BioInvent International AB: Interim Report January – June 2025

On August 26, 2025 BioInvent reported interim report for the period January to June 2025 (Presentation, BioInvent, AUG 26, 2025, https://www.bioinvent.com/sites/bioinvent/files/pr/20250826-b8958ea1-a830-41b4-871e-759ffd4abac0-1.pdf?ts=1756189813 [SID1234656794]).

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Abdera Therapeutics to Present Early Pharmacokinetics, Dosimetry and Safety Data from Ongoing Phase 1 Trial of ABD-147 at the IASLC 2025 World Conference on Lung Cancer and Participate in Upcoming Investor Conferences

On August 26, 2025 Abdera Therapeutics Inc., a clinical-stage biopharmaceutical company leveraging its advanced antibody engineering ROVEr platform to design and develop tunable precision radiopharmaceuticals for cancer, reported that initial pharmacokinetics, dosimetry and safety data from the company’s ongoing first-in-human Phase 1 dose-escalation trial of ABD-147, a novel DLL3-targeting radiopharmaceutical, will be presented at the IASLC 2025 World Conference on Lung Cancer (WCLC), being held September 6-9 in Barcelona, Spain (Press release, Abdera Therapeutics, AUG 26, 2025, View Source [SID1234655498]).

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Details for the presentation at the IASLC 2025 WCLC are as follows:

Title: First-in-Human Study of 225Ac-ABD147 for SCLC and LCNEC Post-Chemotherapy: Pharmacokinetics, Biodistribution and Safety Insights
Presenter: Sean Carlin, Ph.D., vice president, translational sciences, Abdera Therapeutics
Session: P3.13 – Small Cell Lung Cancer and Neuroendocrine Tumors
Session Date and Time: Tuesday, September 9, 2025, from 10:00 a.m. – 11:30 a.m. CEST

In addition, Abdera management will participate in the following investor conferences in September:

2025 Wells Fargo Healthcare Conference
Presentation: Thursday, September 4, 2025, at 10:15 a.m. ET
Location: Boston, MA
Participants: Lori Lyons-Williams, president and chief executive officer; Rachael Brake, Ph.D., chief scientific officer

2025 Cantor Global Healthcare Conference
1×1 meetings: Friday, September 5, 2025
Location: New York, NY
Participant: Lori Lyons-Williams, president and chief executive officer

23rd Annual Morgan Stanley Healthcare Conference
Fireside chat: Monday, September 8, 2025, at 1:05 p.m. ET
Location: New York, NY
Participant: Lori Lyons-Williams, president and chief executive officer

Oppenheimer 3rd Annual Targeted Radiopharmaceutical Therapies in Oncology Summit
Panel discussion: Thursday, September 11, 2025, at 9:30 a.m. ET
Location: New York, NY
Participant: Rachael Brake, Ph.D., chief scientific officer

About ABD-147

ABD-147 is a targeted radiopharmaceutical biologic therapy designed to deliver Actinium-225 (225Ac), a highly potent alpha-emitting radioisotope, to solid tumors expressing delta-like ligand 3 (DLL3) with high affinity. DLL3 is a protein in the Notch pathway that is critical for the development and regulation of neuroendocrine versus epithelial cell differentiation in the lungs. In certain high grade neuroendocrine carcinomas including small cell lung cancer (SCLC), DLL3 is upregulated and specifically expressed on the cell surface in more than 80% of cases. In contrast, DLL3 is absent or very rarely expressed on the surface of nonmalignant cells. Given the high specificity of DLL3 expression on cancer cells and the distinct mechanism of action, DLL3 represents a compelling target for treating SCLC and other DLL3+ solid tumors with targeted radiotherapy.

The U.S. Food and Drug Administration (FDA) has granted Fast Track designation to ABD-147 for the treatment of patients with extensive stage small cell lung cancer (ES-SCLC) who have progressed on or after platinum-based chemotherapy and Orphan Drug Designation to ABD-147 for the treatment of neuroendocrine carcinoma. ABD-147 is currently being evaluated in a first-in-human Phase 1 clinical trial in patients with SCLC or large cell neuroendocrine carcinoma of the lung who have previously received platinum-based therapy.

BostonGene to Participate in the 2025 IASLC World Conference on Lung Cancer

On August 26, 2025 BostonGene, a leader in AI-powered solutions for drug discovery and development, reported its participation in the 2025 IASLC World Conference on Lung Cancer (WCLC), taking place September 6–9, 2025, at the Fira de Barcelona Gran Via in Barcelona, Spain (Press release, BostonGene, AUG 26, 2025, View Source [SID1234655497]). Hosted by the International Association for the Study of Lung Cancer, WCLC is the world’s largest multidisciplinary meeting dedicated to lung cancer and other thoracic malignancies, drawing thousands of clinicians, researchers, industry leaders and patient advocates from more than 100 countries to share cutting-edge science and collaborate on improving outcomes for patients worldwide.

