Zetagen Announces Publication in Pain Management of Early Data Using ZetaMet™ (Zeta-BC-003) as a Potential Treatment for Bone Metastases

On October 10, 2023 Zetagen Therapeutics, a private, clinical-stage, biopharmaceutical company focused on driving breakthrough innovation in the treatment of metastatic cancers to bone and soft tissue organs as well as osteologic interventions, reported publication of early, human clinical data in the peer-reviewed journal Pain Management on ZetaMet (Zeta-BC-003) for the treatment bone metastases (Press release, Zetagen Therapeutics, OCT 10, 2023, View Source [SID1234647528]).

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This case study, entitled Treating Bone Metastases with Local Therapy in a Breast Cancer Patient Resulted in Decrease Pain and Prevented Fracture, demonstrated resolution of lytic lesions, significant reduction in pain and prevention of fracture in a patient living with Stage 4 breast cancer being treated with ZetaMet (Zeta-BC-003).

To view the publication via open access, go to: View Source

ZetaMet (Zeta-BC-003) is a synthetic, small-molecule, inductive biologic technology being developed to target and resolve metastatic bone lesions while inhibiting future tumor growth and regenerating bone. The small molecule has been approved by the U.S. Food and Drug Administration (FDA) since 1971. Zetagen scientists have discovered an entirely new pathway for this established molecule which, if proven successful in human clinical trials, could create a new treatment paradigm for patients living with metastatic bone lesions and other osteologic conditions.

"Recently, I had the opportunity to spend some time with this patient. I will always remember what she said to me: ‘thank you for giving me more time’," said Joe C. Loy, Chief Executive Officer of Zetagen Therapeutics. "We are grateful to have had the opportunity to provide ZetaMet (Zeta-BC-003) to this patient and we remain cautiously hopeful as we await results from our on-going Phase 2 clinical trial."

"We recognize that these results are from a single patient and are prudently hopeful for similar outcomes from our ongoing ZetaMet (Zeta-BC-003) clinical trial," said Bryan Margulies, PhD, Chief Scientific Officer of Zetagen Therapeutics. "I am encouraged that at the two-year time period this patient does not have active tumor at the treatment sites, and that the sacral lesion which was not treated with fractionated radiation completely resolved."

Lytic lesions can cause severe, debilitating pain in patients with advanced cancer. Patients with these lesions often experience a reduced quality of life with multiple skeletal-related events (SREs), including fractures, spinal cord compression, elevated levels of calcium in the blood or "hypercalcemia", bone marrow infiltration and severe bone pain.[i] Bone metastases are also a major cause for morbidity in patients with advanced stage cancer.[ii]

"We are inspired with these initial results and thankful this patient was able to experience such pain relief and avoid a skeletal related event (SRE)," said Nikhil Thakur, MD, Chief Medical Officer of Zetagen Therapeutics.

"The ease of administering of the ZetaMet (Zeta-BC-003) product, via a percutaneous outpatient procedure could benefit these very ill patients and accelerate physician adoption," said David Palma, MD, interventional radiologist administering the therapy in this case study.

Zetagen is focused on the more than 620,000 people in the United States, and more globally, living with metastatic cancers. This number is expected to reach more than 690,000 by the year 2025.[iii] Bone metastases are common among cancer patients and occur when cells from the primary cancerous tumor relocate to the bone. When these cancers relocate, they can cause changes to the bone, damaging it in a process called osteolysis. Osteolysis can cause small holes within the bone, weakening it and increasing the risk of breakage. These holes are called "lytic lesions." Among cancers which metastasize to bone, Breast and Prostate are most prevalent, amounting to approximately 70-percent of cases.[iv]

The Company has been issued two Breakthrough Device Designations from the U.S. Food and Drug Administration (FDA) for ZetaMet (Zeta-BC-003) and ZetaFuse and issued multiple patents from the U.S. Patent and Trademark Office (USPTO). Zetagen is funded through Series A and B rounds of funding, Phase I and II National Institute of Health (NIH) / National Cancer Institute (NCI) grants and angel investors.

[i] Ibrahim T, Mercatali L, Amadori D. A new emergency in oncology: Bone metastases in breast cancer patients (Review). Oncol Lett. 2013;6(2):306-310. doi:10.3892/ol.2013.1372

[ii] Cecchini M, Wetterwald A, Pluijm G, Thalmann G. Molecular and biological mechanisms of bone metastasis. EAU Update Series 2005;3:214-26. [Google Scholar]

[iii] Gallicchio L, Devasia TP, Tonorezos E, Mollica MA, Mariotto A. Estimation of the Number of Individuals Living With Metastatic Cancer in the United States, JNCI: Journal of the National Cancer Institute, 2022;, djac158, View Source

[iv] Li S, Peng Y, Weinhandl ED, et al. Estimated number of prevalent cases of metastatic bone disease in the US adult population. Clin Epidemiol. 2012;4:87-93. doi:10.2147/CLEP.S28339

