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RECOVERY Trial Data Monitoring Committee Recommends Continuing Evaluation of REGN-COV2 in All Hospitalized Patients

The Pharma Data

About the Trial The RECOVERY trial is conducted by the registered clinical trials units in the Nuffield Department of Population Health in partnership with the Nuffield Department of Medicine. The DMC letter is available here: [link]. Department of Health and Human Services under OT number: HHSO100201700020C.

Trials 52
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Philips on designing innovation and cultivating partnerships – part two

pharmaphorum

It’s a package, and sometimes we deploy one or two modules, sometimes multiple modules in a project. It all depends on the needs and the available budget in a particular project,” Kroezen says. “If you have a health issue in Africa and you’re low income, you go to a primary care clinic.

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Ep. 003 – Ritesh Patel Podcast Transcript

Pharma Marketing Network

Most recently, telemedicine and specialty pharmacy connected together to create a product that a consumer can get directly. Where you can get ED medication, hair loss, medication, that sort of thing, all packaged together. You go online, you talk to a doctor via telemedicine, and a specialty pharmacy then delivers it for you.

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Ep. 003 – Ritesh Patel Podcast Transcript

Pharma Marketing Network

Most recently, telemedicine and specialty pharmacy connected together to create a product that a consumer can get directly. Where you can get ED medication, hair loss, medication, that sort of thing, all packaged together. You go online, you talk to a doctor via telemedicine, and a specialty pharmacy then delivers it for you.

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Regeneron Announces U.S. Government Agreement to Purchase Additional COVID-19 Antibody Cocktail Doses

The Pharma Data

“Patients in our antibody cocktail outpatient clinical trial experienced significant reductions in virus levels and required fewer medical visits for COVID-19, suggesting the therapy can help reduce the current burden on hospitals and healthcare systems,” said George D.

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New England Journal of Medicine Publishes Positive Initial Regeneron Antibody Cocktail Results in Non-hospitalized Patients with COVID-19

The Pharma Data

Data from the Phase 1/2/3 clinical trial supported an Emergency Use Authorization for casirivimab and imdevimab administered together, granted by the U.S. If the therapy proves safe and effective in clinical trials and regulatory approvals are granted, Regeneron will manufacture and distribute it in the U.S. ,

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Regeneron Announces Encouraging Initial Data from COVID-19 Antibody Cocktail Trial in Hospitalized Patients on Low-flow Oxygen

The Pharma Data

NASDAQ: REGN) today announced encouraging initial data from an ongoing Phase 1/2/3 clinical trial of the Regeneron antibody cocktail, casirivimab and imdevimab, in hospitalized COVID-19 patients requiring low-flow oxygen. Evaluation of its safety and efficacy is ongoing in multiple clinical trials. In the U.S.