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.

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.