Case Western Reserve awarded $3 million National Cancer Institute grant to apply AI to immunotherapy in lung cancer patients

On April 9, 2021 Medical researchers from Case Western Reserve University, New York University (NYU), and University Hospitals reported that have been awarded a five-year, $3 million National Cancer Institute grant to develop and apply artificial intelligence (AI) tools for predicting which lung cancer patients will respond to immunotherapy (Press release, Case Western Reserve University, APR 9, 2021, View Source [SID1234577779]).

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A unique aspect of the Case Western Reserve-led study is that it will involve testing of their specific AI tools—for the first time during an ongoing clinical trial.

While these real-time treatment predictions will be used exclusively for research–and not for clinical diagnosis or treatment–the work is the next step toward trials that would allow physicians to apply the tools with participating patients.

"Clinical trials down the road will be our biggest test, but now we will be—for the first time—studying changes in the tissue-scan patterns of patients as they are being treated, and that will provide real-world context of our tools," said Anant Madabhushi, director of Case Western Reserve’s Center for Computational Imaging and Personalized Medicine . "Our AI tools have excelled in previous studies, but they have all been after-the-fact."

The researchers hope to predict which patients will have successful immunotherapy treatments based on previously unseen indicators in their initial computerized tomography (CT) scans. If successful, they will have more data to support using the AI diagnosis for lung cancer patients in clinical trials.

Madabhushi will again work with longtime collaborator Vamsidhar Velcheti, MD, director of thoracic oncology at NYU Langone’s Perlmutter Cancer Center, who previously worked in Cleveland.

Lung cancer remains the leading cause of cancer-related deaths worldwide, according to the World Health Organization. Dr. Velcheti said advances like the work by our team "to match patients to the right treatment—can improve outcomes and significantly reduce costs for patients with lung cancer" and that "tests to identify patients for appropriate immunotherapy treatments are a critical unmet need in the field of oncology.

"Using novel and sophisticated AI approaches, we are developing personalized strategies to identify patients who may benefit from combination-based immunotherapy approaches," Velcheti said. "This NIH grant will help advance our efforts to developing innovative approaches for patient selection and monitor patients on immunotherapy."

The team will also include the University Hospitals Radiology Department Amit Gupta, MD, and Robert Gilkeson, MD, both professors at the Case Western Reserve School of Medicine; Pingfu Fu, PhD, professor of Population and Quantitative Health Sciences at the School of Medicine.

AI and immunotherapy
The CCIPD digital imaging lab has become a global leader in using machine learning to discern patterns in digital images of tissue scans that can’t be seen by the human eye, including for various cancers.

The lab pioneered the use of AI to predict which patients would benefit from chemotherapy. And recent research by CCIPD scientists has demonstrated that AI and machine learning can help predict which lung cancer patients will benefit from immunotherapy.

Immunotherapy uses drugs to help the immune system fight the cancer, while chemotherapy uses drugs to directly kill cancer cells, according to the National Cancer Institute.

As with their chemotherapy work, the researchers can accurately predict who will or won’t benefit from immunotherapy by training a computer to find minuscule changes in patterns in CT scans taken when the lung cancer is first diagnosed. Those scans are then compared to scans taken after the first two to three cycles of immunotherapy.

Many cancer patients benefit from immunotherapy, but the treatment is expensive. Researchers hope to find a better way to identify which cancer patients would likely benefit. And those who wouldn’t avoid having to pay for what turns out to be ineffective and costly treatment.

Multiple partners, sites
The Case Western Reserve-led team will also work with the ECOG-ACRIN cancer research group, a membership-based organization that oversees scientific programs and research into cancer control and outcomes, therapeutic studies and biomarker sciences. Its members include the Case Comprehensive Cancer Center.

Stanton Gerson, director of the center and interim dean of the Case Western Reserve School of Medicine, called the new work a "pivotal study."

"When these data mature, we hope they will lead to improved clinical decision-making," Gerson said. "Such an advance could be transformative for physicians making those complex decisions on which treatment is best for a patient."

Madabhushi said the partnership with ECOG-ACRIN is significant because it marks the first time his center will work with a broader, cooperative oncology group. It would also further establish the "generalizability of our tools," he said, meaning the AI analysis developed at one site or with one set of patients should also be valid at a second testing site—something that has yet to be proven in AI-driven precision medicine.

Madabhushi said his team would also benefit from partnerships with pharmaceutical partners who provide researchers with access to completed retrospective clinical trial datasets of lung cancer patients previously treated with immunotherapy. This data will also help the researchers validate their tools.

The new work will also investigate how lung cancer tumors change in size and shape during immunotherapy. Oncologists now rely on whether tumors shrink or grow to determine whether treatment is working.

"But it turns out that is not a good way of assessing treatment response, and our AI research has shown that," Madabhushi said. "There are a certain percentage of patients whose tumors grow in size, but the immunotherapy is working, a phenomenon called ‘pseudoprogression.’ There are now other features that the computer can pull from the CT scan—both inside and in the vessels outside the tumor—that will give us a better indication."

He also said the AI would reveal the less frequent but troubling cases of "hyper-progression," in which a patient’s condition is actually worsened by immunotherapy.

Moderna to Present at the 20th Annual Needham Virtual Healthcare Conference

On April 9, 2021 Moderna, Inc. (Nasdaq: MRNA), a biotechnology company pioneering messenger RNA (mRNA) therapeutics and vaccines, reported that David Meline, Chief Financial Officer, and Lavina Talukdar, Senior Vice President & Head of Investor Relations, will participate in a fireside chat at the 20th Annual Needham Virtual Healthcare Conference on April 15th, 2021 at 11:45 a.m. ET.

