Three Complete Responses in Azer-Cel Allogeneic CD19 CAR T Phase 1b
Trial in Blood Cancer (Diffuse Large B-Cell Lymphoma)

On September 2, 2024 : Imugene Limited (ASX:IMU), a clinical stage immuno-oncology company, reported promising results from its Phase 1b clinical trial with azer-cel (azercabtagene zapreleucel, an allogeneic off-the-shelf CD19 CAR T), in patients with relapsed/refractory diffuse large B cell lymphoma (DLBCL), a type of non-Hodgkin’s lymphoma (NHL) (Press release, Imugene, SEP 2, 2024, View Source [SID1234646253]). All enrolled patients had cancer that had returned following autologous CAR T therapy, a high unmet need for this patient population.

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"We are delighted that the first 2 patients in the Cohort B in our azer-cel Phase 1b trial achieved a complete response and continue to maintain their complete responses, one for over 120 days and the other for over 90 days," said Paul Woodard, MD, Imugene’s Chief Medical Officer. "All four patients enrolled in Cohort B have failed 4 to 5 prior treatments, including autologous CAR T therapy. All 4 patients remain on the study and given the robust response rates and durability seen to date, we will continue to enrol patients in the azer-cel plus IL-2 cohort and will closely follow all patients for further responses and durability."

Patients in the trial are being recruited across 15 leading cancer centres in the U.S. including, Columbia University, University of Minnesota, Emory, and Moffitt Cancer Centres and plans are ongoing to open up to 5 sites in Australia.

Nine (9) patients total from Cohorts A and B are considered evaluable (qualified for at least day 28 scan). One (1) patient (Cohort B) has been treated and is awaiting their 28- day scan:

• Of the 6 evaluable patients in Cohort A:
o 1 CR, 1 PR = 33% Overall Response Rate (ORR)
o 1 CR = 17% CR
o Durability of response was < 60 days o All patients no longer on trial

• Of the 3 evaluable patients in Cohort B:
o 2 CRs = 67% ORR o 2 CRs = 67% CR
o 1 Stable Disease (SD)*: On PET/CT scan imaging, patient’s tumour has decreased however, due to potential T-cell infiltration, noted an increase in signal intensity. This could represent pseudoprogression. The patient remains on trial and continues to be assessed for response at the follow up scans.
o Durability of response thus far: >120 days and >90 days (all patients are ongoing)
o All 4 patients (including 1 patient awaiting 28-day scan) continue on trial.

"I am proud of our clinical development team who assessed ways to enhance azer-cel’s durability of response, as one of the biggest challenges in CAR T therapy is ensuring that the modified T-cells stay in the body long enough to kill cancer cells," said Leslie Chong, Managing Director and CEO of Imugene. "

To maximise the response rates and durability further, we added a very low dose of IL-2 to the regimen in Cohort B. We are pleased with the results, which suggest improved outcomes in patients, and we look forward to amassing more data using this dosing regimen. We will continue to seek biomarker evidence from Cohort B patients that suggest our strategy is improving the performance of azer-cel."

The company will continue to enrol additional patients in Cohort B and follow patients for durability of response with the goal of providing a comprehensive package to the FDA for the potential Phase 2/3 registrational trial. Subject to patient recruitment, the company aims to provide an interim Phase 1b data update.

If successful, azer-cel has the potential to become the first approved allogeneic CAR T cell therapy for blood cancer. Beyond studying its efficacy in blood cancers, in the future, Imugene plans to combine azer-cel with its novel onCARlytics program for the treatment of patients with solid tumours, opening a potentially large market for azer-cel in the 90% of cancer not classified as blood cancers.

About the Phase 1b azer-cel trial

acceptable safety profile. In addition, the current patients in Cohort B, treated with azercel, LD, and IL-2 are demonstrating clinically meaningful activity and durability.

About diffuse large B cell lymphoma (DLBCL)

DLBCL is an aggressive and fast-growing type of non-Hodgkin’s lymphoma (NHL), a type of blood cancer. DLBCL is the most common type of NHL, with approximately 80,500 cases per year and approximately 30,000 new cases per year in the U.S.2 Relapsed/refractory DLBCL has a high unmet medical need; 60-65% of patients treated with treatments, including autologous CD19 CAR T, relapse.

About Interleukin 2 (IL-2)

IL-2 is a cytokine (a protein that affects what happens between cells in the immune system) that helps T-cells (which are part of the immune system that help fight cancer) grow and survive. IL-2 has been shown to help T cells live longer and to enhance the cancer killing functions of CAR T cells, making them more effective at targeting and killing cancer cells.

