Arovella Licenses the Rights to a Novel Monoclonal Antibody Targeting a DKK1 Peptide

On December 13, 2021 Arovella Therapeutics, (ASX: ALA), a biotechnology company focused on developing its invariant Natural Killer T (iNKT) cell therapy platform, reported that it has signed a global, exclusive licence agreement with The University of Texas MD Anderson Cancer Center for the patent rights to a novel mAb developed for cancer treatment (Press release, Arovella Therapeutics, DEC 13, 2021, View Source [SID1234629025]).

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This is the first monoclonal antibody directed against a DKK1 peptide found in complex with HLA-A2 on the surface of cancer cells (DKK1). DKK1 is a target that is found in many cancer types, including blood cancers and solid tumours and 40-50% of the population is HLA-A2 positive, meaning that this technology may be applicable across a wide spectrum of cancers that affect a significant proportion of the population.

Higher levels of DKK1 in cancer patients may serve as a prognostic biomarker for cancers such as Multiple Myeloma, Head and Neck Squamous Cell Carcinoma (HNSCC), Pancreatic Adenocarcinoma (PAAD), and Lung Squamous Cell Carcinoma (LUSC). Higher DKK1 production has been observed in bladder cancer and increased production of DKK1 may assist Non-small Cell Lung Carcinoma (NSCLC) cell invasion and migration. It has also been suggested that increased DKK1 levels may cause resistance to chemotherapy in cancers such as ovarian cancer.

Arovella’s CEO and MD, Dr Michael Baker, commented: "The data that we have seen for the DKK1- CAR is compelling. We see a lot of promise in combining DKK1-CAR with our iNKT cell therapy platform and expect synergistic effects for the treatment of certain cancers. The next steps are to confirm the specificity, safety and proof-of-concept data in animal models before advancing this into manufacturing."

Numerous studies have shown that multiple myeloma cells overproduce DKK1. It is also documented that multiple myeloma cells produce CD1d, which is recognised by invariant Natural Killer T (iNKT) cells, the core of Arovella’s iNKT cell therapy platform. Arovella expects that by combing the DKK1- CAR with its iNKT cell therapy platform, it will lead to a more effective product to treat multiple myeloma and potentially other cancers. To date, the DKK1 mAb has shown promise in treating multiple myeloma when used as a single agent in mouse models. The DKK1-CAR-T successfully eliminates cancer in numerous cancer models, including multiple myeloma, pancreatic cancer, lung cancer and triple negative breast cancer.

More than a decade of work has gone into the production and testing of the DKK1 mAb. Professor Qing Yi, now at Houston Methodist, developed the technology during his time at MD Anderson as a tenured Professor of Medicine. At Houston Methodist, Professor Yi has continued the research, assessing the potential of the DKK1-CAR. Professor Yi was recruited to Houston Methodist in 2018 through a US$6m Cancer Prevention and Research Institute of Texas (CPRIT) award.

Professor Yi commented: "We have been working on the role of DKK1 for more than a decade. To target a range of cancers, we knew we needed to target something unique on the surface of different cancer types. That is why we generated the DKK1-peptide targeting mAb and CAR, because the DKK1 peptide in complex with HLA-A2 is found on many cancers and as expected, we see robust data treating several cancer types."

Key terms of the Licence Agreement

Under the terms of the licence agreement, Arovella has secured the right to use the technology for the treatment of human disease, for which it has agreed to pay MD Anderson license fees, development milestones and single digit royalty payments based on net sales. Upfront fees associated with the license agreement will be funded entirely from existing cash reserves. The licence agreement commences with an effective date of 13 December 2021 and extends to the later of the expiration of applicable patent rights or agreed upon number of years.

Arovella’s role in the oncology market

The Licence Agreement involving the DKK1 mAb adds substantially to Arovella’s existing exposure to the immuno-oncology market. The Company acquired the licence for a novel iNKT cell therapy platform in June 2021 and is developing a CD19 targeting CAR to treat haematological malignancies.

