Oncoinvent patent issues in the USA

On January 18, 2017 Oncoinvent reported that US Patent 9,539,346 entitled "Radiotherapeutic particles and suspensions" has issued (Press release, Oncoinvent, JAN 18, 2017, http://www.oncoinvent.com/pdf.cfm?dok_id=481 [SID1234517439]). The patent relates to a particle or pharmaceutical composition comprising one or more particles, or a suspension of same or different particles comprising a degradable compound and an alpha emitting radionuclide and/or a radionuclide generating alpha emitting daughter. The particles are beneficial for use in the treatment of cancer.

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Jan A. Alfheim, Oncoinvent’s CEO commented: "This is a significant milestone in the development of our lead product candidate, Radspherin. With this first patent we have gained a solid protection of Radspherin until 2035 in what we believe will be a very significant future market for the product. Our Radspherin patent applications include claims on composition of matter as well as various medical and medical device applications. The current applications and this issued patent are therefore very broad and cover a wide spectrum of Radspherin particle variants and applications."

About Radspherin

Radspherin is a novel alpha-emitting radioactive microsphere designed for treatment of metastatic cancers in body cavities. The radium based therapeutic, Radspherin has shown strong and consistent anticancer activity at doses being essentially non-toxic in preclinical studies. It is anticipated that the product can potentially treat several forms of metastatic cancer. The first clinical indication for Radspherin will be treatment of peritoneal carcinomatosis originating from ovarian cancer. Peritoneal carcinomatosis is one of the most serious complications of gastrointestinal and gynecological malignancies.

New Outcomes Data Using Delcath’s Melphalan/HDS To Treat Unresectable Metastatic Ocular Melanoma To The Liver Accepted For Oral Presentation At Regional Cancer Therapies Symposium

On Jan 18, 2017 Delcath Systems, Inc. (NASDAQ: DCTH), an interventional oncology Company focused on the treatment of primary and metastatic liver cancers, reported that new data from a retrospective study of Melphalan/HDS, entitled "Percutaneous Hepatic Perfusion For Unresectable Metastatic Ocular Melanoma To The Liver: A Multi-Institutional Report Of Outcomes," has been accepted for oral presentation at the Regional Cancer Therapies 12th International Symposium, taking place February 18 – 20, 2017 at the Snowbird Ski and Summer Resort in Snowbird, UT (Press release, Delcath Systems, JAN 18, 2017, View Source;p=RssLanding&cat=news&id=2238088 [SID1234517438]).

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The retrospective study was conducted by teams from Moffitt Cancer Center in Tampa, FL and the University of Southampton in the United Kingdom. The study explores patient treatment outcomes with Percutaneous Hepatic Perfusion (PHP Therapy) with Melphalan/HDS in patients with primary metastatic ocular melanoma (OM) with liver metastasis treated between 2008 and 2016. The study was led by Dr. Alexandra Gangi of the Moffitt Cancer Center.

"We are very pleased that Dr. Gangi and her team’s research has been accepted for oral presentation at this prestigious event and believe that their research results will further inform on the use of Melphalan/HDS as a potentially viable additional option for treatment of hepatic metastases in patients with metastatic ocular melanoma," said Jennifer K. Simpson, Ph.D., MSN, CRNP, President and Chief Executive Officer of Delcath. "We look forward to announcing the details of these new data after they are presented."

Celsion Corporation Announces Issuance of Two New Patents for ThermoDox®

On January 18, 2017 Celsion Corporation (NASDAQ:CLSN), a clinical stage oncology drug development company, reported that the United States Patent and Trademark Office has granted U.S Utility Patent No. 9,492,385 B2 – Temperature-Sensitive Liposomal Formulation, which is directly applicable to the method of treating cancer using the Company’s current ThermoDox formulation (Press release, Celsion, JAN 18, 2017, View Source [SID1234517437]). The claims cover intravenous or direct (to the tumor) administration of the formulation followed by heating and extends coverage time over ThermoDox’s current parent patents. The Company also announced the issuance of Korean Patent No. 1652126 – Novel Thermosensitive Liposomes Containing Therapeutic Agents, which relates to composition claims directed to a thermally sensitive liposome that contains all of the components in the Company’s ThermoDox liposome as well as one additional lipid (DSPG).

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These two new patents strengthen the global coverage of ThermoDox, Celsion’s proprietary dose form of doxorubicin based on a heat-activated liposomal platform technology, currently in Phase III development for the treatment of primary liver cancer, also known as hepatocellular carcinoma (HCC). The Company’s Phase III OPTIMA Study is expected to enroll up to 550 patients at up to 75 clinical sites in the North America, Europe, China, S. Korea, Taiwan, and Southeast Asia, and will evaluate ThermoDox in combination with optimized RFA, which will be standardized to a minimum of 45 minutes across all investigators and clinical sites for treating HCC lesions three to seven centimeters, versus standardized RFA alone.

