Alligator Bioscience Announces Publication Highlighting ATOR-1017 Preclinical Data in the Scientific Journal "Cancer Immunology, Immunotherapy"

On October 5, 2023 Alligator Bioscience (Nasdaq Stockholm: ATORX) reported the publication of a scientific article highlighting the 4-1BB FcγR-conditional agonist antibody ATOR-1017, which is being developed as a tumor-directed therapy for advanced/metastatic cancer (Press release, Alligator Bioscience, OCT 5, 2023, View Source [SID1234635673]).

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The publication in the journal Cancer Immunology, Immunotherapy demonstrates how the design, detailed binding epitope (binding site) on 4-1BB and molecular properties of ATOR-1017 translate into very potent activity both in vitro and in vivo, as monotherapy and in combination with anti-PD-1 treatment, while being well tolerated in preclinical models.

ATOR-1017 binds to a unique epitope on 4-1BB enabling the activation of T cells, including cells with an exhausted phenotype, and NK cells, in a cross-linking dependent, FcγR-conditional manner. This translates into a tumor-directed and potent anti-tumor therapeutic effect in vivo, which is further enhanced with anti-PD-1 treatment.

The full article, entitled "ATOR-1017, an Fc-gamma receptor conditional 4-1BB agonist designed for optimal safety and efficacy, activates exhausted T cells in combination with anti-PD-1", is available online via this link.

"The publication of this article in the renowned scientific journal Cancer Immunology, Immunotherapy is an important recognition of our research into 4-1BB as a target for cancer immunotherapy," said Søren Bregenholt, CEO of Alligator Bioscience. "The first generation of 4-1BB agonists were limited by poor efficacy and unacceptable safety profiles but the preclinical data presented in this article, and the results of our recent Phase 1 dose-escalation study, demonstrate how ATOR-1017 is both a potent 4-1BB agonist and a safe and well tolerated drug candidate with a significant therapeutic potential."
In September 2022, Alligator announced that its Phase 1 open-label dose-escalation study of ATOR-1017 in patients with histologically confirmed, advanced, and/or refractory solid cancer (NCT04144842) had successfully met its primary objective to investigate the safety and tolerability of ATOR-1017 at therapeutic doses. ATOR-1017 demonstrated excellent safety and tolerability at doses up to 900 mg and stable disease as the best tumor response confirmed its previously reported indications on clinical benefit.

Novartis to present new oncology data at ESMO 2023 demonstrating practice-changing innovation in advanced prostate and early breast cancer

On October 5, 2023 Novartis reported that it will present new data from 29 Novartis and investigator-led abstracts at the European Society for Medical Oncology (ESMO) (Free ESMO Whitepaper) Congress 2023, highlighting latest developments from across its oncology portfolio and addressing unmet needs of patients diagnosed with some of the most prevalent cancers, including prostate and breast (Press release, Novartis, OCT 5, 2023, View Source,some%20of%20the%20most%20prevalent [SID1234635654]).

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Key data from the Phase III PSMAfore trial investigating PluvictoTM (INN: lutetium (177Lu) vipivotide tetraxetan) as an earlier line of treatment for patients with prostate-specific membrane antigen (PSMA)-positive metastatic castration-resistant prostate cancer (mCRPC) who have not been exposed to a taxane-containing regimen will be presented. PSMAfore met its primary endpoint of radiographic progression-free survival (rPFS) in December 2022, and data collection for the key secondary endpoint of overall survival (OS) is ongoing. Data from the primary rPFS analysis and the second interim OS analysis will be presented at ESMO (Free ESMO Whitepaper).

"Metastatic prostate cancer has a five-year survival rate of about 30 percent, and patients who progress despite taking androgen-receptor pathway inhibitor therapy need additional treatment options with reduced toxicity," said Jeff Legos, Executive Vice President, Global Head of Oncology and Hematology Development at Novartis. "Pluvicto is the first and only approved, targeted radioligand therapy to significantly extend life in patients with mCRPC who have been treated with ARPI therapy and taxane-based chemotherapy. We look forward to sharing new data from the Phase III PSMAfore trial, which adds to the growing body of evidence demonstrating the potential of our radioligand therapy platform in earlier lines of therapy."

