Highlights

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  [1]=>
  string(81) "Axcella achieves initial milestones with its hematology product candidate AXA4010"
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  string(81) "Axcella achieves initial milestones with its hematology product candidate AXA4010"
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  string(155) "Mechanistic data on AXA4010 will be presented at the American Society of Hematology’s (ASH) 2019 Annual Meeting. Additionally, the company has initi"
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  string(155) "Mechanistic data on AXA4010 will be presented at the American Society of Hematology’s (ASH) 2019 Annual Meeting. Additionally, the company has initi"
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Mechanistic data on AXA4010 will be presented at the American Society of Hematology’s (ASH) 2019 Annual Meeting. Additionally, the company has initiated enrollment of subjects with sickle cell

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Mechanistic data on AXA4010 will be presented at the American Society of Hematology’s (ASH) 2019 Annual Meeting. Additionally, the company has initiated enrollment of subjects with sickle cell

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The post Axcella achieves initial milestones with its hematology product candidate AXA4010 appeared first on Pharmaceutical Business review.

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Axcella achieves initial milestones with its hematology product candidate AXA4010

Mechanistic data on AXA4010 will be presented at the American Society of Hematology’s (ASH) 2019 Annual Meetin

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  string(4) "5790"
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  string(4) "5790"
  [1]=>
  string(71) "Regeneron, Vyriad sign deal to develop oncolytic virus-based treatments"
  ["article_title"]=>
  string(71) "Regeneron, Vyriad sign deal to develop oncolytic virus-based treatments"
  [2]=>
  string(155) "Both firms will also sign a five-year research agreement to use Regeneron’s VelociSuite technologies to jointly design and validate Vesicular Stomat"
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  string(155) "Both firms will also sign a five-year research agreement to use Regeneron’s VelociSuite technologies to jointly design and validate Vesicular Stomat"
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Both firms will also sign a five-year research agreement to use Regeneron’s VelociSuite technologies to jointly design and validate Vesicular Stomatitis Virus (VSV)-based oncolytic virus treatments. Under the

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The post Regeneron, Vyriad sign deal to develop oncolytic virus-based treatments appeared first on Pharmaceutical Business review.

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Both firms will also sign a five-year research agreement to use Regeneron’s VelociSuite technologies to jointly design and validate Vesicular Stomatitis Virus (VSV)-based oncolytic virus treatments. Under the

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The post Regeneron, Vyriad sign deal to develop oncolytic virus-based treatments appeared first on Pharmaceutical Business review.

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Regeneron, Vyriad sign deal to develop oncolytic virus-based treatments

Both firms will also sign a five-year research agreement to use Regeneron’s VelociSuite technologies to jointl

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  [1]=>
  string(139) "SOTIO exercises second target option under existing collaboration with NBE-Therapeutics to develop next-generation antibody-drug conjugates"
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  string(139) "SOTIO exercises second target option under existing collaboration with NBE-Therapeutics to develop next-generation antibody-drug conjugates"
  [2]=>
  string(150) "Basel, Switzerland & Prague, Czech Republic – November 7, 2019 – NBE-Therapeutics AG and SOTIO a.s. today announced that SOTIO has ele"
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  string(150) "Basel, Switzerland & Prague, Czech Republic – November 7, 2019 – NBE-Therapeutics AG and SOTIO a.s. today announced that SOTIO has ele"
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  string(603) "Basel, Switzerland & Prague, Czech Republic – November 7, 2019 – NBE-Therapeutics AG and SOTIO a.s. today announced that SOTIO has elected a second target for the development of a next generation antibody-drug conjugate (ADC) under their existing license and collaboration agreement. NBE and SOTIO will collaborate on the discovery, non-clinical development and manufacturing of this second undisclosed target. The development will be based on NBE’s proprietary antibody drug conjugate platform, including NBE’s site-specific SMAC-technology™...&#nl&#nlSource: RealWire"
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  string(603) "Basel, Switzerland & Prague, Czech Republic – November 7, 2019 – NBE-Therapeutics AG and SOTIO a.s. today announced that SOTIO has elected a second target for the development of a next generation antibody-drug conjugate (ADC) under their existing license and collaboration agreement. NBE and SOTIO will collaborate on the discovery, non-clinical development and manufacturing of this second undisclosed target. The development will be based on NBE’s proprietary antibody drug conjugate platform, including NBE’s site-specific SMAC-technology™...&#nl&#nlSource: RealWire"
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  string(107) "http://www.realwire.com/releases/SOTIO-exercises-second-target-option-under-existing-collaboration-with-NBE"
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SOTIO exercises second target option under existing collaboration with NBE-Therapeutics to

Basel, Switzerland & Prague, Czech Republic – November 7, 2019 – NBE-Therapeutics AG and SOTIO a.s. toda