Helix Biopharma Announces Upcoming Poster Presentation at the AACR-NCI-EORTC International Conference on Molecular Targets and Cancer Therapeutics

On October 10, 2023 Helix BioPharma Corp. (TSX:HBP) ("Helix" or the "Company"), an immune-oncology antibody-drug-conjugate company developing an innovative drug platform for the treatment of cancer, reported that the Company will present new preclinical data on L-DOS47 in combination with PD1 checkpoint inhibition at the 2023 AACR (Free AACR Whitepaper)-NCI-EORTC AACR-NCI-EORTC (Free AACR-NCI-EORTC Whitepaper) International Conference on Molecular Targets and Cancer Therapeutics (EORTC-NCI-AACR) (Free ASGCT Whitepaper) (Free EORTC-NCI-AACR Whitepaper) in the Hynes Convention Center, Boston, via in person attendance, October 11-15, 2023 (Press release, Helix BioPharma, OCT 10, 2023, View Source [SID1234635947]).

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Poster Presentation Details:

Title: Neutralizing Acidosis with ADC L-DOS47 Urease Immunoconjugate Enhances Response to Anti-PD1 Checkpoint Blockade in A Preclinical Orthotopic Model of Pancreatic Adenocarcinoma
Abstract Number: 35494
Poster Presentation Date and Time: Friday, October 13, 12:30 pm – 4:00 pm
Location: Level 2, Exhibit Hall D Poster Session B,

Poster Number: B125

During the conference, Helix will highlight the enhanced effects of anti-PD1 immunotherapy when combined with L-DOS47 in an orthotopic Pancreatic tumor model in mice. The drug has already been administered to over 120 patients in the clinic across 4 Toronto, Ontario | October 10, 2023 07:01 AM Eastern Daylight Time clinical trials and has been shown to be safe and well tolerated. Additionally, L-DOS47 has also demonstrated promising anti-tumor activity across a range of doses, both as monotherapy and in combination with chemotherapy agents. The Company is open to collaborating with the right partner(s) to explore potential synergies with anti-PD1 and other treatment regimens.

"We are enthusiastic about the results of these studies, which showcase a distinctive ADC platform. This platform has the capability to synergize effectively with a wide range of approaches, such as chemotherapy, radiation therapy, immunotherapy, and emerging cell therapies. This synergy aims to boost effectiveness while minimizing safety issues." said Jacek Antas, Helix’s Chief Executive Officer. More details about the AACR (Free AACR Whitepaper)-NCI-EORTC Conference are available on the official website.

TME Pharma Provides Positive Update on 18-Month Survival for NOX-A12 Combination Regimen in Brain Cancer and Provides Strategic Update Including Decision to Engage with US FDA

On October 10, 2023 TME Pharma N.V. (Euronext Growth Paris: ALTME), a biotechnology company focused on developing novel therapies for treatment of cancer by targeting the tumor microenvironment (TME), reported a positive update on survival at 18 months for patients receiving NOX-A12 with the VEGF inhibitor bevacizumab and radiotherapy, and provides an overview on upcoming clinical development plans for NOX-A12 in the aggressive adult brain cancer, glioblastoma (Press release, TME Pharma, OCT 10, 2023, View Source [SID1234635840]).

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The percentage of patients who were alive 18 months after start of therapy of NOX-A12 with the VEGF inhibitor bevacizumab and radiotherapy is currently 50% (with the possibility to increase to 67% with the next patient reaching 18 months) which exceeds by 10-fold the 18-month survival of 5% observed in the matched group of patients receiving standard of care1. Since neither bevacizumab (anti-VEGF) alone, nor bevacizumab plus radiotherapy have previously shown to extend survival, the strong increase in survival can be attributed to the complementary mechanism of action of NOX-A12 with bevacizumab and radiotherapy2. The survival rate of the NOX-A12 triple combination also exceeds the 18-month survival of 20% seen in the patients with high levels of the NOX-A12 predictive biomarker EG12 receiving NOX-A12 + radiotherapy alone3, which further supports NOX-A12’s potential to synergize with VEGF inhibition in glioblastoma (see figure below).

The median overall survival has now reached 18 months and is expected to improve further as the remaining patients continue to receive treatment or follow-up care4. Two of the three living patients are clinically stable despite radiographic tumor progression at last report from treating clinicians, including the patient who achieved complete response, now completing 22 months therapy. As a reminder, the matched standard of care reference cohort achieved a median overall survival of 10.5 months.

The NOX-A12-based therapy has now delivered median overall survival exceeding all the relevant competitor studies conducted in the US or EU involving newly diagnosed, chemotherapy-resistant (MGMT unmethylated) glioblastoma patients despite recruiting more difficult to treat patients whose tumors could not be fully removed by surgery5. NOX-A12 in combination with bevacizumab and radiotherapy continues to show an excellent safety and tolerability profile similar to that noted in previous publications.

