Domain Therapeutics receives development milestone payment from Merck KGaA, Darmstadt, Germany, for collaboration on adenosine receptor antagonists

On May 4, 2020 Domain Therapeutics, a biopharmaceutical company specializing in the discovery and development of new drugs targeting G Protein-Coupled Receptors (GPCRs) in immuno-oncology, neurology and rare diseases, reported that the decision of Merck KGaA, Darmstadt, Germany, to enter into a regulatory phase of drug development with its candidate, triggers an undisclosed milestone payment to Domain Therapeutics (Press release, Domain Therapeutics, MAY 4, 2020, View Source [SID1234606731]).

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The candidate was identified during a collaboration with Merck KGaA, Darmstadt, Germany, that was initiated in 2017, making Domain Therapeutics eligible for more than €240 million ($261M) in development milestones, as well as undisclosed royalties. The compound is an orally available small molecule antagonist of adenosine receptors. It fulfils all the criteria defined by Merck KGaA, Darmstadt, Germany, to become a valuable drug candidate and to be developed as a differentiated immunotherapeutic agent in multiple cancers.

The adenosine receptor antagonist program brought to the collaboration by Domain Therapeutics was the first asset from its immuno-oncology franchise, which has significantly expanded over the years. Today, the company has other assets from hit-to-lead to candidate stage and has secured exclusive access to a target validation approach to identify GPCR modulation in the immuno-oncology field.

"This new adenosine receptor antagonist is one of the strategic assets in our immuno-oncology pipeline," said Joern-Peter Halle, senior vice president, head of immuno-oncology research at Merck KGaA, Darmstadt, Germany. "It results from a successful and productive collaboration between the Domain and Merck KGaA, Darmstadt, Germany teams. We are eager to see the compound progressing through regulatory development and entering the clinic for the benefit of cancer patients."

"We are delighted to have contributed to the strengthening of Merck KGaA, Darmstadt, Germany’s portfolio in immuno-oncology with a new adenosine receptor antagonist," said Pascal Neuville, CEO of Domain Therapeutics. "This is a great achievement for Domain. It illustrates its capacity to discover and deliver valuable clinical candidates and highlights Domain’s innovation capacity in immunotherapies."

About adenosine receptor antagonists in immuno-oncology
Adenosine is a powerful immunosuppressive substance produced inside tumors as a result of rapid cancer cell turnover. In some cases, it is responsible for resistance to certain anti-tumor interventions, such as chemotherapy and radiation. The adenosine receptors, expressed on the surface of immune cells, mediate the immunosuppressive effects of adenosine. The adenosine-driven impairment of tumor-infiltrating lymphocytes (mainly CD8+ T cells and NK cells) and myeloid cells (dendritic cells, macrophages), mediated by adenosine receptors, requires the development of specific inhibitors. For the last few years, the pharma industry has been investigating the benefit of combining adenosine receptor antagonists with ICI in order to decrease adenosine-mediated resistance and restore ICI antitumor activity.

Turning Point Therapeutics to Host First Quarter Conference Call

On May 4, 2020 Turning Point Therapeutics, Inc. (NASDAQ: TPTX), a precision oncology company developing next-generation therapies that target genetic drivers of cancer, reported that it will report first quarter financial results following the close of U.S. financial markets on May 12 and host a conference call at 1:30 p.m. PT/4:30 p.m. ET to discuss the results and provide operational updates (Press release, Turning Point Therapeutics, MAY 4, 2020, View Source [SID1234564375]). President and CEO Athena Countouriotis, M.D., will host the call, which will include a question and answer session.

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The update will be accessible via audio webcast through the "Investors" section of www.tptherapeutics.com or by dialing (877) 388-2118 (in the United States) or (470) 495-9489 (outside the U.S.) using conference ID 6135289. A replay will be available through the "Investors" section of www.tptherapeutics.com.

Kezar Life Sciences Strengthens Executive Team with the Appointment of Noreen R. Henig, MD as Chief Medical Officer

On May 4, 2020 Kezar Life Sciences, Inc. (Nasdaq: KZR), a clinical-stage biotechnology company discovering and developing novel small molecule therapeutics to treat unmet needs in autoimmunity and cancer, reported the appointment of Noreen R. Henig, MD as its Chief Medical Officer (Press release, Kezar Life Sciences, MAY 4, 2020, View Source [SID1234557124]). As an integral member of the Company’s Executive Leadership team, Dr. Henig will oversee all aspects of the Company’s clinical development, regulatory and medical affairs.

