Apros Therapeutics Announces IND Clearance from U.S. FDA to Initiate the Trial of APR003, an Orally-Administered Gastrointestinal/Liver-Targeted TLR7 Agonist for Treatment of Advanced Colorectal Cancer (CRC) with Malignant Liver Lesions

On September 9, 2020 Apros Therapeutics, Inc., a drug discovery and development company focused on tissue-targeted Toll-Like Receptor 7 (TLR7) agonists for the treatment of cancer and infectious diseases, reported that its Investigational New Drug (IND) application for a Phase 1 dose escalation trial of APR003, the company’s first-in-class orally-administered gastrointestinal- and liver-targeted TLR7 agonist development candidate, was cleared by the FDA (Press release, Apros Therapeutics, SEP 9, 2020, View Source [SID1234564866]). The Phase 1 trial aims to evaluate safety, tolerability, pharmacokinetics, pharmacodynamics, and initial anti-tumor activity of APR003 in patients with advanced unresectable CRC with malignant liver lesions. The trial will be conducted at multiple sites in the United States, and the company intends to report top-line results upon completion.

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"We are excited to enter the clinic with our lead drug APR003 that was designed utilizing our tissue-targeted chemistry to deliver a TLR7 agonist in abundance to liver and GI tissue with little-to-no systemic distribution," stated Dr. Aaron Weitzman, M.D., FACP, Acting Chief Medical Officer at Apros Therapeutics. "We are encouraged by APR003’s unique profile and significant single agent efficacy at well-tolerated doses observed in our preclinical studies, and we are pleased to advance this program into the clinic as we believe it will offer an important step forward in creating a new immunotherapeutic treatment option for advanced colorectal cancer patients, a disease with a large unmet medical need."

ABOUT APR003

APR003 is a first-in-class, orally-administered, TLR7 agonist designed specifically to localize to the GI and liver to promote local immune activation in the targeted tissues and drive tumor eradication. Given the immune-activating capacity of this class of drugs, the tissue-targeted approach taken with APR003 is predicted to exhibit an improved tolerability profile compared to other oral non-targeted approaches, which possess side effects associated with systemic immune activation and inflammation. TLR7 activation in the liver of patients with malignancies that are metastatic to the liver may lead to innate immune priming, release of cytokines and, ultimately, enhanced anti-tumor immune responses. Although APR003 may have applications in several GI and liver malignancies, Apros will focus the initial evaluation of APR003 in patients with unresectable CRC that is metastatic to the liver given the unique bio-distribution and mechanism of action of this first-in-human investigational agent. CRC is the 3rd most common cancer in the world, and 50% of patients with advanced disease will develop liver metastasis. While most patients with CRC are non-responsive to immunotherapies, largely due to the immune-quiescent nature of the disease, APR003 aims to turn these "cold" tumors into "hot" immune-permissive tumors.

Jon DeVries Named Qlarity Imaging Chief Executive Officer

On September 9, 2020 Life science innovator Paragon Biosciences reported the appointment of Jon T. DeVries as the new chief executive officer of its portfolio company, Qlarity Imaging, a leading artificial intelligence (AI) diagnostics company (Press release, Paragon Biosciences, SEP 9, 2020, View Source [SID1234564899]). A proven leader with in-depth expertise in developing and commercializing medical imaging and AI solutions, Mr. DeVries will be responsible for executing Qlarity Imaging’s mission to advance breast cancer diagnosis through AI-driven technology.

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"Paragon serves as a catalyst and advisor to our portfolio companies to accelerate groundbreaking discoveries that help patients in need. With breast cancer remaining the second leading cause of cancer deaths in women, the need for improved care is undeniable," said Jeff Aronin, founder, chairman and chief executive officer of Paragon Biosciences. "Jon’s impressive background, along with his patient-centered approach and outstanding leadership talents, makes him well-suited to be at the helm of Qlarity Imaging as we seek to help patients live longer, healthier lives."

Mr. DeVries has more than 20 years of experience spearheading the creation and release of innovative cloud-based healthcare initiatives that bring advanced services and technologies to providers and researchers, with the ultimate goal of improving patient care. For example, at Massachusetts General Hospital he launched a Tele3D service that provides any hospital in the country access to three-dimensional (3D) image analytics without incurring the substantial cost of cultivating in-house 3D capabilities. While at IBM, he developed technologies that deliver medical images anywhere at anytime, giving providers a complete view of patients and their histories, and he created software that reduces the time and cost of clinical trials. He also developed the first AI offering at IBM Watson Health Imaging that identifies patients with a potential misdiagnosis to ensure they receive the necessary cardiac care.

