Will Genentech's eye implant be a tough sell?
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Today's Rundown

Featured Story

Merck taps Xeris for ready-to-use versions of antibody products

Merck has tapped Xeris Pharmaceuticals to help reformulate some of its drugs. The deal gives Merck a chance to license a Xeris technology to develop ultra-high concentration, ready-to-use formulations of certain monoclonal antibodies.

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Top Stories

Novartis-backed Credence taps Phillips-Medisize to step up production drug delivery system

Credence MedSystems has hit upon a way to scale up production of its drug delivery system. Weeks after disclosing $40 million from investors including Novartis, Credence has unveiled a partnership with Phillips-Medisize to step up from a clinical line to large-scale manufacturing.

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FDA greenlights Genentech's eye implant for macular degeneration. Will it be a tough sell?

The FDA has approved Genentech’s Susvimo, a port delivery system with Roche’s ranibizumab in patients with wet age-related macular degeneration. Now the trick could be to get patients to accept an implant the size of a grain of rice placed under the upper eyelid that delivers doses of Lucentis and is refilled every six months.

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AmMax, targeting a Daiichi market, posts data on delivery of rare tumor drug

AmMax Bio's attempt to muscle in on a market monopolized by Daiichi Sankyo has advanced, with the biotech posting midphase data on the effect of injecting an antibody into the joints of patients with rare tumors.

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Ligand licenses prodrug tech to oral COVID-19 antiviral project

Ligand Pharmaceuticals wants another piece of the COVID-19 pie. Having been one of the companies behind Gilead’s Veklury, Ligand has positioned itself to support an oral COVID-19 antiviral through a deal with China Resources Double-Crane Pharmaceutical (CRDC).

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Top 10 drug launch disasters

An estimated 40% of drugs approved between 2004 and 2016 underperformed, according to Wall Street’s prelaunch sales forecasts. That's a lousy track record, given that a strong launch is critical to a drug's success. Here, we list 10 drug launches from the past five years that suffered the most noteworthy failures.

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Resources

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Report: New research indicates an accelerated shift to decentralized clinical trials

New research indicates an accelerated adoption of decentralized clinical trials due to COVID-19.

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Integrate supply chain simulation into your early clinical trial planning to minimize risk in an uncertain supply chain environment, improve supply chain outcomes, and help streamline time-to-market for innovative therapies.

Whitepaper: Big Challenges for Small Sponsors: Competition in Oncology Research

Every biopharma sponsor faces the challenge of initiating, running and closing trials on time, but oncology studies pose several unique hurdles.

eBook: Get solutions to market faster

Read Get to Know Cloud Content Management for Life Sciences and learn how to eliminate silos across all workflows, from R&D to commercialization.

Content Hub: Remarque Systems Resource Hub

Remarque Systems consolidates data, then layers on visualization and automated metrics to generate consistent, actionable data insights in real-time. Click here for more info. 

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