"The issuance of these patents further strengthens Celsion’s growing position as a leader in the development of directed chemotherapeutics designed to address some of the most difficult-to-treat cancers. In conjunction with its composition of matter patents, these new issuances broaden our intellectual property portfolio and provides for life cycle management of ThermoDox well into the next decade. Additionally by covering the use of ThermoDox, Celsion reinforces its exclusivity in many of the major markets around the world where HCC approaches epidemic proportions," said Michael H. Tardugno, chairman, president and CEO. "HCC has the fastest rate of growth of all cancers with annual incidence of over 800,000 new cases and is projected to be the most prevalent form of cancer by 2020."

ThermoDox is currently in late stage clinical trials in primary liver cancer and recurrent chest wall breast cancer. It is positioned for use with multiple heating technologies, and has the potential for applications in the treatment of other forms of cancer including metastatic liver and non-muscle invading bladder cancers.

About ThermoDox
Celsion’s most advanced program is a heat-mediated drug delivery technology that employs a novel heat-sensitive liposome engineered to address a range of difficult-to-treat cancers. The first application of this platform is ThermoDox, a lyso-thermosensitive liposomal doxorubicin (LTLD), whose novel mechanism of action delivers high concentrations of doxorubicin to a region targeted with the application of localized heat at 40°C, just above body temperature. ThermoDox has the potential to address a broad range of cancers.

Celsion’s LTLD technology leverages two mechanisms of tumor biology to deliver higher concentrations of drug directly to the tumor site. In the first mechanism, rapidly growing tumors have leaky vasculature, which is permeable to liposomes and enables their accumulation within tumors. Leaky vasculature influences a number of factors within the tumor, including the access of therapeutic agents to tumor cells. Administered intravenously, ThermoDox is engineered with a half-life to allow significant accumulation of liposomes at the tumor site as these liposomes recirculate in the blood stream. In the second mechanism, when an external heating device heats tumor tissue to a temperature of 40°C or greater, the heat-sensitive liposome rapidly changes structure and the liposomal membrane selectively dissolves, creating openings that can release a chemotherapeutic agent directly into the tumor and into the surrounding vasculature. Drug concentration increases as a function of the accumulation of liposomes at the tumor site, but only where the heat is present. This method damages only the tumor and the area related to tumor invasion, supporting more precise drug targeting.

MRC Technology, Cancer Research UK and Cancer Research Technology collaborate to focus on cancer immunotherapies

On January 18, 2017 Cancer Research UK, Cancer Research Technology and MRC Technology reported that they are joining forces to identify and validate novel drug discovery targets that could lead to new immunotherapy treatments (Press release, Cancer Research Technology, 18 18, 2017, View Source [SID1234523172]).

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The partnership brings together Cancer Research UK’s network of leading scientists with CRT’s cancer-focused target selection and validation expertise, and MRCT’s antibody screening and development capability. The collaboration will identify possible targets for the development of both antibody and small molecule therapeutics. The next stage of the collaboration will be to seek a clinical partner to accelerate the progress of promising compounds into the clinic.

New targets that increase cancer’s susceptibility to the immune system will be identified from Cancer Research UK’s funded research. MRC Technology will develop antibodies for suitable targets via its antibody screening platform, while CRT will focus on small molecule approaches.

Dr Hamish Ryder, director of discovery, Cancer Research Technology, said: "Immunotherapy is a hugely promising approach to cancer treatment and we’re delighted to extend our research in this area by partnering with MRC Technology.

"The aim of this alliance is to work together to identify highly novel immunotherapy targets and develop treatments that will complement the checkpoint inhibitors that are already having such an impact on patients.

"We want to move quickly to bring promising new drugs forward to treat cancer patients as soon as possible."

Dr Justin Bryans, director, drug discovery at MRC Technology said: "Bringing together MRC Technology’s antibody drug discovery and CRT’s cancer biology expertise and applying them to cutting-edge discoveries from the Cancer Research UK network represents a very exciting prospect and will help us identify and develop new immune-oncology therapies, which already have a significant impact on cancer patients’ lives."

CRT and MRC Technology will be joint commercialisation partners for the collaboration and any resulting immunotherapy treatments.

Telix Pharmaceuticals and Atlab Pharma Conclude Therapeutic Product Development Agreement for Prostate Cancer

On January 18, 2017 (GLOBE NEWSWIRE) — Telix Pharmaceuticals Limited ("Telix") reported the completion of a product collaboration and purchase option agreement with Atlab Pharma SAS ("Atlab") (Press release, Telix Pharmaceuticals, JAN 18, 2017, View Source [SID1234519564]). Under the terms of the agreement, Telix will finance the manufacturing and clinical development of the huJ591 monoclonal antibody (mAb) radiolabelled with 177Lu (Lutetium) and 211At (Astatine), both promising "theranostic" products for the treatment of metastatic prostate cancer. The huJ591 mAb was originally developed by Dr. Neil Bander at the Weill Cornell Graduate School of Medical Sciences (New York, NY) and targets Prostate-Specific Membrane Antigen (PSMA), a well-validated target in prostate cancer.

