Gritstone Announces Presentations during Three Upcoming Investor Conferences

On December 30, 2021 Gritstone bio, Inc. (Nasdaq: GRTS), a clinical-stage biotechnology company developing the next generation of cancer and infectious disease immunotherapies, reported that Gritstone management will participate in the following upcoming investor conferences in January (Press release, Gritstone Oncology, DEC 30, 2021, View Source [SID1234597854]).

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Conference: JP Morgan 40th Annual Global Healthcare Conference
Presentation Date and Time: Thursday, January 13, 2022 at 8:15 a.m. ET
Presenter: Andrew Allen, M.D., Ph.D., co-founder, president, and chief executive officer

Conference: H.C. Wainwright BioConnect Conference 2022
Presentation Date and Time: Available beginning Monday, January 10, 2022 at 7:00 a.m. ET
Presenter: Andrew Allen, M.D., Ph.D., co-founder, president, and chief executive officer

Conference: B. Riley Securities’ 2022 Virtual Oncology Conference
Presentation Date and Time: Thursday, January 27, 2022 at 1:30 p.m. ET
Presenter: Andrew Allen, M.D., Ph.D., co-founder, president, and chief executive officer

Live webcasts of all presentations will be accessible via the Investors & Media section of the company’s website at View Source An archived replay will be accessible for 30 days following each event.

Thermo Fisher Scientific to Present at the 2022 Goldman Healthcare CEOs Unscripted Conference

On December 30, 2021 Thermo Fisher Scientific Inc. (NYSE: TMO), the world leader in serving science, announced that Marc N. Casper, chairman, president and chief executive officer, reported that it will present virtually at the 2022 Goldman Healthcare CEOs Unscripted Conference on Thursday, January 6, 2022, at 9:00 a.m. (EDT) (Press release, Thermo Fisher Scientific, DEC 30, 2021, View Source [SID1234597858]).

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You can access the webcast of the presentation via the Investors section of our website, www.thermofisher.com.

Mission Bio and SequMed Sign Collaboration Agreement Announcing Partnership to Provide Tapestri Services and Co-Develop Clinical Applications in China

On December 30, 2021 Mission Bio, the pioneer in high-throughput single-cell DNA and multi-omics analysis, reported that it has signed an agreement with SequMed, a pioneer in single-cell omics technology innovation and applications in China (Press release, Mission Bio, DEC 30, 2021, View Source [SID1234597860]). The agreement will allow Mission Bio to expand its product and services offerings into China, a key region of growth for its geographical expansion strategy, enabling high quality single-cell sequence services using Mission Bio’s products to customers in mainland China.

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With this new and important collaboration, Mission Bio and SequMed will work jointly by integrating Mission Bio’s technology platform into SequMed’s clinical assay development and data analysis capabilities to co-develop novel single cell assays for early detection, medication guidance, and prognostic monitoring of cancers, as well as reproductive genetics applications. This partnership builds on Mission Bio’s commitment to providing high quality single-cell multi-omics with the Tapestri platform in China, where there is an increasing demand for single-cell innovation for clinical diagnosis.

"Tumor heterogeneity is always one of the biggest challenges for cancer therapy and the development of treatment resistance," said Yan Zhang, CEO of Mission Bio. "Our Tapestri single-cell sequencing solutions enable us to detect the co-occurring mutations within cancer cells, allowing us to understand the mechanisms of resistance at a granular level. We are excited to collaborate with SequMed. By integrating our single-cell technology with SequMed’s expertise in clinical assay development, we are committed to improving diagnosis, prognosis, and treatment of diseases in China."

Prof. Xinghua Victor Pan, Chairman of Technology Committee of SequMed, said, "We are dedicated to promoting the development and application of next-generation single-cell multi-omics technology in scientific and clinical research. We look forward to working with Mission Bio to develop novel single-cell assays for different diseases, from molecular mechanism elucidation to clinical medicine acceleration. With the synergies between the two collaborating parties, SequMed will enter into a new era, providing our customers in China with comprehensive solutions for personalized medicine."

Sumgen Completed Series B+ Financing of RMB ¥200 million

On December 30, 2021 Hangzhou Sumgen Biotech Co., Ltd. (hereinafter referred to as "Sumgen") reported that it has completed the series B + funding with over RMB 200 million (Press release, Sumgen Biotech, DEC 30, 2021, View Source;a=nav&id=247 [SID1234656269]). This funding is jointly invested by Junchuan Capital, Zheshang Venture Capital, Qianhai Wanhui and Wuxi Shangtong, and the existing investors Sinopharm CNBG, Hankang Capital and Addor Capital continue to add on. StartPointAdvisors has served as the exclusive financial adviser for this round of financing.

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Sumgen is an innovation-driven biopharmaceutical company, which is committed to the development and commercialization of innovative antibody drugs for major diseases such as tumors. The company has continuous innovation capability and product export capability, and has established several innovation platforms, including several antibody discovery platforms such as mammalian cell display platform and BIMA (BI-specific/functional Macrophage Activator), BITA(BI-specific/functional T cell Activator).

