Agitated Solutions receives fast track designation for investigational drug ASI-02

23 October 2025 - ASI-02 is a novel contrast agent for cardiac bubble studies. ...

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Azurity Pharmaceuticals announces the FDA approval of Ferabright (ferumoxytol injection), the first and only iron-based contrast agent indicated for magnetic resonance imaging of the brain

17 October 2025 - Azurity Pharmaceuticals announced today that the US FDA has approved Ferabright (ferumoxytol injection), the first and only ...

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Roche's Elecsys pTau181 becomes the only FDA cleared blood test for use in primary care to rule out Alzheimer's related amyloid pathology

13 October 2025 - Roche today announced that the US FDA has cleared its Elecsys pTau181 test, the only blood ...

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Telix provides regulatory update on TLX250-CDx

28 August 2025 - Telix Pharmaceuticals today announces that it has received a complete response letter from the US FDA ...

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Gadoquatrane new drug application accepted for review by US FDA

26 August 2025 - Bayer today announced that a new drug application for its investigational contrast agent gadoquatrane has been accepted ...

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Thermo Fisher receives FDA approval for NGS based companion diagnostic for new non-small cell lung cancer treatment

11 August 2025 - Thermo Fisher Scientific has received approval from the US FDA for its Oncomine Dx Target Test as ...

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Bayer files for EU approval of gadoquatrane

10 July 2025 - Submission of marketing authorization application to the EMA seeking approval for investigational low dose gadoquatrane for contrast-enhanced ...

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FDA approves updated label for Lilly’s Amyvid (florbetapir F 18 injection) to support diagnosis of Alzheimer’s disease in patients

25 June 2025 -  Eli Lilly announced that the US FDA has approved a label update for Amyvid (florbetapir F ...

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Bayer files for approval of gadoquatrane in the US

17 June 2025 - Bayer today announced the submission of a new drug application to the US FDA for its ...

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Radiopharm Theranostics granted US FDA fast track designation for RAD101 imaging in brain metastases

11 June 2025 - Radiopharm Theranostics today announced that the US FDA has granted fast track designation for RAD101 to ...

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FDA clears first blood test used in diagnosing Alzheimer’s disease

16 May 2025 - New test provides less invasive option, reduces reliance on PET scans and increases diagnosis accessibility. ...

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Roche granted FDA breakthrough device designation for first AI-driven companion diagnostic for non-small cell lung cancer

29 April 2025 - The VENTANA TROP2 (EPR20043) RxDx device is an immunohistochemistry assay combined with a digital pathology algorithm to ...

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Telix provides regulatory update on TLX101-CDx

28 April 2028 - Telix Pharmaceuticals today announces that it has received a complete response letter from the US FDA ...

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World first as MHRA approves trofolastat for diagnostic imaging of prostate cancer in men

28 March 2025 - The MHRA has approved trofolastat (RoTecPSMA), the first prostate-specific membrane antigen (PSMA)-targeting product authorised for use with ...

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FDA approves new prostate cancer imaging agent Gozellix

21 March 2025 - Telix Pharmaceuticals today announces that the US FDA has approved its new drug application for Gozellix ...

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