Intercept announces voluntary withdrawal of Ocaliva for primary biliary cholangitis from the US market

11 September 2025 -  Intercept Pharmaceuticals today announced its decision to voluntarily withdraw Ocaliva (obeticholic acid) from the US market ...

Read more →

Sanofi’s SAR402663 earns fast track designation in the US for neovascular age-related macular degeneration

11 September 2025 - Designation earned for a one time intravitreal gene therapy with the potential to eliminate treatment burden for ...

Read more →

FDA files Corcept’s new drug application for relacorilant as a treatment for patients with platinum-resistant ovarian cancer

10 September 2025 - Corcept Therapeutics today announced that the US FDA has accepted Corcept’s new drug application for relacorilant as ...

Read more →

Greenwich LifeSciences’ GLSI-100 granted US FDA fast track designation

10 September 2025 - Greenwich LifeSciences today announced that FDA has granted fast track designation for GLSI-100 in the HLA-A*02 patient ...

Read more →

FDA approves selumetinib for pediatric patients 1 year of age and older with neurofibromatosis type 1 with symptomatic, inoperable plexiform neurofibromas

10 September 2025 - Today, the FDA approved selumetinib (Koselugo, AstraZeneca Pharmaceuticals) granules and capsules for paediatric patients 1 year ...

Read more →

FDA accepts biologics license application for Sobi's NASP for patients with uncontrolled gout

10 September 2025 - Sobi today announced that the US FDA has accepted the biologics license application seeking approval for Nanoecapsulated ...

Read more →

US FDA approval of Inlexzo (gemcitabine intravesical system) set to transform how certain bladder cancers are treated

9 September 2025 - First and only drug releasing system to provide extended local delivery of a cancer medication into the ...

Read more →

Teva’s emrusolmin granted US FDA fast track designation for treatment of multiple system atrophy

9 September 2025 - Teva Pharmaceuticals today announced that the US FDA granted fast track designation for Teva’s investigational therapy emrusolmin ...

Read more →

FDA grants fast track designation to NS-229 for the treatment of eosinophilic granulomatosis with polyangiitis

9 September 2025 - NS Pharma, a subsidiary of Nippon Shinyaku, announced today that the US FDA has granted fast track ...

Read more →

Ionis receives US FDA breakthrough therapy designation for ION582 in Angelman syndrome

9 September 2025 - Pivotal Phase 3 REVEAL study enrollment on track to complete in 2026. ...

Read more →

ICER releases draft evidence report on treatments for obesity

9 September 2025 - Public comment period now open until 6 October 2025; requests to make oral comment during public ...

Read more →

FDA approves gemcitabine intravesical system for non-muscle invasive bladder cancer

9 September 2025 - Today, the FDA approved gemcitabine intravesical system (Inlexzo, Janssen) for adults with Bacillus Calmette-Guérin unresponsive non-muscle ...

Read more →

Revisiting the FDA’s accelerated approval pathway

8 September 2025 - After aducanumab’s accelerated approval for Alzheimer's disease, and prompted by long standing concerns regarding the accelerated approval pathway ...

Read more →

Saol Therapeutics receives complete response letter from FDA for SL1009 (DCA) for the treatment of pyruvate dehydrogenase complex feficiency

8 September 2025 - Saol is seeking a path forward with the FDA that does not require an additional trial ...

Read more →

ICER publishes evidence report on treatment for non-cystic fibrosis bronchiectasis

8 September 2025 - There are significant uncertainties regarding long term efficacy of brensocatib; ICER estimates that treatment would achieve ...

Read more →