On June 30, 2023 Castle Biosciences, Inc. (Nasdaq: CSTL), a company improving health through innovative tests that guide patient care, reported the publication of a study in JCO Precision Oncology1 in which DecisionDx-Melanoma provided significant, independent risk stratification of patients with cutaneous melanoma (CM), beyond American Joint Committee on Cancer Eighth Edition (AJCC8) stage, which may help inform more personalized patient management decisions (Press release, Castle Biosciences, JUN 30, 2023, View Source [SID1234633018]). Additionally, data from the study shows that testing with DecisionDx-Melanoma was associated with lower melanoma-specific and overall mortality relative to untested patients. The study can be found here.

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!

"Management decisions for melanoma patients, such as referrals for sentinel lymph node biopsy or frequency and intensity of surveillance, are guided by a patient’s risk of disease recurrence or metastasis, and improvements in the accuracy of risk prediction can inform these decisions," said Matthew Goldberg, M.D., F.A.A.D., board-certified dermatologist and dermatopathologist, and senior vice president, medical, of Castle Biosciences. "The independent risk-stratification provided by DecisionDx-Melanoma has already been demonstrated in numerous retrospective and prospective studies. This large study of real-world, unselected, clinically tested patients who received our test as part of their ongoing melanoma care further supports these findings.

"The statistically significant risk stratification for survival between patients who received a Class 1A test result (lowest risk of metastasis) and those with a Class 2B test result (highest risk of metastasis) highlights the value that testing with DecisionDx-Melanoma can bring to personalizing patient care decisions when interpreted in the context of the extensive, published clinical utility data for DecisionDx-Melanoma, including the recently published study from Dhillon et al."2

In the study, to assess the effect of the DecisionDx-Melanoma test on survival outcomes, a group of tested patients (n=3,258) was matched to a group of patients who did not receive DecisionDx-Melanoma test results as part of their clinical care (n=9,774); the matching was performed using propensity score matching with three untested patients for each tested patient and was based on 11 clinicopathologic and socioeconomic variables.

Key findings of the study include:

DecisionDx-Melanoma independently risk-stratified patients according to their risk of dying from melanoma, consistent with previously published retrospective and prospective studies.
DecisionDx-Melanoma was an independent predictor of patient outcomes; a Class 2B (high risk) DecisionDx-Melanoma test result was an independent predictor of melanoma-specific survival (HR= 7.00, 95% CI 2.70-18.00) and overall survival (HR= 2.39, 95% CI 1.54-3.70). Additionally, a Class 2B result conferred the highest risk of all clinicopathologic factors included in multivariable analyses that included ulceration status, Breslow thickness and nodal status, the three risk factors used in the AJCC8 staging system.
DecisionDx-Melanoma testing was associated with 29% lower melanoma-specific mortality (HR=0.71, 95% CI 0.53-0.94) and 17% lower overall mortality (HR=0.83, 95% CI 0.70-0.99) relative to patients who did not receive DecisionDx-Melanoma testing.
"We believe that DecisionDx-Melanoma will be a practice-changing test, providing personalized information based on the genomic profile of a patient’s tumor that can help guide more informed and risk-aligned patient care decisions," said Derek Maetzold, president and chief executive officer of Castle Biosciences. "We are looking forward to continuing our collaboration with the NCI SEER Program’s Registries to provide DecisionDx Melanoma data to the SEER registries as part of public health reporting to further advance research and patient care."

About DecisionDx-Melanoma

DecisionDx-Melanoma is a gene expression profile risk stratification test. It is designed to inform two clinical questions in the management of cutaneous melanoma: a patient’s individual risk of sentinel lymph node (SLN) positivity and a patient’s personal risk of melanoma recurrence and/or metastasis. By integrating tumor biology with clinical and pathologic factors using a validated proprietary algorithm, DecisionDx-Melanoma is designed to provide a comprehensive and clinically actionable result to guide risk-aligned patient care. DecisionDx-Melanoma has been shown to be associated with improved patient survival and has been studied in more than 10,000 patient samples. DecisionDx-Melanoma’s clinical value is supported by more than 40 peer-reviewed and published studies, providing confidence in disease management plans that incorporate the test’s results. Through March 31, 2023, DecisionDx-Melanoma has been ordered more than 128,000 times for patients diagnosed with cutaneous melanoma. More information about the test and disease can be found at www.CastleTestInfo.com.

