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CPHI North America - thank you for visiting Polpharma booth!

CPHI North America - thank you for visiting Polpharma booth!

25 May 2017

Dear Customers and Business Partners! Thank you all for visiting Polpharma’s booth in Philadelphia during CPHI North America, the latest addition to key global events for the pharmaceutical industry! We hope it was as fruitful for you as for us! Our...

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WuXi STA, CFDA and Jinshan Government to co-host Marketing Authorization Holder regulatory summit in Shanghai

WuXi STA, CFDA and Jinshan Government to co-host Marketing Authorization Holder regulatory summit in Shanghai

25 May 2017

Industry and regulators combine to run afternoon congress on the implications of regulatory changes.

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Hovione starts clinical trial of its proprietary minocycline sterile ointment to treat a subset of anterior ocular inflammation

Hovione starts clinical trial of its proprietary minocycline sterile ointment to treat a subset of anterior ocular inflammation

25 May 2017

First clinical study using a patent protected minocycline API and formulation developed by Hovione.

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PharmaMar and Eczacıbaşı sign a licensing agreement for Aplidin in Turkey

PharmaMar and Eczacıbaşı sign a licensing agreement for Aplidin in Turkey

25 May 2017

Aplidin is PharmaMar's second most advanced anticancer drug currently under development for the treatment of multiple myeloma and angioimmunoblastic T-cell lymphoma.

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IPF patients treated with Ofev vs placebo twice as likely to have improved or stable lung function

IPF patients treated with Ofev vs placebo twice as likely to have improved or stable lung function

25 May 2017

Separate subgroup analysis demonstrates long-term efficacy of Ofev in slowing disease progression is maintained for up to 96 weeks in IPF patients who require dose adjustments to manage adverse events.

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Bioverativ to acquire clinical-stage rare disease biotechnology company, True North Therapeutics

Bioverativ to acquire clinical-stage rare disease biotechnology company, True North Therapeutics

25 May 2017

Strengthens pipeline with lead candidate TNT009 in cold agglutinin disease, a rare and chronic autoimmune hemolytic anemia with no approved therapies.

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FDA approves Kevzara for the treatment of moderately to severely active RA in adults

FDA approves Kevzara for the treatment of moderately to severely active RA in adults

23 May 2017

Kevzara is now available to US patients.

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New analyses reinforce the potential of Ultibro Breezhaler for COPD patients historically treated with steroids

New analyses reinforce the potential of Ultibro Breezhaler for COPD patients historically treated with steroids

23 May 2017

New analyses from the FLAME study suggest dual bronchodilator Ultibro Breezhaler provides similar or better efficacy versus steroid-containing therapies, regardless of blood eosinophil counts.

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Spiriva Respimat inhalation spray improves breathing for people with asthma regardless of BMI or allergic status

Spiriva Respimat inhalation spray improves breathing for people with asthma regardless of BMI or allergic status

23 May 2017

In all analyses, people experiencing uncontrolled asthma symptoms saw improvements in their breathing by adding Spiriva Respimat to an ICS or combination ICS/LABA.

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FDA approves Genentech’s Actemra for giant cell arteritis

FDA approves Genentech’s Actemra for giant cell arteritis

22 May 2017

Sixth FDA approval for Actemra since its US launch in 2010,

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Thermo Fisher Scientific to acquire Patheon

Thermo Fisher Scientific to acquire Patheon

22 May 2017

Patheon provides entry into the attractive, high-growth CDMO market.

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Boehringer Ingelheim inaugurates biopharmaceutical manufacturing facility in China

Boehringer Ingelheim inaugurates biopharmaceutical manufacturing facility in China

22 May 2017

It is the first and only biopharmaceutical manufacturing site established by a multinational active pharmaceutical company in China.

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