Highlights

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  [1]=>
  string(93) "Hansoh Pharma, Atomwise launch AI drug discovery collaboration for multiple therapeutic areas"
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  string(93) "Hansoh Pharma, Atomwise launch AI drug discovery collaboration for multiple therapeutic areas"
  [2]=>
  string(150) "Scientific teams from Atomwise and Hansoh Pharma will work closely together on the programs. The combination of complementary expertise and technologi"
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  string(150) "Scientific teams from Atomwise and Hansoh Pharma will work closely together on the programs. The combination of complementary expertise and technologi"
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Scientific teams from Atomwise and Hansoh Pharma will work closely together on the programs. The combination of complementary expertise and technologies has the potential to dramatically increase success

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Scientific teams from Atomwise and Hansoh Pharma will work closely together on the programs. The combination of complementary expertise and technologies has the potential to dramatically increase success

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The post Hansoh Pharma, Atomwise launch AI drug discovery collaboration for multiple therapeutic areas appeared first on Pharmaceutical Business review.

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Hansoh Pharma, Atomwise launch AI drug discovery collaboration for multiple therapeutic ar

Scientific teams from Atomwise and Hansoh Pharma will work closely together on the programs. The combination of compl

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  [1]=>
  string(93) "Roche’s Tecentriq monotherapy significantly improves OS in phase III lung cancer study"
  ["article_title"]=>
  string(93) "Roche’s Tecentriq monotherapy significantly improves OS in phase III lung cancer study"
  [2]=>
  string(150) "The trial is evaluating Tecentriq as a first-line (initial) monotherapy compared against cisplatin or carboplatin and pemetrexed or gemcitabine (chemo"
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  string(150) "The trial is evaluating Tecentriq as a first-line (initial) monotherapy compared against cisplatin or carboplatin and pemetrexed or gemcitabine (chemo"
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The trial is evaluating Tecentriq as a first-line (initial) monotherapy compared against cisplatin or carboplatin and pemetrexed or gemcitabine (chemotherapy) in advanced non-squamous and squamous non-small cell lung

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The post Roche’s Tecentriq monotherapy significantly improves OS in phase III lung cancer study appeared first on Pharmaceutical Business review.

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The trial is evaluating Tecentriq as a first-line (initial) monotherapy compared against cisplatin or carboplatin and pemetrexed or gemcitabine (chemotherapy) in advanced non-squamous and squamous non-small cell lung

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The post Roche’s Tecentriq monotherapy significantly improves OS in phase III lung cancer study appeared first on Pharmaceutical Business review.

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Roche’s Tecentriq monotherapy significantly improves OS in phase III lung cancer st

The trial is evaluating Tecentriq as a first-line (initial) monotherapy compared against cisplatin or carboplatin and

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  string(4) "4377"
  [1]=>
  string(81) "Merck initiates phase 3 programme for evobrutinib in relapsing multiple sclerosis"
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  string(81) "Merck initiates phase 3 programme for evobrutinib in relapsing multiple sclerosis"
  [2]=>
  string(154) "“Evobrutinib is a potential innovation for people living with MS, as it may offer a novel dual mechanism of action that is thought to impact myeloid"
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  string(154) "“Evobrutinib is a potential innovation for people living with MS, as it may offer a novel dual mechanism of action that is thought to impact myeloid"
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“Evobrutinib is a potential innovation for people living with MS, as it may offer a novel dual mechanism of action that is thought to impact myeloid cells in

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The post Merck initiates phase 3 programme for evobrutinib in relapsing multiple sclerosis appeared first on Pharmaceutical Business review.

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“Evobrutinib is a potential innovation for people living with MS, as it may offer a novel dual mechanism of action that is thought to impact myeloid cells in

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The post Merck initiates phase 3 programme for evobrutinib in relapsing multiple sclerosis appeared first on Pharmaceutical Business review.

