On May 15, 2024 Innate Pharma SA (Euronext Paris: IPH; Nasdaq: IPHA) ("Innate" or the "Company") reported that four abstracts with Innate’s drug candidates have been accepted for the European Association of Hematology (EHA) (Free EHA Whitepaper) 2024 Congress, taking place June 13-16, 2024 in Madrid, Spain (Press release, Innate Pharma, MAY 15, 2024, View Source [SID1234643377]).

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Two abstracts are related to SAR443579 (IPH6101), an investigational trifunctional anti-CD123 NKp46xCD16 NK cell engager from a joint research collaboration between Innate Pharma and Sanofi and currently being evaluated as a monotherapy in a Sanofi-sponsored Phase 1/2 clinical trial for the treatment of blood cancers with high unmet needs.
Two abstracts are related to IPH6501, Innate’s second generation ANKET for the treatment of relapsed or refractory CD20-expressing B-cell Non-Hodgkin’s Lymphoma, currently in Phase 1/2 clinical trial.
"We’re pleased to see a continued momentum around our ANKET platform assets, SAR443579 and IPH6501," said Dr. Sonia Quaratino, Chief Medical Officer of Innate Pharma. "With their innovative format, we believe that NK Cell Engagers will benefit for patients who are in high unmet medical need, and we look forward to continue the studies with these assets."

EHA abstract details:

SAR443579 / IPH6101 (under development by Sanofi)

Abstract: S146
Abstract Title: Completed dose-escalation from the First-in-Human, Phase 1/2 Study of CD123 NK Cell Engager SAR443579 in Relapsed or Refractory Acute Myeloid Leukemia or High Risk-Myelodysplasia
Abstract type: Oral Presentation

Abstract: P475
Abstract Title: Exploring Dose-response Relationship of a Novel CD123 NK Cell Engager SAR443579 in Acute Myeloid Leukemia (AML) Models
Abstract type: Poster Presentation

IPH6501

Abstract: P1251
Abstract Title: Preclinical assessment of IPH6501, a first-in-class IL2V-armed tetraspecific NK Cell Engager directed against CD20 for R/R B-NHL, in comparison with a CD20-targeting T Cell Engager
Abstract type: Poster Presentation
This abstract is embargoed until 23.05.2024 23:00 CEST, until publication by the American Society of Clinical Oncology (ASCO) (Free ASCO Whitepaper), Inc. for their 2024 ASCO (Free ASCO Whitepaper) Annual Meeting.

The Abstract PB3041, "A Phase 1/2 trial investigating safety, tolerability, and preliminary antitumor activity of IPH6501, a first-in-class NK Cell Engager, in patients with R/R CD20-expressing NHL" will be available in the EHA (Free EHA Whitepaper) abstracts book.

About ANKET

ANKET (Antibody-based NK cell Engager Therapeutics) is Innate’s proprietary platform for developing next-generation, multi-specific natural killer (NK) cell engagers to treat certain types of cancer. This versatile, fit-for-purpose technology is creating an entirely new class of molecules to induce synthetic immunity against cancer.

About IPH6501

IPH6501 is the first Antibody-based NK cell Engager Therapeutic to co-engage activating receptors on NK cells (NKp46 and CD16), IL-2R (but not α subunit) through a variant of human IL-2, and a tumor antigen (CD20) via a single molecule, hence providing proliferation and activation signals targeted to NK cells and promoting their cytotoxic activity against CD20 expressing malignant cells. IPH6501 has shown better anti-tumor efficacy than approved benchmark antibodies in preclinical tumor models (Demaria, EHA (Free EHA Whitepaper) 2023).

About the Innate-Sanofi research collaboration and licensing agreements

The Company has a research collaboration and license agreement with Sanofi to apply Innate’s proprietary technology to the development of innovative multi-specific antibody formats engaging NK cells through the activating receptors NKp46 and CD16 to kill tumor cells.

Under the terms of the 2016 research collaboration and license agreement, Sanofi is responsible for the development, manufacturing and commercialization of products resulting from the research collaboration, which includes SAR443579/IPH6101 (Trifunctional anti-CD123 NKp46xCD16 NK cell engager) and SAR445514/IPH6401 (Trifunctional anti-BCMA NKp46xCD16 NK cell engager). As part of the 2016 agreement, Innate Pharma is eligible to up to €400m in development and commercial milestone payments as well as royalties on net sales.

