Abcuro Announces Participation in Upcoming Investor Conferences

On November 11, 2024 Abcuro, Inc., a clinical-stage biotechnology company developing therapies for the treatment of autoimmune diseases and cancer through precise modulation of cytotoxic T cells, reported that Alex Martin, Chief Executive Officer, will present at the following investor conferences (Press release, Abcuro, NOV 11, 2024, View Source [SID1234648065]).

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Stifel 2024 Healthcare Conference: Presentation on November 18, 2024, at 3:00 pm E.T.
Piper Sandler 36th Annual Healthcare Conference: Presentation on December 3, 2024, at 4:10 pm E.T.

Phase 1 onCARlytics Trial Doses First Patient in Intratumoural (IT) Combination Arm

On November 11, 2024 Imugene Limited (ASX: IMU), a clinical stage immuno-oncology company, reported the dosing of the first patient in the intratumoural (IT) combination arm of its Phase 1 onCARlytics (CF33-CD19) clinical trial (Press release, Imugene, NOV 11, 2024, https://mcusercontent.com/e38c43331936a9627acb6427c/files/0b72d5aa-3410-e210-9537-71ef3b912378/onCARlytics_Trial_Doses_First_Patient_in_IT_Combination_Arm.pdf [SID1234648060]). This development is part of the OASIS trial, which is designed to assess the safety and efficacy of Imugene’s CD19 oncolytic virotherapy in patients with advanced or metastatic solid tumours.

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The OASIS trial is a Phase 1 dose escalation study that explores two routes of administration, intratumoural (IT) injection and intravenous (IV) infusion. onCARlytics, a CD19-expressing oncolytic virus, is being investigated both as a monotherapy and in combination with the CD19-targeting bispecific antibody blinatumomab, an established cancer immunotherapy.

Imugene Managing Director & CEO Leslie Chong said: "We are pleased to have dosed the first patient in the intratumoural arm of our OASIS trial. With CD19 being a well-established target in blood cancers, we are optimistic about the effectiveness it could show in solid tumours. onCARlytics has the potential to induce expression of CD19 on the surface of solid tumours and allowing existing CD19 therapies to recognise and attack the cancer. We’re pleased to continue advancing this prospective new treatment option for those in need."

OASIS is currently being conducted at seven sites in the U.S. including City of Hope, University of Cincinnati, and MD Anderson Cancer Center, with the potential to open a total of 10 sites to recruit up to approximately 40 patients with advanced solid cancers that have spread. The primary objective of the trial is to evaluate the safety and efficacy of onCARlytics, either by IT injection or IV infusion, either alone, or in combination with blinatumomab. In February, the first patient with bile tract cancer was dosed in the IV monotherapy arm of the trial at City of Hope in California. Subject to the rate of patient enrolment, preliminary IT and/or IV combination status is expected in the fourth quarter of 2024.

The trial is titled: "A Phase I, Dose Escalation and Dose Expansion, Safety and Tolerability Study of onCARlytics (CF33-CD19), Administered Intravenously or Intratumorally in Combination with Blinatumomab in Adults with Advanced or Metastatic Solid Tumors." See View Source

Alteogen enters into an Exclusive License Agreement to Develop and Commercialize Subcutaneous ENHERTU® Enabled by Alteogen’s Hybrozyme™ Technology

On November 10, 2024 Alteogen Inc. (KOSDAQ:196170) reported that the company has entered into an exclusive license agreement with Daiichi Sankyo (TSE: 4568) (Press release, Alteogen, NOV 10, 2024, View Source [SID1234648061]). Under the terms of the agreement, Daiichi Sankyo will acquire world-wide rights to use ALT-B4, Alteogen’s novel hyaluronidase utilizing Hybrozyme Technology, to develop and commercialize a subcutaneous version of ENHERTU (fam-trastuzumab deruxtecan-nxki), a HER2 directed antibody drug conjugate (ADC) that has been jointly developed and commercialized by Daiichi Sankyo and AstraZeneca.

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Alteogen will receive an upfront payment and is eligible to receive milestone payments upon Daiichi Sankyo’s achievement of specified development, regulatory and sales milestones. Additionally, Alteogen will be entitled to receive tiered royalties on the sales of the commercialized product. Alteogen will be responsible for clinical and commercial supply of ALT-B4 to Daiichi Sankyo.

"Our collaboration with Daiichi Sankyo is groundbreaking in the ADC field, being the first to use hyaluronidase for a subcutaneous ADC marks a significant milestone in the oncology field, and we look forward to our collaboration with Daiichi Sankyo in bringing this product to the market." said Dr. Soon Jae Park, Chief Executive Officer of Alteogen.