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Merck initiates phase 3 programme for evobrutinib in relapsing multiple sclerosis

“Evobrutinib is a potential innovation for people living with MS, as it may offer a novel dual mechanism of act

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  string(4) "4378"
  [1]=>
  string(93) "Avalon Ventures and COI Pharmaceuticals announce acquisition of Sitari Pharmaceuticals by GSK"
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  string(93) "Avalon Ventures and COI Pharmaceuticals announce acquisition of Sitari Pharmaceuticals by GSK"
  [2]=>
  string(150) "Sitari has been developing a novel treatment for celiac disease and was the first company formed under the GSK-Avalon venture collaboration in 2013. S"
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  string(150) "Sitari has been developing a novel treatment for celiac disease and was the first company formed under the GSK-Avalon venture collaboration in 2013. S"
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Sitari has been developing a novel treatment for celiac disease and was the first company formed under the GSK-Avalon venture collaboration in 2013. Sitari was incubated at COI

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The post Avalon Ventures and COI Pharmaceuticals announce acquisition of Sitari Pharmaceuticals by GSK appeared first on Pharmaceutical Business review.

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Sitari has been developing a novel treatment for celiac disease and was the first company formed under the GSK-Avalon venture collaboration in 2013. Sitari was incubated at COI

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The post Avalon Ventures and COI Pharmaceuticals announce acquisition of Sitari Pharmaceuticals by GSK appeared first on Pharmaceutical Business review.

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Avalon Ventures and COI Pharmaceuticals announce acquisition of Sitari Pharmaceuticals by

Sitari has been developing a novel treatment for celiac disease and was the first company formed under the GSK-Avalon

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  string(4) "4379"
  [1]=>
  string(45) "Mallinckrodt to divest BioVectra for £202m"
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  string(45) "Mallinckrodt to divest BioVectra for £202m"
  [2]=>
  string(156) "The deal includes a fixed consideration of $175m (£141m), comprised of an upfront payment of $135 (£109m) and a long-term note for $40m (£32m), as "
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  string(156) "The deal includes a fixed consideration of $175m (£141m), comprised of an upfront payment of $135 (£109m) and a long-term note for $40m (£32m), as "
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The deal includes a fixed consideration of $175m (£141m), comprised of an upfront payment of $135 (£109m) and a long-term note for $40m (£32m), as well as contingent

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The post Mallinckrodt to divest BioVectra for £202m appeared first on Pharmaceutical Business review.

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The deal includes a fixed consideration of $175m (£141m), comprised of an upfront payment of $135 (£109m) and a long-term note for $40m (£32m), as well as contingent

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The post Mallinckrodt to divest BioVectra for £202m appeared first on Pharmaceutical Business review.

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Mallinckrodt to divest BioVectra for £202m

The deal includes a fixed consideration of $175m (£141m), comprised of an upfront payment of $135 (£109m) and a

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  string(4) "4380"
  [1]=>
  string(80) "FDA approves Xeris’ GVOKE injection for treatment of severe hypoglycaemia"
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  string(80) "FDA approves Xeris’ GVOKE injection for treatment of severe hypoglycaemia"
  [2]=>
  string(150) "GVOKE is a ready-to-use, room-temperature stable liquid glucagon product, which can be administered to the patient using a prefilled syringe or auto-i"
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  string(150) "GVOKE is a ready-to-use, room-temperature stable liquid glucagon product, which can be administered to the patient using a prefilled syringe or auto-i"
  [3]=>
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GVOKE is a ready-to-use, room-temperature stable liquid glucagon product, which can be administered to the patient using a prefilled syringe or auto-injector. The liquid glucagon product will be

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The post FDA approves Xeris’ GVOKE injection for treatment of severe hypoglycaemia appeared first on Pharmaceutical Business review.

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GVOKE is a ready-to-use, room-temperature stable liquid glucagon product, which can be administered to the patient using a prefilled syringe or auto-injector. The liquid glucagon product will be

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The post FDA approves Xeris’ GVOKE injection for treatment of severe hypoglycaemia appeared first on Pharmaceutical Business review.