Median Technologies to host two webcasts on September 5, 2024

On September 2, 2024 Median Technologies (FR0011049824, ALMDT, PEA/SME eligible, "Median" or "The Company") reported that it will host two live webcasts on September 5, 2024 (Press release, MEDIAN Technologies, SEP 2, 2024, View Source [SID1234646271]).

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Following the recent release of results of the eyonis LCS REALITY study, Fredrik Brag, CEO and Founder of Median Technologies, will offer further insights into the significance of eyonis LCS and discuss the next steps for Median’s novel Software as a Medical Device.

September 5, 2024 – 4:00 pm CEST / 10:00 am EDT (English)
September 5, 2024 – 6:00 pm CEST / 12:00 pm EDT (French)

Webcast replays will be available on Median’s corporate website shortly after the live sessions.

Lumina Pharmaceuticals Awarded $2 million SBIR Phase II Fast Track NIH Grant to Support the Development of Novel Therapeutics to Solid Tumor Cancer

On September 1, 2024 Collagen Medical, dba Lumina Pharmaceuticals, reported that the company has been awarded a $2 million Small Business Innovation Research (SBIR) Phase II Fast Track grant from the National Cancer Institute (NCI), a member of the US National Institutes of Health (NIH) (Press release, Lumina Pharmaceuticals, SEP 1, 2024, View Source [SID1234656611]). This award will focus on the development of an image-guided therapy paradigm for improving the management of gastric cancer by targeting fibrin in the tumor microenvironment. This SBIR grant follows numerous earlier NIH grants awarded to Lumina.

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"The Fast Track award from NCI represents another important milestone for Lumina as we continue to advance our platform of targeted molecular probes for medical imaging and radioligand therapy," said co-founder Dr. Gregory Sorensen. "This award will enable Lumina to further optimize our lead theranostic pair and acquire additional early clinical imaging data to inform our development plan."

Gastric cancer ranks as the fifth most prevalent malignancy and is the third leading cause of cancer-related mortality globally. Despite advancements in the management of advanced gastric cancer, prognosis remains unfavorable, with median survival limited to 12–14 months even with combination chemotherapy.

Lumina’s theranostic strategy holds the potential to significantly enhance the quality of patient care in solid tumor cancers with high unmet need such as gastric cancer. The approach combines the use of a diagnostic imaging agent for patient selection with a precision medicine of targeted radioligand therapy.

This grant is provided by the National Cancer Institute under Award Number R44CA275590. The content of this release is solely the responsibility of the authors and does not necessarily represent the official views of the National Institutes of Health.

Kuano makes significant strides towards novel bowel cancer therapy

On August 30, 2024 Kuano reported the successful completion of their Innovate UK funded project "Streamlined and Targeted Design of NOTUM Inhibitors as Colorectal Cancer Drugs" (Press release, Kuano, AUG 30, 2024, View Source [SID1234646235]).

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This work delivered in-vivo efficacy data for compounds designed using their computational platform. Launched in December 2022, the programme exceeded initial goals to demonstrate efficacy in cellular assays and validated the ability of Kuano’s combination of quantum simulation and artificial intelligence to accelerate drug discovery. These results provide the basis for the company to develop the lead molecule, further to provide a first in class drug addressing the challenge of treatment resistance in colorectal cancer.

The project funding not only allowed the development of novel drug candidates but the enhancement of the computational platform used to produce them. Kuano’s "Quantum Pharmacophore" provides unique insights into how molecules bind to target enzymes, enabling the identification of potential drug molecules in new areas of chemical space and facilitating their rapid refinement. Use of this approach enables Kuano to identify a lead molecule capable of reducing tumour size in less than 200 molecules, more than an order of magnitude more efficient than conventional approaches.

Molecules designed in-silico by the platform were tested in-vitro using a bespoke assay cascade developed during the project. The most advanced compound was as effective as a highly toxic chemotherapy agent (cisplatin) at killing bowel cancer cells, but had a much improved safety profile for healthy cells. This success provided us with the confidence to test the compound in mouse models (a cell derived xenograft). The data produced showed our compound is tolerated at high doses and reduced tumour size. To enable further development of the compound, and identification of the patient populations most likely to benefit, Kuano is planning further experiments (including organoid studies) starting in August 2024.

Vid Stojevic, CEO of Kuano Ltd, expressed his enthusiasm for the project’s progress:

"This project provides the first evidence that our vision for quantum informed drug design can provide transformational impacts by tailoring chemistry to meet the needs of specific targets. Ultimately this will enable us to develop a new generation of drugs to save and improve the lives of patients with hard to treat cancers."

Chris Sawyer, Innovation Lead, Digital Health at Innovate UK, added:

"Innovate UK is delighted to be able to support innovative projects like Kuano’s that is designed to meet the needs of patients with major diseases like bowel cancer."

