Lantern Pharma to Present AI-Driven Cancer Drug Development & Research Platforms at Inaugural AI for Biology and Medicine Symposium at UNT

On October 30, 2025 Lantern reported it will present two commercially deployed AI research platforms at the inaugural AI for Biology and Medicine (AI4BM) symposium at the University of North Texas. The symposium, hosted by Dr. Serdar Bozdag and the newly established Center for Computational Life Sciences, brings together leading researchers advancing the intersection of artificial intelligence and biomedicine.

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The Lantern Pharma team will deliver two presentations demonstrating how machine learning is transforming drug development and precision oncology through specific AI modules that are already delivering value to Lantern’s drug development efforts and other pharmaceutical companies and researchers:

"Machine Learning Ensemble Models for In Silico Screening and Prediction of Blood-Brain Barrier Permeability: A Comprehensive Approach Using Molecular Fingerprints and Descriptors". This presentation will showcase predictBBB.ai, Lantern’s commercially deployed platform that achieves 94.1% accuracy in predicting blood-brain barrier permeability—placing it at the top of the Therapeutic Data Commons leaderboard. The platform predicts BBB permeability in days rather than the months or years required by traditional methods, with the ability to screen 200,000 drug candidates in under a week. The ensemble model has been blindly validated on over 1,300 unseen molecules, demonstrating both accuracy and scalability for pharmaceutical companies developing CNS-targeted therapeutics and is available now as a commercial-ready resource.
"Machine Learning Models for Liquid Biopsy-Based Treatment Response Prediction and Biomarker Discovery in Cancer" Lantern will demonstrate LBx-AI, a production-ready platform that transforms liquid biopsy data into actionable insights with 86% accuracy in predicting treatment response for non-small cell lung cancer patients. Using a novel pathway-level engineering approach, the platform identifies complex biomarkers and pathway analytics that would be missed by traditional single-mutation analysis—with 20 out of 21 significant predictive markers being engineered pathway features. Beyond treatment prediction, LBx-AI can infer solid tumor characteristics from circulating tumor DNA, including accurate prediction of PD-L1 expression levels (0.76 Pearson correlation). Lantern is actively collaborating with world-class research institutions to further validate and improve the models’ performance across a number of tumor types, including GBM, and breast cancer.
Lantern believes that the platforms stand apart through three key differentiators: proven commercial deployment, dramatically compressed drug development timelines, and the generation of novel insights previously inaccessible through conventional methods. While traditional BBB permeability testing and biomarker discovery require months to years of laboratory work, Lantern’s AI models deliver comprehensive insights for drug development, candidate optimization, and target identification within days—maintaining enterprise-level scalability throughout. This transformation from lengthy experimental cycles to rapid computational analysis represents a fundamental shift in how pharmaceutical companies can approach drug discovery and development.

These advanced AI models power Lantern’s comprehensive cancer drug development ecosystem, which was initially developed as RADR. LBx-AI serves as a core component of RADR, Lantern’s AI-driven platform that accelerates precision oncology drug development, while predictBBB.ai operates as a standalone service helping pharmaceutical companies and research teams reduce development costs and improve success rates for CNS-targeted therapeutics.

"Our team is excited to share our efforts and platforms with leading researchers at this inaugural AI symposium," said Panna Sharma, President and CEO at Lantern Pharma. "We’re honored to present alongside distinguished researchers and look forward to engaging with the scientific community. Our vision extends beyond these current capabilities—we’re committed to making these powerful AI tools available as open-access platforms, democratizing advanced computational methods for researchers worldwide."

The symposium will feature keynote speaker Dr. Iman Hajirasouliha, Associate Professor of Systems and Computational Biomedicine at Weill Cornell Medicine, member of the Englander Institute for Precision Medicine and the Meyer Cancer Center, and Co-Director of the Tri-I Computational Biology and Medicine Ph.D. program.

For more information about the AI4BM symposium, visit: View Source

(Press release, Lantern Pharma, OCT 30, 2025, View Source;Research-Platforms-at-Inaugural-AI-for-Biology-and-Medicine-Symposium-at-UNT/default.aspx [SID1234657170])

Sapu Nano to present at the 2025 San Antonio Breast Cancer Symposium (SABCS) Highlighting Sapu003 (Deciparticle™ Everolimus)

On October 30, 2025 Oncotelic Therapeutics, Inc. (OTCQB: OTLC), a biopharmaceutical company founded to discover, create, test, and deliver transformative medicines to treat cancer patients by leveraging its novel PDAOAI platform and deep knowledge in nanomedicines and the tumor microenvironment, reported that Sapu Nano will be featuring its investigational intravenous Deciparticle everolimus (Sapu003) have been accepted for presentation at the 2025 San Antonio Breast Cancer Symposium (SABCS), to be held December 9-12, 2025, at the Henry B. Gonzalez Convention Center, San Antonio, Texas. Sapu Nano is the developer of DeciparticleTM and is part of Sapu family of companies and a joint venture between Oncotelic (OTCQB:OTLC) and Dragon Oversea.