On June 30, 2023 Toragen, Inc., a San Diego-based clinical-stage biotechnology company focused on developing uniquely selective drugs targeting cancers caused by viruses, reported that it has initiated a Phase 1 clinical trial to evaluate its first drug candidate (TGN-S11) (Press release, Toragen, JUN 30, 2023, View Source [SID1234633017]). It is believed that HPV survives within the cells and can eventually cause cancer by blocking immune responses and going undetected by the immune system. Toragen’s drug candidate, TGN-S11, inhibits the E5 oncogene of HPV in pre-clinical studies. Toragen believes this will allow the HPV-infected cancer cells to be detected by killer T-cells which could trigger an immune response that could be beneficial in cancer treatment.

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!

This Phase 1 trial is an open-label, non-randomized, dose escalation/dose expansion trial in cohorts of patients with relapsed, resistant, or metastatic HPV-associated cancers. The expansion phase will begin in parallel, one dose level lower than the highest dose deemed safe in the dose escalation phase in combination with a PD-1 checkpoint inhibitor. The trial is anticipated to enroll up to 55 patients at approximately six sites in the United States.

"We are excited to announce the enrollment of our first patient in our first clinical trial with TGN-S11. Not only were we able to rapidly achieve our goal of beginning this clinical trial, but we are thrilled to transition Toragen to a clinical-stage company," said Dr. Sandra Coufal, Toragen’s CEO. "This is a historic milestone for the company and moves forward our mission to improve outcomes for patients with HPV-induced cancers."

On June 30, 2023 Rakuten Medical, Inc., a global biotechnology company developing and commercializing precision, cell targeting therapies based on its proprietary Alluminox platform, reported that new interim evaluation data from the ASP-1929-103 study has been presented at the Society of Nuclear Medicine and Molecular Imaging (SNMMI) 2023 Annual Meeting held from June 24 to 27 (Press release, Rakuten Medical, JUN 30, 2023, View Source [SID1234633016]). ASP-1929-103 is a Phase 2, open-label, single-arm, window of opportunity study* of Alluminox treatment (photoimmunotherapy: PIT) using an antibody-dye conjugate ASP-1929 with fluorescence imaging (ClinicalTrials.gov Identifier: NCT05182866) in patients with operable primary or recurrent head and neck squamous cell carcinoma (HNSCC) or cutaneous squamous cell carcinoma (cuSCC).

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 oral presentation was given by Liza Lindenberg, M.D., of the National Cancer Institute (NCI), which has a Cooperative Research and Development Agreement to conduct ASP-1929-103 study. ASP-1929-103 is the very first clinical trial of Alluminox treatment in operable cancer. As part of this trial, early time point (1 day) 18F-FDG PET/CT imaging was investigated as a potential response indicator of Alluminox treatment.

The preliminary, descriptive imaging analysis based on interim evaluation of 6 patients in ASP-1929-103 study presented during the meeting showed that 18F-FDG PET/CT imaging demonstrates a therapeutic response 1 day after Alluminox treatment using ASP-1929. PET/CT is an imaging modality for combined acquisition of positron emission tomography (PET) and computed tomography (CT) pictures. 18F-fluorodeoxyglucose (18F-FDG) is the radiotracer used for this PET study. Like glucose (sugar), 18F-FDG is taken up by cells, particularly rapidly dividing cells such as cancer cells. Following uptake, 18F-FDG accumulates in the cytoplasm rather than undergoing further metabolism which results in signal amplification from labeled cells.