Since acquiring the licence to the iNKT cell therapy platform, Arovella has added new members to its Board of Directors, its Scientific Advisory Board and its management team. Arovella believes that acquiring the licence to another CAR adds substantial value to its iNKT cell therapy platform.

HARPOON THERAPEUTICS PROVIDES PIPELINE UPDATE FOR TRITAC® CLINICAL PROGRAMS AND T CELL ENGAGER PLATFORMS

On December 13, 2021 Harpoon Therapeutics, Inc. (NASDAQ: HARP), a clinical-stage immunotherapy company developing novel T cell engagers, reported a pipeline update on its programs, including the interim data presented from the ongoing dose-escalation portion of the Phase 1/2 trial for HPN217 in patients with relapsed/refractory multiple myeloma (R/R MM) at the 63rd American Society for Hematology (ASH) (Free ASH Whitepaper) Annual Meeting and Exposition (Press release, Harpoon Therapeutics, DEC 13, 2021, View Source [SID1234597098]). Harpoon has four product candidates in clinical trials that are based on its proprietary Tri-specific T cell Activating Construct (TriTAC) platform designed to recruit a patient’s own immune cells to kill tumor cells.

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"We are focused on advancing our clinical programs in 2022 and are pleased to see the HPN217 and HPN328 programs showing clinical activity at well tolerated dose levels, indicating a threshold effect," stated Julie Eastland, President and CEO, Harpoon Therapeutics. "We look forward to the initiation of expansion cohorts to learn more about these promising TriTAC programs while building our future clinical pipeline with our first ProTriTAC candidate, HPN601 targeting EpCAM, currently in IND-enabling studies."

"The interim clinical data from the escalation portion of the HPN217 trial shows robust anti-myeloma activity that is encouraging," said Natalie Sacks, M.D., Chief Medical Officer of Harpoon. "In addition, we are observing tumor shrinkage in small lung cancer patients in the HPN328 trial, and we are excited to see validation of the TriTAC platform in both solid tumors and hematologic malignancies. We continue to investigate the performance of our novel technology in multiple indications and are encouraged by the signs of clinical activity and manageable tolerability profiles."

Dose escalation for HPN217 (BCMA TriTAC) Phase 1/2 clinical trial Ongoing
Relapsed/refractory multiple myeloma patients (N=37) have been treated across 9 fixed dose cohorts of 5 to 2860 µg/week, and 1 step dose cohort of 1620 (priming) and 3240 (target) µg/week reflecting rapid dose expansion since the trial began. HPN217 has been well tolerated, with one DLT, Grade 4 AST which resolved, as of the November 10, 2021 data cutoff date.

The ASH (Free ASH Whitepaper) poster presentation, included the following observations:

Encouraging clinical activity in higher dose cohorts including a 63% ORR and 88% DCR reported in the 2150 µg/week cohort with 8 disease evaluable patients with R/R MM, including one minimal residual disease (MRD) negative, stringent CR.
HPN217 shows tolerable safety profile with cytokine release syndrome (all Grade 1 or 2) observed in 9 of 37 patients (24%)
Patient enrollment and dose escalation is ongoing to define the RP2D and MTD
Introduction of step dose regimens has allowed for the administration of higher target doses.
Dose escalation for HPN328 (DLL3 TriTAC) Phase 1/2 clinical trial making rapid progress. Fifteen patients have been enrolled in dose cohorts ranging from 15 µg to 7200 µg per week in both fixed and step dose cohorts administered once weekly by intravenous infusion. Fifteen patients with a median of 2 lines (range 1 to 5) of prior therapy have been enrolled and eligible patients include small cell lung cancer patients who have relapsed after platinum chemotherapy and patients with other malignancies with high grade neuroendocrine tumors associated with DLL3 expression. HPN328 has been well tolerated with Grade 1-2 CRS reported in 33% of patients, no DLTs observed and MTD has not been reached. Among four patients with small cell lung cancer receiving the two highest doses tested to date, 1215 µg fixed dose and 3600-7200 µg step dose, three had target lesion reduction, including 1 confirmed RECIST partial response. The patient with a cPR experienced a target lesion reduction of 53% at week 10. Presentation of initial interim clinical data is planned for 2022.

