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.

Schedule your 30 min Free 1stOncology Demo!
Discover why more than 1,500 members use 1stOncology™ to excel in:

Early/Late Stage Pipeline Development - Target Scouting - Clinical Biomarkers - Indication Selection & Expansion - BD&L Contacts - Conference Reports - Combinatorial Drug Settings - Companion Diagnostics - Drug Repositioning - First-in-class Analysis - Competitive Analysis - Deals & Licensing

                  Schedule Your 30 min Free Demo!

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]).

Schedule your 30 min Free 1stOncology Demo!
Discover why more than 1,500 members use 1stOncology™ to excel in:

Early/Late Stage Pipeline Development - Target Scouting - Clinical Biomarkers - Indication Selection & Expansion - BD&L Contacts - Conference Reports - Combinatorial Drug Settings - Companion Diagnostics - Drug Repositioning - First-in-class Analysis - Competitive Analysis - Deals & Licensing

                  Schedule Your 30 min Free Demo!

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]).

Schedule your 30 min Free 1stOncology Demo!
Discover why more than 1,500 members use 1stOncology™ to excel in:

Early/Late Stage Pipeline Development - Target Scouting - Clinical Biomarkers - Indication Selection & Expansion - BD&L Contacts - Conference Reports - Combinatorial Drug Settings - Companion Diagnostics - Drug Repositioning - First-in-class Analysis - Competitive Analysis - Deals & Licensing

                  Schedule Your 30 min Free Demo!

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."

Ankyra Therapeutics Announces Clinical Trial Collaboration and Supply Agreement with Merck to Evaluate ANK-101 in Combination with KEYTRUDA® (pembrolizumab) in Patients with Advanced Solid Tumors

On October 4, 2023 Ankyra Therapeutics, a clinical biotechnology company developing a new form of local immunotherapy termed "anchored immunotherapy," reported a clinical trial collaboration and supply agreement with Merck (known as MSD outside of the US and Canada) to evaluate ANK-101 in combination with Merck’s anti-PD-1 therapy, KEYTRUDA (pembrolizumab) following the completion of a first-in-human phase I study of ANK-101 alone in patients with advanced solid tumors (Press release, Ankyra Therapeutics, OCT 4, 2023, View Source [SID1234635666]).

Schedule your 30 min Free 1stOncology Demo!
Discover why more than 1,500 members use 1stOncology™ to excel in:

Early/Late Stage Pipeline Development - Target Scouting - Clinical Biomarkers - Indication Selection & Expansion - BD&L Contacts - Conference Reports - Combinatorial Drug Settings - Companion Diagnostics - Drug Repositioning - First-in-class Analysis - Competitive Analysis - Deals & Licensing

                  Schedule Your 30 min Free Demo!

Pending completion of a first-in-human phase I study, ANK-101 would advance to KEYNOTE-E56, a clinical trial designed to evaluate ANK-101 in combination with pembrolizumab in patients with advanced solid tumors. The study is anticipated to begin enrollment in 2024.

The Ankyra platform uses an inert scaffolding composed of aluminum hydroxide, a well-known vaccine adjuvant, and links bioactive immune agents to the anchor. Preclinical studies of ANK-101, a functional human interleukin-12 (IL-12) cytokine, have demonstrated retention within the tumor microenvironment for up to 28 days with limited diffusion and systemic toxicity. Significant monotherapy anti-tumor activity has been seen in multiple murine tumor models and in a Phase I clinical trial of canine melanoma. Further studies have shown that ANK-101 drives expression of local PD-L1 and pre-clinical combination studies with PD-1 blockade have demonstrated improved therapeutic activity in PD-1-refractory tumor models.

"ANK-101 has demonstrated therapeutic activity in several preclinical models and has been shown to strongly induce expression of PD-1 within the tumor microenvironment," said Robert Tighe, CSO at Ankyra. "We have also seen significant improvement in tumor responses and abscopal activity in the preclinical models when murine ANK-101 is combined with PD-1 blockade without increased toxicity."

"We are especially excited about evaluating our drug in combination with pembrolizumab in the KEYNOTE-E56 trial," stated Dr. Joe Elassal, CMO at Ankyra. "Pembrolizumab has changed the clinical landscape for many different cancers, and we anticipate that the combination of ANK-101 and pembrolizumab may allow more patients to benefit from immunotherapy."

KEYTRUDA is a registered trademark of Merck Sharp & Dohme LLC, a subsidiary of Merck & Co., Inc., Rahway, NJ, USA.