As part of the license agreement entered in December 2022, Sanofi licensed IPH62 and IPH67 and has the option for one additional target. Under the terms of the 2022 agreement, Innate Pharma is eligible to up to €1.35bn in development and commercial milestone payments as well as royalties on net sales.

On May 15, 2024 Rondo Therapeutics, a biopharmaceutical company pioneering next-generation bispecific antibodies, reported oral presentations at both Protein & Antibody Engineering Summit (PEGS) and Antibody Engineering & Therapeutics (AET) EU (Press release, Rondo Therapeutics, MAY 15, 2024, View Source [SID1234643376]).

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Rondo Therapeutics will describe its immune-cell engaging bispecific antibody platforms and how it is building a clinical pipeline with a focus on treating solid tumors. The company will provide an update on its lead program, RNDO-564, a co-stimulatory T-cell engaging bispecific antibody targeting CD28 and Nectin-4 for the treatment of bladder cancer.

"Presenting our data at PEGS and AET EU represents a significant milestone for our company. This is a golden age for bispecific antibodies and we are delighted to be driving innovation in the field. Targeted signaling through the CD28 pathway is showing a lot of promise as an effective strategy for overcoming the challenges presented by solid tumors. We look forward to sharing our unique approach and commitment to developing novel immunotherapy options for patients with solid tumors," said Shelley Force Aldred, co-founder, and CEO of Rondo Therapeutics.

Presentation Details

Protein & Antibody Engineering Society (Boston, MA)
Date: Wednesday, May 15
Title: Bispecific Antibody Combination Strategies for Treating Solid Tumors
Presenter: Nathan D. Trinklein, PhD, Co-Founder and President, Rondo Therapeutics
Conference Link: https://www.pegsummit.com/

Antibody Engineering & Therapeutics EU (London, UK)
Date: Tuesday, June 5
Title: Co-stimulatory Bispecific Antibody Strategies for Treating Solid Tumors
Presenter: Starlynn Clarke, PhD, Director of Preclinical Biology, Rondo Therapeutics
Conference Link: https://informaconnect.com/antibody-engineering-europe/

On May 15, 2024 TriSalus Life Sciences Inc., (Nasdaq: TLSI), reported its financial results for the first quarter ended March 31, 2024, and provided a business update (Press release, TriSalus Life Sciences, MAY 15, 2024, View Source [SID1234643375]).

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"I’m proud to highlight our strong start in the first quarter of 2024 with 116% growth in revenues compared to the first quarter of 2023 and significantly improving our financial position with our debt financing facility with OrbiMed," said Mary Szela, Chief Executive Officer of TriSalus. "With our recent positive developments in reimbursement, clinical data, and the dedication of our seasoned executive team, we’re confident in our ability to execute our company-building strategy. Our objectives of achieving over 50% top-line revenue growth, advancing our pipeline, and strengthening our operational foundations remain firmly on track."

First Quarter 2024 and Subsequent Highlights

Secured up to $50 million of debt financing with OrbiMed to support TriNav Infusion System growth initiatives

In April, TriSalus announced the closing of a debt financing facility with OrbiMed, a healthcare investment firm. Under the terms of the Credit Agreement with OrbiMed, the Company borrowed $25 million at closing. In addition, an aggregate of up to an additional $25 million is available in two tranches at the Company’s option, subject to the Company’s achievement of certain revenue thresholds.

The $25 million draw, along with cash and cash equivalents on hand of $4 million at March 31, 2024, are expected to provide sufficient cash runway to fund the Company’s operations through the end of 2024. Including our SEPA agreement and other existing sources of liquidity and assuming we achieve the revenue targets and borrow the remaining $25 million of the debt financing, the Company expects to have sufficient cash runway to fund operations through the end of 2025.

Liselotte Hyveled appointed to the Board of Directors

In May, TriSalus announced the appointment of Liselotte Hyveled to its Board of Directors. Ms. Hyveled currently serves as the Chief Patient Officer at Novo Nordisk, where she is responsible for ensuring the integration of patient needs and perspectives into the company’s decision-making processes and operations. She brings over two decades of experience stimulating scientific innovation and advancing pharmaceutical pipelines through research and development excellence.

