQ: ACTU) ("Actuate" or the "Company"), a clinical-stage biopharmaceutical company focused on developing therapies for the treatment of high-impact, difficult-to-treat cancers through the inhibition of glycogen synthase kinase-3 beta (GSK-3β), reported the publication of new data in Nature Medicine from a randomized phase 2 clinical trial (NCT03678883) evaluating elraglusib in combination with the gemcitabine-Nab-paclitaxel (GnP) chemotherapy compared to GnP alone in patients with previously untreated metastatic pancreatic cancer. The peer-reviewed paper (DOI: 10.1038/s41591-026-04327-4), entitled "Elraglusib and Chemotherapy in Metastatic Pancreatic Ductal Adenocarcinoma: A Randomized Controlled Phase 2 Trial" is available here.

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"These Phase 2 results continue to reinforce elraglusib’s potential as a combination-ready, first-line therapy with the ability to enhance the activity of standard of care chemotherapeutic backbones," said Daniel Schmitt, Chief Executive Officer of Actuate. "The significant improvement in overall survival with an acceptable safety profile marks an important milestone for patients facing metastatic pancreatic cancer, historically one of the most difficult to treat diseases. The elraglusib containing regimen delivered a 40% improvement in median overall survival, a 38% lower risk of death, and doubled the survival rate at one year compared to the current first-line chemotherapy regimen of GnP alone.

By targeting a central signaling node such as GSK-3β, elraglusib may modulate tumor cell survival, reshape tumor microenvironment, and suppress adaptive resistance pathways, enabling a broader biological impact across a broad range of cancers. Importantly, we are also advancing our research focused on exploring the expected synergistic potential of elraglusib in combination with RAS and MEK/RAF inhibitors, with the goal of further enhancing anti-tumor activity and broadening elraglusib’s therapeutic potential for patients. We remain deeply committed to advancing treatments that can improve patients’ lives and are grateful to the investigators and families who made this study possible."

Pancreatic cancer remains one of the deadliest malignancies worldwide. Pancreatic ductal adenocarcinoma (PDAC), which accounts for the majority of cases, is often diagnosed at a metastatic stage, where survival outcomes remain poor. For these patients, GnP is a commonly used first‑line regimen, yet median overall survival typically remains limited to approximately seven to ten months. Despite advances in understanding the molecular drivers of pancreatic cancer, meaningful therapeutic progress has been scarce, and immunotherapies successful in other solid tumors have not delivered similar benefits in PDAC, highlighting the urgent need for novel treatment approaches.

Elraglusib (9‑ING‑41), a first‑in‑class GSK‑3β inhibitor, was evaluated in combination with GnP in a global, open‑label, phase 2 study in previously untreated metastatic pancreatic ductal adenocarcinoma. Patients were randomized 2:1 to receive elraglusib plus GnP or GnP alone. The combination improved median overall survival to 10.1 months versus 7.2 months and reduced the risk of death by 38% (HR 0.62; p=0.01), with one‑year survival rates of 44.1% and 22.3%, respectively. Safety was generally manageable in the elraglusib/GnP combination, with the most common Grade ≥3 adverse events including neutropenia, anemia, and fatigue. Exploratory analyses identified cytokine biomarkers and immune‑cell changes consistent with the immunomodulatory effect of elraglusib.

Key Highlights and Readouts:

Among the 286 patients enrolled across 60 global sites, efficacy analyses focused on 155 patients treated with once‑weekly elraglusib plus GnP and 78 patients receiving GnP alone in the modified intent‑to‑treat population, the study’s prespecified population for efficacy and safety analyses.
Median overall survival (OS) was 10.1 months in the elraglusib/GnP arm (95% CI, 7.7–12.5) vs 7.2 months on the GnP arm (95% CI, 5.7–9.0), corresponding to a 2.9‑month improvement and a 38% reduction in risk of death (HR 0.62; p=0.01).
A 1-year survival rate of 44.1% was observed in patients receiving elraglusib/GnP compared with 22.3% treated with GnP alone; at 18 and 24 months, landmark survival rates were 20.5% and 13.2% vs 4.4% and 0%, respectively.
Survival benefits were consistent across poor prognosis subgroups; in patients with liver metastases, median OS was 8.3 vs 6.6 months (HR 0.62; p=0.008), and 1‑year survival rates were 39.2% vs 15.2%.
Exploratory immunophenotyping demonstrated 7–40X increases in intratumoral CD8⁺ T cells, granzyme‑B⁺ cells, and CD56⁺ NK cells following elraglusib/GnP, with no comparable increases observed with GnP alone.
High pre‑dose cytokine levels correlated with improved survival only in the elraglusib/GnP arm, indicating emerging predictive biomarker associations.
The combination was well tolerated; the most common ≥Grade 3 TEAEs with elraglusib/GnP vs GnP were neutropenia (52.3% vs 30.8%), anemia (25.2% vs 29.5%), and fatigue (16.8% vs 5.1%). The mild to moderate visual changes observed in the elraglusib arm were transient and reversible.

