FDA approves erdafitinib for locally advanced or metastatic urothelial carcinoma

19 January 2024 - Today, the FDA approved erdafitinib (Balversa, Janssen Biotech) for adult patients with locally advanced or metastatic ...

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Verastem Oncology granted fast track designation for combination of avutometinib and sotorasib for the treatment of KRAS G12C mutant non-small-cell lung cancer

18 January 2024 - On-going RAMP 203 trial assessing a more complete vertical blockade with RAF/MEK and KRAS G12C inhibition along ...

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European Commission approves Roche’s Tecentriq SC, the EU's first PD-(L)1 cancer immunotherapy subcutaneous injection for multiple cancer types

16 January 2024 - Roche is working closely with national health systems in Europe to ensure patients can access Tecentriq ...

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Nurix Therapeutics receives US FDA fast track designation for NX-5948 for the treatment of relapsed or refractory CLL and SLL

16 January 2024 - Fast track designation follows positive Phase 1 data presented at the American Society of Hematology that supports ...

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RemeGen's RC88 obtained FDA fast track designation, heralds new hope for ovarian cancer patients

12 January 2024 - RemeGen announced recently that its independently developed mesothelin targeting antibody drug conjugate RC88 has been granted fast ...

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Shorla Oncology announces FDA filing acceptance of new drug application for novel formulation to treat breast and ovarian cancer

9 January 2024 - Shorla Oncology announced today that the US FDA has accepted for review the company’s new drug application ...

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FDA approves pembrolizumab with chemoradiotherapy for FIGO 2014 stage III-IVA cervical cancer

15 January 2024 - On 12 January 2024, the FDA approved pembrolizumab (Keytruda) with chemoradiotherapy for patients with FIGO 2014 stage ...

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European Commission approves Krazati (adagrasib) as a targeted treatment option for patients with advanced non-small-cell lung cancer with a KRAS G12C mutation

10 January 2024 - Mirati Therapeutics today announced that the European Commission granted conditional marketing authorisation for Krazati (adagrasib) as ...

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Tivdak supplemental biologics license application accepted for priority review by FDA for patients with recurrent or metastatic cervical cancer

9 January 2024 - Submission based on positive results from global Phase 3 study demonstrating overall survival benefit of TIVDAK ...

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European Commission approves Pfizer’s Talzenna in combination with Xtandi for adult patients with metastatic castration resistant prostate cancer

8 January 2024 - Talzenna is the first and only PARP inhibitor approved in combination with standard of care Xtandi ...

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Sellas Life Sciences receives FDA fast track designation for SLS009 for treatment of relapsed/refractory acute myeloid leukaemia

9 January 2024 - Sellas Life Sciences Group today announced that the US FDA has granted fast track designation to SLS009 ...

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Astellas provides update on zolbetuximab biologics license application in US

8 January 2024 - Astellas Pharma today announced the US FDA issued a complete response letter on 4 January 2024, ...

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ProfoundBio announces rinatabart sesutecan FDA fast track designation for patients with advanced ovarian cancer

5 January 2023 - ProfoundBio today announced that the US FDA has granted fast track designation for rinatabart sesutecan (Rina-S; ...

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European Medicines Agency validates Bristol Myers Squibb’s application for repotrectinib for the treatment of locally advanced or metastatic ROS1 positive non-small cell lung cancer and NTRK positive solid tumours

2 January 2024 - Application based on data from the registrational TRIDENT-1 and CARE trials showing robust responses and durable activity ...

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Imaging Biometrics granted FDA fast track

19 December 2023 - Imaging Biometrics is pleased to announce that the US FDA has granted fast track designation for oral ...

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