Mr. DeVries has earned eight patents in the areas of superconducting electronics, medical imaging and AI. He has served on the HIMSS Interoperability & Standards Committee, a collective effort to improve patient care delivery through the advancement of semantic interoperability and standards-based health IT systems.

"Developing the first diagnostic AI technology to be cleared by the U.S. Food and Drug Administration speaks volumes to Qlarity Imaging’s commitment to innovation in improving breast cancer diagnosis," said Mr. DeVries. "Forward thinking is necessary to make bold scientific breakthroughs, and with Paragon’s support, we are poised to deliver better outcomes for the hundreds of thousands of women who are diagnosed with breast cancer each year."

Mr. DeVries has a Bachelor of Science in Physics from Harvey Mudd College and a Master of Business Administration in Finance and Operations from Columbia University-Columbia Business School.

NICE turns down Celgene’s Revlimid as multiple myeloma maintenance treatment

On September 9, 2020 The National Institute for Heath and Care Excellence (NICE) reported that it has turned down NHS funding of Revlimid (lenalidomide) as maintenance treatment after an autologous stem cell transplant for newly diagnosed multiple myeloma in adults (Press release, Celgene, SEP 9, 2020, View Source [SID1234564993]).

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There is currently no maintenance treatment for newly diagnosed multiple myeloma in people who have had an autologous stem cell transplant; the condition is usually monitored until it gets worse.

Clinical trial results show that, compared with monitoring alone, Revlimid increases how long people live and also extends the time before the condition gets worse.

However, NICE has concluded in preliminary guidelines that cost-effectiveness estimates for the drug in this setting "are uncertain".

"This is because of limitations in the cost-effectiveness model, and because the model might not reflect what happens in the NHS in England," it said.

Therefore, Revlimid could not be considered value for money for the NHS when used for this indication, it noted.

AMAG Pharmaceuticals to Participate in H.C. Wainwright 22nd Annual Global Investment Conference

On September 9, 2020 AMAG Pharmaceuticals, Inc. (NASDAQ: AMAG) reported that Scott Myers, Chief Executive Officer, and Brian Piekos, Chief Financial Officer, will participate in a fireside chat at the H.C. Wainwright 22nd Annual Global Investment Conference on Tuesday, September 15, 2020 at 10:30 a.m. Eastern Time (Press release, AMAG Pharmaceuticals, SEP 9, 2020, View Source [SID1234565143]).

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A live audio webcast of the virtual event will be accessible through the Investors section of the company’s website at www.amagpharma.com. A replay of the webcast will be archived on the company’s website for 30 days.

Oasmia Pharmaceutical AB (publ) Interim report for the period May 1 – July 31, 2020

On September 9, 2020 Oasmia Pharmaceutical AB (publ)reported that Interim report for the period May 1 – July 31, 2020 (Press release, Oasmia, SEP 9, 2020, View Source [SID1234564799])

