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CHMP positive opinion recommending approval of Benlysta for adult patients with active lupus nephritis

The Pharma Data

The CHMP opinion is one of the final steps in the marketing authorisation procedure prior to approval by the European Commission. The adverse reactions observed in BLISS-LN were consistent with the known safety profile of Benlysta administered intravenously plus standard therapy in patients with SLE. About the BLISS-LN study.

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European Commission approves Benlysta for adult patients with active lupus nephritis

The Pharma Data

GlaxoSmithKline plc (GSK) today announced the European Commission has approved the expanded use of intravenous and subcutaneous BENLYSTA (belimumab) in combination with background immunosuppressive therapies for the treatment of adult patients with active lupus nephritis (LN) in Europe, in addition to systemic lupus erythematosus (SLE).

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Alzheimer’s disease community from our Head of Research and Development, Alfred Sandrock, M.D., Ph.D.

The Pharma Data

We believe patients, family members and physicians deserve the facts about the therapy and the process by which it was approved so they may make informed decisions. We believe that this will be further established as we collect more data from the ongoing EMBARK study and the post-marketing confirmatory trial.

Disease 52
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Women in Stem with Andrea Pfeifer

Drug Target Review

On my return to Europe, I took a position at Nestlé as Head of the Research Centre, where I led the scientific development of several highly innovative health promoting food products from laboratory to market. Then I was approached to co-found AC Immune in 2003. COVID-19 has shown the revolutionary impact of vaccines.

Disease 95
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U.S. FDA ACCEPTS FOR PRIORITY REVIEW

The Pharma Data

FDA ACCEPTS FOR PRIORITY REVIEW PFIZER’S APPLICATION FOR TICOVAC (TICK-BORNE ENCEPHALITIS VACCINE). If approved, the vaccine may help reduce the risk of TBE for people traveling to endemic areas, potentially including military personnel serving in these locations. 1,2 If approved, TicoVac would be the first vaccine in the U.S.

FDA 52
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Nirsevimab demonstrated protection against respiratory syncytial virus disease in healthy infants in Phase 3 trial

The Pharma Data

In contrast to other options for RSV under development, such as maternal vaccines, nirsevimab was designed to be administered at birth to infants born during the RSV season or at the season’s start for infants born prior to the season. We prevent illness with vaccines, provide innovative treatments to fight pain and ease suffering.

Virus 40
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Muscle Imbalances RevealedMuscle Imbalances Revealed

The Pharma Data

Clients who get results will rave about your skills and nothing beats word of mouth marketing. Nutritional Therapy Practitioner. 2003 ACE Personal Trainer of the Year. ve built a six figure business by providing great service to my clients. This course will help you do that. Curb Ivanic, MS, CSCS. Jeff Salzenstein. Stephen Holt.