Key findings presented at SNMMI 2023
"Early 18F-FDG Response after Near-Infrared Photoimmunotherapy for Head and Neck and Cutaneous Squamous Cell Carcinoma" (Abstract: P50) presented by Liza Lindenberg, M.D., Molecular Imaging Branch, NCI, NIH

– 18F FDG PET/CT demonstrates a therapeutic response 1 day after a single ASP-1929 PIT treatment
– Delayed 18F-FDG PET/CT imaging may decrease confounding inflammatory uptake on scans
– Pathologic tumor response may add complementary information to 18F-FDG PET/CT in PIT

Disclaimer: These early findings may change upon trial completion and final data analysis.

ASP-1929-103 study overview
ASP-1929-103 is a Phase 2, open-label, single-arm, window of opportunity study* of Alluminox treatment (PIT) using an anti-EGFR antibody-dye conjugate, ASP-1929 with fluorescence imaging in patients with operable primary or recurrent HNSCC or cuSCC. The study, sponsored by Rakuten Medical in collaboration with NCI and Shimadzu Corporation (Shimadzu), will enroll 22 patients in the US to evaluate the efficacy and safety of a single Alluminox treatment using ASP-1929 administered prior to standard of care surgical tumor resection. The feasibility of the Shimadzu fluorescence imaging system for real-time monitoring and recording of the fluorescence of the IRDye 700DX portion of ASP-1929 will also be assessed.

* Window of opportunity study takes place in the period between a cancer diagnosis and the subsequent initiation of standard treatment, during which, the patient receives a non-standard drug or treatment of interest over a short period of time 1.2.
1. Aroldi F, Lord SR. Window of opportunity clinical trial designs to study cancer metabolism. Br J Cancer. 2020;122(1):45-51. doi:10.1038/s41416-019-0621-4.
2. Schmitz S, Duhoux F, Machiels JP. Window of opportunity studies: Do they fulfil our expectations? Cancer Treat Rev. 2016 Feb;43:50-7. doi: 10.1016/j.ctrv.2015.12.005. Epub 2015 Dec 31. PMID: 26827692.

On June 30, 2023 Transcenta Holding Limited ("Transcenta") (HKEX: 06628), a clinical stage biopharmaceutical company with fully-integrated capabilities in discovery, research, development and manufacturing of antibody-based therapeutics, reported progression free survival (PFS) data by CLDN18.2 expression level from Phase I/II study of Osemitamab (TST001) plus Capecitabine and Oxaliplatin (CAPOX) as the first-line treatment of advanced gastric/gastroesophageal junction (G/GEJ) cancer at ESMO (Free ESMO Whitepaper) World Congress on Gastrointestinal Cancer 2023. These data will support the upcoming global Phase III pivotal trial to be initiated in the second half of 2023.

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!

Title

Osemitamab (TST001) plus Capecitabine and Oxaliplatin (CAPOX) as the First-Line Treatment of Advanced G/GEJ Cancer – Updated Efficacy Data per Claudin 18.2 Expression Level from Study TranStar102/TST001-1002-Cohort C.

Study Design

The efficacy and safety of Osemitamab (TST001) plus CAPOX as the first-line treatment for patients with advanced G/GEJ cancer was explored in a dose escalation and expansion Phase I/II study in China (Cohort C of TranStar102, NCT04495296). In the expansion phase (except 8 patients from a safety run-in), CLDN18.2 positive was required, which is defined as IHC membrane staining ≥10% tumor cells with ≥1+ intensity per LDT assay, selecting approximately 55% of the screened patients.

