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hereditary angioedema

This page shows the latest hereditary angioedema news and features for those working in and with pharma, biotech and healthcare.

Takeda’s HAE drug Takhzyro backed by NICE

Takeda’s HAE drug Takhzyro backed by NICE

New treatment option for rare, hereditary disease. Takeda’s drug for the rare disease hereditary angioedema (HAE) should be made available routinely on the NHS in England and Wales, says NICE.

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  • Drug launches to watch in 2019 Drug launches to watch in 2019

    The first test of this will be Shire’s new blockbuster-in-waiting Takhzyro, which gained EMA approval in November, for the rare disease hereditary angioedema (HAE).

  • ‘How is your day?’ ‘How is your day?’

    These are: Primary Immunodeficiency Diseases (PID – causes severe infections); Chronic Inflammatory Demyelinating Polyneuropathy (CIDP – causes of loss of limb function/disability); bleeding disorders (haemophilia and related conditions);

  • Deal Watch August 2016 Deal Watch August 2016

    151. Valeant (US). Pharming (NL). Asset acquisition North America. Ruconest (recombinant human C1 esterase inhibitor) for treatment of acute Hereditary Angioedema with sales of $25m.

  • Deal Watch February 2016 Deal Watch February 2016

    Annapurna brings a portfolio of four AAV-based gene therapy programmes at the preclinical stage for alpha-1 antitrypsin deficiency, hereditary angioedema, cardiomyopathy associated with Friedreich's ataxia and severe allergy.

  • Deal Watch November 2015 Deal Watch November 2015

    hereditary angioedema (HAE). ... US. Abbreviations: HAE, Hereditary angioedema. 14th December 2015.

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