Pharmaceutical

Roche records 4% decline in H1 2024 net income

Roche has reported a net income of SFr6.6bn ($7.4bn) in H1 2024, a 4% decline co...

Mankind Pharma acquires Bharat Serums and Vaccines for ...

Mankind Pharma has announced a definitive agreement for the acquisition of Bhara...

AbbVie’s Q2 2024 net earnings drop to $1.37bn

AbbVie has reported a 32.1% decrease in net earnings attributable to the company...

EC conditionally approves Pfizer’s haemophilia B gene t...

The European Commission has awarded conditional marketing authorisation for Pfiz...

FDA committee proposes overhaul of perioperative lung c...

The ODAC highlighted that perioperative trials should separately evaluate the ef...

EMA backs Wegovy cardiovascular label update as Novo se...

The EMA recommended a label update that allows the drug to be used to reduce car...

FDA approves Sun Pharma’s JAK inhibitor for alopecia

The FDA approval is based on data gathered from two Phase III studies where over...

Bavarian Nordic wins positive CHMP opinion to amend Imv...

The current approval, which is based on data from non-human primates and healthy...

MHRA approves Pfizer-BioNTech’s Comirnaty JN.1 vaccine

The UK MHRA has authorised Pfizer-BioNTech’s adapted Comirnaty vaccine against t...

BioAtla receives FDA fast track designation for ozurift...

The Phase II antibody drug conjugate received FDA fast track designation against...

The potential of 3D printing in drug development and de...

3D printing is replacing traditional prototype development approaches across var...

AC Immune wins FDA fast track for Alzheimer’s vaccine c...

JNJ-2056 is being investigated in the Phase IIb ReTain study which enrols partic...

Ipsen outlines $461m for ex-US rights to Day One’s glio...

Ipsen will pay $111m in cash and equity upfront to gain the global rights, exclu...

Sandoz launches ustekinumab biosimilar in Europe 

Sandoz launched the biosimilar of J&J’s Stelara in Europe in partnership with Sa...

ConSynance wins FDA designation for Prader-Willi syndro...

A Phase II study for ConSynance’s triple monoamine reuptake inhibitor CSTI-500 i...

FDA agrees wider use of BioMarin’s BRINEURA for CLN2

The US FDA has expanded approval to BioMarin Pharmaceutical's BRINEURA to includ...