Newly combined with Baxalta, Shire is now the leading global biotechnology company focused on serving people affected by rare diseases and other highly specialized conditions. These diseases are often misunderstood, under-diagnosed, and potentially life-threatening.

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SHIRE’S EXPERIMENTAL HAE DRUG HITS PHASE 3 MARKS

Fiercebiotech | September 11, 2017

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Shire has posted positive results for its late-stage hereditary angioedema candidate SHP616 against a dummy treatment. The biopharma’s subcutaneous C1 esterase inhibitor significantly lowered hereditary angioedema (HAE) monthly attack rate against placebo in the pivotal phase 3. Data from the Sahara test show that median HAE attack reduction hit 79% from day 0, and 85% from day 14. Shire also found that 38% of patients were HAE attack free while on its med....

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SHIRE REAFFIRMS COMMITMENT TO DUNBOYNE DEVELOPMENT

biotech | May 03, 2017

news image

Shire’s proposed 400-job plant at Dunboyne is fully on track, with the company moving to put fears to rest that work on the new facility would stop or that the project would continue on a smaller scale...

Read More

SHIRE FILES INJUNCTION AGAINST ROCHE HEMOPHILIA COMPETITOR

biopharmadive | July 10, 2017

news image

In an unexpected move, Shire International has secured an injunction in a Hamburg, Germany court against Roche for the Swiss pharma's as yet unmarketed hemophilia drug, emicizumab. The injunction claims Roche is disseminating "inaccurate and misleading characterization of the serious adverse events that occurred in the HAVEN 1 Phase 3 trial of emicizumab, as well as misinformation about "the appropriate management of breakthrough bleeds uncontrolled by emicizumab....

Read More

A FUTURE GENE THERAPY COULD BE DELIVERED IN TINY ‘NANOCONTAINERS’

Labiotech.eu | January 28, 2020

news image

A Swiss research group has developed tiny plastic particles that could carry gene therapies to the center of the cell with less risk of getting attacked by the immune system than conventional gene therapies. The majority of gene therapies in use today are delivered to the DNA of target cells using viral vectors. While efficient at their job, viral vectors can risk triggering the immune system to destroy them. This can lead to the therapy becoming ineffective....

Read More
news image

SHIRE’S EXPERIMENTAL HAE DRUG HITS PHASE 3 MARKS

Fiercebiotech | September 11, 2017

Shire has posted positive results for its late-stage hereditary angioedema candidate SHP616 against a dummy treatment. The biopharma’s subcutaneous C1 esterase inhibitor significantly lowered hereditary angioedema (HAE) monthly attack rate against placebo in the pivotal phase 3. Data from the Sahara test show that median HAE attack reduction hit 79% from day 0, and 85% from day 14. Shire also found that 38% of patients were HAE attack free while on its med....

Read More
news image

SHIRE REAFFIRMS COMMITMENT TO DUNBOYNE DEVELOPMENT

biotech | May 03, 2017

Shire’s proposed 400-job plant at Dunboyne is fully on track, with the company moving to put fears to rest that work on the new facility would stop or that the project would continue on a smaller scale...

Read More
news image

SHIRE FILES INJUNCTION AGAINST ROCHE HEMOPHILIA COMPETITOR

biopharmadive | July 10, 2017

In an unexpected move, Shire International has secured an injunction in a Hamburg, Germany court against Roche for the Swiss pharma's as yet unmarketed hemophilia drug, emicizumab. The injunction claims Roche is disseminating "inaccurate and misleading characterization of the serious adverse events that occurred in the HAVEN 1 Phase 3 trial of emicizumab, as well as misinformation about "the appropriate management of breakthrough bleeds uncontrolled by emicizumab....

Read More
news image

A FUTURE GENE THERAPY COULD BE DELIVERED IN TINY ‘NANOCONTAINERS’

Labiotech.eu | January 28, 2020

A Swiss research group has developed tiny plastic particles that could carry gene therapies to the center of the cell with less risk of getting attacked by the immune system than conventional gene therapies. The majority of gene therapies in use today are delivered to the DNA of target cells using viral vectors. While efficient at their job, viral vectors can risk triggering the immune system to destroy them. This can lead to the therapy becoming ineffective....

Read More

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Feature market insights and perspectives from top C-Level executives, elite technology influencers and thought leaders from your company here. This signature initiative has garnered immense support...

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