FDA grants fast track designation to Spinogenix's SPG601 for treatment of Fragile X syndrome, a common inherited form of autism

13 January 2025 - -- Spinogenix today announced that the US FDA has granted fast track designation to SPG601 for the ...

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Datopotamab deruxtecan granted priority review in the US for patients with previously treated advanced EGFR mutated non-small cell lung cancer

13 January 2025 - Application based on TROPION-Lung05 Phase 2 trial and supported by data from TROPION-Lung01 Phase 3 and ...

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GSK’s Shingrix new pre-filled syringe presentation accepted for review by US FDA

10 January 2025 - An FDA decision on the application is expected by 20 June 2025. ...

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Bayer submits application to US FDA and to China’s CDE for new indication of finerenone for patients with common form of heart failure with high unmet medical need

10 January 2025 - Regulatory submissions are based on positive data from the Phase 3 FINEARTS-HF study recently presented at ESC ...

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Important milestone for Biotest: biologics license application for fibrinogen submitted to the US FDA

9 January 2025 - The biologics license application for Biotest’s fibrinogen has been submitted to the US FDA.  ...

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Vanda's letter to FDA Commissioner highlights faulty gastroparesis NDA review

 8 January 2025 - Vanda Pharmaceuticals letter to FDA Commissioner highlights faulty gastroparesis NDA review. ...

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BridgeBio Oncology Therapeutics granted US FDA fast track designation for BBO-8520 for KRASG12C mutated metastatic non-small cell lung cancer

9 January 2025 - The US FDA has granted fast track designation to BBO-8520 for the treatment of adult patients with ...

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Mersana Therapeutics announces additional FDA fast track designation granted to emiltatug ledadotin (XMT-1660)

10 January 2025 - Mersana Therapeutics today announced the US FDA recently granted an additional fast track designation to XMT-1660. ...

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ViGeneron announces FDA rare paediatric disease designation for VG901

8 January 2025 - ViGeneron today announced two important milestones for its novel gene therapy candidate VG901, to treat patients ...

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Nipocalimab granted US FDA priority review for the treatment of generalized myasthenia gravis

9 January 2024 - Biologics license application acceptance supported by results from the Phase 3 Vivacity-MG3 study. ...

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FDA accepts Agios’ supplemental new drug application for Pyrukynd (mitapivat) in adult patients with non-transfusion-dependent and transfusion-dependent alpha- or beta-thalassemia

8 January 2025 - Agios Pharmaceuticals today announced that the US FDA accepted the company’s supplemental new drug application for Pyrukynd ...

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PureTech receives FDA fast track designation for LYT-200 in acute myeloid leukaemia

9 January 2024 - Single agent and combination data from Phase 1b AML/MDS trial presented at ASH 2024 showed potential of ...

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CDER brings many safe and effective therapies to patients and consumers in 2024

8 January 2024 - Each year, the US FSA’s Center for Drug Evaluation and Research (CDER) evaluates and, as appropriate, approves ...

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Marengo’s first in class invikafusp alfa (STAR0602) receives US FDA fast track designation for treatment of unresectable, locally advanced, or metastatic colorectal cancers with high tumour mutational burden

8 January 2025 - Initial safety and efficacy data from Phase 1 STARt-001 trial showed promising single agent clinical activity ...

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Johnson & Johnson’s posdinemab and tau active immunotherapy receive US FDA fast track designations for the treatment of Alzheimer’s disease

8 January 2025 - Building on decades of the Company’s Alzheimer’s research, two differentiated investigational therapies aim to slow pathological tau ...

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