VERAXA Biotech Provides Overview on Implementation of FDA-Aligned Human-Relevant Models into R&D Strategy

On October 7, 2026 VERAXA Biotech AG (NASDAQ: VRXA; "VERAXA" or the "Company"), a leading developer of next-generation antibody-based cancer therapies, reported an update on its strategy and progress to implement a suite of U.S. Food and Drug Administration (FDA) aligned New Approach Methodologies (NAMs) across its preclinical research and development programs, potentially enabling faster clinical advancement while significantly reducing animal testing. This strategic implementation positions VERAXA ahead of the FDA’s 2025 roadmap, which encourages the phased reduction and ultimate replacement of animal testing in favor of human-relevant, non-animal and non-clinical test methods for developing safe and effective therapies.

Schedule your 30 min Free 1stOncology Demo!
Discover why more than 1,500 members use 1stOncology™ to excel in:

Early/Late Stage Pipeline Development - Target Scouting - Clinical Biomarkers - Indication Selection & Expansion - BD&L Contacts - Conference Reports - Combinatorial Drug Settings - Companion Diagnostics - Drug Repositioning - First-in-class Analysis - Competitive Analysis - Deals & Licensing

                  Schedule Your 30 min Free Demo!

NAMs encompass a range of technologies, including cell-based assays, organ-on-chip systems, computational modeling and ex vivo tissue models, designed to more accurately predict human biological responses while reducing dependence on animal models. Beyond this regulatory alignment, the shift toward more sustainable and ethical research practices is also expected to reduce development costs and timelines, for example, by bypassing certain non-human primate (NHP) toxicology studies traditionally required ahead of clinical development.

"We see NAMs as not just a regulatory obligation, but also as a scientific opportunity," said Christoph Erkel, Ph.D., Chief Scientific Officer of VERAXA. "We’ve been investing in translational, human-relevant model systems well ahead of the FDA’s 2025 roadmap, and we see this shift as beneficial and a win-win situation for both science and sustainability. Reducing our reliance on animal studies, particularly NHP toxicology testing, allows us to generate more clinically predictive data, move faster, and do so more efficiently and sustainably."

VERAXA has been building a multi-layered panel of NAMs to characterize and de-risk its pipeline of BiTAC (bi-targeted tumor-associated cytotoxicity) based T cell engagers (BiTAC-TCEs), BiTAC-based antibody drug conjugates (BiTAC-ADCs) and bispecific antibody-drug conjugates (bsADCs) technologies. At the AACR (Free AACR Whitepaper) Annual Meeting 2026, the Company presented initial data on its most advanced BiTAC-TCE program. In those studies, the candidate performed as intended in vitro and in vivo, attacking cancer cells that displayed both target molecules while sparing cells expressing only one of the two, with a safety profile that was superior, and efficacy that matched, a more traditional TCE, pointing to the possibility of a meaningfully improved therapeutic index. The in vitro results came from three-dimensional, cell line-derived spheroid models, which recapitulate solid tumor architecture more closely than two-dimensional culture. VERAXA has since generated new spheroid data demonstrating consistent predictivity of T cell engagement specificity across diverse cancer cell lines and validating the model for IND-enabling studies, further reinforcing this model’s translational value ahead of clinical development.

VERAXA further evaluated its lead BiTAC-TCE and bsADC candidates in an ex vivo panel of ten low-passage patient-derived xenograft models of non-small cell lung cancer, models that closely preserve the molecular characteristics, heterogeneity, and therapeutic response of the original tumors. Because these assays draw on tumor material from a small number of donor mice and can be split into many parallel patient samples, the panel required only about ten mice in total, versus an estimated 200 or more for comparable in vivo efficacy studies.

Across the panel, the combined BiTAC consistently induced potent T cell-mediated killing, while relevant controls, including commercial T cell engagers against non-expressed targets, showed only minimal activity, providing strong evidence that VERAXA’s dual-targeting approach extends beyond cell line models into clinically meaningful anti-tumor activity, validating the need for simultaneous dual-target engagement and reinforcing BiTAC as a next-generation approach to T cell redirection. This ex vivo platform demonstrates how VERAXA’s NAM strategy reduces both animal use and preclinical cycle time without compromising clinical relevance.

