G1 Therapeutics Announces Upcoming Presentations at the 2023 ASCO Quality Care Symposium

On October 16, 2023 G1 Therapeutics, Inc. (Nasdaq: GTHX), a commercial-stage oncology company, reported that multiple abstracts have been accepted for poster presentation at the upcoming 2023 American Society of Clinical Oncology (ASCO) (Free ASCO Whitepaper) Quality Care Symposium, held October 27th and 28th in Boston, MA (Press release, G1 Therapeutics, OCT 16, 2023, View Source [SID1234635997]). A copy of the posters will be made available on the G1 Therapeutics website following the presentations here.

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"The important research being presented at this year’s ASCO (Free ASCO Whitepaper) Quality Care Symposium highlights the significant burden of chemotherapy-induced myelosuppression and the real-world clinical impact of treatment with trilaciclib in patients with extensive-stage small cell lung cancer," said Raj Malik, M.D., Chief Medical Officer of G1 Therapeutics. "Real-world evidence is essential to deepening our collective understanding of the impact of treatment on patient outcomes."

Burden of Myelosuppression in Extensive-Stage Small-Cell Lung Cancer Patients Receiving Chemotherapy: Retrospective Analysis of Real-World Data from Tennessee Oncology. Blakely, L.J. et al.
Abstract 364. Poster Session A, Poster Board F21.
Friday October 27: 11:30 AM – 1:00 PM ET; 5:30 – 6:30 PM ET

Myelosuppression and Healthcare Utilization Among Patients with Chemotherapy-Treated Extensive-Stage Small Cell Lung Cancer (ES-SCLC) with and without Trilaciclib from Community Oncology Practices. Gajra, A. et al.
Abstract 527. Poster Session B, Poster Board L2.
Saturday, October 28: 7:00 AM – 8:00 AM; 11:45 AM – 1:00 PM ET

Assessment Of Hospitalizations and Cytopenia Events Among Patients with Extensive Stage Small Cell Lung Cancer (ES-SCLC) Receiving Chemotherapy with Trilaciclib. Huang, H. et al.
Abstract 531. Poster Session B, Poster Board L6.
Saturday, October 28: 7:00 AM – 8:00 AM; 11:45 AM – 1:00 PM ET

Patient Characteristics Associated with Myelosuppression Among Patients with Extensive-Stage Small Cell Lung Cancer Treated with Chemotherapy in The Community Oncology Setting. Goldschmidt, J. et al.
Abstract 289. Poster Session B, Poster Board J24.
Saturday, October 28: 7:00 AM – 8:00 AM; 11:45 AM – 1:00 PM ET

Enterome to Present Data on EO2401 in Adrenal Tumors at the European Society for Medical Oncology (ESMO) 2023 Congress

On October 16, 2023 Enterome, a clinical-stage company developing first-in-class immunomodulatory drugs for solid and liquid malignancies and inflammatory diseases based on its unique Mimicry platform, reported that updated data from its Phase 1/2 SPENCER study on EO2401 in combination with nivolumab, in patients with adrenal tumors, will be presented in an oral session at the European Society for Medical Oncology (ESMO) (Free ESMO Whitepaper) Congress 2023, to take place on October 20-23, 2023 in Madrid, Spain (Press release, Enterome, OCT 16, 2023, View Source [SID1234635996]).

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Oral Presentation details – Abstract 724O

Title: EO2401 (E) peptide immunotherapy + nivolumab (N) in adrenocortical carcinoma (ACC) and metastatic pheochromocytoma/paraganglioma (MPP); EOADR1-19/SPENCER

Presenter: Dr. Eric Baudin, Associate Professor and Head of the Endocrine Oncology Unit at Gustave Roussy (Villejuif, France)

Session Title: Proffered Paper Session – NETs and endocrine tumors

Presentation Date and Time: Sunday, October 22, 2023, at 9.30 am CET

Location: Toledo Auditorium – Hall 3

The abstract was published today and is available online in the ESMO (Free ESMO Whitepaper) Congress 2023 Abstract Book (a supplement to the official ESMO (Free ESMO Whitepaper) journal, Annals of Oncology).