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Alexander Bagaev, PhD, Chief Product Officer at BostonGene, will participate in the session, "Personalizing Approaches to SCLC: Translating New Understandings of SCLC Heterogeneity into Biomarker-Driven Small Cell Lung Cancer Therapies," alongside experts from Yale University, MD Anderson Cancer Center and Moffitt Cancer Center. The discussion will address recent advances in small cell lung cancer (SCLC), focusing on biomarker-defined subtypes, multiomic tumor profiling, integration of tissue and liquid biopsy data and the role of AI-based platforms in delivering advanced patient stratification to inform trial design and improve the precision of therapeutic development.

Date and time: Saturday, September 6 | 8:15 AM
Location: Room 09
BostonGene will highlight its clinically validated assay that identifies transcriptional subtypes of SCLC, leveraging its AI-powered multiomic platform to support biomarker strategy, refine trial cohorts and strengthen therapeutic alignment. Already deployed in clinical settings, the platform is streamlining patient matching, enabling flexible trial designs and helping accelerate evaluation of investigational agents in biomarker-enriched programs.

"The IASLC WCLC provides a unique platform to present how BostonGene is applying multiomic profiling and AI-driven analytics to deliver regulatory-grade patient stratification in SCLC," said Dr. Bagaev. "By enabling precise identification of biomarker-defined subgroups, we support drug developers in optimizing trial design, accelerating development timelines, and increasing the probability of success for novel therapies targeting this aggressive disease."

Guardant Health to Participate in the Morgan Stanley 23rd Annual Global Healthcare Conference

On August 26, 2025 Guardant Health, Inc. (Nasdaq: GH), a leading precision oncology company, reported the company will participate in the upcoming Morgan Stanley 23rd Annual Global Healthcare Conference in New York, NY (Press release, Guardant Health, AUG 26, 2025, View Source [SID1234655496]).

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Guardant Health’s management is scheduled to participate in a fireside chat on Monday, September 8th at 4:05 p.m. ET. Interested parties may access live and archived webcasts of the sessions on the "Investors" section of the company website at: www.guardanthealth.com.

Curasight announces acceptance of clinical trial application (CTA) for phase 1 trial with uTREAT® in brain cancer patients

On August 26, 2025 Curasight A/S ("Curasight" or "the Company") (CPH: CURAS), a clinical stage radiopharmaceuticals company, reported the European Medicines Agency (EMA) has approved the company’s clinical trial application (CTA) for the investigation of uTREAT in a phase 1 trial (Press release, Curasight, AUG 26, 2025, View Source [SID1234655495]).

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The phase 1 trial is part of Curasight’s theranostic strategy developing more gentle and targeted diagnosis and treatment of certain types of cancer. Dosing the first patient in the trial is expected to occur before the end of the year.

Today’s news means Curasight is now in clinical development with both its diagnostic (uTRACE) and therapeutic (uTREAT) platforms.

"The approval of the CTA underlines the strong progress being made in developing uTREAT as a potential more targeted therapeutic solution for patients with aggressive brain cancer, where there is a strong unmet medical need," said Curasight’s CEO Ulrich Krasilnikoff and continues, "There has been little progress in treating glioblastoma over the last decades but recently published data from an investigator-initiated Phase II study highlighted the potential of both uTRACE and uTREAT in diagnosing and treating brain cancer where 94% of Grade 4 gliomas -including glioblastomas – were uPAR-positive.".

About the Phase 1 trial with uTREAT in brain cancer

The trial aims to investigate Curasight’s uTREAT as a new type of targeted radiopharmaceutical therapy in glioblastoma patients. Participants in the trial are patients with newly diagnosed verified or suspected GBM. The trial design is informed from research and earlier studies with uTRACE as well as protocol discussions with Key Opinion Leaders.

About the uPAR theranostic platform

Curasight’s uPAR theranostic platform combines two key technologies – uTRACE and uTREAT both targeting the uPAR receptor. uTRACE is designed to deliver sensitive imaging for diagnosis, while uTREAT offers a targeted radiopharmaceutical solution. Together, they form an integrated approach to improving the diagnosis and treatment of cancers that express uPAR. Curasight’s ambition is to develop both uTRACE and uTREAT to improve diagnosis and treatment of uPAR-expressing cancers.

About high grade glioma

Treatment of glioblastoma and other high-grade gliomas (WHO grades 3 or 4) presents a significant unmet medical need, necessitating innovative and effective treatments. A total of approx. 65,000 patients are diagnosed with primary brain tumors and more than 30,000 patients are diagnosed annually with the most aggressive form, glioblastoma, in the US and EU. Approximately 10 % of the patients are children. The prognosis for individuals with glioblastoma is very poor as approximately 50% of the patients die within 14 months and after five years from diagnosis only 5% are still alive. External beam radiation is a cornerstone in the therapy of brain cancers. uTREAT could potentially replace or reduce the use of external beam radiation and thereby lower side effects to the healthy brain due to more specific tumor tissue targeting.