(Press release, Veraxa Biotech, OCT 7, 2026, View Source [SID1234673278])

Byondis to Profile Potential of Platform Technologies at World ADC San Diego, Advancing Strategy to Lead the Antibody-Drug Conjugate Field

On October 7, 2026 Byondis B.V., a private biopharmaceutical company engineering antibody-drug conjugates (ADCs) to tackle the cancers that current therapies cannot reach, reported it will share progress from its platform technology portfolio at World ADC San Diego, the world’s largest ADC conference, being held from 12-15 October in San Diego, USA.

Schedule your 30 min Free 1stOncology Demo!
Discover why more than 1,500 members use 1stOncology™ to excel in:

Early/Late Stage Pipeline Development - Target Scouting - Clinical Biomarkers - Indication Selection & Expansion - BD&L Contacts - Conference Reports - Combinatorial Drug Settings - Companion Diagnostics - Drug Repositioning - First-in-class Analysis - Competitive Analysis - Deals & Licensing

                  Schedule Your 30 min Free Demo!

With more than 20 years of in-house ADC expertise, Byondis is evolving the ADC field with novel payload platforms, advanced masking technology and optimized linker and conjugation strategies. These enable ADC solutions that can overcome the critical limitations of current and next-generation therapies with the potential for superior efficacy, duration of response and safety, to improve clinical outcomes in patients with difficult-to-treat tumor types.

Overcoming ADC Resistance
The company is advancing an IND-enabling (regulatory non-clinical) package to completion for its lead proprietary ADC candidate, BYON14156, marking a key step towards clinical trial authorization. Harnessing the company’s first-in-class antifolate payload and targeting an antigen highly expressed across multiple tumor types, BYON14156 is engineered to overcome the major challenge seen in current and next-generation ADCs with payload resistance. Dose range-finding toxicity studies in non-human primates have shown a benign toxicity profile and a favorable therapeutic window. Earlier studies have demonstrated efficacy across a range of tumor models in vitro and in vivo, including topoisomerase and tubulin inhibitor-resistant models.

Wim Dokter, PhD, Chief Scientific Officer at Byondis, will share a presentation at World ADC entitled Spotlighting Comprehensive Preclinical Development of Antifolate ADCs to Enter IND Phase for a Novel Drug-Linker Mechanism on Wednesday 14 October at 11.00am PDT, in which he will profile the development of BYON14156, ahead of its advancement into the clinic, anticipated in 2027.

The advancement of BYON14156 is a key part of the company’s strategy to establish itself as a leader in the development of ADCs, through its platform technologies and the modular, end-to-end capabilities that underpin the company.

A Universal Solution to Reduce Off-Tumor Toxicity
Byondis’ best-in-class steric masking technology, ByonGuard, which is designed to improve the therapeutic index of ADCs, T cell engagers and other antibody-based therapies, and provide a universal solution to reduce off-tumor toxicity, will be highlighted on Monday 12 October at 10.30am PDT in the presentation, Introducing ByonGuard: Conditional Activation Technology that Improves the Safety Profile & Therapeutic Index of ADCs. Wim Dokter will explore the rationale to develop conditionally active ADCs to overcome challenges with target-mediated toxicity and improve therapeutic index, and share safety and efficacy findings from Byondis’ latest research.

Christoph Korpus, PhD, MBA, Chief Executive Officer of Byondis, said: "The progress of our first-in-class antifolate payload ADC candidate towards the clinic is a clear demonstration of the strength of our platform technologies in action. It reflects the focused strategy we have built over the past year: prioritizing the proprietary platforms with the greatest potential to address the limitations of current and next-generation ADCs, while pursuing partnerships that can accelerate the impact of our technologies for patients. This candidate brings forward Byondis’ most advanced platform technology, and its progress reinforces our conviction as we continue to engage with potential partners across our platform portfolio."

Under the leadership of Christoph Korpus, PhD, MBA, who was appointed as Chief Executive Officer in April 2026, Byondis has sharpened its focus on the continued development of its proprietary technology platforms, each of which are engineered to work independently or in combination to address multiple hallmarks of cancer, alongside the pursuit of partnering, licensing and co-development opportunities to maximize value.

Byondis’ fully integrated discovery, development and manufacturing capabilities give the company the flexibility to advance its proprietary pipeline independently, while its modular platform approach enables broad partnering flexibility through co-development, licensing and strategic collaboration. The company continues to actively engage with prospective partners across its antifolate, immunostimulatory phosphonate and dual payload platforms, and its steric masking technology.