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  string(4) "5879"
  [1]=>
  string(140) "Roxadustat significantly increased hemoglobin levels for chronic kidney disease patients with anemia in phase III OLYMPUS and ROCKIES trials"
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  string(140) "Roxadustat significantly increased hemoglobin levels for chronic kidney disease patients with anemia in phase III OLYMPUS and ROCKIES trials"
  [2]=>
  string(150) "The OLYMPUS trial compared roxadustat to placebo while the ROCKIES trial compared roxadustat to epoetin alfa. The results were presented today during "
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  string(150) "The OLYMPUS trial compared roxadustat to placebo while the ROCKIES trial compared roxadustat to epoetin alfa. The results were presented today during "
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The OLYMPUS trial compared roxadustat to placebo while the ROCKIES trial compared roxadustat to epoetin alfa. The results were presented today during two oral sessions at the American

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The OLYMPUS trial compared roxadustat to placebo while the ROCKIES trial compared roxadustat to epoetin alfa. The results were presented today during two oral sessions at the American

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The post Roxadustat significantly increased hemoglobin levels for chronic kidney disease patients with anemia in phase III OLYMPUS and ROCKIES trials appeared first on Pharmaceutical Business review.

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Roxadustat significantly increased hemoglobin levels for chronic kidney disease patients w

The OLYMPUS trial compared roxadustat to placebo while the ROCKIES trial compared roxadustat to epoetin alfa. The res

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  string(4) "5880"
  ["article_id"]=>
  string(4) "5880"
  [1]=>
  string(62) "Johnson & Johnson seeks EMA approval for Ebola vaccine regimen"
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  string(62) "Johnson & Johnson seeks EMA approval for Ebola vaccine regimen"
  [2]=>
  string(150) "The company has submitted marketing authorisation applications (MAAs) to the EMA to prevent Ebola Virus Disease (EVD) caused by Zaire ebolavirus speci"
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  string(150) "The company has submitted marketing authorisation applications (MAAs) to the EMA to prevent Ebola Virus Disease (EVD) caused by Zaire ebolavirus speci"
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The company has submitted marketing authorisation applications (MAAs) to the EMA to prevent Ebola Virus Disease (EVD) caused by Zaire ebolavirus species. Janssen has submitted two MAAs in

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The post Johnson & Johnson seeks EMA approval for Ebola vaccine regimen appeared first on Pharmaceutical Business review.

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The company has submitted marketing authorisation applications (MAAs) to the EMA to prevent Ebola Virus Disease (EVD) caused by Zaire ebolavirus species. Janssen has submitted two MAAs in

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The post Johnson & Johnson seeks EMA approval for Ebola vaccine regimen appeared first on Pharmaceutical Business review.

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Johnson & Johnson seeks EMA approval for Ebola vaccine regimen

The company has submitted marketing authorisation applications (MAAs) to the EMA to prevent Ebola Virus Disease (EVD)

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  string(4) "5881"
  [1]=>
  string(98) "Takeda’s dengue vaccine candidate demonstrates protection in children ages four to 16 years"
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  string(98) "Takeda’s dengue vaccine candidate demonstrates protection in children ages four to 16 years"
  [2]=>
  string(155) "Takeda’s dengue vaccine candidate demonstrated protection against virologically-confirmed dengue (VCD), the trial primary endpoint, in children ages"
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  string(155) "Takeda’s dengue vaccine candidate demonstrated protection against virologically-confirmed dengue (VCD), the trial primary endpoint, in children ages"
  [3]=>
  string(682) "

Takeda’s dengue vaccine candidate demonstrated protection against virologically-confirmed dengue (VCD), the trial primary endpoint, in children ages four to 16 years. Vaccine efficacy (VE) was 80.2% (95% confidence

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The post Takeda’s dengue vaccine candidate demonstrates protection in children ages four to 16 years appeared first on Pharmaceutical Business review.

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Takeda’s dengue vaccine candidate demonstrated protection against virologically-confirmed dengue (VCD), the trial primary endpoint, in children ages four to 16 years. Vaccine efficacy (VE) was 80.2% (95% confidence

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The post Takeda’s dengue vaccine candidate demonstrates protection in children ages four to 16 years appeared first on Pharmaceutical Business review.

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Takeda’s dengue vaccine candidate demonstrates protection in children ages four to

Takeda’s dengue vaccine candidate demonstrated protection against virologically-confirmed dengue (VCD), the tr

array(40) {
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  string(4) "6069"
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  string(4) "6069"
  [1]=>
  string(80) "GSK’s mepolizumab succeeds in phase 3 trial in hypereosinophilic syndrome"
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  string(80) "GSK’s mepolizumab succeeds in phase 3 trial in hypereosinophilic syndrome"
  [2]=>
  string(150) "The late-stage study evaluated subcutaneously administered mepolizumab 300mg (3x100mg) every four weeks against placebo in 108 adolescent and adult pa"
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  string(150) "The late-stage study evaluated subcutaneously administered mepolizumab 300mg (3x100mg) every four weeks against placebo in 108 adolescent and adult pa"
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The late-stage study evaluated subcutaneously administered mepolizumab 300mg (3x100mg) every four weeks against placebo in 108 adolescent and adult patients with severe HES. The HES trial met its

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The post GSK’s mepolizumab succeeds in phase 3 trial in hypereosinophilic syndrome appeared first on Pharmaceutical Business review.

