UNITED THERAPEUTICS CORPORATION REPORTS
THIRD QUARTER 2017 FINANCIAL RESULTS

On October 25, 2017 United Therapeutics Corporation (NASDAQ: UTHR) reported its financial results for the third quarter ended September 30, 2017 (Press release, United Therapeutics, OCT 25, 2017, View Source [SID1234521159]).

"Our third quarter net revenues totaled $446 million," said Martine Rothblatt, Ph.D., United Therapeutics Chairman and Chief Executive Officer. "In addition, Orenitram’s third quarter net revenues grew 29%, as compared to the same period in the prior year, resulting in two consecutive quarters of greater than 20% net revenue growth for this product. This further confirms our belief in the organic growth opportunity of Orenitram, which is the only true oral prostacyclin analog therapy for the large and increasing number of pulmonary arterial hypertension (PAH) patients. We also continued to invest in our growing pipeline of late stage programs in cardiopulmonary diseases and oncology, including the initial enrollment of patients into our phase III DISTINCT study of dinutuximab in small cell lung cancer, and our SOUTHPAW study of Orenitram in patients with WHO Group 2 pulmonary hypertension associated with left heart failure. Finally, we have continued to invest in our regenerative medicine and organ manufacturing programs to ultimately find a cure for PAH and other end-stage organ diseases."

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TESARO to Announce Third-Quarter 2017 Financial Results on November 7, 2017

On October 24, 2017 TESARO, Inc. (NASDAQ:TSRO) reported that it will announce its third-quarter 2017 financial results on Tuesday, November 7, 2017, after the close of the U.S. financial markets (Press release, TESARO, OCT 24, 2017, View Source [SID1234521279]). TESARO’s senior management team will host a conference call and live audio webcast at 4:15 p.m. ET on November 7, 2017 to discuss the Company’s operating results in greater detail, as well as the status of its development programs and the VARUBI/Y and ZEJULA launches.

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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

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This quarterly earnings call will be available via phone and webcast. The conference call dial-in information is listed below. To access the webcast, please log on to the TESARO website at www.tesarobio.com at least 15 minutes prior to the start of the call to ensure adequate time for any software downloads that may be required.

CONFERENCE CALL & WEBCAST INFORMATION

TESARO will host a conference call and live audio webcast to discuss its third-quarter financial results.

WHEN: Tuesday, November 7, 2017 at 4:15 p.m. ET
LIVE DOMESTIC & CANADA CALL-IN: (877) 853-5334
LIVE INTERNATIONAL CALL-IN: (970) 315-0307
THIS CALL WILL ALSO BE BROADCAST LIVE, LISTEN ONLY, VIA THE WEB AT: www.tesarobio.com

A replay will be available for 30 days at www.tesarobio.com.

Genmab Announces Additional Information Concerning Net Sales of DARZALEX® (daratumumab) for Third Quarter of 2017

On October 24, 2017 Genmab A/S (Nasdaq Copenhagen: GEN) reported that Johnson & Johnson has given additional information relating to rest of world sales of DARZALEX (daratumumab) in the third quarter of 2017 (Press release, Genmab, OCT 24, 2017, View Source [SID1234521141]). As previously reported, net sales were USD 87 million in the rest of the world. This figure was negatively impacted by a one-time adjustment of approximately USD 20 million related to accruals for retroactive reimbursement matters in Germany and France. Genmab receives royalties on the worldwide net sales of DARZALEX under the exclusive worldwide license to Janssen Biotech, Inc. to develop, manufacture and commercialize DARZALEX.

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Bruno Lucidi Appointed Chief Executive Officer of AgenTus Therapeutics, The Cell Therapy Subsidiary of Agenus

On October 23, 2017 Agenus Inc. (NASDAQ: AGEN) Chairman and Chief Executive Officer (CEO) Garo Armen Ph.D. announces the appointment of Bruno Lucidi as CEO of AgenTus Therapeutics, Inc., a subsidiary of Agenus that has been established as a dedicated cell therapy company, which will focus on the discovery, development, and commercialization of Adoptive Cell Therapy (ACT) (Press release, AgenTus Therapeutics, OCT 24, 2017, View Source [SID1234521135]). Lucidi brings extensive expertise in drug development and more than 30 years of experience in the biopharmaceutical industry.

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Lucidi’s leadership record includes Head of Pediatric Vaccines at GSK Biologicals, where he was in charge of developing a global business of more than $3 billion. Lucidi was Worldwide Vice-President Virology & Oncology at Johnson & Johnson where he led portfolio strategy from drug discovery to market and served in senior leadership at Bristol-Myers Squibb where he was responsible for the strategy and launch of several new antiviral and oncology products, including but not limited to Videx (didanosine), Zerit (stavudine), Paraplatin (carboplatin) and Taxol (paclitaxel).

