Alessa Therapeutics announces FDA fast track designation for Enolen, a first of its kind treatment for localised prostate cancer

8 January 2026 - Alessa Therapeutics today announced that the US FDA has granted fast track designation for Enolen, the ...

Read more →

Bayer receives breakthrough therapy designation in the US and China for sevabertinib as a first-line treatment for patients with HER2-mutant non-small cell lung cancer

6 January 2026 - Bayer receives breakthrough therapy designation in the US and China for sevabertinib as a first-line treatment for ...

Read more →

Protara Therapeutics receives both FDA breakthrough therapy and fast track designations for TARA-002 in paediatric patients with lymphatic malformations

5 January 2026 - Protara Therapeutics today announced that the US FDA has granted both breakthrough therapy and fast track designations ...

Read more →

FDA approves Roche’s Lunsumio Velo for subcutaneous use in relapsed or refractory follicular lymphoma

22 December 2025 - Approval supported by data demonstrating compelling complete response rate in third-line or later follicular lymphoma, which ...

Read more →

Enhertu granted breakthrough therapy designation in the US as post-neo-adjuvant therapy for patients with HER2 positive early breast cancer

22 December 2025 - Tenth breakthrough therapy designation for Daiichi Sankyo and AstraZeneca’s Enhertu with the latest based on DESTINY-Breast05 ...

Read more →

Alphamab Oncology announces biparatopic HER2 targeting ADC JSKN003 was granted breakthrough therapy designation by the FDA for the treatment of PROC

20 December 2025 - Alphamab Oncology announced that the biparatopic HER2 targeting antibody drug conjugate JSKN003, independently by the US FDA ...

Read more →

BeOne Medicines granted US FDA fast track designation for BGB-B2033 as treatment for hepatocellular carcinoma

18 December 2025 - BGB-B2033 is a bispecific antibody directed at GPC3 and 4-1BB; key targets in the most common liver ...

Read more →

FDA approves amivantamab and hyaluronidase-lpuj for subcutaneous injection

17 December 2025 - Today, the FDA approved amivantamab and hyaluronidase-lpuj (Rybrevant Faspro, Janssen Biotech) for subcutaneous injection for adult ...

Read more →

FDA grants regular approval to rucaparib for metastatic castration-resistant prostate cancer

17 December 2025 - Today, the FDA approved rucaparib (Rubraca, pharmaand) for adults with a deleterious BRCA mutation (germline and/or ...

Read more →

Palvella Therapeutics granted FDA fast track designation for Qtorin 3.9% rapamycin anhydrous gel for the treatment of angiokeratomas

16 December 2025 - Angiokeratomas are characterised by lymphatic-derived skin lesions that can persistently bleed and significantly impact quality of ...

Read more →

Adagene announces FDA fast track designation for muzastotug (ADG126)

16 December 2025 - Adagene today announced that the US FDA has designated muzastotug, in combination with Merck’s anti-PD-1 therapy, Keytruda ...

Read more →

Tecvayli and Darzalex Faspro combination selected for Commissioner’s National Priority Voucher Pilot program

15 December 2025 - We are pleased the US FDA has selected the teclistamab MajesTEC-3 supplemental biologics license application to participate ...

Read more →

FDA approves fam-trastuzumab deruxtecan-nxki with pertuzumab for unresectable or metastatic HER2-positive breast cancer

15 December 2025 - Today, the FDA approved fam-trastuzumab deruxtecan-nxki (Enhertu, Daiichi Sankyo) in combination with pertuzumab for the first-line ...

Read more →

FDA approves niraparib and abiraterone acetate plus prednisone for BRCA2-mutated metastatic castration-sensitive prostate cancer

12 December 2025 - Today, the FDA approved niraparib and abiraterone acetate (Akeega, Janssen Biotech) with prednisone for adults with ...

Read more →

US FDA grants priority review to Bristol Myers Squibb's application for Opdivo (nivolumab) plus chemotherapy combination for classical Hodgkin's lymphoma

11 December 2025 - Bristol Myers Squibb today announced that the US FDA has accepted and granted priority review to ...

Read more →