IND-enabling studies for HPN601 (EpCAM ProTriTAC) are progressing as planned. HPN601 is the first conditionally active T cell engager based on the ProTriTAC platform. EpCAM is expressed in a broad range of solid tumors, including gastrointestinal cancers, potentially enabling HPN601 to address multiple indications with high unmet medical need. By the end of 2022, an IND submission for HPN601 is expected as well as identification of a second IND candidate from the ProTriTAC platform.

Harpoon’s T cell engager platforms, TriTAC, ProTriTAC, and TriTAC XR, are designed to mitigate different target toxicities across a range of disease indications, including solid and hematologic malignancies.

Next generation T cell engager platforms advancing. Harpoon continues to discover new technologies to improve the therapeutic application of T cell engagers. We recently introduced the TriTAC XR platform, which is designed to minimize on-target cytokine release syndrome. Nomination of an IND candidate from the TriTAC XR platform is also expected by the end of 2022.

Conference Call and Webcast Today

Harpoon’s management will host a webcast and conference call at 4:30 p.m. ET / 1:30 p.m. PT on Monday, December 13, 2021 to review the data presented at ASH (Free ASH Whitepaper) and provide an update on its other pipeline programs. The live call may be accessed by dialing 866-951-6894 for domestic callers or 409-216-0624 for international callers and using conference ID # 2760075.

A live webcast of the call will be available from the Events and Presentations section of the company’s website at View Source and will be archived there shortly after the live event.

The Second Generation RET Inhibitor APS03118 Completing FDA’s Declaration of IND

On December 13, 2021 APS reported the application for clinical trial of APS second generation RET inhibitor APS03118 without cancer limitation was accepted by the United States Food and Drug Administration (FDA) (Press release, Applied Pharmaceutical Science, DEC 13, 2021, View Source [SID1234613104]). APS03118 is an oral second-generation RET kinase inhibitor independently developed by APS. Preclinical studies indicated that APS03118 could effectively inhibit solvent frontier RET G810R/S mutation and was expected to overcome drug resistance of existing selective RET inhibitors.

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The approval of selective RET inhibitors brings significant improvements to the treatment of aberrant RET positive patients, including non-small cell lung cancer and thyroid cancer. However, the drug resistance of these first-generation selective RET inhibitors was reported recently. Compared with EGFR, ALK and other targets, there are no drugs targeting RET resistant mutations, and patients usually have disease progression again after experiencing effective treatment. The reported drug resistance mechanism is the on target mutation represented by the RET G810R/S solvent frontier mutations, which hinders the binding of first-generation RET inhibitors to the target and finally results in drug resistance. APS03118, with unique structural advantages, can effectively inhibit RET solvent frontier mutations and displays remarkable anti-tumor effect in multiple mouse models with good tolerance.

2022 French delegation JP Morgan week

On December 13, 2021 Brenus Pharma reported that it will be attenting the #JPMweek2022 from January 10 to 12 in San Francisco; We are proud to be part of the 2022 French delegation of this major networking event for the healthcare ecosystem (Press release, Brenus Pharma, DEC 13, 2021, View Source [SID1234598462]). This JP Morgan week is an opportunity to meet investors, business partners and make new connections. Follow us, and contact us to learn and see more !!

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Rospatent Grants AskAt a Patent for the Use of EP4 Receptor Antagonists in the Treatment of NASH-Associated Liver Cancer

On December 13, 2021 AskAt reported that it received an Official Decision of Grant dated November 19, 2021 of a use patent for its EP4 receptor antagonist in the treatment of NASH-associated liver cancer (Press release, AskAt, DEC 13, 2021, View Source [SID1234596829]). The notice was issued by the Russian Federal Service for Intellectual Property, Patents and Trademarks (Rospatent), in connection with Russian Patent Application No. 2020109376 (Filing Date: November 2, 2017). In addition to Russia, the use patent has been granted in Canada, China, Europe, Japan, Mexico, and the U.S.

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