Highlights

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  [1]=>
  string(76) "Switching to smart charging electric vehicles could save the UK over £1bn"
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  string(76) "Switching to smart charging electric vehicles could save the UK over £1bn"
  [2]=>
  string(150) "Introducing smart charging infrastructure for electric vehicles could reduce the need to build extra storage into the National Grid – saving the"
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  string(150) "Introducing smart charging infrastructure for electric vehicles could reduce the need to build extra storage into the National Grid – saving the"
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  string(576) "

Introducing smart charging infrastructure for electric vehicles could reduce the need to build extra storage into the National Grid – saving the UK power network £1.16bn a year,

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The post Switching to smart charging electric vehicles could save the UK over £1bn appeared first on Compelo - latest news, features and insight on influencers and innovators within business.

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Introducing smart charging infrastructure for electric vehicles could reduce the need to build extra storage into the National Grid – saving the UK power network £1.16bn a year,

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The post Switching to smart charging electric vehicles could save the UK over £1bn appeared first on Compelo - latest news, features and insight on influencers and innovators within business.

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Switching to smart charging electric vehicles could save the UK over £1bn

Introducing smart charging infrastructure for electric vehicles could reduce the need to build extra storage into the

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  string(4) "3332"
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  string(4) "3332"
  [1]=>
  string(103) "Sensorion receives EMA agreement on the pediatric investigation plan for Arazasetron in two indications"
  ["article_title"]=>
  string(103) "Sensorion receives EMA agreement on the pediatric investigation plan for Arazasetron in two indications"
  [2]=>
  string(154) "“We are delighted by this outcome which we regard as an important stage for Sensorion and young patients. Indeed, this approval will allow Sensorion"
  ["short_description"]=>
  string(154) "“We are delighted by this outcome which we regard as an important stage for Sensorion and young patients. Indeed, this approval will allow Sensorion"
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  string(657) "

“We are delighted by this outcome which we regard as an important stage for Sensorion and young patients. Indeed, this approval will allow Sensorion to develop SENS-401 for

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The post Sensorion receives EMA agreement on the pediatric investigation plan for Arazasetron in two indications appeared first on Pharmaceutical Business review.

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“We are delighted by this outcome which we regard as an important stage for Sensorion and young patients. Indeed, this approval will allow Sensorion to develop SENS-401 for

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The post Sensorion receives EMA agreement on the pediatric investigation plan for Arazasetron in two indications appeared first on Pharmaceutical Business review.

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Sensorion receives EMA agreement on the pediatric investigation plan for Arazasetron in tw

“We are delighted by this outcome which we regard as an important stage for Sensorion and young patients. Indee

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  [1]=>
  string(89) "CHMP recommends EU approval of Roche’s Tecentriq plus Abraxane for metastatic TNBC"
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  string(89) "CHMP recommends EU approval of Roche’s Tecentriq plus Abraxane for metastatic TNBC"
  [2]=>
  string(154) "“This CHMP recommendation marks a breakthrough in the treatment of triple-negative breast cancer, an aggressive type of breast cancer with high unme"
  ["short_description"]=>
  string(154) "“This CHMP recommendation marks a breakthrough in the treatment of triple-negative breast cancer, an aggressive type of breast cancer with high unme"
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“This CHMP recommendation marks a breakthrough in the treatment of triple-negative breast cancer, an aggressive type of breast cancer with high unmet medical need,” said Sandra Horning, MD,

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The post CHMP recommends EU approval of Roche’s Tecentriq plus Abraxane for metastatic TNBC appeared first on Pharmaceutical Business review.

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“This CHMP recommendation marks a breakthrough in the treatment of triple-negative breast cancer, an aggressive type of breast cancer with high unmet medical need,” said Sandra Horning, MD,

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The post CHMP recommends EU approval of Roche’s Tecentriq plus Abraxane for metastatic TNBC appeared first on Pharmaceutical Business review.

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CHMP recommends EU approval of Roche’s Tecentriq plus Abraxane for metastatic TNBC

“This CHMP recommendation marks a breakthrough in the treatment of triple-negative breast cancer, an aggressive

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  string(4) "3334"
  [1]=>
  string(59) "Pfizer gets FDA nod for Avastin’s biosimilar Zirabev"
  ["article_title"]=>
  string(59) "Pfizer gets FDA nod for Avastin’s biosimilar Zirabev"
  [2]=>
  string(150) "Pfizer said that Zirabev has been approved to treat five types of cancer, including metastatic colorectal cancer; unresectable, locally advanced, recu"
  ["short_description"]=>
  string(150) "Pfizer said that Zirabev has been approved to treat five types of cancer, including metastatic colorectal cancer; unresectable, locally advanced, recu"
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Pfizer said that Zirabev has been approved to treat five types of cancer, including metastatic colorectal cancer; unresectable, locally advanced, recurrent or metastatic non-squamous non-small cell lung cancer

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The post Pfizer gets FDA nod for Avastin’s biosimilar Zirabev appeared first on Pharmaceutical Business review.