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SIGNIFICANT EVENTS DURING THE FIRST QUARTER
Oasmia announced in May the outcome of a strategic review to deliver long-term, profitable growth as a specialty pharma company. As a result of the review, Oasmia will discontinue commercial manufacturing and implement cost reductions that will result in savings of MSEK 100 on an annual basis and a monthly burn rate of below MSEK 10.
An Extraordinary General Meeting in May elected existing Board member Anders Härfstrand as new Chairman of the Board and Birgit Stattin Norinder as new member of the Board. Jörgen Olsson, former Chairman of the Board, and Gunilla Öhman, former Board member, stepped down from the Board.
Oasmia signed in June a Phase 1b Trial Agreement with SAKK, the Swiss Group for Clinical Cancer Research, for evaluation of docetaxel micellar for the treatment of metastatic prostate cancer.
In July Oasmia’s partner Elevar Therapeutics and Tanner Pharma Group announced a global Named Patient Program to provide access to Apealea in areas outside of the United States.
The outbreak of COVID-19 and its effects around the world accelerated during the first quarter of the financial year. The pandemic has entailed heavily reduced access to health care providers and oncologists, which continues to have a profound negative impact on the marketing activities of the company.
SIGNIFICANT EVENTS AFTER THE REPORTING PERIOD
In August Oasmia appointed Peter Selin as Chief Business Officer.
Oasmia’s CFO Michael af Winklerfelt resigned from his role in August.
In September Oasmia’s Nomination Committee revised its proposal for the AGM regarding Board of Directors and Sven Rohmann notified that he is no longer available for re-election.
In September Oasmia appointed Fredrik Järrsten as Chief Financial Officer.
FIRST QUARTER: MAY 1, 2020 – JULY 31, 2020
Consolidated net sales amounted to TSEK 208 (182)
Operating income was TSEK -49,220 (-35,764)[3]
Net income after tax amounted to TSEK -53,105 (-39,783)[3]
Earnings per share was SEK -0.12 (-0.13)[3,4]
CEO’S COMMENTS
During the first quarter at Oasmia, we continued to work to deliver the strategic vision we set out following the announcement of the global strategic partnership with Elevar Therapeutics to commercialize our anti-cancer therapy Apealea.

Oasmia retains the rights to Apealea in the Nordic countries under the agreement with Elevar and is now making the product commercially available. The Covid-19 pandemic has inevitably impacted the ability of our medical scientific liaisons to meet oncologists during the quarter. An easing of lockdown restrictions will help resuming medical activities to return to more normal levels during the rest of the year.

Elevar entered into an agreement with Tanner Pharma Group in July to establish a named patient program that will facilitate patient access to Apealea in countries outside the US where it is not yet commercially available. The goal of the program is to assist cancer patients who have no alternative therapeutic options to get access to the drug. Apealea is the only cremophor-free product approved in Europe for use in combination with carboplatin for the treatment of adults with first relapse of platinum-sensitive epithelial ovarian cancer, primary peritoneal cancer and fallopian tube cancer. The initial target population for ovarian cancer is therefore patients with potential or previously established hypersensitivity reactions to currently used solubility enhancer containing paclitaxel formulations. We hope that this will make them particularly eligible to our XR-17 based paclitaxel formulation.

The collaboration with Elevar that started in 2020, as well as the transfer of all commercial manufacturing of Apealea to Baxter at the end of 2018, were important developments in realigning our growth strategy, enabling us to focus resources where they can bring the best return for shareholders.

The Board’s long-term vision is to build a cash flow-positive specialty pharmaceutical company. To help achieve this, we have implemented a strategic reorganization of Oasmia to focus on R&D and Business Development and to reduce unnecessary expenditure. With a proven technology in XR-17, a highly promising approved anti-cancer product, Apealea, and a global commercialisation agreement worth up to $678 million plus royalties, we are well positioned to grow through M&A and licensing deals for late-stage and marketed products. We will seek further opportunities to apply our proprietary XR-17 solubility-enhancing technology platform, primarily in oncology but also in other therapeutic areas. We are also looking at the potential to out-license the technology in non-core applications. We are already in the process of reviewing strategic options for our Animal Health business.

We will continue to drive the development of our pipeline of XR-17-based products and leverage the Company’s manufacturing expertise for R&D. Current promising lead programs include docetaxel micellar in metastatic prostate cancer. In June, we signed an agreement with the Swiss research group SAKK to conduct the first clinical trial of docetaxel micellar in advanced prostate cancer. Oasmia’s docetaxel micellar formulation is based on XR-17, which enables greater use of otherwise water-insoluble cancer drugs while reducing the side effects or need for additional medications associated with traditional solubility enhancers. In addition, we continue the assessment of XR-19, the dual encapsulation technology platform.

During the rest of 2020 we will continue to advance key areas of our growth strategy, including working closely with Elevar to deliver key milestones for Apealea and support efforts to identify the most appropriate commercial partners for the product in Europe and China. The appointment of Peter Selin as Chief Business Officer, announced a few weeks ago, together with our strong cash position, will be invaluable as we continue to pursue growth through M&A and in- and out-licensing opportunities that complement our technology and business model.

I look forward to keeping you updated on our progress. Please accept my thanks for your patience and continued support as we further transform Oasmia into a sustainable and profitable growth business with long-term potential. Above all, we are here to help patients to better manage their cancer diseases.