Key highlights of data accepted by ESMO (Free ESMO Whitepaper) include:

Medicine Abstract title Presentation Number / Presentation Details
Pluvicto (lutetium Lu 177 vipivotide tetraxetan) Phase 3 trial of [177Lu]Lu-PSMA-617 in taxane-naïve patients with metastatic castration-resistant prostate cancer (PSMAfore) Presentation Number #LBA13
Presidential 3 (Proffered Paper session):
Monday, October 23,
17:10 – 17:22 CEST
Pluvicto (lutetium Lu 177 vipivotide tetraxetan) First real life data on [177Lu]Lu-PSMA-617: Descriptive analysis on the largest metastatic castration-resistant prostate cancer (mCRPC) cohort treated in early access in France Presentation Number #1814P
Poster available:
Sunday, October 22,
9:00 – 17:00 CEST
Pluvicto (lutetium Lu 177 vipivotide tetraxetan) Enzalutamide and 177Lu-PSMA-617 in poor-risk metastatic, castration-resistant prostate cancer (mCRPC): a randomized phase 2 trial: ENZA-p (ANZUP 1901) Presentation Number #LBA84
Proffered Paper session:
Friday, October 20,
16:40 – 16:50 CEST
Pluvicto (lutetium Lu 177 vipivotide tetraxetan) Prognostic value of neutrophil-to-lymphocyte ratio and lymphopenia in patients with metastatic castration-resistant prostate cancer (mCRPC) treated with [177Lu]Lu-PSMA-617: VISION post-hoc analysis Presentation Number #1838P
Poster available:
Sunday, October 22,
9:00 – 17:00 CEST
Pluvicto (lutetium Lu 177 vipivotide tetraxetan) Association of health-related quality of life with efficacy outcomes in the VISION study of patients with metastatic castration-resistant prostate cancer Presentation Number #1810P
Poster available:
Sunday, October 22,
9:00 – 17:00 CEST
Pluvicto (lutetium Lu 177 vipivotide tetraxetan) Molecular features of circulating tumour cells (CTCs) associate with response to 177Lu PSMA 617 plus pembrolizumab for metastatic castration resistant prostate cancer (mCRPC). Presentation Number #1825P
Poster available:
Sunday, October 22,
9:00 – 17:00 CEST
Kisqali (ribociclib)* Invasive disease-free survival (iDFS) across key subgroups from the Phase III NATALEE study of ribociclib (RIB) + a nonsteroidal aromatase inhibitor (NSAI) in patients (pts) with HR+/HER2- early breast cancer (EBC) Presentation Number #LBA23
Mini oral session:
Monday, October 23,
17:05 – 17:10 CEST
Kisqali (ribociclib)* First-line ribociclib (RIB) + endocrine therapy (ET) vs combination chemotherapy (combo CT) in aggressive HR+/HER2- advanced breast cancer (ABC): a subgroup analysis of patients (pts) with or without visceral crisis from the Phase II RIGHT Choice study Presentation Number #402P
Poster available:
Saturday, October 21,
9:00 – 17:00 CEST
Kisqali (ribociclib)* Quality of life (QOL) analysis from the Phase II RIGHT Choice study of first-line ribociclib (RIB) + endocrine therapy (ET) vs combination chemotherapy (combo CT) in aggressive HR+/HER2- advanced breast cancer (ABC) Presentation Number #456P
Poster available:
Saturday, October 21,
9:00 – 17:00 CEST
Lutathera (lutetium Lu 177 dotatate) A Prospective Phase II Single-Arm Trial on Neoadjuvant Peptide Receptor Radionuclide Therapy (PRRT) with 177Lu-DOTATATE Followed by Surgery for Pancreatic Neuroendocrine Tumors (NeoLuPaNET) Presentation Number #1186MO
Mini oral session:
Sunday, October 22,
17:25 – 17:30 CEST

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Already Partnered With Nvidia, Iambic Adds $100M for AI Drug Discovery

On October 4, 2023 Iambic Therapeutics reported the company brings together software engineers and drug-hunting scientists, all sharing the goal of using artificial intelligence to optimize properties of small molecule drugs (Press release, Iambic Therapeutics, OCT 4, 2023, View Source [SID1234637213]). The startup will apply its Series B financing to a cancer drug pipeline that includes two candidates on track for the clinic in 2024.