"Metastatic pancreatic cancer remains one of the most therapeutically challenging solid tumors, with few interventions demonstrating meaningful improvements in survival," said Dr. Devalingam Mahalingam, MD, PhD, lead author of the manuscript. "The 2.9-month improvement in median overall survival observed with elraglusib plus gemcitabine and nab-paclitaxel, together with early and sustained signals of benefit across poor-prognosis subgroups, is encouraging and supports further clinical evaluation. The observed increases in tumor-infiltrating cytotoxic immune cells provide preliminary biologic context for the clinical findings and raise the possibility of an immunomodulatory effect, although these exploratory observations will require confirmation in future studies. Collectively, these results provide a rationale for continued investigation of elraglusib-based combinations in pancreatic cancer and potentially other difficult-to-treat malignancies."

(Press release, Actuate Therapeutics, APR 14, 2026, View Source [SID1234664390])

EpimAb Biotherapeutics to Present a Novel Prodrug T-Cell Engager (ProTCE) Platform at the 2026 American Association for Cancer Research Annual Meeting

On April 14, 2026 EpimAb Biotherapeutics, a clinical stage biotechnology company specializing in the development of bispecific antibodies and T-cell engagers, reported that the company will be presenting a Novel Prodrug T-Cell Engager (ProTCE) Platform poster presentation at the upcoming 2026 American Association for Cancer Research (AACR) (Free AACR Whitepaper) Annual Meeting taking place at the San Diego Convention Center in San Diego, California, from April 17-22, 2026.

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The posters will feature: ProTCE Platform and Initial Pre-clinical Proof of Concept for EM33. Details for the presentation are as follows:

ProTCE Platform and its Candidate ProTCE EM33

Title: A novel and versatile Prodrug T cell engager platform with a novel candidate demonstrating potent and tumor-restricted activity
Presentation Number: 1610
Presentation Date: Monday, April 20, 2026
Presentation Time: 9:00AM – 12:00PM, local time (Location: Poster Section 10)

"We are pleased to present our Prodrug T-cell engager technology platform at AACR (Free AACR Whitepaper) annual conference. This achievement validates the global competitiveness and clinical translation potential of our proprietary innovations, marking a key milestone in advancing the company’s R&D capabilities," said Dr. Chengbin Wu, Founder and CEO of EpimAb. "Moving forward, the platform aims to address key unmet medical needs and advance the development of safer and more effective therapeutic options for patients worldwide."

(Press release, EpimAb Biotherapeutics, APR 14, 2026, View Source [SID1234664389])

EvolveImmune Therapeutics to Present Update on Lead Asset EVOLVE104 and New Data for EVOLVE T Cell Engager Platform at 2026 AACR Annual Meeting

On April 14, 2026 EvolveImmune Therapeutics, a clinical-stage immuno-oncology company developing a new class of multi-specific T cell engagers with integrated CD2 costimulation, reported that new data highlighting its novel EVOLVE T cell engager platform will be presented at the 2026 American Association for Cancer Research (AACR) (Free AACR Whitepaper) Annual Meeting. The conference is being held April 17-22, 2026, in San Diego, California.