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Sapu003 is a novel Deciparticle formulation of everolimus for intravenous administration, designed to overcome the pharmacologic limitations of oral mTOR inhibitors (Afinitor), including poor bioavailability, dose-limiting toxicity, and restricted tumor penetration. Collectively, the accepted abstracts highlight the clinical rationale, molecular biomarkers, and pharmacokinetic justification supporting the ongoing Phase 1 trial of Sapu003 in hormone receptor-positive (HR )/HER2 metastatic breast cancer and RCC and NET.

Renal Cell Carcinoma (RCC): FDA approved oral Everolimus for advanced RCC after failure of sunitinib and/or sorafenib. Approval was based on RECORD-1 randomized phase III (everolimus 10 mg PO daily vs placebo + best supportive care) showing a PFS benefit (median 4.9 vs 1.9 mo; HR 0.33).
Pancreatic NET (pNET): FDA approved Everolimus for Pancreatic NET (pNET). Approval was based on RADIANT-3 (everolimus vs placebo in progressive, advanced pNET), which significantly prolonged PFS.
GI and Lung NET (lNET): FDA approved Everolimus for GI & lung NET. Approval was based on RADIANT-4 (non-functional, well-differentiated, nonresectable/metastatic GI or lung NET), showing a PFS benefit.
Patients and Investigators – please contact Ingenu for trial participation.

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Phone: 1300 633 226
Email: [email protected]

Presentation Session:
Thursday, December 11, 2025 | 5:00 PM – 6:30 PM CST

Abstract Number Presentation Number Title
1834 PS4-04-04 High RICTOR / Low RPTOR Gene Expression Signature as a Predictive Biomarker for Intravenous Everolimus Nanoparticle (Sapu003): Rationale for the First in Human Trial
1702 PS4-04-21 Deciparticle Everolimus (Sapu003): From Cytostasis to Cytotoxicity via a Single mPEG Polymer and Clinic-Ready Manufacturing
1811 PS4-06-05 Sapu003: Everolimus for Injection – Pharmacokinetic Rationale for Phase I Evaluation in HR /HER2 Metastatic Breast Cancer

The studies were conducted in collaboration with Southern Oncology Clinical Research Unit (SOCRU), Ingenu CRO, and Medicilon, and reflect a coordinated clinical-translational effort bridging molecular biomarker discovery, pharmacokinetic modeling, and scalable GMP manufacturing of Deciparticle everolimus.

(Press release, Oncotelic, OCT 30, 2025, View Source [SID1234657169])

Nurix Therapeutics to Participate in Upcoming Investor Conferences

On October 30, 2025 Nurix Therapeutics, Inc. (Nasdaq: NRIX), a clinical-stage biopharmaceutical company focused on the discovery, development and commercialization of targeted protein degradation medicines, reported that Arthur T. Sands, M.D., Ph.D., president and chief executive officer of Nurix, will participate in fireside chats at the following investor conferences in November.

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Stifel 2025 Healthcare Conference, New York, NY
Thursday, November 13, 2025, from 9:20 – 9:50 a.m. ET
Jefferies Global Healthcare Conference – London, UK
Wednesday, November 19, 2025, from 11:00 – 11:25 a.m. GMT
The fireside chats will be webcast live and can be accessed via a link in the Investors section of the Nurix website. The archived webcasts will be available for 30 days after the event.

(Press release, Nurix Therapeutics, OCT 30, 2025, View Source [SID1234657168])

Syndax Announces Participation in November Investor Conferences

On October 30, 2025 Syndax Pharmaceuticals (Nasdaq: SNDX), a commercial-stage biopharmaceutical company advancing innovative cancer therapies, reported that Michael A. Metzger, Chief Executive Officer, as well as members of the Syndax management team, will participate in the following upcoming investor conferences:

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UBS Global Healthcare Conference 2025 with a fireside chat on Monday, November 10, 2025, at 11:00 a.m. ET.
Guggenheim Second Annual Healthcare Innovation Conference with a fireside chat on Tuesday, November 11, 2025, at 3:00 p.m. ET.
Stifel 2025 Healthcare Conference with a fireside chat on Thursday, November 13, 2025, at 10:00 a.m. ET.
Jefferies 2025 London Healthcare Conference with a fireside chat on Thursday, November 20, 2025, at 10:00 a.m. GMT/ 5:00 a.m. ET.
A live webcast of the fireside chats will be available in the Investor section of the Company’s website at www.syndax.com, where a replay will also be available for a limited time.