About ALT-B4

ALT-B4 is Alteogen’s proprietary human recombinant hyaluronidase enzyme developed utilizing Hybrozyme technology. ALT-B4 can enable the large volume subcutaneous administration of drugs that are typically administered as an IV infusion. ALT-B4 does this by temporarily hydrolyzing hyaluronan in the extracellular matrix.

Clarity and Nucleus RadioPharma sign Master Services Agreement and Cu-67 SAR-bisPSMA Clinical Supply Agreement

On November 10, 2024 Clarity Pharmaceuticals (ASX: CU6) ("Clarity" or "Company"), a clinical-stage radiopharmaceutical company with a mission to develop next-generation products that improve treatment outcomes for children and adults with cancer, reported that it has entered into an MSA and Clinical Manufacturing Agreement for 67Cu-SAR-bisPSMA with Nucleus RadioPharma, an innovative contract development and manufacturing organisation (CDMO) in the radiopharmaceutical industry, dedicated to the development and manufacturing of targeted radiotherapies (Press release, Clarity Pharmaceuticals, NOV 10, 2024, View Source [SID1234648058]).

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This agreement builds on the earlier MSA and Clinical Supply Agreements with NorthStar for the production of 67Cu-SAR-bisPSMA1, allowing Clarity to continue building supply chain capacity ahead of a Phase III trial and commercialisation with this product.

Nucleus RadioPharma’s facility in Minnesota enables 67Cu-SAR-bisPSMA manufacturing and distribution to all 50 states in the U.S. Their recently announced expansion plans for building additional manufacturing capacity in Arizona and Pennsylvania2 are also in line with the timelines for development of Clarity’s 67Cu-SAR-bisPSMA product, ensuring broad drug supply throughout the U.S.

Clarity’s Executive Chairperson, Dr Alan Taylor, commented, "We continue to strengthen our manufacturing network, ensuring prostate cancer patients in need of novel radiopharmaceutical treatments can get access to what we believe is a best-in-class product, on time and on demand. We have seen excellent data from the SECuRE3 trial and in case studies as part of the U.S. Food and Drug Administration (FDA) Expanded Access Program (EAP) with 67Cu-SAR-bisPSMA and look forward to progressing the development of this important therapy to address the large unmet need in prostate cancer care.

"The strong demand from investigators for 67Cu-SAR-bisPSMA and our accelerating pace of the SECuRE trial recruitment make this the right time to invest in additional manufacturing capacity. Our long-standing relationship with NorthStar has put us in a very unique position in radiopharmaceuticals, having both the therapeutic isotope and finished product manufactured at one site. We have seen the failures in the supply of Pluvicto by Novartis where vulnerable patients were left waiting for their treatments4-5 and have learnt from these mistakes.

"At Clarity, we know that employing a layered supply strategy in anticipation of future demand is essential in radiopharmaceuticals. The use of the true theranostic pair, copper-64 and copper-67, allows for a readily scalable approach to product manufacture, which stands in stark contrast to currently used isotopes, such as gallium-68, fluorine-18 and lutetium-177, where supply and logistical complications are common. As we continue to progress our development of Targeted Copper Theranostics (TCTs) and scale our supply in support of later-phase clinical trials and eventual commercialisation, we intend to make logistical interruptions affecting patient care a thing of the past."

Nucleus RadioPharma’s Chief Scientific Officer, Dr Geoffrey Johnson, commented, "I am excited to continue my collaboration with Clarity on the development of its SAR-bisPSMA theranostic product. Being a Principal Investigator on the SECuRE trial, I have seen first-hand how my patients have benefited from the 67Cu-SAR-bisPSMA therapy. I am now pleased to support the development of this product on the supply chain side as well and that Nucleus RadioPharma will be producing doses of this novel drug for patients in the SECuRE trial and beyond as it continues to generate strong data. Having the therapeutic copper-67 isotope produced domestically on purpose-built electron accelerators allows for reliable and scalable supply, free from the challenges of other therapeutic isotopes at this time, and Nucleus RadioPharma’s location in Rochester, MN allows seamless access to prestigious medical centres in the vicinity."

The Master Services Agreement and Clinical Supply Agreement are effective as of 8 November 2024 and are for an initial period of 36 months. Cancellation and extension provisions are aligned with industry standard rates.