About SPENCER

SPENCER (EOADR1-19) is a multicenter, open-label, first-in-human, Phase 1/2 study of EO2401 in combination with an immune checkpoint inhibitor (nivolumab) for the treatment of patients with locally advanced or metastatic adrenocortical carcinoma (ACC), or malignant pheochromocytoma/paraganglioma (MPP). The study aims to assess the safety, tolerability, immunogenicity, and preliminary efficacy of the combination at sites in Europe and the US.

For more information on the Phase 1/2 trial of EO2401 in adrenal tumors, please refer to ClinicalTrials.gov Identifier: NCT04187404

About EO2401

EO2401 is Enterome’s first-in-class off-the-shelf OncoMimics peptide-based immunotherapy. It combines three microbial-derived OncoMimics peptides that closely mimic specific cytotoxic T cell (CD8+ T cell) epitopes on the Tumor-Associated Antigens IL13Ra2, BIRC5, and FOXM1, combined with the helper peptide (CD4+ T cell epitope) Universal Cancer Peptide 2 (UCP2).

About OncoMimics

OncoMimics immunotherapies are designed to activate pre-existing effector memory T cells that target bacterial (non-self) peptides, which are strongly cross-reactive against selected Tumor-Associated Antigens (TAAs), or B cell markers expressed on tumoral cells, resulting in a rapid, targeted cytotoxic response against cancer.

Delcath Systems Announces a Comparative Study of Chemosat and SIRT Published in the Journal Cancers

On October 16, 2023 Delcath Systems, Inc. (Nasdaq: DCTH), an interventional oncology company focused on the treatment of primary and metastatic cancers of the liver, reported the publication of an article entitled "Selective Internal Radiotherapy (SIRT) and Chemosaturation Percutaneous Hepatic Perfusion (CS-PHP) for Metastasized Uveal Melanoma: A Retrospective Comparative Study" in the peer reviewed oncology journal Cancers (Press release, Delcath Systems, OCT 16, 2023, View Source [SID1234635995]). CS-PHP utilizes CHEMOSAT, Delcath’s proprietary European CE Marked Hepatic Delivery System (HDS), to administer high-dose chemotherapy (melphalan) to the liver, while controlling systemic exposure and associated side effects during a PHP procedure. Initial findings were previously presented on September 9, 2023 at the Cardiovascular and Interventional Radiological Society of Europe (CIRSE) Annual Meeting held in Copenhagen, Denmark.

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Uveal melanoma usually shows a liver-dominant metastasis spread and is often treated with liver directed therapies. This retrospective study compared two cohorts of patients with liver dominant uveal melanoma treated at the University Hospitals Tubingen, Germany with multiple cycles of either CS-PHP (N=28) or SIRT (N=34).

Patients included in the study were treated between December 2013 and February 2020. Allocation to treatment was determined by a multidisciplinary team.

Presence of extrahepatic disease at baseline favored the SIRT group (68% and 41%, CS-PHP and SIRT, respectively), as did the hepatic tumor load (0-25%: 57% and 76%; 26%-50%: 29% and 24%; >50%: 14% and 0%, for CS-PHP and SIRT, respectively). Tumor responses were evaluated by consensus reading by two experienced radiologists.

Disease control rates (DCR) were 30% and 18%, for CS-PHP and SIRT, respectively. Median overall survival (mOS) was 516 days for CS-PHP and 300.5 days for SIRT. In a Cox regression model, there was a significant difference between SIRT and CS-PHP treatment, HR = 0.46, CI 95% (0.23; 0.93), p = 0.030.

Descriptive Survival by Treatment.

An adjusted Cox regression analysis, including the variables age, sex, presence of extrahepatic metastasis and hepatic load at baseline, also showed a significant effect of choice of treatment, HR = 0.32, CI 95% (0.14; 0.73), p = 0.006.

Adjusted Conditional Survival by Treatment.

Median progression-free survival (mPFS) was 408.5 days for CS-PHP and 127.5 days for SIRT; the adjusted Cox regression analysis showed a trend favoring CS-PHP (p=0.090).

When initially presented at the 2023 CIRSE Annual Meeting held in Copenhagen, Denmark, presenting author Prof. Dr. Med. Gerd Groezinger, stated "Liver directed treatment, including transarterial radioembolization and CS-PHP, is a critical treatment modality for patients with metastatic uveal melanoma, given the longer overall survival seen in the CS-PHP cohort, we conclude that for metastatic uveal melanoma patients, CS-PHP might be the superior liver directed treatment option."

