Selecta Biosciences to Participate at the 2022 H.C. Wainwright BioConnect Conference

On January 5, 2022 Selecta Biosciences, Inc. (NASDAQ: SELB), a biotechnology company leveraging its clinically validated ImmTOR platform to develop tolerogenic therapies that selectively mitigate unwanted immune responses, reported that Company’s Management will provide a corporate update at the H.C. Wainwright BioConnect Conference, to be held virtually January 10-13, 2022 (Press release, Selecta Biosciences, JAN 5, 2022, View Source [SID1234598169]).

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The presentation will be available on-demand through the H.C. Wainwright conference portal, starting at 7 a.m. ET on Monday, January 10, 2022.

The webcast can be accessed here and an archived webcast will also be accessible in the Investors & Media section of the company’s website at www.selectabio.com.

Lexicon Pharmaceuticals to Participate in the 40th Annual J.P. Morgan Healthcare Conference

On January 5, 2022 Lexicon Pharmaceuticals, Inc. (Nasdaq: LXRX) reported that Lonnel Coats, Lexicon’s chief executive officer, will present at the 40th Annual J.P. Morgan Healthcare Conference on Thursday, January 13, 2022 at 10:30 a.m. ET (Press release, Lexicon Pharmaceuticals, JAN 5, 2022, View Source [SID1234598163]).

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A webcast of the event will be available in the "Events" section of the Lexicon website at www.lexpharma.com. An archived version of the webcast will be available on the website for two weeks.

Transfer of global rights for Eklira and Duaklir to Covis Pharma completed

On January 5, 2022 AstraZeneca reported that it has completed the transfer of its global rights to Eklira (aclidinium bromide), known as Tudorza in the US, and Duaklir (aclidinium bromide/formoterol) to Covis Pharma Group (Covis Pharma) (Press release, AstraZeneca, JAN 5, 2022, View Source [SID1234598160]).

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Financial considerations
Under the terms of the agreement, AstraZeneca received a payment of $270m from Covis Pharma. AstraZeneca will also receive payments in respect of certain ongoing development costs related to the medicines. The income arising from the upfront payment will be fully offset by a charge for derecognition of the associated intangible asset and therefore no Other Operating Income will be recognised in AstraZeneca’s financial statements.

Notes

Eklira and Duaklir
Eklira (aclidinium bromide) and Duaklir (aclidinium bromide/formoterol) are inhaled respiratory medicines used for the maintenance treatment of chronic obstructive pulmonary disease. Eklira is a long-acting muscarinic antagonist (LAMA), which is marketed in the US as Tudorza and in some countries as Bretaris.

Duaklir is a combination therapy that contains both a LAMA and a long-acting beta2-agonist (LABA). It is marketed in some countries as Brimica.

Both medicines are presented as a dry powder for inhalation and are delivered via a breath-actuated multi-dose dry powder inhaler, Genuair (Pressair in the US). AstraZeneca licensed the global rights to both products from Almirall S.A. in 2014.

Legend Biotech to Participate in the 40th Annual J.P. Morgan Healthcare Conference

On January 5, 2021 Legend Biotech Corporation (NASDAQ: LEGN) (Legend Biotech), a global, clinical-stage biotechnology company developing and manufacturing novel therapies, reported that it will virtually participate in the 40th Annual J.P. Morgan Healthcare Conference (Press release, Legend Biotech, JAN 5, 2022, View Source [SID1234598124]).
. Ying Huang, PhD, CEO and CFO of Legend Biotech, will deliver the company presentation on Tuesday, January 11, 2022 at 2:15 p.m. (Eastern Time).

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A live webcast of the presentation will be available to investors and other interested parties at the Legend Biotech website at View Source

Wheeler Bio Announces $14M Seed Round To Expand Access To Portable CMC™

On January 04, 2022 Wheeler Bio, a biomanufacturing company built to accelerate the translation of therapeutic innovation into clinical impact, reported the closing of a $14M Seed financing round (Press release, Wheeler Bio, JAN 4, 2022, View Source [SID1234642126]). The round was co-led by Echo Investment Capital and Alloy Therapeutics, with participation from Floating Point and Presbyterian Health Foundation.

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The new funding will be used by Wheeler Bio to expand its team and make its Portable CMC solution more broadly available, partnering with more preclinical CROs and antibody drug developers. Through parallel integration with preclinical drug discovery groups, Portable CMC provides a faster, easier, and more predictable discovery-to-IND path for drug developers.

"We are delighted to have the continued support of partners and investors as we work to solve the biggest problems associated with tech transfer," said Dr. Jesse McCool, Co-founder and CEO of Wheeler Bio. "With Portable CMC, we can empower preclinical CROs to halve the time to clinical supply for their customers, while significantly de-risking program onboarding for our CDMO partners. This means more medicines reach more patients faster."

By integrating discovery capabilities with Wheeler Bio’s open source biomanufacturing processes and platforms, preclinical CRO partners can extend their offering beyond drug candidate lead selection, providing drug developers with a clearer path to IND clinical manufacturing. Wheeler’s first partner is Alloy Therapeutics—a Boston-headquartered biotechnology company providing antibody discovery platforms and services to a community of more than 100 developers.

Errik Anderson, Founder and CEO of Alloy Therapeutics, said, "We are very enthusiastic about our partnership with Wheeler Bio because its unique approach and high-quality Portable CMC services address the problems our partners face regularly when moving into the IND-enabling phase. Differentiating speed, predictability, and cost benefits amplify our mission to democratize access to foundational drug development capabilities and reduce barriers in the pursuit of making medicine."

Scientific and operation leadership for the development and implementation of Portable CMC falls to Dr. Stephen Hamilton, Chief Technical Officer of Wheeler Bio, and a veteran of 20 years in industrial R&D and platform engineering. Dr. Hamilton said, "Over the course of my career, I have experienced firsthand the complexities of tech transfer and outsourcing. I am therefore very excited by the unique model that Wheeler Bio is implementing because it provides the next-generation CDMO services that will be critical to the success of emerging biopharma."

More information on Wheeler Bio and Portable CMC can be found on its website at www.wheelerbio.com.