Insmed to Present at the 39th Annual J.P. Morgan Healthcare Conference

On January 5, 2021 Insmed Incorporated (Nasdaq: INSM), a global biopharmaceutical company on a mission to transform the lives of patients with serious and rare diseases, reported that management will present at the virtual 39th Annual J.P. Morgan Healthcare Conference on Tuesday, January 12, 2021 at 7:30 a.m. ET (Press release, Insmed, JAN 5, 2021, View Source [SID1234573520]).

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The presentation will be webcast live and can be accessed by visiting the investor relations section of the company’s website at www.insmed.com. The webcast will be archived for a period of 30 days following the conclusion of each live event.

Regulus Therapeutics to Present at the H.C. Wainwright Virtual BioConnect Conference

On January 5, 2021 Regulus Therapeutics Inc. (Nasdaq: RGLS), a biopharmaceutical company focused on the discovery and development of innovative medicines targeting microRNAs ("Regulus"), reported that Jay Hagan, President and Chief Executive Officer of Regulus, will present at the H.C. Wainwright Virtual BioConnect Conference being held from January 11-14, 2021 (Press release, Regulus, JAN 5, 2021, https://www.prnewswire.com/news-releases/regulus-therapeutics-to-present-at-the-hc-wainwright-virtual-bioconnect-conference-301200819.html [SID1234573519]).

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A webcast of the on-demand presentation will be available beginning Monday, January 11, 2021 through the investor relations section of the Company’s website at www.regulusrx.com.

Y-Biologics signed License Agreement with 3D Medicines for T cell bispecific engager in Greater China territory

On January 5, 2021 The South Korean biotech company Y-Biologics and the China-based biopharmaceutical company 3D Medicines reported that have entered into a License Agreement granting exclusive rights to develop, manufacture, and commercialize YBL-013, a T cell bi-specific engager based on ALiCE platform technology, in the Territory of Greater China (mainland China, Hong Kong, Macau and Taiwan) (Press release, Y-Biologic, JAN 5, 2021, View Source [SID1234573518]).

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Under the terms of this Agreement, Y-Biologics will receive an upfront fee of $2 million and is eligible to receive up to $85 million in additional development, regulatory, commercialization and sales milestone payments as well as up to double-digit royalties on net sales in the Territory. Both Parties will share part of IND development cost. In the meantime, 3D Medicines will have an exclusive right to develop, manufacture, and commercialize for YBL-013 in Greater China, with potential expansion collaboration opportunity in US and other regions.

YBL-013, a novel I/O therapeutic candidate which simultaneously targets CD3 on T cell and PD-L1 on cancer cell, is the first candidate developed based on Y-Biologics’ proprietary T cell bispecific engager technology, namely ‘ALiCE’ (Antibody Like Cell Engager). The technology is the CD3-based bispecific antibody engineered to have a unique 2 versus 1 structure with two Fab regions targeting for a tumor antigen and Fv region specific for CD3 by placing between T cell and cancer cell. Notably, it shows a higher binding affinity to tumor antigens and activates mainly T cells around the tumor. This is an innovative technology that can significantly reduce the toxicity which current T cell bispecific antibodies have.

"We are very pleased to enter into this exclusive license agreement with Y-Biologics," said John Gong, M.D., Ph.D., Chairman and Chief Executive Officer of 3D Medicines. "We believe that YBL-013, bi-specific engager, a next generation T cell bi-specific engager, together with Envafolimab, the global first subcutaneous PD-L1 antibody to be launched in China, and other innovative products in our pipelines, could alter the treatment paradigm across various tumor types. We are committed to working closely with Y-Biologics to further advance the development of YBL-013, which has great potential to help patients living with cancer.

Young Woo Park, CEO of Y-Biologics, stated "We have focused our capabilities on the development of ALiCE, T cell bispecific engager technology, and we are extremely pleased that the output has emerged as the global license agreement. Through ALiCE technology, we will strengthen our novel therapeutic portfolio by presenting a variety of competitive novel I/O therapeutic candidates in the CD3-based T cell bispecific engager market, which is a key trend in the field of bispecific antibody. In addition, starting from China, we will put our efforts to present our highly skilled technology to an international market."

Meanwhile, Y-Biologics has licensed out YBL-001, which is an ADC candidate co-developed with LegoChem Bioscience, to Pyxis Oncology in early December. On the other hand, 3D Medicines recently licensed-in AVB-500 from Aravive and galinpepimut-S (GPS) from SELLAS Life Sciences for both hematological malignancies and solid tumors.

About ALiCE

ALiCE, a novel T cell bispecific antibody format, is designed to overcome immune evasion in cancer. This format allows T cells to directly engage to target cancer cells and thereby activates the cytotoxic immune responses. The ALiCE molecules are engineered to have a unique 2 by 1 structure with two Fab regions targeting for a tumor antigen and Fv region specific for CD3 found on T cells.

