Karyopharm to Participate at Upcoming Investor Conferences

On September 7, 2022 Karyopharm Therapeutics Inc. (Nasdaq: KPTI), a commercial-stage pharmaceutical company pioneering novel cancer therapies, reported that the Company’s senior management team will participate in the following investor conferences in September (Press release, Karyopharm, SEP 7, 2022, View Source [SID1234619162]):

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Morgan Stanley 20th Annual Global Healthcare Conference
Format: Fireside chat
Date: Monday, September 12, 2022
Time: 12:30 p.m. ET

Baird 2022 Global Healthcare Conference
Format: Fireside chat
Date: Tuesday, September 13, 2022
Time: 12:50 p.m. ET

A live webcast of the fireside chats, along with accompanying slides, can be accessed under "Events & Presentations" in the Investor section of the Company’s website, View Source, and will be available for replay for 90 days following each fireside chat.

Cue Biopharma to Present at Two September 2022 Scientific Conferences

On September 7, 2022 Cue Biopharma, Inc. (Nasdaq: CUE), a clinical-stage biopharmaceutical company developing a novel class of injectable biologics to selectively engage and modulate tumor-specific T cells directly within the patient’s body, reported members of their management and scientific teams will participate in two scientific conferences this September, The Promise of Interleukin-2 Therapy taking place September 14-17 in Paris, France and the Next Generation Protein Therapeutics Summit, held in Boston, Massachusetts and virtually on September 28-30 (Press release, Cue Biopharma, SEP 7, 2022, View Source [SID1234619179]).

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Presentation Details

The Promise of IL-2 Therapy
Location: Centre international de Conférence Sorbonne Université, Paris, France
Presentation title: Leveraging the Immuno-STAT platform to enhance anti-tumor immunity by selectively delivering IL-2 to tumor-specific T cells
Presenter: Matteo Levisetti, M.D., senior vice president, Clinical Development, Cue Biopharma
Session: Session IX – IL-2 in Cancer Therapy
Date and time: September 17, 2022, 9:00 am CET

Dr. Levisetti will present an overview of Cue Biopharma’s Immuno-STAT (Selective Targeting and Alteration of T cells) platform including the interleukin 2 (IL-2)-based CUE-100 series of biologics designed to enable selective targeting of IL-2 to tumor-specific T cells. The presentation will highlight data from clinical trials evaluating CUE-101, the company’s lead clinical candidate from the CUE-100 series, in patients with human papilloma virus positive recurrent/metastatic head and neck squamous cell carcinoma (HPV+ R/M HNSCC) as a monotherapy and in combination with pembrolizumab. Dr. Levisetti will also discuss the company’s second clinical candidate, CUE-102, currently in evaluation in a Phase 1 trial for patients with Wilms’ Tumor 1 (WT1)-positive cancers as well as other platform developments that support versatility for the potential treatment of several diverse cancers.

Presentation title: CUE-401: a novel IL-2/TGF-beta fusion protein for induction and expansion of regulatory T cells
Presenter: Steven Quayle, Ph.D., vice president Translational Pharmacology, Translational Medicine, Cue Biopharma
Session: Session X – Novel IL-2s and Combination Therapies
Date and time: September 17, 2022, 11:30 am CET

Dr. Quayle will provide an overview on the Company’s lead CUE-400 series drug product candidate CUE-401, a novel bispecific molecule designed for differentiation and expansion of induced regulatory T cells (iTregs). Dr. Quayle will discuss preclinical data supporting CUE-401’s mechanism of action and potential opportunity for the treatment of patients with autoimmune and graft-versus-host disease. Cue Biopharma plans to advance the CUE-400 series programs through strategic partnerships.