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Pfizer said that Zirabev has been approved to treat five types of cancer, including metastatic colorectal cancer; unresectable, locally advanced, recurrent or metastatic non-squamous non-small cell lung cancer

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The post Pfizer gets FDA nod for Avastin’s biosimilar Zirabev appeared first on Pharmaceutical Business review.

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Pfizer gets FDA nod for Avastin’s biosimilar Zirabev

Pfizer said that Zirabev has been approved to treat five types of cancer, including metastatic colorectal cancer; unr

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  string(4) "3335"
  [1]=>
  string(88) "Xeris doses first patient in phase 2 trial of developmental ready-to-use glucagon in PBH"
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  string(88) "Xeris doses first patient in phase 2 trial of developmental ready-to-use glucagon in PBH"
  [2]=>
  string(150) "Post-bariatric hypoglycemia (PBH) is a complication of bariatric surgery thought to be related to excessive insulin secretion in response to a meal. P"
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  string(150) "Post-bariatric hypoglycemia (PBH) is a complication of bariatric surgery thought to be related to excessive insulin secretion in response to a meal. P"
  [3]=>
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Post-bariatric hypoglycemia (PBH) is a complication of bariatric surgery thought to be related to excessive insulin secretion in response to a meal. PBH can begin to occur one

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The post Xeris doses first patient in phase 2 trial of developmental ready-to-use glucagon in PBH appeared first on Pharmaceutical Business review.

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Post-bariatric hypoglycemia (PBH) is a complication of bariatric surgery thought to be related to excessive insulin secretion in response to a meal. PBH can begin to occur one

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The post Xeris doses first patient in phase 2 trial of developmental ready-to-use glucagon in PBH appeared first on Pharmaceutical Business review.

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Xeris doses first patient in phase 2 trial of developmental ready-to-use glucagon in PBH

Post-bariatric hypoglycemia (PBH) is a complication of bariatric surgery thought to be related to excessive insulin s

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  string(4) "3336"
  [1]=>
  string(97) "Lung cancer drug Imfinzi improves overall survival at interim analysis in phase III CASPIAN trial"
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  string(97) "Lung cancer drug Imfinzi improves overall survival at interim analysis in phase III CASPIAN trial"
  [2]=>
  string(152) "A planned interim analysis conducted by an Independent Data Monitoring Committee concluded that the trial has met its primary endpoint by showing a s"
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  string(152) "A planned interim analysis conducted by an Independent Data Monitoring Committee concluded that the trial has met its primary endpoint by showing a s"
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A planned interim analysis conducted by an Independent Data Monitoring Committee concluded that the trial has met its primary endpoint by showing a statistically-significant and clinically-meaningful improvement in OS

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The post Lung cancer drug Imfinzi improves overall survival at interim analysis in phase III CASPIAN trial appeared first on Pharmaceutical Business review.

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A planned interim analysis conducted by an Independent Data Monitoring Committee concluded that the trial has met its primary endpoint by showing a statistically-significant and clinically-meaningful improvement in OS

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The post Lung cancer drug Imfinzi improves overall survival at interim analysis in phase III CASPIAN trial appeared first on Pharmaceutical Business review.

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Lung cancer drug Imfinzi improves overall survival at interim analysis in phase III CASPIA

A planned interim analysis conducted by an Independent Data Monitoring Committee concluded that the trial has met

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  string(4) "3337"
  ["article_id"]=>
  string(4) "3337"
  [1]=>
  string(97) "FDA approves Alexion’s Soliris to treat adults with neuromyelitis optica spectrum disorder"
  ["article_title"]=>
  string(97) "FDA approves Alexion’s Soliris to treat adults with neuromyelitis optica spectrum disorder"
  [2]=>
  string(150) "The NMOSD is a rare and severe autoimmune disease, which attacks the central nervous system without warning. Also referred as relapses, the attacks ma"
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  string(150) "The NMOSD is a rare and severe autoimmune disease, which attacks the central nervous system without warning. Also referred as relapses, the attacks ma"
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  string(567) "

The NMOSD is a rare and severe autoimmune disease, which attacks the central nervous system without warning. Also referred as relapses, the attacks may result in progressive and

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The post FDA approves Alexion’s Soliris to treat adults with neuromyelitis optica spectrum disorder appeared first on Pharmaceutical Business review.