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Details of the company’s presentations at the AACR (Free AACR Whitepaper) conference are as follows:

Oral Minisymposium Presentation #4055:

Title: Integrated CD2-costimulation on CD3 T cell engager EVOLVE platform yields differentiated and superior T cell effector profile
Presenting Author: Emma Stewart, Ph.D., EvolveImmune Therapeutics
Session Title: Advances in Therapeutic Antibodies
Session Date/Time: Monday, April 20, 2026, 2:30 – 4:30 p.m. PT
Location: Ballroom 20 CD – Upper Level – Convention Center
Poster Presentation #CT079:

Title: EIU-104101: A first-in-human phase 1a/1b study of EVOLVE104, a trispecific CD3×CD2×ULBP2/5/6 T cell engager, in advanced urothelial and squamous cell carcinomas
Presenting Author: Tony Fiorino, M.D., Ph.D., EvolveImmune Therapeutics
Session Title: Phase I Clinical Trials in Progress
Session Date/Time: Monday, April 20, 2026, 9:00 a.m. – 12:00 p.m. PT
Location: Poster Section 51; Poster Board #10
Poster Presentation #5594:

Title: Pharmacological integration of CD3 and CD2 signaling triggers formation of a CD2 corolla that boosts T cell activation
Presenting Author: Sergio Trombetta, Ph.D., EvolveImmune Therapeutics
Session Title: T Cell Engagers 2/Antibody-Drug Conjugates 1
Session Date/Time: Tuesday, April 21, 2026, 2:00 – 5:00 p.m. PT
Location: Poster Section 8; Poster Board #13
About EVOLVE104
EVOLVE104 is a next-generation trispecific T cell engager that binds CD3 and CD2 on T cells and the tumor-associated antigens ULBP2/5/6, which have limited expression in normal human tissues and are found on a number of epithelial-derived malignancies, including urothelial carcinoma and a broad array of squamous cell carcinomas. In preclinical studies, EVOLVE104 has demonstrated compelling single-agent activity and combination activity with anti-PD-1 therapy, the ability to reinvigorate dysfunctional T cells, and a promising safety profile. EVOLVE104 is currently being studied in a first-in-human phase 1 clinical trial in subjects with advanced, relapsed or refractory solid tumors (NCT07217171).

(Press release, EvolveImmune Therapeutics, APR 14, 2026, View Source [SID1234664388])

Er-Kim Signs Exclusive Distribution Agreement with LEO Pharma A/S to Commercialize LOQTORZI® (toripalimab) for Nasopharyngeal and Oesophageal Cancers

On April 14, 2026 Er-Kim, an international pharmaceutical company specializing in the commercialization of novel therapies in the EMEA region, reported that it has signed an exclusive agreement with LEO Pharma A/S to commercialize LOQTORZI (toripalimab) in select regions in Central and Eastern Europe (CEE).

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Under the terms of the agreement, Er-Kim will serve as the exclusive commercial partner for LOQTORZI in the following markets: Bulgaria, Croatia, Czechia, Estonia, Hungary, Latvia, Lithuania, Poland, Romania, Slovakia, and Slovenia.

This PD-1 inhibitor is an intravenous immunotherapy that harnesses the body’s immune system to identify and attack cancer cells. In the European Union, the treatment is indicated for two distinct, hard-to-treat malignancies:

Nasopharyngeal Carcinoma (NPC): A rare and aggressive cancer of the head and neck. The therapy is used in combination with cisplatin and gemcitabine for adults with recurrent (non-resectable) or metastatic NPC as a first-line option, or as a monotherapy for those who have previously undergone chemotherapy.
Oesophageal Squamous Cell Carcinoma (OSCC): For patients with advanced, recurrent, or metastatic OSCC that cannot be removed by surgery. In these cases, it is used in combination with cisplatin and paclitaxel.
Cem Zorlular, Chief Executive Officer of Er-Kim, said, "Advancements in immunotherapy are fundamentally changing the outlook for patients with nasopharyngeal carcinoma and oesophageal squamous cell carcinoma, but innovation only matters when it reaches the people who need it. By leveraging our deep infrastructure and relationships in Central and Eastern Europe, we are pleased to partner with LEO Pharma to bridge this access gap and bring LOQTORZI to oncology patients throughout the CEE region."

