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AZD 1222 US Phase III primary analysis confirms safety and efficacy for prevention of COVID-19 – AstraZeneca

Written by | 27 Mar 2021

Positive high-level results from the primary analysis of the Phase III trial of AZD 1222 in the US have confirmed vaccine efficacy consistent with the pre-specified interim analysis… read more.

AbbVie announces extension of review for supplemental NDA of upadacitinib to treat psoriatic arthritis

Written by | 26 Mar 2021

AbbVie announced that the FDA has extended the review period for the supplemental New Drug Application (sNDA) for upadacitinib in the treatment of adult patients with active psoriatic… read more.

Real world evidence from Israeli Ministry of Health analysis confirms high effectiveness of the Pfizer-BioNTech COVID 19 vaccine

Written by | 24 Mar 2021

The Israel Ministry of Health (MoH), Pfizer Inc. and BioNTech SE announced real-world evidence demonstrating dramatically lower incidence rates of COVID-19 disease in individuals fully vaccinated with the… read more.

UK and EU regulatory agencies confirm COVID-19 Vaccine AstraZeneca is safe and effective

Written by | 22 Mar 2021

The Medicines Health Regulatory Authority (MHRA) and European Medicines Agency (EMA) reaffirmed the benefits of COVID-19 Vaccine AstraZeneca continue to far outweigh the risks.

Allarity Therapeutics initiates phase II trial of Ixempra in Europe for the treatment of metastatic breast cancer

Written by | 21 Mar 2021

Allarity Therapeutics A/S announced that it has enrolled the first patient in its European Phase II clinical trial of Ixempra (ixabepilone) for the treatment of metastatic breast cancer.

Lupin will partner with Endoceutics to commercialise Intrarosa for postmenopausal vulvovaginal atrophy in Canada

Written by | 20 Mar 2021

Lupin Pharma, a subsidiary of global pharma major Lupin Ltd, announced a partnership with Endoceutics, a women’s health focused innovative Canadian biotech company, to commercialize Intrarosa in Canada.

FDA approves Kimyrsa to treat acute bacterial skin and skin structure infections (ABSSSI) – Melinta Therapeutics

Written by | 19 Mar 2021

Melinta Therapeutics, LLC announced that the FDA has approved Kimyrsa (oritavancin) for the treatment of adult patients with acute bacterial skin and skin structure infections (ABSSSI) caused by… read more.

Interim SAGE/WHO recommendation supporting the use of the Johnson & Johnson COVID-19 Vaccine

Written by | 18 Mar 2021

Johnson & Johnson welcomes the interim recommendation by the Strategic Advisory Group of Experts (SAGE) on Immunization for the World Health Organization (WHO) supporting the use of Johnson… read more.

EU grants conditional approval for single-dose COVID-19 vaccine JNJ 78436735 – Johnson & Johnson

Written by | 18 Mar 2021

Johnson & Johnson announced that the European Commission (EC) has granted a Conditional Marketing Authorization (CMA) for its single-dose COVID-19 vaccine JNJ 78436735, developed by the Janssen Pharmaceutical… read more.

Health Canada approves COVID 19 AstraZeneca vaccine to prevent COVID-19

Written by | 17 Mar 2021

Health Canada has approved the Oxford-AstraZeneca COVID-19 vaccine (ChAdOx1 nCoV-19) and a related shot by the Serum Institute of India for use in Canada.

Update on the safety of COVID-19 Vaccine AstraZeneca

Written by | 16 Mar 2021

Following a recent concern raised around thrombotic events, AstraZeneca would like to offer its reassurance on the safety of its COVID-19 vaccine based on clear scientific evidence. Safety… read more.

FDA approves Azstarys to treat attention deficit hyperactivity disorder – Kem Pharma Inc

Written by | 15 Mar 2021

KemPharm, Inc. has announced that the FDA has approved the New Drug Application for Azstarys (formerly referred to as KP 415), a once-daily product for the treatment of… read more.

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