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Business as usual: bank climate commitments, lending, and engagement

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tisdag, april 2, 2024
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Key Points: 

    GSK shares positive data for AREXVY, its respiratory syncytial virus (RSV) older adult vaccine, indicating protection over two RSV seasons

    Retrieved on: 
    onsdag, juni 21, 2023

    The trial also evaluated efficacy following an annual revaccination schedule as a confirmatory secondary endpoint.

    Key Points: 
    • The trial also evaluated efficacy following an annual revaccination schedule as a confirmatory secondary endpoint.
    • The clinical development program will continue to evaluate longer term follow up and the optimal timing for potential revaccination.
    • Tony Wood, Chief Scientific Officer, GSK, said: “Our goal is to provide a high level of protection for older adults most at risk from RSV.
    • These data will be submitted to the US Food and Drug Administration (FDA) and other regulators for review.

    Kiboko Gold Drills Multiple High-grade Intervals Including 8.7 g/t Au Over 9 m and 23.9 g/t Au Over 3 m at its Harricana Gold Project

    Retrieved on: 
    torsdag, januari 26, 2023

    As shown in figures 1 and 2, the Harricana Project (the “Project” or “Harricana Project”) is located 55 kilometres north of Val-d’Or, Québec, in the world-renowned Abitibi gold belt.

    Key Points: 
    • As shown in figures 1 and 2, the Harricana Project (the “Project” or “Harricana Project”) is located 55 kilometres north of Val-d’Or, Québec, in the world-renowned Abitibi gold belt.
    • To date, 2 holes (totalling 540 m of drilling) have been completed as part of the Company’s ongoing 12-hole / 2,800 m winter diamond drilling program.
    • In addition to intercepting several exciting high-grade intervals, many lower grade intervals were intersected in this first batch of assay results.
    • Further investigation is necessary, including the study of gold grain size distribution, gold content, and representative sub-sample sizes for assaying is necessary.

    Ipsen Announces Withdrawal of Palovarotene NDA, Confirming Intention to Re-submit Following Additional Data Analyses

    Retrieved on: 
    fredag, augusti 13, 2021

    Ipsen (Euronext: IPN; ADR: IPSEY) today announced, following very recent discussions with the U.S. Food and Drug Administration (FDA), withdrawal of the New Drug Application (NDA) for palovarotene.

    Key Points: 
    • Ipsen (Euronext: IPN; ADR: IPSEY) today announced, following very recent discussions with the U.S. Food and Drug Administration (FDA), withdrawal of the New Drug Application (NDA) for palovarotene.
    • As a result, Ipsen has therefore confirmed their withdrawal of the NDA for palovarotene.
    • After recent discussion with FDA, Ipsen plans to resubmit to the FDA upon completion of the additional data analyses.
    • The target regulatory action date assigned by the FDA under a Priority Review status for palovarotene was 30 November 2021.