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A live webcast will be available under "Events and Presentations" in the Investors section of the Moderna website at investors.modernatx.com. A replay of the webcast will be archived on Moderna’s website for 30 days following the presentation.

Sanofi acquires Tidal Therapeutics, adding innovative mRNA-based research platform with applications in oncology, immunology, and other disease areas

On April 9, 2021 Sanofi acquired Tidal Therapeutics, a privately owned, pre-clinical stage biotech company with a novel mRNA-based approach for in vivo reprogramming of immune cells (Press release, Sanofi, APR 9, 2021, View Source [SID1234577780]). The new technology platform will expand Sanofi’s research capabilities in both immuno-oncology and inflammatory diseases, while likely having broad applicability to other disease areas as well. Sanofi acquired Tidal Therapeutics for an upfront payment of $160 million and up to $310 million upon achievement of certain milestones.

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"We anticipate that this next generation, off-the-shelf approach has the potential to bring CAR-T cell therapy to a much broader patient population," said Frank Nestle, Global Head of Research and Chief Scientific Officer at Sanofi. "We believe that the underlying mRNA targeting platform will create disruptive therapeutic approaches across a variety of oncology and autoimmune conditions."

Tidal Therapeutics utilizes a novel mRNA-based approach to in vivo reprogramming of immune cells. The technology is based on proprietary nanoparticles that deliver mRNA (messages) to reprogram immune cells inside the body. The technology delivers mRNA cargos selectively to designated types of cells in the body, with initial applications targeting specific types of immune cells. The in vivo approach is designed to provide similar efficacy to current ex vivo (outside the body) approaches where immune cells are genetically modified to enhance their therapeutic properties (such as chimeric antigen receptor [CAR]-expressing T-cells), with the potential for improved safety, outpatient dosing, and repeat dosing. Currently, Tidal Therapeutics has ongoing pre-clinical programs including in vivo re-programming of T cells or other types of immune cells for cancer indications.

"Teaming up with Sanofi gives us the opportunity to further develop our unique platform and rapidly apply it to ultimately help patients across a range of diseases," said Ulrik Nielsen, President and CEO, Tidal Therapeutics.

IntelGenx Announces Intention to Amend Convertible Unsecured Promissory Notes

On April 9, 2021 IntelGenx Technologies Corp. (TSX-V:IGX) (OTCQB:IGXT) ("IntelGenx"), a leader in pharmaceutical films, reported that it is proposing to amend the terms of its 6.0% convertible unsecured promissory notes due June 1, 2021, originally issued by private placement on May 8, 2018 (the "Notes"), to (i) extend the maturity date to October 31, 2024, (ii) change the conversion ratio for conversions at the option of the holders of the Notes from 6,250 fully paid and non-assessable shares of common stock for each U.S.$5,000 aggregate principal amount of the Notes then outstanding to 11,363 fully paid and non-assessable shares of common stock for each U.S.$5,000 aggregate principal amount of the Notes then outstanding, effectively representing a reduction of the conversion price from U.S.$0.80 to U.S.$0.44, and (iii) reduce the trigger price for a conversion at the option of IntelGenx from U.S.$1.40 or greater for 20 consecutive trading days to U.S.$0.88 or greater for 20 consecutive trading days (Press release, IntelGenx, APR 9, 2021, View Source(TSX%2DV%3AIGX),date%20to%20October%2031%2C%202024%2C [SID1234577797]). The proposed amendments are subject to approval of the TSX Venture Exchange and holders holding a majority of the aggregate outstanding principal amount of the Notes.

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An aggregate principal amount of U.S.$1,600,000 of Notes is outstanding as of the date hereof.

Werewolf Therapeutics looks to make a killing in the public markets with a $100M IPO

On April 9, 2021 Werewolf Therapeutics reported that now wants an IPO (Press release, Werewolf Therapeutics, APR 9, 2021, View Source [SID1234577882]).

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The early-stage biotech is working on shape-shifting cytokine drugs, i.e., ones that deliver the promise of cytokines without their nasty side effects. Known as Indukines, Werewolf’s candidates are "switched off" when they’re given to patients and activate only when they arrive in cancer cells.

Cytokines, such as interleukin-2, emerged decades ago as promising cancer treatments. But they evolved as signaling molecules and not as drugs, so it’s no surprise that they’re missing some key pharmaceutical features that would make them good medicines.

"These mechanisms are a very powerful way to stimulate the immune system to attack tumors, but unfortunately, a number of cytokines can activate the immune system in an adverse way where it can attack normal tissues," Werewolf CEO Daniel Hicklin, Ph.D., said in January. Werewolf’s protein engineering technology is designed to limit its drugs’ effects on healthy tissues.

The biotech, which is preclinical but wants the cash to chase these drugs into the clinic, got off a $72 million raise in January just over a year after it nabbed $56 million series A back in November 2019. Now, according to its SEC-1 filing, it wants a $100 million IPO, though don’t be surprised if, like so many other biotechs over the past year, it ends up getting more than that.

Its two leading assets, WTX-124 and WTX-330, are seeking INDs with the FDA from next year, according to its filing, after which it plans to conduct phase 1/1b trials in patients with multiple tumor types both as standalone treatments and in combination with an immune checkpoint inhibitor.

It also has a third asset, WTX-613, which is much further back in the pipeline, with clinical trials not slated until 2023. This drug is designed to be a systemically delivered, conditionally activated interferon alpha, or IFN-a, molecule for the treatment of solid tumors and blood cancers.

Other players hoping to make better cytokines for cancer treatment include Synthekine, which launched in September with $82 million, and Bright Peak Therapeutics, which debuted in July with $35 million.

And Sanofi bet big on the approach in December 2019 when it inked a $2.5 billion deal to acquire Synthorx, with some early data dropping this weekend at the American Association for Cancer Research (AACR) (Free AACR Whitepaper).