FDA approval of Leqembi subcutaneous formulation charts path to combination therapies for Alzheimer's disease

29 August 2025 - Subcutaneous delivery increases accessibility and introduces potential for at home administration, following model of diabetes and ...

Read more →

High dose regimen of nusinersen receives positive CHMP opinion for the treatment of spinal muscular atrophy

17 November 2025 - Positive CHMP opinion is based on data from the DEVOTE study which evaluated the high dose regimen ...

Read more →

Henlius and Organon announce US FDA approval of Poherdy (pertuzumab-dpzb), the first Perjeta (pertuzumab) biosimilar in the US

17 November 2025 - Shanghai Henlius Biotech and Organon today announced that the US FDA has approved the biologics license application ...

Read more →

Celcuity announces completion of submission of its new drug application to the US FDA for gedatolisib in HR+/HER2-/PIK3CA wild type advanced breast cancer

17 November 2025 - Celcuity today announced the completion of the submission of its new drug application to the US FDA ...

Read more →

FDA grants fast track designation to Dewpoint Therapeutics’ DPTX3186 for the treatment of gastric cancer

17 November 2025 - Dewpoint Therapeutics announced today that the US FDA has granted fast track designation to DPTX3186, the company’s ...

Read more →

Business Council urges unlocking ‘Aladdin's cave’ of Medicare data to save lives, health system

17 November 2025 - Unlocking an “Aladdin’s cave” of Medicare data is the key to saving Australia’s celebrated health system ...

Read more →

Ascelia Pharma announces FDA acceptance of Orviglance new drug application for review

15 November 2025 - Ascelia Pharma today announced that the US FDA has accepted the new drug application for Orviglance for ...

Read more →

FDA’s new plausible mechanism pathway

12 November 2025 - Personalised therapies hold tremendous promise but challenge traditional models of drug and biologic development.  ...

Read more →

CHMP positive opinion for Waskyra, a gene therapy for the treatment of Wiskott-Aldrich syndrome

14 November 2025 - Fondazione Telethon announces the positive opinion issued by the CHMP of the EMA, recommending marketing authorisation in ...

Read more →

Highlights from the 10-13 November 2025 CHMP meeting

14 November 2025 - The  EMA’s CHMP recommended ten medicines for approval at its November 2025 meeting. ...

Read more →

Sanofi’s Teizeild recommended for EU approval by the CHMP for patients with stage 2 type 1 diabetes

14 November 2025 - The EMA’s CHMP has adopted a positive opinion recommending the approval of Teizeild (teplizumab) to delay ...

Read more →

Sarepta announces FDA’s approval of updated Elevidys Prescribing Information

14 November 2025 - Sarepta Therapeutics today announced an update to the prescribing information for Elevidys (delandistrogene moxeparvovec-rokl), the only ...

Read more →

Outcome statement - DUSC October 2025 meeting

14 November 2025 - The outcome statement from the October 2025 DUSC meeting is now available. ...

Read more →

Public Summary Documents (first time decisions not to recommend and deferrals) – July 2025 PBAC meeting

14 November 2025 - The Public Summary Documents (first time decisions not to recommend and deferrals) from the July 2025 PBAC ...

Read more →

Outlook Therapeutics announces acceptance of biologics license application by FDA for ONS-5010 as a treatment for wet AMD

13 November 2025 -  Outlook Therapeutics today announced that the US FDA has acknowledged receipt of the resubmission of the ...

Read more →

Arcutis Canada announces Health Canada approval of Zorvye 0.3% topical foam, the first steroid-free topical foam for scalp and body psoriasis, for adults and adolescents ages 12 and older

13 November 2025 - Approval supported by pivotal Phase 3 and Phase 2 data demonstrating rapid improvement in skin clearance and ...

Read more →