Presentation Details

Next Generation Protein Therapeutics Summit
Location: Boston Convention and Exhibition Center & virtual. The event will be simultaneously live streamed: https://informaconnect.com/next-gen-protein/
Presentation title: Immuno-STATs: TCR-selective engagers and activators of anti-tumor T cells
Presenter: Anish Suri, President and chief scientific officer, Cue Biopharma
Session: T Cell Engager Design and Challenges
Date and time: September 28, 2022, 4:30 pm ET

Dr. Suri will present an overview of Cue Biopharma’s Immuno-STAT platform and biologics designed to present tumor-specific proteins to T cell receptors (TCR) of the target tumor-specific T cells, to modulate that T cell repertoire for the anti-cancer response, as well as clinical data demonstrating the single-agent anti-tumor activity of CUE-101, the Company’s first IL-2 based clinical candidate, in late-stage head and neck cancer patients.

About Immuno-STAT
The company’s Immuno-STAT (Selective Targeting and Alteration of T cells) biologics are designed for targeted modulation of disease-associated T cells in the areas of immuno-oncology and autoimmune disease. Each of our biologic drugs is designed using our proprietary scaffold comprising: 1) a pMHC to provide selectivity through interaction with the T cell receptor (TCR), and 2) a unique co-stimulatory signaling molecule to modulate the activity of the target T cells. The simultaneous engagement of co-regulatory molecules and pMHC binding mimics the signals delivered by antigen presenting cells (APCs) to T cells during a natural immune response. This design enables Immuno-STAT biologics to engage with the T cell population of interest, resulting in selective T cell modulation. Because our drug candidates are delivered directly in the patient’s body (in vivo), they are fundamentally different from other T cell therapeutic approaches that require the patients’ T cells to be extracted, modified outside the body (ex vivo), and reinfused.

CytoImmune Therapeutics Appoints Remus Vezan, M.D., Ph.D., as Chief Medical Officer

On September 7, 2022 CytoImmune Therapeutics, a clinical-stage immuno-oncology company that is developing a novel class of engineered natural killer (NK) cell-based cancer therapies, reported the appointment of Remus Vezan, M.D., Ph.D., as Chief Medical Officer (Press release, CytoImmune Therapeutics, SEP 7, 2022, View Source [SID1234619196]). Dr. Vezan is an industry leader who has been responsible for the successful advancement of numerous cell therapies from early-stage development through commercialization, including one of the first U.S. Food and Drug Administration (FDA)- approved CAR T-cell therapies for hematologic malignancies.

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"Remus brings an ideal combination of expertise to CytoImmune, having led the successful implementation and execution of clinical development strategies for several biopharmaceutical companies focused on both immuno-oncology and cell therapies," said Christina Coughlin, M.D., Ph.D., Chief Executive Officer of CytoImmune. "We recently made the important transition to a clinical-stage company with the initiation of our Phase 1 trial of CYTO-102 for non-small cell lung cancer, and I am excited to partner with Remus as we advance this program and others in our pipeline."

"CytoImmune is taking a novel approach to developing cell therapies, leveraging NK cells to create medicines that directly attack cancer cells and broadly stimulate both the innate and adaptive arms of the immune system," said Dr. Vezan. "Cell therapies have proven highly effective in treating various hematologic malignancies, with several approved products available today, however, the results obtained in solid tumors to date are underwhelming. Through novel engineering and manufacturing strategies, CytoImmune’s engineered NK cell therapies have the potential to overcome key challenges that have been observed in solid tumors. This will greatly expand the number of patients who could benefit from this therapy. I am pleased to join the team at this exciting time in the evolution of the company."

Dr. Vezan joins CytoImmune from CERo Therapeutics where he served as Chief Medical Officer. Prior to that, he served as Executive Director of clinical development at Kite, a Gilead company, where he oversaw the clinical development of CAR T-cell products, including axi- cell/YESCARTA, the first CAR T-cell therapy approved for relapsed/refractory B-cell lymphoma and brexu-cell/TECARTUS, the first CAR T-cell therapy approved for mantle cell lymphoma and adult acute lymphoblastic leukemia. In this role, Dr. Vezan supported the overall clinical development strategy and execution of numerous registrational clinical trials and under his leadership, YESCARTA and TECARTUS were granted various global approvals. Before Kite, Dr. Vezan served as Medical Director at Pharmacyclics, an AbbVie Company, where he was the clinical lead for HDACi-abexinostat program and ibrutinib (IMBRUVICA) in lymphoplasmacytic lymphomas (Waldenstrom Macroglobulinemia). Dr. Vezan completed his medical training (M.D. and Ph.D.) at the University of Medicine and Pharmacy Cluj, Romania and University of Bern, Switzerland.