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"Noreen brings with her a depth and breadth of expertise in clinical practice, translational science, clinical development, and medical affairs, and we are thrilled to welcome her to the Kezar team," said John Fowler, Kezar’s Chief Executive Officer. "Her proven leadership skills, deep understanding of immunology and rare diseases, and profound appreciation of the patient voice will make a significant impact, and I look forward to working in partnership with her as we continue to advance our novel therapies for a wide range of autoimmune diseases and cancers."

Noreen Roth Henig, M.D. is a seasoned leader whose career spans clinical practice, academic medicine, translational science, clinical development, medical and regulatory affairs. She currently serves on the Board of Avidity Biosciences and most recently served as Chief Medical Officer of Breath Therapeutics, which was acquired by Zambon SpA in 2019. As CMO, Dr. Henig built and led the clinical team and was responsible for all development activities including clinical and non-clinical science, clinical operations, regulatory, project management, and medical affairs. Prior to joining Breath, Dr. Henig was Chief Medical Officer at ProQR Therapeutics where she brought two unique RNA oligonucleotides through early clinical trials in rare diseases. Before ProQR, Dr. Henig spent 2008 through 2014 at Gilead Sciences where she held roles with increasing responsibility, including building and leading a global medical affairs organization, strategic development of clinical trials Phase 2-4, regulatory strategy, corporate development, leadership of key alliances and commercial strategy. Prior to joining industry, Dr. Henig spent nearly 10 years in leadership roles within academic medicine at Stanford University and California Pacific Medical Center. She is a board-certified physician in Pulmonary, Critical Care and board eligible in Allergy and Immunology. Dr. Henig received her B.A. from Yale University and her M.D. from Albert Einstein College of Medicine of Yeshiva University in 1991 with a distinction in immunology. She trained in Internal Medicine at University of California, San Francisco and in Pulmonary/Critical Care and Allergy/Immunology at University of Washington, Seattle.

"I am excited to join Kezar at such an important time in the company’s growth," said Dr. Henig. "Kezar’s scientific excellence in protein homeostasis via protein degradation and secretion presents tremendous opportunity to create elegant therapies for those living with serious and often debilitating diseases. It will be a joy to work alongside Kezar’s talented and dynamic team to realize our full potential by combining science with innovative approaches to development and patient engagement."

CymaBay Therapeutics to Report First Quarter 2020 Financial Results on Monday, May 11

On May 4, 2020 CymaBay Therapeutics, Inc. (NASDAQ: CBAY), a clinical-stage biopharmaceutical company focused on developing therapies for liver and other chronic diseases with high unmet need, reported that it will host a conference call and live audio webcast on Monday, May 11, 2020 at 4:30 p.m. Eastern Time to discuss financial results for the first quarter ended March 31, 2020 and to provide a business update (Press release, CymaBay Therapeutics, MAY 4, 2020, View Source [SID1234557046]).

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Conference Call Details
To access the live conference call, please dial 855-327-6837 from the U.S. and Canada, or 631-891-4304 internationally, Conference ID# 10009543. To access the live and subsequently archived webcast of the conference call, go to the Investors section of the company’s website at View Source

Sangamo Therapeutics Announces First Quarter 2020 Conference Call and Webcast

On May 4, 2020 Sangamo Therapeutics, Inc. (Nasdaq: SGMO), a genomic medicine company, reported that the Company has scheduled the release of its first quarter 2020 financial results after the market closes on Monday, May 11, 2020 (Press release, Sangamo Therapeutics, MAY 4, 2020, View Source [SID1234557045]). The press release will be followed by a conference call at 5:00 p.m. ET, which will be open to the public via telephone and webcast. During the conference call, the Company will review its financial results and provide a business update.

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The conference call dial-in numbers are (877) 377-7553 for domestic callers and (678) 894-3968 for international callers. The conference ID number for the call is 6043504. Participants may access the live webcast via a link on the Sangamo Therapeutics website in the Investors and Media section under Events and Presentations. A conference call replay will be available for one week following the conference call. The conference call replay numbers for domestic and international callers are (855) 859-2056 and (404) 537-3406, respectively. The conference ID number for the replay is 6043504.