A2 Bio Highlights Progress of Tmod™ CAR T-Cell Clinical Programs During 2024 Annual Meeting of the Society for Immunotherapy of Cancer

On November 9, 2024 A2 Biotherapeutics, Inc. (A2 Bio), a clinical-stage cell therapy company developing first-in-class logic-gated cell therapies to selectively target tumor cells and protect normal cells, reported progress of its Tmod CAR T-cell clinical programs during the 39th Annual Meeting of the Society for Immunotherapy of Cancer (SITC) (Free SITC Whitepaper) taking place November 8-10, 2024 (Press release, A2 Biotherapeutics, NOV 10, 2024, View Source [SID1234648064]). In an oral presentation today, the company shared continued progress in increasing the diversity of participants enrolled in the BASECAMP-1 nationwide prescreening study for all Tmod CAR T-cell trials. A2 Bio also shared posters highlighting early safety and biomarker data from the ongoing EVEREST-1 clinical study, an enrollment update for the EVEREST-2 clinical study, and updates on adaptations to boost potency and preserve selectivity of its Tmod-based precision cell therapies.

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The BASECAMP-1 abstract (number 589: "BASECAMP-1 is an efficient pre-screening study that identifies patients with HLA LOH and provides mutational, RNA-Seq, and microbiome data for precision logic-gated CAR T therapeutic trials") was recognized by SITC (Free SITC Whitepaper) as a top 100 abstract during the 2024 annual meeting.

"A2 Bio is very pleased to present progress of our clinical trials at SITC (Free SITC Whitepaper) 2024 as we advance our innovative Tmod logic-gated CAR T-cell therapies to help patients with today’s most challenging cancers. We are pioneering a new participant-recruitment model to enhance safety, efficiency and diversity in the interventional trials of our Tmod precision cell therapies," said William Go, M.D., Ph.D., chief medical officer of A2 Bio.

The Tmod platform solves the problem of on-target, off-tumor toxicity with a dual-receptor system that targets two (or more) antigens to confer selective tumor killing. Normal cells are protected from cytotoxicity by the Tmod blocker that recognizes antigens expressed only on normal tissues.1 A2 Bio is sponsoring two investigational Tmod therapies in separate trials: EVEREST-1 that utilizes A2B530 to target carcinoembryonic antigen (CEA); and EVEREST-2 that utilizes A2B694 to target mesothelin (MSLN). Patients are enrolled in EVEREST-1 and EVEREST-2 through the BASECAMP-1 prescreening study. BASECAMP-1 utilizes artificial intelligence (AI)-enabled precision diagnostics in partnership with Tempus AI, as a cost-effective, high-yield approach to identify eligible patients for all A2 Bio clinical studies.2

BASECAMP-1 Oral Presentation Summary

In an oral presentation today, Julian R. Molina, M.D., Ph.D., professor of oncology, Mayo Clinic, Rochester, Minn., presented an update on the BASECAMP-1 prescreening study, highlighting innovative advancements that improve participant diversity in clinical trials and operational efficiency in patient recruitment. BASECAMP-1 is an ongoing, nationwide prescreening study featuring an innovative approach to overcome the operational burden of finding eligible participants for precision medicine studies. BASECAMP-1 uses a single next-generation sequencing (NGS) test from Tempus AI to efficiently screen for participants with tumor-associated HLA-A*02 LOH. Such screening identifies participants eligible for multiple current and future interventional trials of Tmod logic-gated CAR T therapies, improves trial diversity, and enhances the dataset and statistical power for translational studies. As of September 1, 2024, 70 participants have been enrolled in the BASECAMP-1 prescreening study.

A participants-matching program has been implemented to accelerate the identification and enrollment of participants whose tumors have HLA-A*02 LOH. Careful evaluation of the Tmod blocker has demonstrated that it functions well against HLA-A*02 subtypes beyond HLA-A*02:01, thus providing the impetus to enroll additional participants with broader ethnic and racial diversity. Based on these data, eligibility criteria have been amended to enroll patients with germline HLA-A*02:XX heterozygosity. As of July 1, 2024, this amendment has led to the potential enrollment of 16% more Hispanic, 43% more African American, and 112% more Asian and Pacific Islander participants, improving the racial and ethnic diversity of the BASECAMP-1 study population. Furthermore, information captured in the BASECAMP-1 study provides a large dataset for correlative analysis to further characterize tumors of patients with and without LOH.

"The wealth of data generated from the multicenter BASECAMP-1 prescreening study will enable more efficient identification and enrollment of patients undergoing cancer treatment at leading academic centers across the United States. Additional strategies to enhance access to BASECAMP-1 include increasing the geographic location of study sites; leveraging NGS across the US in both academic and community practices; and creating materials to help patients understand complex clinical trials," Dr. Molina said.