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The late-stage study evaluated subcutaneously administered mepolizumab 300mg (3x100mg) every four weeks against placebo in 108 adolescent and adult patients with severe HES. The HES trial met its

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The post GSK’s mepolizumab succeeds in phase 3 trial in hypereosinophilic syndrome appeared first on Pharmaceutical Business review.

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GSK’s mepolizumab succeeds in phase 3 trial in hypereosinophilic syndrome

The late-stage study evaluated subcutaneously administered mepolizumab 300mg (3x100mg) every four weeks against place

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  string(4) "6070"
  ["article_id"]=>
  string(4) "6070"
  [1]=>
  string(82) "Finch Therapeutics, Takeda expand collaboration to develop microbiome therapeutics"
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  string(82) "Finch Therapeutics, Takeda expand collaboration to develop microbiome therapeutics"
  [2]=>
  string(160) "Under the terms of the expanded agreement, Finch and Takeda will utilize Finch’s platform to target Crohn’s disease, a form of inflammatory bowel "
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  string(160) "Under the terms of the expanded agreement, Finch and Takeda will utilize Finch’s platform to target Crohn’s disease, a form of inflammatory bowel "
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Under the terms of the expanded agreement, Finch and Takeda will utilize Finch’s platform to target Crohn’s disease, a form of inflammatory bowel disease. Finch’s Human-First Discovery platform

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Under the terms of the expanded agreement, Finch and Takeda will utilize Finch’s platform to target Crohn’s disease, a form of inflammatory bowel disease. Finch’s Human-First Discovery platform

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The post Finch Therapeutics, Takeda expand collaboration to develop microbiome therapeutics appeared first on Pharmaceutical Business review.

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Finch Therapeutics, Takeda expand collaboration to develop microbiome therapeutics

Under the terms of the expanded agreement, Finch and Takeda will utilize Finch’s platform to target Crohnâ€

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  [0]=>
  string(4) "6071"
  ["article_id"]=>
  string(4) "6071"
  [1]=>
  string(50) "RDD Pharma signs LOI to acquire Naia Rare Diseases"
  ["article_title"]=>
  string(50) "RDD Pharma signs LOI to acquire Naia Rare Diseases"
  [2]=>
  string(150) "Closing of the transaction is anticipated to occur after the consummation of the proposed merger of RDD and Innovate Biopharmaceuticals, Inc. (Nasdaq:"
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  string(150) "Closing of the transaction is anticipated to occur after the consummation of the proposed merger of RDD and Innovate Biopharmaceuticals, Inc. (Nasdaq:"
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Closing of the transaction is anticipated to occur after the consummation of the proposed merger of RDD and Innovate Biopharmaceuticals, Inc. (Nasdaq: INNT) which will form a combined

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The post RDD Pharma signs LOI to acquire Naia Rare Diseases appeared first on Pharmaceutical Business review.

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Closing of the transaction is anticipated to occur after the consummation of the proposed merger of RDD and Innovate Biopharmaceuticals, Inc. (Nasdaq: INNT) which will form a combined

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The post RDD Pharma signs LOI to acquire Naia Rare Diseases appeared first on Pharmaceutical Business review.

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RDD Pharma signs LOI to acquire Naia Rare Diseases

Closing of the transaction is anticipated to occur after the consummation of the proposed merger of RDD and Innovate

array(40) {
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  string(4) "6072"
  ["article_id"]=>
  string(4) "6072"
  [1]=>
  string(48) "Merck to acquire Calporta Therapeutics for $576m"
  ["article_title"]=>
  string(48) "Merck to acquire Calporta Therapeutics for $576m"
  [2]=>
  string(150) "The transaction includes an upfront payment and contingent milestone payments. Calporta is involved in the development of selective small-molecule ago"
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  string(150) "The transaction includes an upfront payment and contingent milestone payments. Calporta is involved in the development of selective small-molecule ago"
  [3]=>
  string(569) "

The transaction includes an upfront payment and contingent milestone payments. Calporta is involved in the development of selective small-molecule agonists to TRPML1 (transient receptor potential cation channel, mucolipin

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The transaction includes an upfront payment and contingent milestone payments. Calporta is involved in the development of selective small-molecule agonists to TRPML1 (transient receptor potential cation channel, mucolipin

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