"There is a scarcity of comparative studies between liver directed therapies. This peer reviewed publication authored by experienced investigators, supports that the PHP procedure, whether utilizing melphalan delivered by Delcath’s CE marked Chemosat or the FDA approved HEPZATO KIT, may be the preferred liver directed treatment option for patients with liver-dominant metastatic uveal melanoma," said Dr. Vojo Vukovic, Delcath’s Chief Medical Officer. "We remain committed to making this treatment option available to patients in the US by the end of this year."

The full article can be viewed by clicking here.

About Chemosat and HEPZATO KIT
CHEMOSAT Hepatic Delivery System for Melphalan percutaneous hepatic perfusion (PHP) is designated under the medical device regulation for use in Europe and the United Kingdom. The Hepatic Delivery System (HDS) is designed to administer high-dose chemotherapy to the liver while controlling systemic exposure and associated side effects during a PHP procedure. The use of the HDS allows a healthcare provider team to surgically isolate the liver while the hepatic venous blood is filtered during melphalan infusion and subsequent washout during a PHP procedure. PHP, which can only be performed with Delcath’s HDS, results in loco-regional delivery of a relatively high melphalan dose. For more information regarding CHEMOSAT and its use, please visit Chemosat.com.

HEPZATO KIT (melphalan for Injection/Hepatic Delivery System), approved for use in the United States by FDA, is a combination drug/device product which administers HEPZATO (melphalan) directly to the liver through the HDS, which permits higher drug exposure in target tissues while limiting systemic toxicity.

HEPZATO KIT is approved in the United States as a liver-directed treatment for adult patients with uveal melanoma with unresectable hepatic metastases affecting less than 50% of the liver and no extrahepatic disease, or extrahepatic disease limited to the bone, lymph nodes, subcutaneous tissues, or lung that is amenable to resection or radiation.

HEPZATO KIT Important Safety Information
Patients eligible for HEPZATO should NOT have any of the following medical conditions:

Active intracranial metastases or brain lesions with a propensity to bleed
Liver failure, portal hypertension, or known varices at risk for bleeding
Surgery or medical treatment of the liver in the previous 4 weeks
Active cardiac conditions including unstable or severe angina or myocardial infarction), worsening or new-onset congestive heart failure, significant arrhythmias, or severe valvular disease
History of allergies or known hypersensitivity to melphalan or a component or material utilized within the HEPZATO KIT including natural rubber latex, heparin, and severe hypersensitivity to iodinated contrast not controlled by antihistamines and steroids
Most common adverse reactions or laboratory abnormalities occurring with HEPZATO treatment are thrombocytopenia, fatigue, anemia, nausea, musculoskeletal pain, leukopenia, abdominal pain, neutropenia, vomiting, increased alanine aminotransferase, prolonged activated partial thromboplastin time, increased alkaline phosphatase, increased aspartate aminotransferase and dyspnea.

Severe peri-procedural complications including hemorrhage, hepatocellular injury, and thromboembolic events may occur via hepatic intra-arterial administration of HEPZATO. HEPZATO is available only through a restricted program under a Risk Evaluation and Mitigation Strategy called the HEPZATO KIT REMS. Myelosuppression with resulting severe infection, bleeding, or symptomatic anemia may occur with HEPZATO. Additional cycles of HEPZATO therapy will be delayed until blood counts have improved.

Please see the full Prescribing Information, including BOXED WARNING for the HEPZATO KIT.

Cimeio Therapeutics Announces Research Collaboration With the University of Pennsylvania

On October 16, 2023 Cimeio Therapeutics reported a preclinical research collaboration with Saar Gill, M.D., Ph.D., an associate professor of medicine and a researcher in the Center for Cellular Immunotherapies in the Perelman School of Medicine at the University of Pennsylvania, to research and evaluate a novel universal immunotherapy with potential to treat multiple blood and bone marrow cancers (Press release, Cimeio Therapeutics, OCT 16, 2023, View Source [SID1234635994]).