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Drug discovery isn’t only about finding new targets. There’s still plenty of opportunity to find better ways to hit targets that are already drugged, according to Tom Miller, CEO of startup Iambic Therapeutics. Understanding how a molecule interacts with a known disease target enables drug hunters to design molecules that could be superior alternatives for patients.

Miller notes that a molecule’s ability to bind to a target protein while leaving related proteins unaffected improves its safety. It’s also important to understand how the distribution of a molecule across tissues in the body affect efficacy. Iambic’s drug discovery research employs artificial intelligence to make predictions about those properties and others.

"With a platform like this, we can not only optimize the molecule, we can [also] optimize the profile," Miller said of Iambic’s technology.

In the span of two years, Iambic has developed four AI-discovered molecules, the most advanced of them now on the cusp of Phase 1 testing. To support those programs and develop more of them, the La Jolla, California-based startup has raised $100 million.

Some companies in the AI space take a "physics-based" approach to drug discovery, using software to run simulations that yield a better understanding of molecular dynamics—how small molecules interact with a protein of interest. Companies in this mold include Nimbus Therapeutics, Schrödinger, and Relay Therapeutics. A different group of AI drug companies run experiments to generate data that they then interrogate to gain biological and chemical insights, an approach taken by companies such as Exscientia and Recursion Pharmaceuticals.

Miller said Iambic brings both worlds together, making the most of physics-based insights that are then augmented with data to make better predictions. The company’s technology enables it to identify new molecules that offer superior efficacy and safety, he said. More than finding out whether a molecule can hit a target, Iambic’s technology reveals insights into other properties, such as potency to its target, its toxicity profile, and how the molecule moves through and interacts with the body.

"It’s the ability to predict across numerous endpoints for a successful drug," Miller said.

Iambic’s technologies can be applied to multiple indications, but the company’s first four programs, including two on pace to reach the clinic next year, are for cancer. IAM-H1 is a small molecule that blocks HER2 and variants of this cancer-driving protein. In addition to its selectivity to this target, Iambic says this molecule also has the ability to penetrate the brain—an important property for treating cancer that has spread to the central nervous system.

IAM-C1 is a small molecule that selectively blocks CDK2 and CDK4, two enzymes associated with tumor growth. The three FDA-approved CDK inhibitors are Pfizer’s Ibrance, Kisqali from Novartis, and the Eli Lilly drug Verzenio. All three are blockbuster products that have become standard of care breast cancer treatments. Iambic claims its drug can selectively block its two enzyme targets while preserving enzymes closely related to those targets. Other properties of this Iambic drug include a better therapeutic window, which is the dose range in which a therapy is effective while causing minimal adverse effects. This molecule is also designed to address drug resistance in cell-cycle-driven cancers.

With the new financing, Iambic aims to advance its two lead programs into Phase 1 testing next year. A third cancer program addressing a yet-to-be-disclosed target could follow them into the clinic. In addition to the clinical trial work, Miller said his company will continue its drug discovery research. While Iambic is flexible in terms of the mechanism of action of potential drugs, Miller said Iambic’s focus is mainly small molecules rather than biologics. Expanding to indications beyond cancer could happen through partnerships.

Iambic’s employee roster is split evenly between software engineers and drug development scientists. Miller said that this composition reflects the reality that AI-driven drug discovery research is interdisciplinary by nature.

"We really do believe that there is a duality that one has to capture to be successful at that interface," he said. "We work hard to embrace the expertise of technology. But we also realize drug discovery and development builds on decades of hard-earned experience. And we need that reflected in the team as well."

Miller co-founded Iambic in 2019 based on research from the University of Bristol and Caltech, where he was a professor of chemistry for 14 years. Iambic’s marriage of technology with biotechnology is reflected in its investor syndicate. In 2021, the startup raised a $53 million Series A round of financing led by Coatue, a technology investment firm, and Catalio Capital Management, which focuses on biomedical technology investments. That financing mainly supported development of the startup’s tech platform.

The company built its AI technology in collaboration with Nvidia, a company whose computing technologies are integral components in the platforms of many AI drug discovery firms. In addition to investing in Iambic, Miller said Nvidia will also continue to work with the startup to develop next-generation technologies for drug development.