Financial Results for Q1 2024

Revenue, all of which is from the sale of the TriNav Infusion System, was $6.5 million in the first quarter ended March 31, 2024. This amount represents growth of 116% compared to the first quarter of 2023, primarily due to increased selling resources and continued market share increases.

Gross margins were 85% in the first quarter ended March 31, 2024, versus 78% in the first quarter of 2023. The improvement is due to increased factory volumes and improved operations efficiency.

Operating losses were $11.7 million in the first quarter ended March 31, 2024, versus $10.1 million in the first quarter of 2023. Increased investment in sales and marketing, research and development, as well as general and administrative costs associated with becoming a public company more than offset increased gross profit in 2024.

Net losses available to common stockholders were $13.2 million in the first quarter ended March 31, 2024, versus $8.3 million in the first quarter of 2023. Net losses in 2024 include the impact of non-cash related gains/(losses) on change in fair value of SEPA and warrant liabilities of $2.5 million and change in fair value of contingent earnout liabilities of ($4.0) million. Net losses in 2023 include the impact of non-cash related gains/(losses) on equity issuance of ($1.5) million, extinguishment of tranche liabilities of $0.9 million, and change in fair value of SEPA and warrant liabilities of $2.4 million.

Basic and diluted loss per share for the first quarter ended March 31, 2024, was $0.60 versus $0.57 per share in the first quarter of 2023.

Conference Call

The event will be webcast live on the investor relations section of TriSalus’ website at View Source on May 15, 2024, at 9:00 a.m. EDT. Following the conclusion of the event, a webcast replay will be available on the website for approximately 90 days. Interested parties participating by phone will need to register using this online form. After registering for the webcast, dial-in details will be provided in an auto-generated e-mail containing a link to the conference phone number along with a personal pin.

On May 15, 2024 Bayer reported initiation of dosing in a Phase I first-in-human clinical study with 225Ac-PSMA-Trillium (BAY 3563254), a next-generation targeted alpha therapy (Press release, Bayer, MAY 15, 2024, View Source [SID1234643373]). The investigational candidate, labeled with actinium-225 and comprising a novel PSMA (prostate-specific membrane antigen) -targeting small molecule with a customized albumin-binding moiety, is designed to potentially improve therapeutic efficacy and reduce side effects in normal organs such as salivary glands. The dose-escalation study (NCT06217822) will evaluate the safety, tolerability and efficacy of 225Ac-PSMA-Trillium in patients with advanced metastatic castration resistant prostate cancer (mCRPC).

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"Despite recent advances in the treatment landscape for prostate cancer, there is still a high unmet need for novel precision therapy options to improve outcomes for patients with metastatic castration-resistant prostate cancer," said Fred Saad, MD, FRCS, Professor and Chairman of Surgery at University of Montreal and Director of Genitourinary Oncology at University of Montreal Hospital Center (CHUM), Canada."225Ac-PSMA-Trillium is a novel approach, which could provide a new treatment to address this unmet need in mCRPC."

"Targeted radionuclide therapy is a strategic pillar of precision oncology at Bayer, holding the promise to shift the treatment paradigm for patients, including those whose disease has developed resistance to other treatments," said Dominik Ruettinger, M.D., Ph.D., Head of Research and Early Development for Oncology at Bayer. "We are excited to announce initiation of the phase I and dosing of the first patient with 225Ac-PSMA-Trillium. With its unique design, we believe it could offer a meaningful benefit for patients with metastatic prostate cancer, and we look forward to advancing the program through clinical development."

Prostate cancer is the second most commonly diagnosed cancer in men1 and a key area of focus at Bayer. Despite significant advances in the last decade, mCRPC remains a deadly disease with a median survival of about 31 months.2 Bayer remains committed to advancing medical innovations for patients across all stages of prostate cancer.

In April, Bayer introduced 225Ac-PSMA-Trillium during the New Drugs on the Horizon session at the AACR (Free AACR Whitepaper) (American Association of Cancer Research) Annual Meeting.3 Along with preclinical in vitro and in vivo characterization, the results were presented for a Phase 0 clinical imaging and dosimetry study conducted in participants with prostate cancer.

