Allarity Therapeutics Submits Premarket Approval Application to U.S. FDA for DRP® Companion Diagnostic for Dovitinib

On April 2, 2021 Allarity Therapeutics A/S ("Allarity" or the "Company") reported the submission of a premarket approval application (PMA) to the U.S. Food and Drug Administration (FDA) for DRP-Dovitinib, the Company’s validated companion diagnostic for the drug dovitinib (Press release, Allarity Therapeutics, APR 2, 2021, View Source [SID1234577544]). Dovitinib is a small molecule, pan-tyrosine kinase inhibitor licensed from Novartis, and is Allarity’s most advanced clinical asset. This milestone marks the first time that Allarity has sought regulatory approval for one of its drug-specific DRPs used to guide patient therapy.

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Allarity’s unique DRP biomarker technology makes it possible to predict whether a particular cancer patient is likely to benefit from treatment with dovitinib, in addition to a broad range of anti-cancer drugs. DRP drug response assessments of the individual patients are done based on a biopsy from the patients’ tumors. The DRP-Dovitinib is intended to be used to identify patients, suffering from renal cell carcinoma (RCC), who by the gene expression signature of their tumor are found to have a high likelihood of responding to dovitinib.

Allarity plans to file a New Drug Application ("NDA") with the FDA for the approval of dovitinib for the treatment of renal cell carcinoma (kidney cancer) during 2021. If the FDA provides the anticipated premarket approval of the dovitinib DRP as a companion diagnostic, as well as an NDA approval for dovitinib, Allarity will be able to market dovitinib to DRP-selected RCC patients as an effective new therapy to treat their disease. The DRP for dovitinib, if approved, will be the first complex, gene expression signature approved by the U.S. FDA as a companion diagnostic to guide patient selection for cancer therapy.

Allarity’s CEO, Steve Carchedi, noted "Our current goal for dovitinib is to make it available to the group of RCC patients for whom a treatment with this particular therapeutic will be the most efficacious treatment for their disease. Today, marks a milestone for the advancement of our unique DRP biomarker technology for dovitinib, and approval of our PMA will enable oncologists to select those patients who are high likelihood responders to this drug." Mr. Carchedi further stated: "Later this year, I look forward to announcing our expected filing of a New Drug Application for dovitinib itself. Ultimately, if both of these filings are approved by the FDA, our Company will be positioned to significantly change how treatment of RCC will be conducted in the future, and help realize the promise of personalized medicine for these patients."

Steen Knudsen, Ph.D., CSO and Co-Founder of the Company, further stated, "I am extremely pleased to reach the milestone event of our first regulatory approval application for a DRP companion diagnostic, following our extensive work, over the past 15 years, developing, validating, and perfecting our DRP technology. I look forward to our Company advancing dovitinib, in combination with the Dovitinib-DRP, through approval and to market, and to similarly advancing the rest of our oncology therapeutics pipeline with DRP companion diagnostics in a true personalize medicine approach."

In October 2020 Allarity announced that the United States Patent and Trademark Office (USPTO) had issued a notice of allowance to the Company on its patent application no 16/444,881 titled "METHODS FOR PREDICTING DRUG RESPONSIVENESS IN CANCER PATIENTS" – directed to a DRP biomarker for dovitinib.

About the Drug Response Predictor – DRP Companion Diagnostic
Allarity uses its drug specific DRP to select those patients who, by the genetic signature of their cancer, are found to have a high likelihood of responding to the specific drug. By screening patients before treatment, the response rate can be significantly increased. The DRP method builds on the comparison of sensitive vs. resistant human cancer cell lines, including genomic information from cell lines combined with clinical tumor biology and prior clinical trial outcomes. DRP is based on messenger RNA from the patient’s biopsies. DRP has proven its ability to provide a statistically significant prediction of the clinical outcome from drug treatment in cancer patients in nearly 40 clinical studies that were examined, including an ongoing, prospective Phase 2 trial. The DRP platform can be used in all cancer types and is patented for more than 70 anti-cancer drugs.

Veracyte to Present at 20th Annual Needham Virtual Healthcare Conference

On April 2, 2021 Veracyte, Inc. (Nasdaq: VCYT), a global genomic diagnostics company, reported that Bonnie Anderson, chairman and chief executive officer, will participate in a fireside chat at the 20th Annual Needham Virtual Healthcare Conference on Tuesday, April 13, 2021 at 2:15 p.m. Eastern Time (Press release, Veracyte, APR 2, 2021, View Source [SID1234577540]).

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The link to the live audio webcast of the company’s presentation will be available by visiting Veracyte’s website at View Source A replay of the webcast will be available for 90 days following the conclusion of the live presentation broadcast.

Celleron Therapeutics publishes new findings showing immune modulation underpins the anti-cancer effects of zabinostat

On April 2, 2021 Celleron Therapeutics, the UK-based company developing personalised medicines for cancer patients, reported that it has worked closely with Oxford University’s Medical Sciences Division to investigate the mechanism of action of zabinostat (previously known as CXD101) (Press release, Celleron, APR 2, 2021, View Source [SID1234577532]).

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The study found that zabinostat enhances immune-relevant gene expression. This effect leads to increased recognition of tumours by the immune system with enhanced anti-cancer activity. The study included a genome‐wide expression analysis and functional profiling, which uncovered enriched gene signatures and pointed towards a role for the immune system in how zabinostat acts. When zabinostat was combined with immune checkpoint inhibitors, such as anti‐PD1 and anti‐CTLA4, using tumour models that are normally unresponsive to mono-therapy, it resulted in enhanced anti‐tumour activity.

The recent scientific findings, published in the latest edition of Molecular Oncology, are highly consistent with the clinical strategy and clinical trial design which Celleron is pursuing in its CAROSELL Phase 2 clincal study, which investigates zabinostat and nivolumab combination treatment in patients with microsatellite-stable colorectal cancer (MSS CRC). MSS CRC, which remains clinically unmet, has been long establised as being unresponsive to immune checkpoint inhibitor monotherapy treatment. In addition to the novel combination therapy deployed in CAROSELL, Celleron plans to translate the key findings on gene signatures described in the study to predictive biomarkers that help identify patients who undergo a favourable response to the combination therapy.

Professor Nick La Thangue, CEO, commented: "This is a truely fascinating study. It represents a major milestone in understanding zabinostat but most importantly opens up new ways of identifying cancer patients that are likely to undergo a good response to the drug. We will deploy the new information to strengthen our precision medicine platform to maximise the therapeutic value of zabinostat for cancer patients".

Professor David Kerr, CMO, commented: "This excellent science provides a platform which we can use to identify patients who are most likely to respond to zabinostat, significantly increasing the likelihood that our clinical trials will yield a positive result and benefit the community of cancer patients whom we serve. Equally as important, it opens up new avenues of clinical research in which we can deploy zabinostat in combination with a wide array of immune therapy approaches to improve their effectiveness".

Up Therapeutics received NCI Phase 1 STTR grant

Up Therapeutics in collaboration with Tuskegee University received NCI STTR phase 1 award to study Up284 efficacy against TNBC.

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Asgard Therapeutics awarded with Sweden’s SWElife Innovation Grant

On April 1, 2021 Asgard Therapeutics reported that it was awarded with Sweden’s SWElife innovation grant. Swelife is a strategic innovation programe, funded by the Swedish Government via the Swedish innovation agency, Vinnova, and by the programe’s partners (Press release, Asgard Therapeutics, APR 1, 2021, View Source [SID1234580066]). Swelife supports collaboration within academia, industry and healthcare, with the goal to strengthen Life Science in Sweden and to improve public health.

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