Lucidi was the Founding CEO of Idenix and the Chairman of Pharmasset, where his contributions at both companies laid the foundation for successful multi-billion dollar companies, which were later acquired by Merck and Gilead for approximately $4bn and $11bn, respectively. Lucidi also served as CEO of several companies in Europe including Karolinska Development AB, KDEV Oncology and Aprea AB. Lucidi is currently an External Expert for the European Commission and Life Sciences Expert at AWEX, Wallonia trade and foreign investment agency in Belgium.

As CEO of AgenTus, Lucidi will lead a team of world-class scientists, while leveraging the proprietary technologies, intellectual property assets, pipeline, and expertise of parent company Agenus.

“Bruno has the ideal mix of industry know-how and business-building expertise to propel AgenTus forward and transform our powerful cell therapy technology into novel treatments for patients with cancer,” said Garo Armen, Ph.D. Chairman and CEO of Agenus. “I am delighted to see Bruno’s appointment to this key role to rapidly translate our cell therapy platforms, novel targets, and innovative delivery format into a pipeline of effective therapies to drive value to patients and AgenTus.”

“AgenTus has the foundational technology and expertise to rapidly become a major player in the field of Cell Therapy. I am honored to work alongside a team of world-class scientists. My objective is to rapidly advance product innovation and create value by bringing effective cell therapies to cancer patients,” said Lucidi. “I look forward to further building and developing this exciting company and to realize the enormous potential of cell therapy as an emerging class of medicines in the immuno-oncology field.”

A Virus, a Gene and a Pill Used to Harness the Immune System to Fight Brain Tumor in Children

ZIOPHARM Oncology is pleased to share a story from the Ann & Robert H. Lurie Children’s Hospital in Chicago on the Ad-RTS-hIL-12 plus veledimex clinical trial for pediatric patients with brain cancer (Press release, Ziopharm, OCT 24, 2017, View Source [SID1234521136]). As we announced last week, Stewart Goldman, M.D., Division Head Hematology-Oncology, Neuro-Oncology & Stem Cell Transplantation at Lurie Children’s dosed the first patient in this pediatric trial.

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First patient on a new Phase 1 pediatric brain tumor study injected with a common cold virus bioengineered to deliver a gene that mobilizes the immune system; a pill is used to control the targeted immune response

The first patient in a new Phase 1 gene therapy trial for pediatric brain tumors underwent a leading-edge procedure at Ann & Robert H. Lurie Children’s Hospital of Chicago. During surgery to remove the brain tumor, the patient was injected with an adenovirus, a common cold virus, at the tumor site. The virus was bioengineered not to cause illness but rather deliver a gene that produces human interleukin 12 (hIL-12), a powerful protein to jumpstart the immune system to kill remaining tumor cells. For the next 14 days, the patient is given a pill – veledimex – to activate the gene and control the immune response, so that the inflammation fights the tumor without overwhelming the rest of the body.

“Using the immune system to fight cancer is one of the most exciting new directions in cancer research,” said Stewart Goldman, MD, Principal Investigator at Lurie Children’s, Division Head of Hematology, Oncology, Neuro-Oncology and Stem Cell Transplantation,​ and Professor of Pediatrics at Northwestern University Feinberg School of Medicine. “What is most challenging is regulating the immune response we unleash, and that is what we are doing in this study. The pill dose acts like a thermostat with which we can adjust the intensity of the patient’s immune response.”

This is the first gene therapy clinical trial of this type for pediatric brain tumors. It will initially include patients with recurrent or progressive glioblastoma multiforme (rGBM) in the cortex of the brain. At a later date, children with diffuse intrinsic pontine glioma (DIPG), an incurable tumor located in the brain stem, will be added.

“Studies of this approach in adults with rGBM are showing promising results,” said Goldman. “We are hopeful that this will offer a viable treatment to children with gliomas who currently do not have any curative options.”

In addition to Lurie Children’s, the Phase 1 study will be conducted at Dana-Farber Cancer Institute in Boston and the University of California, San Francisco. It is sponsored by ZIOPHARM Oncology, Inc. (Nasdaq:ZIOP), a Boston-based biopharmaceutical company focused on developing new gene and cell-based immunotherapies for cancer. Lurie Children’s cancer program is part of Robert H. Lurie Comprehensive Cancer Center of Northwestern University.

Research at Ann & Robert H. Lurie Children’s Hospital of Chicago is conducted through the Stanley Manne Children’s Research Institute. The Manne Research Institute is focused on improving child health, transforming pediatric medicine and ensuring healthier futures through the relentless pursuit of knowledge. Lurie Children’s is ranked as one of the nation’s top children’s hospitals in the U.S.News & World Report. It is the pediatric training ground for Northwestern University Feinberg School of Medicine. Last year, the hospital served more than 208,000 children from 50 states and 58 countries.