The targeting strategy is designed to have a higher binding affinity to a target cancer cell by two arms and a lower binding affinity to CD3 by one arm. Therefore, T cell activation occurs only near the tumor site when the ALiCE molecule bound to the target cancer cell, which is leading to reduced off-tumor toxicity.

ALiCE molecules appear to have more advanced target cancer cell killing mechanism in low doses than other T cell engagers with 1 by 1 structure. The structural feature of bivalent binding and much higher binding affinity to tumor antigens allows T cell engagement to tumor cell efficiently. This clustering formation can generate strong T cell activation signaling and induce cancer cell killing potency.

ALiCE molecules can be formed as heterodimers by harnessing innate assembly mechanisms in mammalian cells and secreted into the culture medium. The molecules can be easily produced and purified with conventional manufacturing procedures.

Thermo Fisher Scientific to Hold Earnings Conference Call on Monday, February 1, 2021

On January 5, 2021 Thermo Fisher Scientific Inc. (NYSE: TMO), the world leader in serving science, reported that it will release its financial results for the fourth quarter and full year 2020 before the market opens on Monday, February 1, 2021, and will hold a conference call on the same day at 8:30 a.m. EDT (Press release, Thermo Fisher Scientific, JAN 5, 2021, View Source [SID1234573516]).

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During the call, the company will discuss its financial performance, as well as future expectations. To listen, call (833) 714-0931 within the U.S. or (778) 560-2662 outside the U.S. The conference ID is 9253945. You may also listen to the call live on the "Investors" section of our website, www.thermofisher.com. The earnings press release and related information can be found in that section of our website under "Financial Results." A replay of the call will be available under "Webcasts and Presentations" through Friday, February 12, 2021.

Nektar Appoints Dr. Brian Kotzin as Interim Chief Medical Officer and Head of Development

On January 5, 2021 Nektar Therapeutics (NASDAQ: NKTR) reported that it has appointed Brian Kotzin, MD as Interim Chief Medical Officer, Head of Development effective immediately (Press release, Nektar Therapeutics, JAN 5, 2021, View Source [SID1234573515]). Since 2017, Dr. Kotzin has served as Senior Vice President, Clinical Development and Head of Immunology at Nektar. Wei Lin will be leaving the company to pursue another opportunity.

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"We are pleased that Dr. Kotzin will take on this key role on our development team at Nektar," said Jonathan Zalevsky, Chief R&D Officer of Nektar Therapeutics. "Since he joined Nektar in 2017, Dr. Kotzin has demonstrated strong leadership and strategic insight. He has extensive development experience and over 30 years of expertise in immunology and his strategic guidance will be invaluable to Nektar as we continue to execute on development activities for our immune-oncology and immunology pipeline."

Brian Kotzin, MD added, "I am honored to expand my role at Nektar and work alongside Dr. Zalevsky. This is an exciting time for the company with multiple registrational studies underway in a range of tumor types for BEMPEG, a broadening clinical program for NKTR-358 in a number of auto-immune disorders, and an emerging opportunity for NKTR-255 in both hematological malignancies and solid tumors."

While at Nektar, Dr. Kotzin has spearheaded the NKTR-358 development program partnered with Eli Lilly & Co. and he has also served as a development program lead for early development of NKTR-255 and NKTR-262. Dr. Kotzin was previously at Amgen for 11 years, where he served as Vice President, Global Clinical Development and Head of the Inflammation Therapeutic area directing the global development efforts for Amgen product candidates, including all immunology programs. During his tenure at Amgen, he also served as Vice President of Translational Sciences and Head of Medical Sciences/Early Development, where he was responsible for the planning and execution of early-phase clinical development in all therapeutic areas as well as the discovery and implementation of pharmacodynamic biomarkers and clinical immunology support for clinical studies. Prior to joining Amgen, Dr. Kotzin served as Head of Clinical Immunology in the Department of Medicine and as director of the Autoimmunity Center of Excellence at the University of Colorado Health Sciences Center in Denver. He previously held the position of Professor in the Departments of Medicine, Pediatrics, and Immunology at the National Jewish Medical and Research Center in Denver. In addition to academic posts in rheumatology and microbiology/immunology, Dr. Kotzin served at the Veterans Administration Medical Center in Denver as chief of the Rheumatology Section. Dr. Kotzin received a B.S. in mathematics from the University of Southern California and an M.D. from Stanford University School of Medicine. He completed a residency in internal medicine and a fellowship in rheumatology and medicine at Beth Israel Hospital in Boston. He was also a postdoctoral fellow in the Division of Immunology and Rheumatology at Stanford University School of Medicine. He is board certified in rheumatology and internal medicine.

"Over the past two years, Wei has played a leadership role in recruiting an experienced clinical development organization and executing a late-stage clinical development strategy for BEMPEG, positioning it for future success. I would like to thank him for his contributions to Nektar, and wish him the best in his next opportunity," continued Zalevsky.