Rakovina Therapeutics Announces 2024 Q2 Financial Results and Provides Corporate Update

On August 30, 2024 Rakovina Therapeutics Inc. (TSX-V: RKV, the "Company") a biopharmaceutical company committed to advancing new cancer therapies based on novel DNA-damage response technologies reported the financial results for the second quarter ending June 30, 2024, and provides an update to corporate activities (Press release, Rakovina Therapeutics, AUG 30, 2024, View Source;utm_medium=rss&utm_campaign=rakovina-therapeutics-announces-2024-q2-financial-results-and-provides-corporate-update [SID1234646237]).

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"We are thrilled by the rapid progress and strategic advancements we’ve made at Rakovina Therapeutics since announcing our collaboration with Prof. Artem Cherkasov and exclusive access to the groundbreaking Deep Docking AI platform. AI has propelled us into an exciting new era of precision medicine, allowing us to screen billions of molecular structures and identify promising candidates for clinical development," said Executive Chairman Jeffrey Bacha.

"The overwhelming support shown through our successful $2 million private placement and the expansion of our research collaborations with UBC and Pharma Inventor Inc. further solidifies our commitment to pioneering innovative cancer therapies. Together, these milestones bring us closer to our goal of delivering life-changing treatments to patients worldwide," added Bacha.

2024 Q2 Highlights and Recent Developments

Earlier this spring, we announced a strategic pivot in our business model that positions Rakovina Therapeutics at the forefront of artificial intelligence-driven (AI) precision medicine through a collaboration with Prof. Artem Cherkasov, which provides us with exclusive access to the proprietary Deep Docking (trademarked) AI platform for DNA-damage response targets. In the past three months, we have evaluated more than 1.5 billion molecular structures against DNA damage response targets as potential lead candidates utilizing the Deep Docking AI platform. This iterative process will eventually screen more than seven billion drug candidates and provide a "short list" of recommended novel small molecule structures for synthesis and validation in our laboratories as potential lead candidates for advancement to human clinical trials in collaboration with pharmaceutical partners.
On July 26, 2024, we announced the final closing of an over-subscribed non-brokered private placement financing of units priced at $0.10 per unit with each unit consisting of one common share and one common share purchase warrant with an exercise price of $0.20 per warrant and a term of three years for gross proceeds to the Company of $2 million (the "2024 Private Placement"). Each Warrant entitles the holder thereof to subscribe for and purchase one Common Share at a purchase price of $0.20 for a period of three years from the date of issuance. If the closing price for the Common Shares on the TSX Venture Exchange is $0.25 or greater for five consecutive trading days, the Company will have the right to accelerate the expiry date of the Warrants, upon written notice to the holder, to the date that is 30 days following such notice.
On May 8, 2024, we announced the expansion of our collaborations with the University of British Columbia ("UBC") and our medicinal chemistry partner, Pharma Inventor Inc. The expansion of our research collaborations was initiated to support our AI Drug Discovery Platform. The wet lab infrastructure at UBC combined with the additional medicinal chemistry resources will allow the Company to quickly synthesize and evaluate lead drug candidates identified by the AI platform.
Summary Financial Results for the quarter ended June 30, 2024

For the three and six months ended June 30, 2024, the Company reported a net loss of $820,580 and $1,572,963, respectively. Research and development expenses were $479,785 and $918,768 for the three and six months ended June 30, 2024, respectively.

General and administrative expenses were $276,184 and $527,274 for the three and six months ended June 30, 2024, respectively. Total cash expenses related to research and development and general and administrative expenses for the three and six months ended June 30, 2024, were $605,465 and $1,128,170, respectively.

Selected Financial Information

As at June 30, 2024 $
Cash & cash equivalents 1,386,372
Working capital 932,980
Intangible assets 4,247,731
Total Assets 6,227,085
Total liabilities 2,420,349
Deficit (12,498,274)
Total equity 3,806,736
Statements of net loss and comprehensive loss data:

Description For the three months ended June 30, 2024 For the six months ended June 30, 2023
Research & Development $479,785 $918,768
General and Administrative $276,184 $527,274
Net loss and comprehensive loss $820,611 $1,572,963
Basic and diluted income (loss) per share $(0.01) $(0.02)
Operating cash burn $605,465 $1,128,170
Weighted average shares outstanding 70,709,288 70,397,106
Rakovina Therapeutics’ financial statements as filed with SEDAR can be accessed from the Company’s website at: View Source

Senior management of Rakovina Therapeutics will hold an information and update webinar on Wednesday, Sept. 4, 2024, at 9:30 A.M. Pacific Time/12:30 P.M. Eastern Time. Interested parties may sign up at https://bit.ly/3ACQCxe