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Late-Breaking Data from First Head-to-Head Study Comparing Dysport and Botox in Adults with Upper Limb Spasticity – Ipsen

Written by | 3 Jun 2026

Ipsen announced results from the only prospective, head-to-head Phase IV DIRECTION trial comparing Dysport (abobotulinumtoxinA) to Botox (onabotulinumtoxinA) in adults living with upper limb spasticity (ULS) will be presented as a late-breaking presentation… read more.

Could shorter working hours cut obesity rates?

Written by | 2 Jun 2026

People who work fewer hours each year appear to have a lower risk of obesity, according to an Australian study presented at the European Congress on Obesity in… read more.

EMA approves eight new medicines

Written by | 2 Jun 2026

The EU drug watchdog, the European Medicines Agency (EMA), has given the green light for eight new medicines at its May meeting. This brings to 36 the number… read more.

CHMP positive for Maviret (glecaprevir/pibrentasvir) to treat acute Hepatitis C – Abbvie

Written by | 2 Jun 2026

AbbVie has announced that the European Medicines Agency’s Committee for Medicinal Products for Human Use (CHMP) adopted a positive opinion recommending the approval of Maviret  (glecaprevir/pibrentasvir), an oral… read more.

Rich countries on course to eliminate cervical cancer

Written by | 1 Jun 2026

The path to wiping out cervical cancer looks increasingly clear – at least for high-income countries with strong uptake of the human papillomavirus (HPV) vaccine and cervical screening…. read more.

EU drug watchdog shortlisted for Ombudsman Award

Written by | 1 Jun 2026

The European Medicines Agency (EMA) has been nominated for the European Ombudsman Award for Good Administration. The Agency’s One Health Instagram account is shortlisted in the ‘Excellence in… read more.

Atea Pharmaceuticals Presents New Drug-Drug Interaction Results Supporting Potential Best-in-Class Profile of the Regimen of Bemnifosbuvir and Ruzasvir for the Treatment of Hepatitis C Virus at EASL Congress 2026

Written by | 1 Jun 2026

Atea Pharmaceuticals, Inc. (Nasdaq: AVIR) (Atea or Company), a late-stage clinical biopharmaceutical company engaged in the discovery and development of oral antiviral therapeutics for serious viral diseases, today… read more.

European Commission approves Hympavzi (marstacimab) for the treatment of adults and adolescents with Hemophilia A or B with inhibitors – Pfizer

Written by | 1 Jun 2026

Pfizer announced that the European Commission has granted marketing authorization to expand the approved indication for Hympavzi (marstacimab) to include patients 12 years of age and older weighing… read more.

Congenital heart defects raise risk of early heart attack

Written by | 31 May 2026

People born with heart defects experience their first acute heart attack at a significantly earlier age than others, according to a new national study from Lund University in… read more.

EMA launches vaccine information initiative

Written by | 31 May 2026

The European Medicines Agency (EMA) has unveiled a new communications effort designed to inform evidence-based decision-making. Vaccine Essentials offers healthcare professionals accessible summaries of how the quality, safety… read more.

New late-breaking data reinforces IQIRVO®’s impact on ALP, fatigue and pruritus in PBC

Written by | 31 May 2026

Ipsen announced the presentation of new late-breaking results from the ELATIVE® Phase III trial and two real-world studies at the European Association for the Study of the Liver (EASL)… read more.

CHMP issues positive opinion for Jascayd (nerandomilast) bringing a new IPF and PPF therapy closer to patients in the EU – Boehringer Ingelheim

Written by | 31 May 2026

Boehringer Ingelheim’s Jascayd (nerandomilast) has been recommended for marketing authorization by the Committee for Medicinal Products for Human Use (CHMP) of the European Medicines Agency for the treatment… read more.

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