About Targeted Alpha Therapy

Targeted alpha therapy is an emerging class of radionuclide therapy that can be used against a variety of tumors. It is designed to deliver alpha particle radiation directly to the tumor inside the body, either via its bone-seeking property (radium-223) or by combining alpha radionuclides, such as actinium-225, with specific targeting moieties. This localized delivery of the radioactive payload induces difficult to repair double-strand DNA breaks in tumor cells; damage that can cause cell cycle arrest or cell death. At the same time, because the energy does not travel very far, there is a potential for reduced damage to nearby normal tissues.

On May 15, 2024 Nutcracker Therapeutics, Inc., a biotechnology company dedicated to developing transformative RNA therapies through its proprietary technology platform, reported data presented by its partners at the University of California, San Francisco (UCSF) on foundational prostate cancer antigen research utilized to inform the development of its mRNA drug candidate, NTX-470 (Press release, Nutcracker Therapeutics, MAY 15, 2024, View Source [SID1234643371]). The data were presented by lead author Elena Montauti, Ph.D., from UCSF on May 4, during the 2024 Annual Meeting of the American Association of Immunologists (AAI) in Chicago.

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It is well established that prostate cancer is a "cold cancer" with low immunogenicity. Its low mutation burden has resulted in very few druggable neoantigens – leaving shared tumor-associated antigens (TAAs) as the primary targets for immunotherapeutic development. However, the larger landscape of which shared prostate TAAs are immunogenic targets is challenging to assess and has not been systemically studied across patients. Further, it is unknown how antigen immunogenicity evolves as the disease progresses. The research presented at AAI aimed to map antigen reactivity in prostate cancer to inform possible combinations of TAAs that could be used as treatment for the disease.

Using its Nutshell technologies, Nutcracker Therapeutics’ scientists worked with UCSF researchers to create mRNAs encoding eight common and shared prostate TAAs, and employed a novel antigen recall assay to systematically study T cell immune responses in blood samples of patients with localized and metastatic prostate cancer. Cellular immune responses to shared TAAs were tracked across cohorts and correlated with treatment and disease outcomes after immunotherapy. Single-cell genomic analysis was used to characterize TAA-reactive T cell effector phenotypes and to track TCR expansion. Together, this in-depth analysis of TAA-reactive cellular responses in prostate cancer patients provides potentially transformative insights for the development of shared antigen-directed immunotherapeutics.

"We’re proud to have a partnership with the talented individuals at the University of California, San Francisco," said Chief Scientific Officer Samuel Deutsch, Ph.D. "The data presented at AAI reflects our deep commitment to new therapeutic strategies for prostate cancer, including the development of NTX-470. We’re hopeful that with our continued work with our partners at UCSF, we can continue conducting research that sheds a light on the unknowns of different cancers, and informs the development of much-needed novel therapeutics – whether by Nutcracker Therapeutics or others in the field."

"There are many knowledge gaps that currently exist in prostate cancer research," said UCSF Assistant Professor of Medicine David Oh, M.D., Ph.D. "The means by which antigen recognition changes as the cancer progresses is still unknown – making it difficult to design and develop effective drugs for more advanced forms of prostate cancer. By systematically researching antigen reactivity using this programmable platform, and relating this to known clinical outcomes after immunotherapy, we aim to lay the groundwork to address these existing knowledge gaps, with the hopes of inspiring the development of a new generation of mRNA-based immunotherapeutics for prostate cancer."

The research presented at AAI was the result of a longstanding partnership between Nutcracker Therapeutics and UCSF. Currently, Nutcracker Therapeutics has partnerships with Dr. Lawrence Fong and Dr. Oh’s labs in cancer immunotherapy. This data – resulting from a collaboration with Dr. Oh – expands upon a previous demonstration of the data by UCSF at last year’s American Association for Cancer Research (AACR) (Free AACR Whitepaper) annual meeting in 2023.

Previously, Nutcracker Therapeutics presented preclinical data at this year’s AACR (Free AACR Whitepaper) Annual Meeting for NTX-470. This multimodal mRNA therapy for prostate cancer encodes both PSMA and STEAP1 antigens, and was shown to effectively engage CD3 T cells with reduced off-tumor binding, which may result in diminished treatment toxicity.