Highlights

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  string(117) "Seattle Genetics gets FDA priority review for tucatinib in locally advanced or metastatic HER2-positive breast cancer"
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  string(117) "Seattle Genetics gets FDA priority review for tucatinib in locally advanced or metastatic HER2-positive breast cancer"
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  string(150) "This NDA requests FDA approval of tucatinib in combination with trastuzumab and capecitabine for treatment of patients with locally advanced unresecta"
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  string(150) "This NDA requests FDA approval of tucatinib in combination with trastuzumab and capecitabine for treatment of patients with locally advanced unresecta"
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This NDA requests FDA approval of tucatinib in combination with trastuzumab and capecitabine for treatment of patients with locally advanced unresectable or metastatic HER2-positive breast cancer, including patients

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This NDA requests FDA approval of tucatinib in combination with trastuzumab and capecitabine for treatment of patients with locally advanced unresectable or metastatic HER2-positive breast cancer, including patients

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The post Seattle Genetics gets FDA priority review for tucatinib in locally advanced or metastatic HER2-positive breast cancer appeared first on Pharmaceutical Business review.

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Seattle Genetics gets FDA priority review for tucatinib in locally advanced or metastatic

This NDA requests FDA approval of tucatinib in combination with trastuzumab and capecitabine for treatment of patient

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  string(4) "7625"
  [1]=>
  string(154) "The US FDA accepts for priority review Bristol-Myers Squibb’s BLA for liso-cel for adult patients with relapsed or refractory large B-cell lymphoma"
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  string(154) "The US FDA accepts for priority review Bristol-Myers Squibb’s BLA for liso-cel for adult patients with relapsed or refractory large B-cell lymphoma"
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  string(154) "The FDA has set a Prescription Drug User Fee Act (PDUFA) goal date of August 17, 2020. “There remains a critical need for additional therapies in la"
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  string(154) "The FDA has set a Prescription Drug User Fee Act (PDUFA) goal date of August 17, 2020. “There remains a critical need for additional therapies in la"
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The FDA has set a Prescription Drug User Fee Act (PDUFA) goal date of August 17, 2020. “There remains a critical need for additional therapies in large B-cell

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The FDA has set a Prescription Drug User Fee Act (PDUFA) goal date of August 17, 2020. “There remains a critical need for additional therapies in large B-cell

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The US FDA accepts for priority review Bristol-Myers Squibb’s BLA for liso-cel for

The FDA has set a Prescription Drug User Fee Act (PDUFA) goal date of August 17, 2020. “There remains a critica

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  string(76) "Roche gets Chinese approval for Tecentriq plus chemotherapy to treat ES-SCLC"
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  string(76) "Roche gets Chinese approval for Tecentriq plus chemotherapy to treat ES-SCLC"
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  string(150) "Tecentriq is a monoclonal antibody designed to bind with PD-L1 protein that is expressed on tumour cells and tumour-infiltrating immune cells, restric"
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  string(150) "Tecentriq is a monoclonal antibody designed to bind with PD-L1 protein that is expressed on tumour cells and tumour-infiltrating immune cells, restric"
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Tecentriq is a monoclonal antibody designed to bind with PD-L1 protein that is expressed on tumour cells and tumour-infiltrating immune cells, restricting its interactions with both PD-1 and

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Tecentriq is a monoclonal antibody designed to bind with PD-L1 protein that is expressed on tumour cells and tumour-infiltrating immune cells, restricting its interactions with both PD-1 and

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Roche gets Chinese approval for Tecentriq plus chemotherapy to treat ES-SCLC

Tecentriq is a monoclonal antibody designed to bind with PD-L1 protein that is expressed on tumour cells and tumour-i

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  [1]=>
  string(58) "ALX Oncology announces closing of $105m Series C financing"
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  string(58) "ALX Oncology announces closing of $105m Series C financing"
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  string(150) "Vivo Capital was the lead investor with other new investors including funds managed by Logos Capital, Janus Henderson, Foresite Capital, Cormorant Ass"
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  string(150) "Vivo Capital was the lead investor with other new investors including funds managed by Logos Capital, Janus Henderson, Foresite Capital, Cormorant Ass"
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Vivo Capital was the lead investor with other new investors including funds managed by Logos Capital, Janus Henderson, Foresite Capital, Cormorant Asset Management, BVF Partners, and investor HBM