(Press release, Byondis, OCT 7, 2026, View Source [SID1234673277])

Artelo Biosciences Selected for its First-Ever Company Presentation at BIO-Europe 2026 to Showcase Clinical Progress and Expanding Potential of its Novel FABP5 Inhibitor Platform

On October 7, 2026 Artelo Biosciences, Inc. (Nasdaq: ARTL) ("Artelo" or the "Company"), a clinical-stage pharmaceutical company focused on modulating lipid-signaling pathways to develop treatments for people living with obesity, cancer, pain, dermatologic and neurological conditions, reported that it has been selected to deliver a company presentation at BIO-Europe 2026, being held November 9-11, 2026, in Cologne, Germany. Artelo will be presenting at 4:15pm CET on November 10th and this will be Artelo’s first company presentation at BIO-Europe.

Schedule your 30 min Free 1stOncology Demo!
Discover why more than 1,500 members use 1stOncology™ to excel in:

Early/Late Stage Pipeline Development - Target Scouting - Clinical Biomarkers - Indication Selection & Expansion - BD&L Contacts - Conference Reports - Combinatorial Drug Settings - Companion Diagnostics - Drug Repositioning - First-in-class Analysis - Competitive Analysis - Deals & Licensing

                  Schedule Your 30 min Free Demo!

The award of the presentation comes at an important point in the advancement of Artelo’s pipeline, following favorable clinical and nonclinical data reported across multiple programs this year. Artelo intends to use BIO-Europe to continue its business development outreach with interested potential partners and to open new conversations around both its clinical-stage and earlier-stage assets.

Artelo’s participation at BIO-Europe follows a series of clinical and nonclinical developments featuring its ART26.12 program, including:

FABP5 – Novel Therapeutic Target: ART26.12 is designed to inhibit fatty acid binding protein 5 ("FABP5"), an emerging therapeutic target that Artelo believes has potential applications in peripheral neuropathy, osteoarthritis and other pain-related conditions.
ART26.12 – Single Ascending Dose study: Phase 1 data in healthy volunteers showed a favorable safety and tolerability profile across all cohorts, with linear, dose-proportional pharmacokinetics. Separately reported human metabolite data demonstrated favorable drug metabolism characteristics.
ART26.12 – Preliminary Food Effect study: Results from healthy volunteers who received ART26.12 under fasted and under fed (low-fat and high-fat) conditions suggest the FABP5 inhibitor can be dosed effectively thereby potentially providing versatility in dosing regimens depending upon the indication.
ART26.12 – Peripheral Neuropathy: In five nonclinical studies, ART26.12 showed both the potential to treat painful neuropathies associated with diabetes or chemotherapy and to prevent its occurrence when dosed concurrently with two commonly used chemotherapies, paclitaxel and oxaliplatin, known to cause high incidences of chemotherapy induced peripheral neuropathy (CIPN).
ART26.12 – Osteoarthritis (OA): A nonclinical OA study demonstrated that oral administration of ART26.12 significantly reduced OA-associated pain over a 4-week period, demonstrating efficacy comparable to naproxen. ART26.12 produced distinct changes in endocannabinoids and other related bioactive lipids and proteins compared to naproxen, supporting a novel mechanism of action for ART26.12. Animals treated with ART26.12 exhibited significantly less stomach tissue damage, including non-glandular hyperkeratosis, compared to those receiving naproxen.
Senior Vice President and Chief Scientific Officer of Artelo Biosciences, Andrew Yates, Ph.D., will deliver the Company’s presentation at BIO-Europe. Dr. Yates also plans to meet with pharmaceutical and biotechnology companies and to seek to establish relationships with prospective partners, particularly in the areas of pain and inflammation.

"BIO-Europe brings together many of the organizations that are actively searching for differentiated programs in the areas where we are generating data," said Dr. Yates. "While we are grateful to feature our clinical experience with the first selective FABP5 inhibitor to enter the clinic, we also expect to advance our business development outreach with interested potential partners during BIO-Europe, and to show the breadth of what we have built across our wider portfolio in pain, cancer cachexia, and obesity."

Pharmaceutical and biotechnology companies interested in meeting with Dr. Yates and learning more about Artelo’s programs are encouraged to request a meeting through the BIO-Europe partnering portal, which is now open. Artelo looks forward to meeting with both existing and prospective partners in Cologne as the Company continues to evaluate partnering opportunities across its portfolio.

