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Johnson & Johnson to Participate in Goldman Sachs 42nd Annual Global Healthcare Virtual Conference

The Pharma Data

Johnson & Johnson to Participate in Goldman Sachs 42nd Annual Global Healthcare Virtual Conference | Johnson & Johnson. Johnson & Johnson COVID-19 Vaccinations Resume Following CDC and FDA Decision. See more information and instructions on how to setup the tag on: [link] >. Learn More.

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Johnson & Johnson to Participate in Wells Fargo 2020 Virtual Healthcare Conference

The Pharma Data

Johnson & Johnson to Participate in Wells Fargo 2020 Virtual Healthcare Conference | Johnson & Johnson. Johnson & Johnson to Participate in Wells Fargo 2020 Virtual Healthcare Conference. Johnson & Johnson to Participate in Wells Fargo 2020 Virtual Healthcare Conference.

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Johnson & Johnson to Participate in Barclays Global Consumer Staples Virtual Conference

The Pharma Data

Johnson & Johnson to Participate in Barclays Global Consumer Staples Virtual Conference | Johnson & Johnson. Johnson & Johnson to Participate in Barclays Global Consumer Staples Virtual Conference. Johnson & Johnson to Participate in Barclays Global Consumer Staples Virtual Conference.

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Johnson & Johnson to Participate in the 18th Annual Morgan Stanley Virtual Global Healthcare Conference

The Pharma Data

Johnson & Johnson to Participate in the 18th Annual Morgan Stanley Virtual Global Healthcare Conference | Johnson & Johnson. Johnson & Johnson to Participate in the 18 th Annual Morgan Stanley Virtual Global Healthcare Conference. Learn More. Our Company. Eastern Time).

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Johnson & Johnson to Participate in Bernstein’s 37th Annual Strategic Decisions Virtual Conference

The Pharma Data

Johnson & Johnson to Participate in Bernstein’s 37th Annual Strategic Decisions Virtual Conference | Johnson & Johnson. Johnson & Johnson Statement on April 23 CDC Advisory Committee Meeting. Johnson & Johnson to Participate in Bernstein’s 37th Annual Strategic Decisions Virtual Conference.

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J&J gets first approval for multiple myeloma bispecific Tecvayli

pharmaphorum

Johnson & Johnson has its first worldwide regulatory approval – in the EU – for Tecvayli, one of two much-anticipated bispecific antibodies the drugmaker has developed for patients with multiple myeloma. Tecvayli previously scored a priority medicines (PRiME) designation from the EMA and a breakthrough-therapy tag from the FDA.

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Axsome bounces back as FDA clears depression drug

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That status goes to Johnson & Johnson’s Spravato (esketamine), which was approved in March 2019 and is administered as a nasal spray twice a week for four weeks. Auvelity isn’t the first NMDA-targeting antidepressant to reach the market.

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