"We are committed to advancing cancer care by making innovative treatments available to this vulnerable group of patients who face limited options. Er‑Kim’s regional knowledge makes them a strong partner to bring LOQTORZI to new markets in Central and Eastern Europe," said Jean Monin, Executive Vice President of the Critical Care Business Unit at LEO Pharma A/S. "Together, we can make a difference for the patients and healthcare professionals we serve."

In 2025, LEO Pharma A/S was granted exclusive distribution and sales rights for LOQTORZI in the European Union (EU), the European Economic Area (EEA), as well as Switzerland and the United Kingdom, while TopAlliance Biosciences remains the Marketing Authorisation Holder (MAH).

(Press release, Erkim Pharmaceuticals, APR 14, 2026, View Source [SID1234664387])

Clinical Data Supporting Targeted Chemotherapeutic Delivery via RenovoRx’s TAMP™ Therapy Platform Presented at 2026 SIR Annual Scientific Meeting

On April 14, 2026 RenovoRx, Inc. ("RenovoRx" or "the Company") (Nasdaq: RNXT), a life-sciences company developing innovative targeted oncology therapies and commercializing RenovoCath, a patented, FDA-cleared drug-delivery device, reported that a clinical data abstract submitted by experts from Moffitt Cancer Center was presented at the 2026 Society of Interventional Radiology (SIR) Annual Scientific Meeting in Toronto, Canada.

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The abstract, entitled "What PET/CT Reveals After Transarterial Microperfusion for Pancreatic Cancer," was presented on April 13, 2026 by a multidisciplinary team of experts, including Dr. Mustafa Al-Roubaie, an Interventional Radiologist at Moffitt Cancer Center and member of RenovoRx’s Medical Advisory Board.

The abstract examined the effectiveness of local, targeted intra-arterial chemotherapy administration using RenovoRx’s patented TAMP (Trans-Arterial Micro-Perfusion) therapy platform. By delivering chemotherapy directly near the tumor site, TAMP helps to overcome the poor vascularity typical of solid tumors like locally advanced pancreatic cancer (LAPC), where intravenous chemotherapy is often less effective. Additionally, the abstract assessed the potential application of metabolic imaging, FDG (fluorodeoxyglucose) PET/CT, in evaluating therapeutic outcomes following targeted intra-arterial drug-delivery via TAMP in patients with refractory disease.

The study concluded that TAMP is a promising approach for localized delivery of chemotherapeutic agents for the treatment of solid tumors such as LAPC, offering the potential for enhanced therapeutic drug-delivery with reduced systemic toxicity. Metabolic imaging further demonstrated dramatic reductions in FDG avidity, suggesting treatment response even when tumor size changed minimally. Eight cycles of intra-arterial chemotherapy were administered over 2 months, using the TAMP therapy platform, which is enabled by the Company’s RenovoCath device. Post-treatment imaging results indicated that PET/CT may detect early treatment response before anatomical changes occur.

"Patients diagnosed with LAPC face a challenging prognosis, due in part to a dense, hypovascular stroma that can restrict the effectiveness of traditional systemic (namely intravenous) chemotherapy," said Dr. Al-Roubaie. "Systemic chemotherapeutic administration is often associated with considerable toxicity and suboptimal tumor penetration. The TAMP therapy platform aims to increase local drug concentration directly near the tumor site while reducing systemic exposure."

Dr. Al-Roubaie continued, "These findings support RenovoRx’s TAMP therapy platform and its ability for local intra-arterial chemotherapeutic delivery directly near the tumor site and the potential for reduced toxicity for patients. These findings may complement RenovoRx’s ongoing Phase III TIGeR-PaC clinical trial evaluating the company’s lead drug-device product candidate (intra-arterial gemcitabine delivered via RenovoCath, known as IAG) for the treatment of LAPC."

About RenovoCath
Based on its FDA clearance, RenovoCath is intended for the isolation of blood flow and delivery of fluids, including diagnostic and/or therapeutic agents, to select sites in the peripheral vascular system. RenovoCath is also indicated for temporary vessel occlusion in applications including arteriography, preoperative occlusion, and chemotherapeutic drug infusion. For further information regarding our RenovoCath Instructions for Use ("IFU"), please see: IFU-10004-Rev.-G-Universal-IFU.pdf.

(Press release, Renovorx, APR 14, 2026, View Source [SID1234664386])