Study Results

As of April 21, 2023, a total number of 64 patients were dosed with Osemitamab (TST001) in combination with CAPOX, 15 patients received Osemitamab (TST001) at doses ranging from 1 to 8 mg/kg Q3W in the dose escalation and 49 patients at 6 mg/kg in the dose expansion. The median follow-up was 195 days.
41 out of 49 patients in the dose expansion at 6mg/kg had CLDN18.2 positive tumor (High: n=9, Medium: n=13, Low: n=19), 8 patients didn’t get their tumor tested (unknown CLDN18.2 expression). The baseline demographics of this dose expansion are similar to that of the overall population published on 2023 ASCO (Free ASCO Whitepaper) (abstract 4046*). There are no clinically significant differences in baseline characteristics across different CLDN18.2 expression levels.
The safety profile of Osemitamab (TST001) is mainly characterized by manageable on-target off-tumor effects and has been presented during at ASCO (Free ASCO Whitepaper) 2023 (abstract 4046*). Most of these AEs are of grade 1 or 2 and occurred during the first 2 cycles.
At the cut-off date of April 21, 2023, 26 out of 64 patients had progression disease or death, with an estimated median progression-free survival (PFS) 9.5 months. There was no clear trend between progression-free survival and the CLDN18.2 expression levels.
"Appropriately selecting the patients is critical to optimize the benefit/risk of treatment with Osemitamab (TST001). Using our proprietary CLDN18.2 assay, we have selected 55% of the G/GEJ cancer patients and shown that the lower expressors amongst these patients derive the same level of durable benefit than the higher expressors. This is a key differentiation and a significant dataset supporting our Phase III design globally." said Dr. Caroline Germa, Transcenta’s Executive Vice President, Global Medicine Development and Chief Medical Officer.

About Osemitamab (TST001)

Osemitamab (TST001) is a high affinity humanized anti- CLDN18.2 monoclonal antibody with enhanced antibody-dependent cellular cytotoxicity ("ADCC"). It has shown potent anti-tumor activities in tumor xenograft models. Osemitamab (TST001) is the second most advanced CLDN18.2 targeting antibody being developed globally. Osemitamab (TST001) was generated using Transcenta’s Immune Tolerance Breaking Technology (IMTB) platform. Osemitamab (TST001) kills CLDN18.2 expressing tumor cells by mechanisms of ADCC. Leveraging advanced bioprocessing technology, the fucose content of Osemitamab (TST001) was significantly reduced during the production, which further enhanced NK cells mediated ADCC activity of Osemitamab (TST001). Clinical trials for Osemitamab (TST001) are ongoing in the U.S. and China (NCT05190575, NCT04396821, NCT04495296, NCT05608785 / CTR20201281). Osemitamab (TST001) was granted Orphan Drug Designation in the U.S. by FDA for the treatment of patients with gastric or gastroesophageal junction (G/GEJ) and pancreatic cancer.

On June 30, 2023 Chime Biologics, a leading CDMO that enables its partners’ success in biologics, reported that it has established 3-way strategic cooperation with Leads Biolabs and BeiGene to accelerate LBL-007 mAb development and manufacturing for speedy clinical advancement (Press release, Nanjing Leads Biolabs, JUN 30, 2023, View Source [SID1234633014]).

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!

LBL-007 is a novel antibody targeting the LAG-3 pathway developed independently by Leads Biolabs. The phase I clinical trial data of LBL-007 in patients with later-stage solid tumors have been announced at the 2021 annual meeting of the American Society of Clinical Oncology (ASCO) (Free ASCO Whitepaper).

Previously, Leads Biolabs and BeiGene reached an authorization and cooperation agreement. Leads Biolabs grants LBL-007 exclusive global development and production license to BeiGene, as well as a commercial manufacturing license outside China.

Leads Biolabs and Chime Biologics initiate strategic cooperation to accelerate IND application and provide clinical trial materials in China.

Leads Biolabs has entrusted Chime Biologics with the file supporting work related to the production of LBL-007 project and clinical trial materials in mainland China. Now, the project is progressing into clinical phase II stage. At 2023 ASCO (Free ASCO Whitepaper) conference in Chicago from June 2 to 6, Leads Biolabs presented a poster summarizing the latest clinical data research results on safety and efficacy of anti-LAG-3 (lymphocyte activating gene-3) antibody LBL-007 in the treatment of advanced or metastatic melanoma. This is an open-label, multicenter, dose-escalation or expansion Phase I clinical trial research conducted in China, focusing on safety, RP2D, pharmacokinetics and pharmacodynamics.