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The NMOSD is a rare and severe autoimmune disease, which attacks the central nervous system without warning. Also referred as relapses, the attacks may result in progressive and

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The post FDA approves Alexion’s Soliris to treat adults with neuromyelitis optica spectrum disorder appeared first on Pharmaceutical Business review.

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FDA approves Alexion’s Soliris to treat adults with neuromyelitis optica spectrum d

The NMOSD is a rare and severe autoimmune disease, which attacks the central nervous system without warning. Also ref

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  string(4) "3338"
  [1]=>
  string(76) "Acceleron completes target enrollment in phase 2 trial of Sotatercept in PAH"
  ["article_title"]=>
  string(76) "Acceleron completes target enrollment in phase 2 trial of Sotatercept in PAH"
  [2]=>
  string(164) "The Company now expects to report top-line results during the first quarter of 2020. “We’re thrilled with PULSAR’s rapid enrollment over the pas"
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  string(164) "The Company now expects to report top-line results during the first quarter of 2020. “We’re thrilled with PULSAR’s rapid enrollment over the pas"
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The Company now expects to report top-line results during the first quarter of 2020. “We’re thrilled with PULSAR’s rapid enrollment over the past 12 months, which underscores the

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The post Acceleron completes target enrollment in phase 2 trial of Sotatercept in PAH appeared first on Pharmaceutical Business review.

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The Company now expects to report top-line results during the first quarter of 2020. “We’re thrilled with PULSAR’s rapid enrollment over the past 12 months, which underscores the

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The post Acceleron completes target enrollment in phase 2 trial of Sotatercept in PAH appeared first on Pharmaceutical Business review.

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Acceleron completes target enrollment in phase 2 trial of Sotatercept in PAH

The Company now expects to report top-line results during the first quarter of 2020. “We’re thrilled wit

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  ["article_id"]=>
  string(4) "3339"
  [1]=>
  string(81) "FDA grants fast track designation to empagliflozin to treat chronic heart failure"
  ["article_title"]=>
  string(81) "FDA grants fast track designation to empagliflozin to treat chronic heart failure"
  [2]=>
  string(150) "The Fast Track designation facilitates the development of new therapies that fill an unmet medical need for serious conditions in an effort to expedit"
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  string(150) "The Fast Track designation facilitates the development of new therapies that fill an unmet medical need for serious conditions in an effort to expedit"
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The Fast Track designation facilitates the development of new therapies that fill an unmet medical need for serious conditions in an effort to expedite the availability of new

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The post FDA grants fast track designation to empagliflozin to treat chronic heart failure appeared first on Pharmaceutical Business review.

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The Fast Track designation facilitates the development of new therapies that fill an unmet medical need for serious conditions in an effort to expedite the availability of new

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The post FDA grants fast track designation to empagliflozin to treat chronic heart failure appeared first on Pharmaceutical Business review.

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FDA grants fast track designation to empagliflozin to treat chronic heart failure

The Fast Track designation facilitates the development of new therapies that fill an unmet medical need for serious c

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  string(4) "3340"
  [1]=>
  string(92) "Regeneron, Sanofi get FDA nod for Dupixent to treat chronic rhinosinusitis with nasal polyps"
  ["article_title"]=>
  string(92) "Regeneron, Sanofi get FDA nod for Dupixent to treat chronic rhinosinusitis with nasal polyps"
  [2]=>
  string(150) "The approval allows the drug firms to use Dupixent with other medicines for the treatment of chronic rhinosinusitis with nasal polyposis (CRSwNP) in a"
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  string(150) "The approval allows the drug firms to use Dupixent with other medicines for the treatment of chronic rhinosinusitis with nasal polyposis (CRSwNP) in a"
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The approval allows the drug firms to use Dupixent with other medicines for the treatment of chronic rhinosinusitis with nasal polyposis (CRSwNP) in adults whose disease is not

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The post Regeneron, Sanofi get FDA nod for Dupixent to treat chronic rhinosinusitis with nasal polyps appeared first on Pharmaceutical Business review.

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The approval allows the drug firms to use Dupixent with other medicines for the treatment of chronic rhinosinusitis with nasal polyposis (CRSwNP) in adults whose disease is not

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The post Regeneron, Sanofi get FDA nod for Dupixent to treat chronic rhinosinusitis with nasal polyps appeared first on Pharmaceutical Business review.

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Regeneron, Sanofi get FDA nod for Dupixent to treat chronic rhinosinusitis with nasal poly

The approval allows the drug firms to use Dupixent with other medicines for the treatment of chronic rhinosinusitis w

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2nd Annual Biotechnology Congress

Conference Series LLC Ltd invites you for the 2nd Annual Biotechnology Congress which is going to be held in July 31-Aug