(Press release, Syndax, OCT 30, 2025, View Source [SID1234657166])

REGiMMUNE presented preclinical data of recent development of its antibody program at Antibody Engineering & Therapeutics Asia 2025 in Kyoto, Japan

On October 30, 2025 REGiMMUNE Limited ("REGiMMUNE" or "the Company"), a clinical stage biopharma company developing novel immune therapeutics targeting regulatory T cells (Treg), reported preclinical data of its antibody program at the meeting of Antibody Engineering & Therapeutics Asia 2025 in Kyoto, Japan from Oct. 20 – 22.

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REGiMMUNE, while pursuing RGI-2001 in advanced clinical development for (Graft vs Host Disease (GvHD), armed with our long-time expertise in human immunology and Treg cells, has been actively developing its therapeutic antibody program. This pipeline currently includes RGI-6004 and AB01, both targeting tumor infiltrating Treg cells, reflecting the two strategies of therapeutic modulation of Treg cells, namely, depleting vs silencing, and AB08-H1 targeting a surface marker shared by blood-borne and solid malignancies.

The presentation in Kyoto included RGI-6004 and AB08-H1. RGI-6004 was developed to highly selectively target tumor infiltrating Treg cells while maintaining all other immune effector cells intact to alleviate the immune suppression in the tumor microenvironment, and consequently enhance anti-cancer immunity. AB08-H1 is an antibody developed to kill malignant cells of Hodgkin & Non-Hodgkin diseases and solid cancer cells via a unique target.

RGI-6004, an Afucosylated Antibody to Target GARP/LAP-TGFβ1 for Selective Depletion of Activated Tregs. RGI-6004, a fully human IgG1 against GARP/Latent-TGFb1 complex, designed to deplete tumor infiltrating activated Treg cells. The antibody specifically binds to activated human Treg cells with high affinity, but none to non-activated Treg cells, and CD4+ and CD8+ T effector cells. The antibody recognizes tumor infiltrating Treg cells in clinical solid tumor tissues. Its afucosylated version highly selectively depletes activated Treg cells with a significantly enhanced efficacy of ~10 pM, but none of CD4+ and CD8+ effector T cells, while granzyme B induction & proliferation of CD4+ and CD8+ effector T cells are not affected. RGI-6004 has minimal impact on platelets (counts and degranulation), minimal binding to major immune cells, nor observable impact on hematological profile of normal human blood. In cynomolgus monkey, its t1/2 is shown to be ~10 days, while its clinical hematology, coagulation, blood chemistry, immunophenotyping in peripheral blood, serum cytokine analysis, and pathology, does not demonstrate safety alarms. In sum, the behavior of RGI-6004 highlights the potential as a next-generation Treg-depleting agent in cancer immunotherapy.

AB08-H1, A humanized antibody that directly kills cancer target cells without ADCC and CDC. AB08-H1 is a humanized IgG that specifically targets pan MHC II (synonym for HLA II, human leukocyte antigen). Upon binding to the cell surface MHC class II molecule, the antibody induces homotypic aggregation, lysosomal membrane permeabilization, and ultimately cell lysis of the target malignant cells directly without the involvement of ADCC and CDC. REGiMMUNE overcame the original bottleneck of protein production of the humanized IgG, developed a high yield method to manufacture it in mammalian cells. As MHC Class II molecules are found highly expressed on lymphoid malignant cells, and have been increasingly recognized to express highly in major solid cancer cells, AB08-H1 is expected to treat various types of lymphoid malignancies (Hodgkin and Non-Hodgkin lymphomas), and solid cancers.

REGiMMUNE is encouraged by the recent news of Nobel Prize in Physiology granted to Dr. Shimon Sakaguchi and others, for their works on Treg cells. We are pleased to see that the fundamental roles of Treg cells in autoimmune disease, GvHD, cancer, and infectious disease are recognized in highest profile. REGiMMUNE is committed to developing therapeutics with, as Dr. Shimon Sakaguchi well put it, Treg-up strategies vs Treg-down strategies.

(Press release, REGimmune, OCT 30, 2025, View Source [SID1234657165])