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Vivo Capital was the lead investor with other new investors including funds managed by Logos Capital, Janus Henderson, Foresite Capital, Cormorant Asset Management, BVF Partners, and investor HBM

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ALX Oncology announces closing of $105m Series C financing

Vivo Capital was the lead investor with other new investors including funds managed by Logos Capital, Janus Henderson

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  [1]=>
  string(154) "Deciphera Pharmaceuticals announces US FDA acceptance of NDA and priority review for ripretinib in patients with advanced gastrointestinal stromal tumours"
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  string(154) "Deciphera Pharmaceuticals announces US FDA acceptance of NDA and priority review for ripretinib in patients with advanced gastrointestinal stromal tumours"
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  string(150) "The FDA granted Priority Review for the NDA, which provides for a six-month review, and assigned a Prescription Drug User Fee Act (PDUFA) target actio"
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The FDA granted Priority Review for the NDA, which provides for a six-month review, and assigned a Prescription Drug User Fee Act (PDUFA) target action date of August

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The FDA granted Priority Review for the NDA, which provides for a six-month review, and assigned a Prescription Drug User Fee Act (PDUFA) target action date of August

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The post Deciphera Pharmaceuticals announces US FDA acceptance of NDA and priority review for ripretinib in patients with advanced gastrointestinal stromal tumours appeared first on Pharmaceutical Business review.

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Deciphera Pharmaceuticals announces US FDA acceptance of NDA and priority review for ripre

The FDA granted Priority Review for the NDA, which provides for a six-month review, and assigned a Prescription Drug

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  [1]=>
  string(79) "Merck’s Keytruda plus chemotherapy meets primary endpoint in mTNBC trial"
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  string(79) "Merck’s Keytruda plus chemotherapy meets primary endpoint in mTNBC trial"
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  string(150) "Keytruda plus chemotherapy achieved one of its dual primary endpoints of PFS in patients with mTNBC whose tumours expressed PD-L1. Keytruda, an anti-P"
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  string(150) "Keytruda plus chemotherapy achieved one of its dual primary endpoints of PFS in patients with mTNBC whose tumours expressed PD-L1. Keytruda, an anti-P"
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Keytruda plus chemotherapy achieved one of its dual primary endpoints of PFS in patients with mTNBC whose tumours expressed PD-L1. Keytruda, an anti-PD-1 therapy, works by blocking the

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Keytruda plus chemotherapy achieved one of its dual primary endpoints of PFS in patients with mTNBC whose tumours expressed PD-L1. Keytruda, an anti-PD-1 therapy, works by blocking the

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The post Merck’s Keytruda plus chemotherapy meets primary endpoint in mTNBC trial appeared first on Pharmaceutical Business review.

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Merck’s Keytruda plus chemotherapy meets primary endpoint in mTNBC trial

Keytruda plus chemotherapy achieved one of its dual primary endpoints of PFS in patients with mTNBC whose tumours exp

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  string(93) "Cornerstone to Showcase AI-powered Innovations Disrupting HR at Learning Technologies UK 2020"
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  string(93) "Cornerstone to Showcase AI-powered Innovations Disrupting HR at Learning Technologies UK 2020"
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  string(150) "Cornerstone client Novartis will also be sharing how the company developed a culture of curiosity amongst its workforce London — 04 February, 20"
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Cornerstone to Showcase AI-powered Innovations Disrupting HR at Learning Technologies UK 2

Cornerstone client Novartis will also be sharing how the company developed a culture of curiosity amongst its workforce

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ASOS and Verint among 300 new customers for e-days as companies double down on absence man

Software provider sees customers like AXA move towards full integration of absence management software ASOS, Campari and

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  string(98) "Harbour BioMed receives FDA IND approval for phase 2 trial and orphan drug designation for HBM9167"
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  string(98) "Harbour BioMed receives FDA IND approval for phase 2 trial and orphan drug designation for HBM9167"
  [2]=>
  string(159) "Separately, the Agency’s Office of Orphan Products Development granted HBM9167 Orphan Drug Designation (ODD) for the use in treating NPC. “Nasopha"
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Separately, the Agency’s Office of Orphan Products Development granted HBM9167 Orphan Drug Designation (ODD) f

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