About ANK-101
ANK-101 is an intratumoral drug complex composed of interleukin-12 (IL-12) linked to aluminum hydroxide. ANK-101 allows local delivery of functional IL-12 to the tumor microenvironment where it remains biologically active for several weeks but does not diffuse into the systemic circulation thereby avoiding systemic toxicity. Treatment with ANK-101 in animal models has been associated with recruitment and retention of tumor-specific CD8+ T cells, NK cells and M1 macrophages activating innate and adaptive anti-tumor immunity. ANK-101 is being evaluated for the treatment of advanced solid tumors alone and in combination with pembrolizumab.

Starton Therapeutics Doses First Patient in Landmark STAR-LLD Lenalidomide Phase 1b Clinical Trial in Multiple Myeloma

On October 4, 2023 Starton Therapeutics Inc. ("Starton" or "the Company"), a clinical-stage biotechnology company focused on transforming standard-of-care therapies with proprietary continuous delivery technology, reported the dosing of the first patient in the STAR-LLD Phase 1b clinical trial, which will assess the safety, efficacy and pharmacokinetics of continuous subcutaneous administration of low-dose lenalidomide (STAR-LLD) for the treatment of multiple myeloma (MM) (Press release, Starton Therapeutics, OCT 4, 2023, View Source [SID1234635665]).

Schedule your 30 min Free 1stOncology Demo!
Discover why more than 1,500 members use 1stOncology™ to excel in:

Early/Late Stage Pipeline Development - Target Scouting - Clinical Biomarkers - Indication Selection & Expansion - BD&L Contacts - Conference Reports - Combinatorial Drug Settings - Companion Diagnostics - Drug Repositioning - First-in-class Analysis - Competitive Analysis - Deals & Licensing

                  Schedule Your 30 min Free Demo!

The study will include six second-line transplant-ineligible patients who will receive lenalidomide by continuous administration daily in a 28-day cycle, in combination with dexamethasone and bortezomib (Velcade), to assess the tolerability and clinical response of the regimen, and will evaluate safety and tolerability, immune biomarkers, and signals of efficacy. The study is also expected to provide signals of efficacy in assessing response rates, duration of response, progression-free survival, and changes in minimal residual disease.

"From its inception, Starton has been focused on execution. We are entering the development stage, in which we expect to achieve the safety and tolerability improvement profile as well signals of efficacy for our proprietary continuous delivery of lenalidomide. We will enable the patient outcomes and quality of life improvements for which we founded Starton," said Pedro Lichtinger, chairman and CEO of Starton Therapeutics. "We are excited to evaluate the potential of STAR-LLD in this trial as a critical step towards delivering on our pipeline of transformative therapies using our continuous delivery technology."

Dr. Nash Gabrail, MD, the study’s principal investigator noted, "Revlimid is an indispensable drug in treating multiple myeloma. Unfortunately, many times patients do not tolerate the side effects associated with oral dosing. I believe the ability to target the precise therapeutic blood levels with continuous administration of the drug may allow an improvement in the therapeutic index of lenalidomide and allow patients to stay on therapy longer."

Dr. Jamie Oliver, Starton’s Chief Medical Officer noted, "This is a major milestone for all of the staff at Starton working to bring new therapies to patients suffering with cancer. Lenalidomide has been an effective immunomodulatory drug in hematologic malignancies for years. However, adverse events have limited its use in certain patient settings, depriving patients of the full benefits the medicine can offer. We believe STAR-LLD may be able to expand the use of lenalidomide where the oral form is not used today."

Starton has signed an agreement for a business combination with Healthwell Acquisition Corp. I (Nasdaq: HWEL) ("Healthwell"). Please see "Additional Information and Where to Find It" below for additional information related to the proposed business combination.

About STAR-LLD

STAR-LLD is a continuous delivery lenalidomide in development to expand and replace the standard of care for the most common blood cancers, multiple myeloma (MM) and chronic lymphocytic leukemia (CLL). A preclinical proof-of-concept study for STAR-LLD demonstrated that MM tumors caused by human myeloma cells grew 25-fold if untreated, five-fold when treated with daily lenalidomide and shrank by 80% with STAR-LLD. The study also showed 100% efficacy (overall response rate ORR) at 144 mcg/day continuous LLD and 20% of animals in this cohort were tumor free after 100 days vs. 0% ORR with active control with daily pulsatile once daily dosing. In addition, a Phase 1 bioavailability study in healthy men comparing STAR-LLD to Revlimid demonstrated the drug is well tolerated and is >91% bioavailable by the subcutaneous route. It was also observed that the Cmax is <90% lower than oral Revlimid. These data support the safety of the planned Phase 1 dose of 400 mcg/hr (9.6 mg a day) versus a standard 25 mg a day dose of Revlimid.