MSAC publishes agenda for April MSAC meeting

22 November 2023 - The MSAC Secretariat has published a list of applications scheduled to be considered by the MSAC on ...

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US FDA approves FoundationOne CDx as a companion diagnostic for AstraZeneca’s Truqap (capivasertib) in combination with Faslodex (fulvestrant) to identify patients with HR positive, HER2 negative advanced breast cancer

20 November 2023 - Foundation Medicine today announced that it has received approval from the US FDA for FoundationOne CDx ...

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US FDA approves FoundationOne CDx as a companion diagnostic for Lilly’s Retevmo (selpercatinib) for certain patients with solid tumours

9 October 2023 - Foundation Medicine’s tissue based comprehensive genomic profiling test is now FDA approved to identify patients with ...

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EntroGen receives FDA approval for CRCdx RAS mutation detection kit as companion diagnostic for Vectibix

3 October 2023 - The US FDA has granted approval for EntroGen's CRCdx RAS Mutation Detection Kit as a companion diagnostic ...

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US FDA approves FoundationOne CDx as a companion diagnostic for Janssen’s Akeega (niraparib and abiraterone acetate dual action tablet) for patients with BRCA positive metastatic castration-resistant prostate cancer

14 August 2023 - Foundation Medicine’s tissue-based comprehensive genomic profiling test is now FDA approved to identify patients with metastatic castration-resistant ...

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Qiagen receives FDA approval for companion diagnostic to Blueprint Medicines’ Ayvakit (avapritinib) in gastro-intestinal stromal tumours

7 August 2023 - QIAGEN’s therascreen PDGFRA RGQ PCR kit approved in US to aid in identifying patients with unresectable or ...

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Invivoscribe announces FDA approval of the LeukoStrat CDx FLT3 mutation assay to select patients with FLT3 ITD positive AML for treatment with Vanflyta

21 July 2023 - Invivoscribe is excited to announce that the LeukoStrat CDx FLT3 mutation assay has been approved by ...

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FDA approves ARUP Laboratories' AAV5 DetectCDx, a first-ever companion diagnostic immunoassay for a gene therapy

29 June 2023 - FDA issues simultaneous approval of Roctavian (valoctocogene roxaparvovec-rvox), BioMarin's gene therapy for severe haemophilia A. ...

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FDA launches pilot program to help reduce risks associated with using laboratory developed tests to identify cancer biomarkers

20 June 2023 - Pilot geared toward sponsors of certain oncology drug products used with certainin vitro diagnostic tests ...

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US FDA approves FoundationOne Liquid CDx as a companion diagnostic for Pfizer’s Braftovi (encorafenib) in combination with cetuximab to identify patients with BRAF V600E alterations in metastatic colorectal cancer

9 June 2023 - Foundation Medicine today announced that it has received approval from the US FDA for FoundationOne Liquid ...

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Qiagen receives FDA approval for companion diagnostic to Mirati Therapeutics’ Krazati in non-small-cell lung cancer

13 December 2022 - therascreen KRAS RGQ PCR kit approved as a companion diagnostic to aid in identifying non-small-cell lung cancer ...

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Agilent Resolution ctDx First receives FDA approval as a liquid biopsy companion diagnostic test for advanced non-small-cell lung cancer

12 December 2022 - Agilent Technologies announced today that the US FDA has approved Agilent Resolution ctDx First as a ...

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Roche receives FDA approval for first companion diagnostic to identify patients with HER2 low metastatic breast cancer eligible for Enhertu

4 October 2022 - Approximately half of all patients with metastatic breast cancer express low levels of HER2. ...

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MSAC publishes agenda for November 2022 meeting

27 July 2022 - 12 agenda items for consideration at the 24-25 November 2022 meeting. ...

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EMA finalises companion diagnostic guidance

7 July 2022 - The EMA) has finalised guidance on companion diagnostics, addressing procedural aspects to facilitate consultation between EMA ...

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