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The Penn team will combine Cimeio Therapeutics’ proprietary epitope-editing and CD45-targeting technologies with Penn Medicine’s epitope-editing and CAR T cell technology to create a CD45-targeting CAR T cell therapy and paired epitope-edited hematopoietic stem cell (HSC). Given that CD45 is highly expressed on nearly all blood cells, this therapy could be a universal CAR T cell therapy for blood cancers.

Recent findings have demonstrated the ability to epitope edit CD45, which is a receptor broadly expressed on the surface of healthy HSCs as well as many blood and bone marrow cancers. A publication from Penn Medicine as well as a presentation by Cimeio Therapeutics and the University of Basel suggested that developing a technology to shield healthy HSCs while leaving malignant cells vulnerable to a CD45-targeting therapy could unlock this target for drug development.

"I am pleased to be working with Cimeio Therapeutics to evaluate a novel immunotherapeutic technology that may have the potential to transform the treatment of multiple blood and bone marrow cancers," said Dr. Gill. "The preclinical research we have each independently advanced fits very well together, and I look forward to joining forces on this endeavor."

"By exchanging a single amino acid on a cell surface receptor, we discovered we could prevent potent immunotherapies from binding to and depleting healthy cells in vitro and in mouse models. It’s exciting to be working with the Penn scientific team to evaluate this novel approach to immunotherapy," said Lukas T. Jeker, M.D., Ph.D., co-founder of Cimeio and professor of experimental transplantation immunology & nephrology at the Department of Biomedicine, University of Basel and at the Basel University Hospital, Switzerland. A foundational patent for epitope editing from the University of Basel is exclusively licensed to Cimeio.

"A CD45-directed CAR T cell therapy enabled via epitope editing has the potential to benefit patients with many types of leukemia, lymphoma, myeloma, and even some autoimmune diseases," said Carl June, M.D., the Richard W. Vague Professor in Immunotherapy in the department of Pathology and Laboratory Medicine and director of the Center for Cellular Immunotherapies at the University of Pennsylvania, and co-senior author of the recent CD45 study with Dr. Gill. "Now the goal is to discover how transformative this potential new therapeutic approach could be."

"The Penn research team is the ideal partner to work with given their shared vision and goals, epitope editing and translational cell therapy expertise," said Thomas Fuchs, Chief Executive Officer of Cimeio Therapeutics. "We hope we can build on these exciting early research findings by developing a CAR T cell that can target multiple hematologic cancers with a single product through our CD45 collaboration."

Cimeio is also developing a CD45-directed antibody-drug conjugate. The company plans to develop that therapy with CD45 epitope shielded cells for blood cancers and autoimmune diseases among other indications.

BioNTech to Present Multiple Program Updates Across Modalities at ESMO Congress 2023

On October 16, 2023 BioNTech SE (Nasdaq: BNTX, "BioNTech" or "the Company") reported that it will present data across its oncology pipeline, covering multiple solid tumor types and novel mechanisms of action, at the European Society for Molecular Oncology ("ESMO") Congress 2023 in Madrid, Spain from October 20-24, 2023 (Press release, BioNTech, OCT 16, 2023, View Source [SID1234635992]). The updates will feature oral and poster presentations for five candidates of BioNTech’s clinical pipeline across the Company’s drug classes, which comprise mRNA-based immunotherapies, cell therapies, protein-based therapeutics, and small molecules.

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"This year’s ESMO (Free ESMO Whitepaper) presentations underline the potential of BioNTech’s precision medicine toolkit for the treatment of solid tumor indications with high unmet medical need, where many patients still remain underserved," said Prof. Özlem Türeci, M.D., Co-Founder and Chief Medical Officer at BioNTech. "We aim to develop and combine innovative immunotherapies for patients at different disease stages, which we believe could increase the likelihood of therapeutic success, reduce the risk of emergence of secondary resistance mechanisms, and unlock a larger potential patient population."