About ART26.12

ART26.12, Artelo’s lead Fatty Acid Binding Protein 5 (FABP5) inhibitor, is under development as a novel, peripherally acting, non-opioid, non-steroidal analgesic, initially for the treatment of chemotherapy-induced peripheral neuropathy. Human studies with ART26.12 have demonstrated a favorable safety profile with no serious adverse events, as well as predictable, linear pharmacokinetics and dosing flexibility in both fed and fasted states. Fatty Acid Binding Proteins (FABPs) are a family of intracellular proteins that chaperone lipids important to normal cellular function. In addition to ART26.12, Artelo’s extensive library of small molecule inhibitors of FABPs has shown therapeutic promise for the treatment of certain cancers, neuropathic and nociceptive pain, psoriasis, and anxiety disorders.

(Press release, Artelo Biosciences, OCT 7, 2026, View Source [SID1234673276])

ITM and Lumara Bio to Announce New Data for ¹⁷⁷Lu-edotreotide (ITM-11) and Ga-DPI-4452 at EANM 2026

On October 7, 2026 ITM Isotope Technologies Munich SE (ITM), a leading radiopharmaceutical biotech company, and Lumara Bio, a dedicated oncology therapeutics division of ITM, reported that new data for 177Lu-edotreotide (ITM-11) and Ga-DPI-4452 (CA-IX peptide) will be unveiled in two top-rated oral presentations at the European Association of Nuclear Medicine (EANM) Congress, held from October 17 – 21, 2026 in Vienna, Austria.

Schedule your 30 min Free 1stOncology Demo!
Discover why more than 1,500 members use 1stOncology™ to excel in:

Early/Late Stage Pipeline Development - Target Scouting - Clinical Biomarkers - Indication Selection & Expansion - BD&L Contacts - Conference Reports - Combinatorial Drug Settings - Companion Diagnostics - Drug Repositioning - First-in-class Analysis - Competitive Analysis - Deals & Licensing

                  Schedule Your 30 min Free Demo!

Anthime Flaus, MD, PhD, of the Hospital Louis Pradel in Bron, France will present dose-response findings from the Phase 3 COMPETE trial, in which patients with gastroenteropancreatic neuroendocrine tumors were treated with 177Lu-edotreotide. Alina Küper, MD, of the University Hospital Essen in Germany will present interim results from an independent, retrospective analysis of the PET/CT imaging agent Ga-DPI-4452 (CA-IX peptide) used for the imaging of clear cell renal cell carcinoma in a bicenter registry.

In addition to the scientific presentations, ITM will host a booth reception and separate Meet the Expert session. At this session, Dr. Neil Quigley will share insights into the production of Actinium-225 (225Ac) using medium-energy cyclotrons and present Actineer’s approach to increase production capacity. Actineer is the joint venture between ITM and Canadian Nuclear Laboratories.

Oral Presentation Details
Title: Ga-DPI-4452 (CA-IX peptide) PET/CT for Imaging Clear Cell Renal Cell Carcinoma: Interim Results from a Bicentre Registry
Session Title: Renal Cell Cancer and Novel Targets
Session Number: 506
Track: Clinical Oncology
Date and Time: Sunday, October 18, 2026, 15:00 – 16:30 CEST
Location: Hall C
Presenter: Dr. Alina Küper, University Hospital Essen, Essen, Germany

Title: Dose-response Analysis in Patients with Gastroenteropancreatic Neuroendocrine Tumors Receiving [¹⁷⁷Lu]Lu-edotreotide
Session Title: From Clinical Dosimetry to Treatment Adaptation in [¹⁷⁷Lu] Therapy
Session Number: 1505
Track: Cutting Edge Science
Date and Time: Tuesday, October 20, 2026, 15:00 – 16:30 CEST
Location: Hall B
Presenter: Dr. Anthime Flaus, Hospital Louis Pradel, Bron, France

Meet the Expert Session
Title: 225Ac Production via Medium-Energy Cyclotrons: Actineer’s Path Towards Increasing Production Capacities
Date and Time: Monday, October 19, 2026, 10:30 – 10:50 CEST
Location: ITM Booth #415, Hall X4
Presenter: Dr. Neil Quigley, Radioisotope Scientific Expert at ITM

Conference attendees will have the opportunity to learn more about ITM and Lumara Bio, a division of ITM, by visiting the company booth, #415 in Hall X4. Attendees are also invited to join the ITM team for an informal booth reception and networking opportunity on Monday, October 19, from 16:00 to 17:00 CEST.

177Lu-edotreotide (ITM-11) and Ga-DPI-4452 (CA-IX peptide) are investigational products and are not approved by any regulatory authority for the safety and/or efficacy of any intended use.

