US FDA approves subcutaneous administration of Takeda’s Entyvio (vedolizumab) for maintenance therapy in moderately to severely active Crohn’s disease

19 April 2024 - Entyvio is now available in the US in both intravenous and subcutaneous administrations for maintenance treatment ...

Read more →

Lumicell’s cutting-edge imaging platform receives historic FDA approval to illuminate residual breast cancer

18 April 2024 - Lumisight and Lumicell DVS previously received FDA fast track and breakthrough device designations, respectively. ...

Read more →

AskBio receives FDA fast track designation for AB-1002 investigational gene therapy program in congestive heart failure

18 April 2024 - AB-1002 is being studied for the treatment of adults with non-ischaemic cardiomyopathy and New York Heart Association ...

Read more →

FDA approves Genentech's Alecensa as first adjuvant treatment for people with ALK positive early stage lung cancer

18 April 2024 - Approval based on Phase 3 ALINA study showing Alecensa reduced the risk of disease recurrence or death ...

Read more →

Alvotech and Teva announce US FDA Approval of Selarsdi (ustekinumab-aekn), biosimilar to Stelara (ustekinumab)

16 April 2024 - Selarsdi is expected to be marketed in the US on or after 21 February 2025, following a ...

Read more →

Lexeo Therapeutics granted FDA fast track designation for LX2006, an AAV based gene therapy candidate for the treatment of Friedreich’s ataxia cardiomyopathy

16 April 2024 - Lexeo Therapeutics today announced the US FDA has granted fast track designation to LX2006, the company’s AAVrh.10hFXN ...

Read more →

GSK’s 5 in 1 meningococcal ABCWY vaccine candidate accepted for regulatory review by US FDA

16 April 2024 - Submission based on results from pivotal Phase III trial showing all primary outcomes met. ...

Read more →

TLX101-CDx (Pixclara) granted FDA fast track designation

16 April 2024 - Telix Pharmaceuticals today announces that the US FDA has granted fast track designation for the Company's investigational ...

Read more →

PureTech receives FDA fast track designation for LYT-200 in head and neck cancers

11 April 2024 - LYT-200 is being evaluated in locally advanced/metastatic solid tumours, including head and neck cancers, as well as ...

Read more →

Fasenra approved for treatment of children aged 6 to 11 with severe asthma

11 April 2024 - AstraZeneca’s Fasenra (benralizumab) is now approved by the US FDA for add-on maintenance treatment for patients ...

Read more →

AdrenoMed receives FDA fast track designation for enibarcimab for treatment of septic shock

10 April 2024 - AdrenoMed today announced that the US FDA has granted fast track designation to its lead product candidate ...

Read more →

FDA accepts filing of new drug application for nalmefene auto-injector for the treatment of known or suspected opioid overdose

8 April 2024 - Purdue Pharma announced today that FDA has accepted for filing the company’s new drug application for the ...

Read more →

Lundbeck and Otsuka submit sNDA for FDA review of brexpiprazole and sertraline combination as potential treatment for PTSD

9 April 2024 - Lundbeck and Otsuka have submitted a supplemental new drug application for US FDA review of brexpiprazole ...

Read more →

Syros receives fast track designation from the FDA for tamibarotene for the treatment of newly diagnosed unfit AML with RARA gene over-expression

9 April 2024 - Syros Pharmaceuticals today announced that the US FDA has granted fast track designation to tamibarotene in ...

Read more →

Using effect scores to characterise heterogeneity of treatment effects

9 April 2024 - It is common for treatments to yield different outcomes in different patients. If patient characteristics that predict ...

Read more →