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The parties will collaborate to manufacture clinical material and work together to execute a multi-centre Phase IIb trial for the treatment of men with metastatic prostate cancer, with and without end-stage chemotherapy (standard care). In financing development, Telix also obtains an exclusive option to acquire Atlab under pre-agreed terms. The financial terms of the option exercise are not publicly disclosed at this time.

CEO Chris Behrenbruch stated, "PSMA targeting radiopharmaceuticals have shown great promise in both the diagnostic and therapeutic setting, dramatically increasing the interest in targeted radionuclide therapy by mainstream biopharma. The 177Lu-huJ591 program is the most clinically advanced PSMA program and has extensive patient experience, including in conjunction with anti-androgens and chemotherapy. We are very pleased to be working with Atlab to add this very promising program to Telix’s development pipeline."

Atlab President, Dr. Jean-Marc Le Doussal commented, "As we learn more about the different strategies to deliver PSMA-targeting radiopharmaceuticals in the clinic, the advantages of antibody-directed approaches have become increasingly apparent. We are pleased to be working with the experienced team at Telix to further progress this very promising program."

Co-Founder and Chief Medical Adviser to Atlab, Professor Jean-François Chatal added, "Radioimmunotherapy is finally starting to hit its stride and garner the interest it deserves. In the clinic, we have seen targeted radionuclide therapy deliver impressive treatment responses, even in late stage patients. We are especially keen to use programs like 177Lu-huJ591 in conjunction with other immuno-oncology agents that have generally demonstrated lackluster performance in the mCRPC setting." Professor Chatal will also join Telix’s scientific advisory board.

About Prostate-Specific Membrane Antigen (PSMA)

PSMA is a cell surface antigen that has relatively little normal expression in normal tissues and represents a validated and highly promising target for a range of therapeutic strategies, especially radiopharmaceuticals. PSMA expression has been detected in a limited range of normal tissues including benign prostatic epithelium, renal proximal tubule, pancreas, small bowel and brain (a subset of astrocytes). However, these normal sites express PSMA at levels 2–3 orders of magnitude lower than that observed in prostate cancer.1

Antibody-directed cytotoxicity (whether from conjugated radiation or other therapeutic payloads) offers several advantages over small molecule or peptide-based delivery approaches. Normal tissue PSMA sites are highly polarized to the apical/luminal aspect of the benign prostatic glands, renal tubules and small bowel, basement membrane and epithelial tight junctions, and as such are effectively inaccessible to circulating mAbs. PSMA expression by astrocytes is similarly sequestered behind the blood-brain barrier. Consequently, antibodies to PSMA are functionally tumor-specific, whereas small molecule PSMA ligands excreted via the renal tubular lumen are not. Small molecule and peptide therapies targeting PSMA, with various isotopes, have demonstrated serious off-target effects, such as pancreatitis, nephrotoxicity and permanent salivary gland ablation. These considerations are particularly important for developing PSMA-targeting agents with high-energy nuclides such as alpha-particle emitters.

About the huJ591 Monoclonal Antibody (mAb)

The huJ591 (humanized) mAb is the most clinically-advanced anti-PSMA antibody, with several hundred patient doses for both imaging and therapy, both as a "naked" antibody and with a wide range of diagnostic and therapeutic payloads. Over 160 patients have been dosed with 177Lu-huJ591 at different dosing levels, and in combination with other standard care therapies in the metastatic castrate-resistant prostate cancer (mCRPC) setting. In over a dozen clinical trials, including with therapeutic radioimmunoconjugate forms, huJ591 has shown excellent immunogenicity, safety and tolerability, including with repeat dosing.

About Telix Pharmaceuticals Limited

Telix Pharmaceuticals Limited ("Telix") is a clinical-stage biopharamaceutical company headquartered in Melbourne, Australia. Telix is developing an advanced portfolio of clinical-stage products that address significant unmet medical need in oncology, particularly renal, prostate and brain (glioblastoma) cancer. Telix’s pipeline consists of "theranostic" radiopharmaceuticals, agents that can be used both diagnostically (via PET imaging) and therapeutically to patient benefit. Telix is an unlisted public company. For more information go to www.telixpharma.com.

About Atlab Pharma SAS

ATLAB Pharma SAS is a privately-owned biotechnology company headquartered in Nantes, France. ATLAB is developing a pipeline of innovative anti-cancer radiopharmaceuticals based on monoclonal antibodies coupled to the beta-emitting radioisotope Lutetium-177 and to the alpha-emitting radioisotope Astatine-211.