About the COMPETE Trial
The COMPETE trial (NCT03049189) evaluated 177Lu-edotreotide (ITM-11), a proprietary, synthetic, targeted radiotherapeutic investigational agent compared to everolimus, a targeted molecular therapy, in patients with inoperable, progressive Grade 1 or Grade 2 gastroenteropancreatic neuroendocrine tumors (GEP-NETs). This trial met its primary endpoint, with 177Lu-edotreotide demonstrating clinically and statistically significant improvement in progression-free survival (PFS) compared to everolimus. 177Lu-edotreotide is an investigational product and is not approved by any regulatory authority for the safety and/or efficacy of any intended use. 177Lu-edotreotide is also being evaluated in COMPOSE, a Phase 3 study in patients with well-differentiated, aggressive Grade 2 or Grade 3, somatostatin receptor (SSTR)-positive GEP-NETs.

About Ga-DPI-4452 (ITM-94)
Ga-DPI-4452 (also known as [68Ga]Ga-DPI-4452, CA-IX peptide, or ITM-94) is an investigational gallium-68-radiolabeled PET imaging agent targeting carbonic anhydrase IX (CAIX), a cell surface protein that plays a key role in tumor growth, invasion, and metastasis. ITM-94 is designed to non-invasively improve the characterization of indeterminate renal masses and enable more accurate diagnosis and disease staging of clear cell renal cell carcinoma (ccRCC). ITM-94 received Fast Track Designation from the FDA in October 2025. [68Ga]Ga-DPI-4452 is an investigational product and is not approved by any regulatory authority for the safety and/or efficacy of any intended use.

(Press release, ITM Isotopen Technologien Munchen, OCT 7, 2026, View Source [SID1234673275])

Perspective Therapeutics Announces Acceptance of [212Pb]VMT-α-NET Data for Presentation at the NANETS 2026 Multidisciplinary NET Medical Symposium

On October 7, 2026 Perspective Therapeutics, Inc. ("Perspective," the "Company," "we," "us," and "our") (NYSE AMERICAN: CATX), a radiopharmaceutical development company pioneering advanced treatments for cancers throughout the body, reported that data from the Company’s [²¹²Pb]VMT-α-NET program have been accepted for presentation at the NANETS 2026 Multidisciplinary NET Medical Symposium taking place November 5 to 7, 2026, in Las Vegas, Nevada.

Schedule your 30 min Free 1stOncology Demo!
Discover why more than 1,500 members use 1stOncology™ to excel in:

Early/Late Stage Pipeline Development - Target Scouting - Clinical Biomarkers - Indication Selection & Expansion - BD&L Contacts - Conference Reports - Combinatorial Drug Settings - Companion Diagnostics - Drug Repositioning - First-in-class Analysis - Competitive Analysis - Deals & Licensing

                  Schedule Your 30 min Free Demo!

Presenter Abstract Title Presentation Details
Thorvardur Halfdanarson, MD, Mayo Clinic Rochester Cohort level safety and efficacy results for [212Pb]VMT-α-NET in advanced somatostatin receptor subtype 2 (SSTR2+)-expressing neuroendocrine tumors (NETs): Cohorts 1–3 Abstract Number: 36595
Presentation type: Oral presentation
Session Name: Featured Abstracts I: Evolving Therapies, Risks, and Outcomes in NETs
Date: November 5, 2026
Time: 4:10 pm – 5:25 pm PST

About [²¹²Pb]VMT-α-NET

Perspective designed [212Pb]VMT-α-NET to target somatostatin receptor subtype 2 (SSTR2), and to deliver the alpha-emitting radioisotope lead-212, or ²¹²Pb, to tumor sites expressing SSTR2. The Company is conducting a multi-center, open-label, dose-escalation and dose-expansion study (clinicaltrials.gov identifier NCT05636618) of [212Pb]VMT-α-NET in patients with unresectable or metastatic SSTR2-positive tumors who have not received prior radiopharmaceutical therapies (RPT).

Interim clinical data from the study, with a data cut-off date of April 17, 2026, were presented at the 2026 American Society of Clinical Oncology (ASCO) (Free ASCO Whitepaper) Annual Meeting in May 2026. These data included efficacy results for half of the patients in Cohort 2 and both patients in Cohort 1. Initial efficacy data for the remaining patients in Cohort 2 and patients in Cohorts 3 and 4 are pending. The Company plans to submit additional data for presentation at future medical conferences in 2026 and 2027.

(Press release, Perspective Therapeutics, OCT 7, 2026, View Source [SID1234673274])