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FDA approves Welireg (belzutifan) to treat advanced, unresectable, or metastatic pheochromocytoma and paraganglioma – Merck Inc

Written by | 16 Jul 2025

Merck Inc., (known as MSD outside of the United States and Canada), announced the FDA  has accepted for priority review a supplemental new drug application (sNDA) seeking approval… read more.

Positive CHMP opinion for Bosulif (bosutinib) on variation to marketing authorisation to extend the use of Bosulif to children aged 6 years and older – Pfizer

Written by | 11 Jul 2025

The Committee for Medicinal Products for Human Use (CHMP) of the EMA adopted a positive opinion, recommending a change to the terms of the marketing authorisation for Bosulif…. read more.

Blenrep (belantamab mafodotin) combinations approved by UK MHRA in relapsed/refractory multiple myeloma – GSK

Written by | 7 Jul 2025

GSK plc announced the authorisation of Blenrep by the Medicines and Healthcare products Regulatory Agency (MHRA). In the UK, Blenrep is approved for the treatment of adults with… read more.

New study results reinforce Tagrisso as the backbone therapy for EGFR-mutated lung cancer across stages and settings – AstraZeneca

Written by | 3 Jul 2025

New study results presented at the European Lung Cancer Congress (ELCC) 2025 demonstrate the role of AstraZeneca’s Tagrisso (osimertinib), as monotherapy and as the backbone for novel combinations,… read more.

Exploring how diet and the gastric microbiome shape gastric cancer risk

Written by | 2 Jul 2025

Gastric cancer (GC), commonly known as stomach cancer, ranks as the world’s fifth most common cancer and the third leading cause of cancer-related deaths, claiming over 784,000 lives… read more.

CHMP recommends EU approval of Itovebi for PIK3CA-mutated, ER-positive, HER2-negative, advanced breast cancer – Roche

Written by | 2 Jul 2025

Roche announced today that the EMA’s Committee for Medicinal Products for Human Use (CHMP) has adopted a positive opinion for Itovebi (inavolisib), in combination with palbociclib (Ibrance) and… read more.

Datroway (datopotamab deruxtecan) is approved in Japan as the first TROP-2 directed therapy for patients with HR positive, HER2 negative breast cancer – Daiichi Sankyo

Written by | 30 Jun 2025

Daiichi Sankyo’s Datroway (datopotamab deruxtecan) has been approved in Japan for the treatment of adult patients with hormone receptor (HR) positive, HER2 negative (IHC 0, IHC 1+ or… read more.

EMA Annual Report: 114 new medicines in 2024

Written by | 27 Jun 2025

The European Medicines Agency (EMA) – the EU’s drug safety watchdog – approved 114 medicines last year, with 46 of these having a new active substance which had… read more.

Cancer screenings continue years after guidelines change to limit unnecessary tests, study finds

Written by | 17 Jun 2025

Stopping the widespread use of unnecessary, potentially even harmful, cancer screenings can take up to 13 years and potentially even longer after new guidelines are put in place, according… read more.

Bristol Myers Squibb to share major Breyanzi updates at ICML 2025

Written by | 17 Jun 2025

BMS announced the first disclosure of the primary analysis results of the marginal zone lymphoma (MZL) cohort of TRANSCEND FL, an open-label, global, multicenter, Phase II, single-arm study… read more.

NICE (UK) recommends Adcetris (brentuximab vedotin) in combination for untreated stage 3 or 4 CD30-positive Hodgkin lymphoma – Takeda

Written by | 16 Jun 2025

NICE(UK): Brentuximab vedotin plus doxorubicin, dacarbazine and vinblastine is recommended, within its marketing authorisation, as an option for untreated stage 3 or 4 CD30‑positive Hodgkin lymphoma in adults. It can… read more.

Program helps cancer survivors return to work with confidence

Written by | 13 Jun 2025

A new pilot project led by McGill University researchers is showing early success in helping cancer survivors return to work, addressing an aspect of recovery they say is… read more.

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