Around the field of cancer, Sumgen has focused on the layout of a series of innovative products. SG301, SG404, SG12473 and other projects have completed the double report between China and the United States, entered the clinical study stage, and made positive progress; In November 2021, SG2501, the world’s first anti-CD38/CD47 bispecific antibody drug wholly developed by the company, was approved by FDA to carry out clinical study, and the clinical preparations for this project in the United States are progressing steadily. The company has carried out a global patent layout for innovative antibody drugs and declared more than 60 invention patents; and reached a number of commercial cooperations with CSPC and Sinopharm CNGB. At present, the company has started the construction of international standard production base, and is committed to providing high-quality Chinese antibodies for patients all over the world.

Dr. Lv Ming, founder and CEO of Sumgen, said: "Thanks to the new and old shareholders for their support to Sumgen. Sumgen will deepen the development of innovative products and accelerate the clinical layout in an all-round way; strengthen the sustainable source innovation ability and drive the development of enterprises with innovation; build industrial transformation ability and commercialization ability, and help enterprises build the whole industrial chain. "

Polyphor closes merger with EnBiotix and is renamed Spexis

On December 30, 2021 Polyphor and EnBiotix Inc. reported the closing of the merger of the two companies and the change of name of the combined company to Spexis AG (Press release, Polyphor, DEC 30, 2021, View Source [SID1234639732]). Pursuant to completion of the capital increase approved at the extraordinary general meeting of shareholders convened on October 28, 2021, Polyphor and EnBiotix, a privately held late clinical-stage rare disease company focused on products for rare, chronic respiratory diseases, have merged, via a transaction whereby Polyphor acquired 99.6% (with the remaining 0.4% expected to follow shortly) of the outstanding capital stock of EnBiotix in exchange for 35’150’961 shares of Polyphor common stock. The acquired capital stock of EnBiotix also includes shares issued by EnBiotix via the full conversion of the USD 11 million convertible debenture financing which was communicated on December 29, 2021.

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Starting January 3, 2022, all 46’375’777 Spexis AG shares recorded in the commercial registry will be listed under the ticker symbol SPEX on the SIX Swiss Exchange under the International Reporting Standard and include all former Polyphor AG shares, which remain listed under the unchanged ISIN number (CH0106213793).

As resolved on October 28, 2021, by the Shareholders’ Meeting, Jeffrey Wager is replacing Kuno Sommer as chairman. Kuno Sommer and Bernard Bollag remain Board members. Dennis Ausiello has been elected vice-chair, Dan Hartman and Robert Clarke have also joined the Board thereby replacing Andreas Wallnöfer, Hugh O’Dowd, and Silvio Inderbitzin. The Executive Committee is led by Jeffrey Wager with Stephan Wehselau, Hernan Levett and Juergen Froehlich, thereby replacing Gökhan Batur, Franziska Müller, Daniel Obrecht and Frank Weber.

"We are pleased with the successful closing of the business combination and welcome the shareholders of EnBiotix and Polyphor to Spexis", said Jeffrey D. Wager, M.D., Chairman and Chief Executive Officer of Spexis. "We believe Spexis will pursue a unique strategy as a rare disease and oncology company. As such, we very much look forward to advancing an innovative R & D pipeline and to engaging in unique strategic corporate development to create long-term shareholder value."

The initial pipeline of Spexis includes:

– ColiFin(R) which EnBiotix has in-licensed from PARI Pharma GmbH, a global leader in nebulized therapies, for worldwide rights ex-Europe. Approved in Europe since 2010 as a front-line therapy for lung infections in cystic fibrosis ("CF"), ColiFin(R) has a proven safety, efficacy and commercial track record which the company aims to leverage towards the U.S. and global markets – and both within and outside the field of CF.

– Inhaled murepavadin, a novel class inhaled antibiotic specifically targeting Pseudomonas aeruginosa ("PA"), is being developed for the treatment of these infections in people with CF and is beginning Phase I development using eFlow(R) Technology nebulizer (PARI Pharma GmbH).

– EBX-002, a combination of amikacin (AMK) and a potentiator molecule for NTM infections which preclinical studies to date have shown potential for superior activity compared to ARYKACE(R).

– Balixafortide, a potent and highly selective blocker of CXCR4. Following the closure of its Phase 3 program in advanced breast cancer, additional oncology and non-oncology indications for balixafortide will be evaluated both alone and in collaboration with Fosun Pharma who owns China rights.

– New CXCR4 inhibitor program focused on orphan, hematological malignancies.

– Preclinical OMPTA BamA and LptA programs funded by CARBX targeting WHO Priority 1 bacterial infections planned to be developed for hospital acquired bacterial infections.

– Company aims to in-license or acquire other rare disease and oncology assets that will consolidate its position in these therapeutic areas.