[Story updated to remove references to Entos Pharmaceuticals, which is a different company than Entos, Inc.] Iambic was initially named Entos, Inc. With the Series B financing announced this week, it revealed the name change to Iambic. The latest financing was co-led by Ascenta Capital and Abingworth. New investors joining the round include Nvidia, Illumina Ventures, Gradiant Corporation, and independent board member Bill Rastetter. Earlier investors that participated in the latest financing include Nexus Ventures, Catalio Capital Management, Coatue, FreeFlow, OrbiMed, and Sequoia Capital.

OncoBone Ventures attends AACR-NCI-EORTC event

On October 4, 2023 OncoBone Ventures reported that the company attends AACR (Free AACR Whitepaper)-NCI-EORTC oncology scientific event in Boston, MA, during October 11-15 and presents a poster titled: ‘Preclinical Bone Metastasis Technology Platform – Predictive evaluation of Experimental Therapies on Bone Metastasis’ (Press release, OncoBone Ventures, OCT 4, 2023, View Source [SID1234636479]).

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The Preclinical Bone Metastasis Technology Platform is a key in drug development activities of OncoBone Ventures that will be utilized to evaluate effects of pipeline therapeutic assets on bone metastases.

If you are interested to learn more, please visit the poster A007 on October 12 at 12:30 – 4:00 pm at the event or reach out via View Source

Orakl Oncology raises €3 million to develop its techbio platform for precision oncology

On October 4, 2023 Orakl Oncology, a precision oncology start-up, today announces that it has raised €3 million to develop its techbio platform that integrates best-in-class biology with real-world patient data at scale to accurately model tumors and accelerate oncology drug development (Press release, Orakl Oncology, OCT 4, 2023, View Source [SID1234635667]).

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A major challenge in oncology is that drug candidates meet patients too late in the development process. This leads to a 96% failure rate in clinical trials and missed treatment opportunities for cancer patients.1

The future of cancer treatment and drug development relies on recognizing that each tumor is different. In response to this unmet need, Orakl Oncology is combining cell biology, engineering and machine learning to build unique tumor avatars for each individual cancer patient that can mimic real-life responses to drugs.

Orakl Oncology’s growing collection of avatars captures the complexity and heterogeneity of cancer at the population scale, helping pharma and biotech companies to identify new therapeutic targets or predictive biomarkers and increase clinical trial success rates.

Dr. Fanny Jaulin, Orakl Oncology CEO & Co-Founder, commented, "Our ambition is to become a world-leading techbio platform leveraging the smartest collection of tumor avatars to transform oncology drug development and bring faster, smarter and more cost-effective treatments to patients. We are delighted with the result of this oversubscribed fundraising round, and we are very grateful to all our investors for their support."

Launched in 2023 as a spin-out from the Gustave Roussy Institute by co-founders Fanny Jaulin, Diane-Laure Pagès and Gustave Ronteix, Orakl Oncology is targeting the global oncology market, with an initial focus on colorectal and pancreatic cancers – the second leading-cause of cancer deaths worldwide.2

Prof. Fabrice Barlesi, General Director of Gustave Roussy, commented, "We are very proud of Gustave-Roussy’s spin-out, Orakl Oncology. They aim to disrupt precision oncology by leveraging major academic and pharma partnerships to accelerate drug development, ultimately leading to better patient outcomes."

The funding will be used to launch the company’s wet and dry lab capabilities and to hire several key team members, including a Senior Oncology Scientist, Organoid Scientists, a Head of Lab, an Automation Engineer and an AI Research Scientist. This will enable Orakl Oncology to execute its first contracts with pharma and biotech partners.

The investment round was led by Speedinvest with additional investment from HCVC and Verve Ventures.

Andrea Zitna, Partner at Speedinvest, commented, "Orakl’s co-founders have a powerful mix of scientific credentials, ambitious vision and entrepreneurial drive. We were impressed by the company’s dry and wet lab techniques, the quality of their biobank and the scope of their exclusive relationship with Gustave Roussy. We’re thrilled to be on this journey with them!"

Xavier Mesnier, Principal at Verve Ventures, commented, "Having an accurate and scalable representation of biology and heterogeneity in the patient population is key to advancing drug discovery. Orakl’s tumor avatar platform delivers this at scale by combining patient samples with automation and machine learning."

Alexis Houssou, Managing Partner at HCVC, commented, "We’re really excited to be supporting Orakl on their mission to accelerate the development of patient-specific tumor therapies. We believe in breakthrough solutions that combine biology, data, and AI – and we’re thrilled to be a part of Orakl’s journey."