EVEREST-1 Poster Presentation Summary

In a poster presentation today, Patrick M. Grierson, M.D., Ph.D., assistant professor in the division of oncology of Washington University in St. Louis, shared safety and early biomarker data from EVEREST-1 (abstract number 588), the first clinical study sponsored by A2 Bio. EVEREST-1 is a first-in-human, phase 1/2, multicenter, open label, nonrandomized study to evaluate the safety and efficacy of a single dose of A2B530 Tmod CAR T cells in adults with recurrent unresectable, locally advanced, or metastatic non-small cell lung, colorectal, pancreatic, or other solid tumors associated with CEA expression.

The first EVEREST-1 patient was dosed in May 2023 and, as of September 1, 2024, 14 patients have been enrolled (four patients with pancreatic cancer and 10 patients with colorectal cancer). Of these, two pancreatic cancer patients have reached one-year survival post-infusion. Pharmacokinetic data from 14 patients show a potential dose-response, with higher doses appearing to have an effect on the peak expansion of Tmod cells. There have been no reports of dose-limiting toxicities, grade >3 serious adverse events, or neurotoxicity related to A2B530, and there have been no significant safety issues in patients at their one-year follow-up visit and beyond. Dose escalation is ongoing, and the maximum tolerated dose has not yet been reached. To date, treatment with A2B530 appears to have a manageable safety profile and to be tolerable.

EVEREST-2 Poster Presentation Summary

In a poster presentation on November 8, Dr. Molina shared an enrollment update on EVEREST-2 (abstract number 627), a seamless, phase 1/2, open-label, nonrandomized study to evaluate the safety and efficacy of A2B694 in adult patients with solid tumors. EVEREST-2 is the second interventional clinical study sponsored by A2 Bio. The first patient was enrolled in EVEREST-2 in April 2024, and dose escalation is ongoing.

For more information about ongoing A2 Bio clinical trials, please visit View Source

About EVEREST-1

EVEREST-1 (NCT05736731) is a seamless Phase 1/2 study for A2B530, an autologous logic-gated investigational cell therapy developed from the A2 Bio proprietary Tmod platform. The Tmod platform provides selective killing of tumor cells and protection of normal cells via a dual-receptor design consisting of an activator that targets tumor cells and a blocker that protects normal cells. A2B530 consists of an activator that targets carcinoembryonic antigen (CEA) and a blocker that targets HLA-A*02. HLA-A*02 is lost in tumor cells and present in normal cells in the eligible patient population. The study is recruiting participants with non-small cell lung, colorectal and pancreatic cancers.

About EVEREST-2

EVEREST-2 (NCT06051695) is a seamless Phase 1/2 study for A2B694, an autologous logic-gated investigational cell therapy developed from the A2 Bio proprietary Tmod platform. The Tmod platform provides selective killing of tumor cells and protection of normal cells via a dual-receptor design consisting of an activator that targets tumor cells and a blocker that protects normal cells. A2B694 consists of an activator that targets mesothelin (MSLN) and a blocker that targets HLA-A*02. HLA-A*02 is lost in tumor cells and present in normal cells in the eligible patient population. The study is recruiting participants with non-small cell lung, colorectal, pancreatic, ovarian and mesothelioma cancers.

About BASECAMP-1

BASECAMP-1 (NCT04981119) is a prescreening study to identify patients for potential treatment in A2 Bio clinical trials. It is a novel approach to help optimize patient treatment outcomes by enabling patients’ immune cells to be stored in their healthiest state earlier in their course of cancer treatment. Next-generation sequencing is used to identify patients who have lost HLA-A*02, the biomarker of interest for the A2 Bio studies. Patients then undergo leukapheresis to collect, process, and store patient T cells for future Tmod CAR T cell therapy. BASECAMP-1 is currently enrolling participants with non-small cell lung, colorectal, pancreatic, ovarian and mesothelioma cancers.

About the Tmod Platform

A2 Bio has pioneered a precision-targeting cellular system – the Tmod platform – that incorporates two receptors, an activator and a blocker, to aim the powerful armaments of immune cells directly at tumors to unequivocally differentiate tumors from normal tissues. The activator recognizes antigens on tumor cells that trigger their destruction, while the blocker recognizes antigens on normal cells that protect them. This novel blocker technology enables precise, personalized and effective T cell targeting. The blocker component equips Tmod cells with the capacity to identify tumors as distinct from normal cells.