Lutris Pharma Reports Positive Top-Line Results From the Open Label Part 1 and Double Blinded Part 2 of Its Phase 1/2 Trial of LUT014 to Treat Radiation Dermatitis in Patients with Breast Cancer

On September 7, 2022 Lutris Pharma, a clinical stage biopharmaceutical company focused on improving anti-cancer therapies by reducing dose limiting side effects, reported positive top-line results from the open label part 1 and double blinded part 2 of its phase 1/2 trial of lead compound, LUT014, a topically applied, novel B-Raf inhibitor, for the treatment of radiation-induced dermatitis (RD) in patients with breast cancer (Press release, Lutris Pharma, SEP 7, 2022, View Source [SID1234619213]).

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Figure 1: Image of the irradiated area of a patient in part 1 of the study at baseline and at each visit (1 week intervals). Courtesy of Lutris Pharma.
Figure 1: Image of the irradiated area of a patient in part 1 of the study at baseline and at each visit (1 week intervals). Courtesy of Lutris Pharma.
Figure 2: Images of 2 patients in part 2 of the study after 1 week of treatment. On the left is a patient in the placebo arm. On the right is a patient treated with LUT014. Courtesy of Lutris Pharma.
Figure 2: Images of 2 patients in part 2 of the study after 1 week of treatment. On the left is a patient in the placebo arm. On the right is a patient treated with LUT014. Courtesy of Lutris Pharma.
Part 1 results showed that, of the eight patients who developed grade 2 RD at baseline, 75% (7/8) had complete resolution, improving to grade 0 dermatitis, and 100% of patients had RD of 1 or 0 as assessed by the Common Terminology Criteria for Adverse Events (CTAE) after 28 days of daily, topically applied LUT014 gel. All of the patients derived benefit in quality of life by day 28 as assessed by the validated, self-reporting Dermatology Life Quality Index (DLQI) questionnaire, with seven of eight patients experiencing no or small effect of the dermatitis on their respective quality of life after the treatment course. The primary endpoint of the open-label part 1 was the incidence of Treatment-Emergent Adverse Events as assessed by CTAE at 12 weeks and the data showed that LUT014 was generally well tolerated, no severe or serious adverse events occurred and no adverse events were associated with discontinuation of the study drug.

The primary endpoint of the double blinded part 2 of the phase 1/2 trial was the change in severity of radiation dermatitis, based on a validated self-reporting DLQI questionnaire at 14 days, as measured by improvement of at least 5 points on the DLQI at day 14. Of note, 8/8 (100%) of patients treated with LUT014 versus 8/11 (73%) of patients treated with placebo achieved the primary endpoint (27% absolute difference, Fisher’s Exact test, p=0.23). Secondary endpoints examined further quality of life variables as well as treatment effect. Improvement in the DLQI score at day 7 was noted by an increase of 30% in the treated arm versus placebo arm; the proportion of patients who showed improvement from grade 2 to grade 1 by day 7 was 75% (6/8) for patients who received LUT014 versus 54% (6/11) for patients who received placebo; and the proportion of patients who achieved complete recovery (grade 0) by day 28 was 50% (4/8) for LUT014 versus 36% (4/11) for placebo.

"We are extremely encouraged by the strong part 1 results and the equally impressive part 2 data, which show 100% of patients with radiation dermatitis in the LUT014 treatment arm experiencing a clinically meaningful treatment effect," stated Noa Shelach, Ph.D., Chief Executive Officer of Lutris Pharma. "The secondary endpoints reported were all supportive, as well, and further highlight the potential, unique ability of LUT014 to expedite patient recovery within just one to two weeks and to make a marked difference in quality of life. Given the fact that the majority of patients with breast cancer will develop radiation dermatitis, these results further empower our thesis about the promise of LUT014 to treat this patient population."