BeiGene and Chime Biologics establish strategic cooperation to facilitate IND applications overseas and clinical trial materials supply.

BeiGene is also entrusting Chime Biologics to provide support for clinical development and manufacturing of clinical trial materials in order to facilitate multiple clinical trials. The indications encompass colorectal cancer, non-small cell lung cancer, head and neck squamous cell carcinoma, as well as other solid tumors. Clinical trials have been conducted in numerous countries worldwide, including Australia and the United States.

The three parties have established a comprehensive strategic partnership based on the principle of "Complementary Advantages, Resource Sharing, Strong Alliance, and Win-win Cooperation". Through 3-way cooperation, multiple clinical studies are advancing rapidly based on the global development distribution of LBL-007. We hope anti-LAG-3 antibodies can bring good news to cancer patients as soon as possible.

A Trusted Partner in Biologics Commercial Manufacturing

Chime Biologics serves as a long-term partner to biopharmaceutical clients with sound solutions for manufacturing and more recently moved into late stage and commercial manufacturing. We support various stages of new drug registration and application, provide production service for preclinical, clinical and listed drugs, including non-GMP standard production and the first modular biopharmaceutical factory in the world which meets the global cGMP standards.

Dr. Kang Xiaoqiang, Founder, Chairman and CEO of Leads Biolabs, stated: "We are so pleased to cooperate with BeiGene, a global leading enterprise in oncology field, and Chime Biologics with extensive antibody production experience. LBL-007 is the first innovative antibody drug with global intellectual property which we developed independently. I believe that the development and commercialization of LBL-007 can be expedited through our triangular cooperation, so we can address unmet medical needs and bring hope to cancer patients."

Dr. Wang Lai, Global R&D Director of BeiGene, said: "The clinical candidate drug developed by Leads Biolabs has a broad prospect, not only enriching our tumor immunotherapy drug pipeline but also supporting us for global clinical development strategic priorities and development opportunities. Chime Biologics has advanced drug commercial manufacturing experience, a sound quality system and efficient production management, providing assurance of LBL-007 for global development. Although the cooperation is not too long, LBL-007 has launched nearly ten Phase I and II clinical trials worldwide in the last year, with indications covering colorectal cancer, non-small cell lung cancer, head and neck squamous cell cancer, melanoma and other solid tumor cancers. I believe that this cooperation will bring new opportunities for the medical community to further conquer cancer."

Dr. Wei Jianzhong, President of Chime Biologics, stated:" We are glad to be the partner of these two leading Biopharma enterprises to provide the IND filing support of LBL-007 project and clinical trial materials production. The three parties will work together to deepen cooperation and promote the clinical trial process of LBL-007 project. Chime Biologics has always focused on quality management and technological innovation. This cooperation project is a remarkable milestone of company’s global development. We are very proud to be able to empower biopharma partners to bring more drugs to the market as soon as possible and benefit patients worldwide."

About LBL-007

LBL-007 is a fully humanized anti-LAG-3 (lymphocyte activating gene-3) monoclonal IgG4 antibody consisting of two IgG4 heavy chains and two κ light chains linked by disulfide bonds, with high affinity to human LAG-3, and exerts antitumor effects by blocking LAG-3 activation of immune function. In preclinical models, LBL-007 in combination with anti-programmed cell death protein 1 (PD-1) showed synergistic antitumor activity. Results from the phase I a study of LBL-007 monotherapy have been published in ASCO (Free ASCO Whitepaper) 2021 (Abstract 2523); preliminary safety and efficacy data for LBL-007 combined with toripalimab in patients with advanced melanoma (Part A) have been reported in ASCO (Free ASCO Whitepaper) 2022 (Abstract 9538/Poster 131), showing a favorable safety profile and better antitumor activity, particularly in anti PD-(L)1 naïve patients with acral melanoma. Several clinical studies of LBL-007 are currently in rapid progress based on global layout.