Highlights of BioNTech’s clinical stage programs to be presented at ESMO (Free ESMO Whitepaper) Congress 2023:

Cell therapies

BioNTech will present new data of its investigational autologous Claudin-6 (CLDN6)-directed CAR-T cell therapy BNT211 (NCT04503278), including data showing the potential of combining these CAR-T cells with a CLDN6-encoding CAR-T cell amplifying mRNA vaccine ("CARVac").
Initial data from BioNTech’s first-in-human Phase 1 study with BNT221 (NCT04625205), a personalized, autologous neoantigen-specific T cell therapy, will be presented. The initial results show a manageable safety profile and tumor regression in several patients with anti-PD-1 and anti-CTLA4 pretreated advanced or metastatic melanoma.
Protein-based therapeutics

The Company will present first-in-human data of BNT325 (DB-1305) (NCT05438329), a next-generation Trop-2-targeting antibody-drug conjugate ("ADC"), which is being jointly developed with Duality Biologics. Initial data with this candidate show encouraging preliminary efficacy and a manageable safety profile in patients with advanced/metastatic non-small cell lung cancer (NSCLC).
mRNA-based immunotherapies

A trial in progress poster will inform on the ongoing EMPOWERVAX Lung 1 Phase 2 trial (NCT05557591), which is being conducted together with Regeneron, evaluating the efficacy and safety of BioNTech’s fully-owned off-the-shelf mRNA cancer vaccine candidate BNT116 in combination with cemiplimab versus cemiplimab alone in the first-line treatment of patients with advanced NSCLC and PD-L1 expression ≥50%.
In addition, BioNTech will also present pre-clinical data from its BNT314 (GEN1059) program, which is being jointly developed with Genmab. BNT314 (GEN1059) is a novel bispecific antibody candidate aimed at boosting antitumor immune responses through EpCAM-dependent 4-1BB agonistic activity. In pre-clinical studies, BNT314 (GEN1059) enhanced T-cell activation, proliferation, and effector functions in vitro and ex vivo and promoted antitumor activity in vivo. A Phase 1/2 trial is planned to start by early 2024 and will assess the safety and preliminary antitumor activity of BNT314 (GEN1059) in patients with advanced or metastatic solid tumors.

BioNTech has established a diversified clinical oncology pipeline of more than 25 programs in high unmet medical need solid tumor indications in more than 30 clinical studies, including seven programs in advanced Phase 2 studies and one candidate in a pivotal Phase 3 study. BioNTech is advancing the Company’s key programs into late-stage development while strengthening its clinical-stage oncology pipeline with synergistic potential, with the aim to deliver the next generation of oncology breakthroughs.

The full abstracts are available on the ESMO (Free ESMO Whitepaper) Congress website. Click here for further information on BioNTech’s pipeline candidates.

Full Presentation Details:

Late-breaking presentation
Candidate: BNT211
Session Title: Developmental Therapeutics
Abstract Title: "BNT211-01: Interim results from a repeat dose escalation study of CLDN6 CAR-T cells manufactured with an automated process ± a CLDN6-encoding CAR-T cell-Amplifying RNA Vaccine (CARVac)"
Abstract Number: LBA35
Date: Monday, October 23, 2023
Time: 4:30-6:00 PM CET

Proffered paper session
Candidate: BNT221
Session title: Investigational Immunotherapy
Abstract Title: "NTC-001: A phase I study to test safety and efficacy of BNT221, a non-engineered neoantigen-specific T cell product, in patients with advanced or metastatic melanoma"
Abstract Number: 1017O
Date: Monday, October 23, 2023
Time: 10:15-11:40 AM CET

Poster
Candidate: BNT325 (DB-1305)
Session Title: Developmental Therapeutics
Abstract Title: "DB-1305 (a Trop-2 targeted antibody-drug-conjugate [ADC]) in patients with advanced solid tumors: Preliminary clinical results from the Phase 1/2a study"
Poster Number: 689P
Date: Monday, October 23, 2023

Candidate: BNT116
Session Title: NSCLC. metastatic
Abstract Title: "A phase 2 study of cemiplimab plus BNT116 versus cemiplimab alone in first-line treatment of patients with advanced non-small cell lung cancer with PD-L1 expression ≥50%"
Poster Number: 1503TiP
Date: Monday, October 23, 2023

Candidate: BNT314 (GEN1059)
Session Title: Investigational Immunotherapy
Abstract Title: "DuoBody-EpCAMx4-1BB mediates conditional T cell co-stimulation and promotes antitumor activity in preclinical models"
Poster Number: 1072P
Date: Monday, October 23, 2023