Benjamin W. Corn, M.D., Chief Medical Officer of Lutris Pharma, added, "Part 2 of the phase 1/2 study provided us with impactful information that supports the need for further study of LUT014 in this radiation-induced dermatitis indication. Based on the top-line results, the 100% success rate indicates that the active arm response is saturated and that there might be an even a greater effect that cannot be detected in the current study design. That said, we believe we may be able to see a higher effect between treatment and placebo arms if LUT014 is started earlier, right after a patient’s radiation treatment."

Antoni Ribas, M.D., Chairman of the Board of Directors of Lutris Pharma, noted, "These favorable results in patients with radiation dermatitis, coupled with the highly encouraging data generated, thus far, in the company’s study of LUT014 in patients with mCRC with EGFR inhibitor induced acneiform lesions, tells us that the LUT014 compound is active to treat skin conditions that could benefit from the topical administration of this small molecule BRAF inhibitor, which opens the door to its use in numerous additional indications, and we look forward to exploring these options and expanding the pipeline in the future."

For more information about this clinical trial, please visit: www.clinicaltrials.gov, NCT04261387.

About LUT014

LUT014 is a novel B-Raf inhibitor which is applied topically on the skin. When the B-Raf protein is mutated, as is the case in some human cancers such as melanoma cancer, blocking this pathway leads to apoptosis of the cells and tumor shrinkage. However, when the same pathway is blocked in normal, non-mutated cells, the opposite happens: the MAPK pathway is activated, and cells start growing. This phenomenon is recognized as the paradoxical effect of B-Raf Inhibitors. LUT014 harnesses the paradoxical effect of B-Raf Inhibitors in order to enhance cell proliferation and balance cell destruction, typical to radiation dermatitis.

About Radiation Dermatitis

Radiation therapy results in ionization events that lead to damage of cellular macromolecules, including double-stranded DNA breaks. Within the epidermis, this DNA damage disrupts the normal proliferation and differentiation of basal keratinocytes, depleting the differentiated epidermal keratinocytes and ultimately resulting in the loss of the protective barrier provided by the skin. This, combined with DNA damage disruption within the dermis, which results in a complex sequence of effects including an immune response cascade, leads to the symptomology associated with radiation dermatitis, which can dramatically diminish a patient’s quality of life.

There is currently no FDA-approved drug whose labelled indication is for the prevention or treatment of radiation-induced dermatitis. Rather, patients are merely treated with supportive cutaneous care. These treatments – which have a weak evidence base — have included topical steroids, non-steroidal anti-inflammatory topicals, and hyaluronic acid derivatives. To date, none has been definitively proved efficacious.

AMGEN TO WEBCAST INVESTOR CALL AT ESMO 2022

On September 7, 2022 Amgen (NASDAQ:AMGN) reported that it will host a webcast call for the investment community in conjunction with the European Society for Medical Oncology Annual Congress (ESMO) (Free ESMO Whitepaper) at 1:30 p.m. ET on Monday, Sept. 12, 2022 (Press release, Amgen, SEP 7, 2022, View Source [SID1234619147]). David M. Reese, M.D., executive vice president of Research and Development at Amgen, along with members of Amgen’s clinical development team, will discuss the data being presented from the LUMAKRAS (sotorasib) CodeBreaK 200 confirmatory Phase 3 study in non-small cell lung cancer and data from the full Phase 1b expansion cohort of LUMAKRAS in combination with Vectibix (panitumumab) in colorectal cancer. The webcast will be broadcast over the internet simultaneously and will be available to members of the news media, investors and the general public.

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The webcast, as with other selected presentations regarding developments in Amgen’s business given by management at certain investor and medical conferences, can be found on Amgen’s website, www.amgen.com, under Investors. Information regarding presentation times, webcast availability and webcast links are noted on Amgen’s Investor Relations Events Calendar. The webcast will be archived and available for replay for at least 90 days after the event.