In the upcoming 6 months the key regulatory steps for NOX-A12 program in brain cancer will include the following:

Q4 2023 – Request advice in October from US Food and Drug Administration (FDA) on next trial design and eligibility for expedited regulatory pathways, such as Fast-Track Designation. Feedback expected in late December.
Q1 2024 – Submit IND6 application for glioblastoma with the US FDA along with expedited regulatory pathway access request. Successful IND filing and feedback targeted by end of Q1 2024.
TME Pharma plans to keep the market updated on the progress of these regulatory discussions. The goal is to have an FDA approved clinical trial protocol in glioblastoma with an expedited regulatory path by the beginning of April 2024 in order to secure the funding for the necessary clinical trial via partnership, investment or other strategic transaction types.

"We believe that survival data from the NOX-A12 bevacizumab expansion arm is now sufficiently mature and have made the decision to request advice from the US regulatory authority in the coming weeks. Once we have feedback from the FDA, we plan to submit an IND and request access to an expedited pathway for approval. We believe that having a clear path to marketing approval in brain cancer, validated by FDA, will significantly increase the attractiveness of NOX-A12 to investors and potential partners." said Aram Mangasarian, CEO of TME Pharma. "While we believe that the FDA will request a randomized clinical trial examining two doses of NOX-A12 combined with bevacizumab and radiotherapy and to compare these two dose regimens against standard of care as a next step, they may also request that these two doses of NOX-A12 be tested only with radiotherapy (without bevacizumab) in order to quantify precisely the benefit of the combination with NOX-A12 and bevacizumab, which would add two additional arms to the clinical trial. We anticipate that an additional trial or an expansion of the upcoming trial would be required for full approval."

BPGbio to Share Updates in Development of Late-Stage AI-Developed Therapeutic Pipeline at the Pharma Partnering Summit

On October 10, 2023 BPGbio, Inc., a leading AI-powered biopharma that focuses on oncology, neurology, and rare diseases, reported plans to present on their groundbreaking AI-developed therapeutics portfolio at the upcoming Pharma Partnering Summit in Boston October 19-20, 2023 (Press release, BPGbio, OCT 10, 2023, View Source [SID1234635839]). At the meeting, BPGbio’s President and CEO, Dr. Niven R. Narain, and Executive Chairman Daniel Elliott will unveil the progress made in advancing their oncology drug candidate BPM31510, currently under investigation for glioblastoma multiforme (GBM) and pancreatic cancer. They will also provide insights into the company’s growing portfolio of AI-discovered therapeutics and diagnostics, identified through the company’s proprietary NAi Interrogative Biology Platform.

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"We are excited to share with industry peers, partners and the investment community about BPGbio’s AI-driven late stage clinical assets at the Pharma Partnering Summit," said Niven R. Narain, Ph.D., President & CEO, BPGbio, Inc. "The positive progress we are making in our clinical trials continue to validate the efficacy of our AI powered NAi Interrogative Biology Platform, with our lead oncology candidatbusine, BPM31510, demonstrating an early indication for potential clinical benefit for both GBM and pancreatic cancer—two of the most aggressive and deadly cancers."

BPM31510, the company’s lead drug candidate is a small molecule compound currently in a Phase 2b clinical trial led by Stanford for glioblastoma multiforme GBM. Notably, BPM31510 has also garnered a favorable recommendation from the medical advisory board to progress into Phase 2b trials for pancreatic cancer. BPM31510 acts by targeting the mitochondrial machinery and tumor microenvironment (TME) to create a metabolic shift in cancer cells, leading to cancer cell death.

In addition, BPGbio’s therapeutic pipeline also includes drug candidates for Epidermolysis Bullosa (EB), Squamous Cell Carcinoma (SCC), Sarcopenia, solid and liquid tumors, Huntington’s disease, and Parkinson’s disease. The company’s diagnostic pipeline includes its prostate cancer diagnostic test pstateDx, which is being launched in Mexico, as well as tests being developed and validated for the detection of Parkinson’s disease (ParkinsonDx), pancreatic cancer (PancDx), breast cancer, and liver disease.

Calidi Biotherapeutics To Present New Preclinical Data Highlighting Cell-based Virotherapy (SuperNova) Platform Technology at SITC 2023

On October 10, 2023 Calidi Biotherapeutics, Inc. (NYSE American: CLDI or "Calidi"), a clinical-stage biotechnology company developing a new generation of targeted immunotherapies, reported a poster highlighting new preclinical data and clinical development plans from the company’s novel SuperNova technology will be presented at the Society for Immunotherapy of Cancer (SITC) (Free SITC Whitepaper)’s (SITC) (Free SITC Whitepaper) 38th Annual Meeting in San Diego, CA, taking place November 1-5, 2023.

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Presentation Details

Title: A Novel Stem Cell-based Platform for Delivery and Potentiation of Oncolytic Virotherapies
Presenting Authors: Antonio F. Santidrian, PharmD, Ph.D., Chief Scientific Officer, Calidi Biotherapeutics
Boris R. Minev, MD. President, Medical & Scientific Affairs, Calidi Biotherapeutics
Abstract Number: 1419
Date: Friday, November 3, 2023
Time: 9:00 AM – 7:00 PM PDT