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FDA approves Xeris’ GVOKE injection for treatment of severe hypoglycaemia

GVOKE is a ready-to-use, room-temperature stable liquid glucagon product, which can be administered to the patient us

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  string(4) "4765"
  [1]=>
  string(118) "Incyte announces first patient treated in phase 3 trial program evaluating Ruxolitinib cream in patients with vitiligo"
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  string(118) "Incyte announces first patient treated in phase 3 trial program evaluating Ruxolitinib cream in patients with vitiligo"
  [2]=>
  string(154) "“Vitiligo is a challenging and life-altering disease further complicated by the lack of effective treatment options available to physicians and thei"
  ["short_description"]=>
  string(154) "“Vitiligo is a challenging and life-altering disease further complicated by the lack of effective treatment options available to physicians and thei"
  [3]=>
  string(714) "

“Vitiligo is a challenging and life-altering disease further complicated by the lack of effective treatment options available to physicians and their patients,” said Jim Lee, M.D., Ph.D., Group

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The post Incyte announces first patient treated in phase 3 trial program evaluating Ruxolitinib cream in patients with vitiligo appeared first on Pharmaceutical Business review.

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“Vitiligo is a challenging and life-altering disease further complicated by the lack of effective treatment options available to physicians and their patients,” said Jim Lee, M.D., Ph.D., Group

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The post Incyte announces first patient treated in phase 3 trial program evaluating Ruxolitinib cream in patients with vitiligo appeared first on Pharmaceutical Business review.

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Incyte announces first patient treated in phase 3 trial program evaluating Ruxolitinib cre

“Vitiligo is a challenging and life-altering disease further complicated by the lack of effective treatment opt

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  [1]=>
  string(103) "Blade Therapeutics expands anti-fibrotic pipeline with acquisition of ATXCo and its autotaxin inhibitor"
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  string(103) "Blade Therapeutics expands anti-fibrotic pipeline with acquisition of ATXCo and its autotaxin inhibitor"
  [2]=>
  string(154) "“With the addition of this IND enabled program to our pipeline, we advance our agenda to bring innovative treatments to patients with fibrotic disor"
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  string(154) "“With the addition of this IND enabled program to our pipeline, we advance our agenda to bring innovative treatments to patients with fibrotic disor"
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“With the addition of this IND enabled program to our pipeline, we advance our agenda to bring innovative treatments to patients with fibrotic disorders,” stated Wendye Robbins, M.D.,

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The post Blade Therapeutics expands anti-fibrotic pipeline with acquisition of ATXCo and its autotaxin inhibitor appeared first on Pharmaceutical Business review.

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“With the addition of this IND enabled program to our pipeline, we advance our agenda to bring innovative treatments to patients with fibrotic disorders,” stated Wendye Robbins, M.D.,

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The post Blade Therapeutics expands anti-fibrotic pipeline with acquisition of ATXCo and its autotaxin inhibitor appeared first on Pharmaceutical Business review.

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Blade Therapeutics expands anti-fibrotic pipeline with acquisition of ATXCo and its autota

“With the addition of this IND enabled program to our pipeline, we advance our agenda to bring innovative treat

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  [1]=>
  string(95) "Jazz’s JZP-258 investigational medicine meets key end points in phase 3 narcolepsy trial"
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  string(95) "Jazz’s JZP-258 investigational medicine meets key end points in phase 3 narcolepsy trial"
  [2]=>
  string(150) "The phase 3 global, double-blind, placebo-controlled, randomised-withdrawal, multicentre study has assessed the efficacy and safety of JZP-258 in the "
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  string(150) "The phase 3 global, double-blind, placebo-controlled, randomised-withdrawal, multicentre study has assessed the efficacy and safety of JZP-258 in the "
  [3]=>
  string(612) "

The phase 3 global, double-blind, placebo-controlled, randomised-withdrawal, multicentre study has assessed the efficacy and safety of JZP-258 in the treatment of cataplexy and excessive daytime sleepiness (EDS) in

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The post Jazz’s JZP-258 investigational medicine meets key end points in phase 3 narcolepsy trial appeared first on Pharmaceutical Business review.

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The phase 3 global, double-blind, placebo-controlled, randomised-withdrawal, multicentre study has assessed the efficacy and safety of JZP-258 in the treatment of cataplexy and excessive daytime sleepiness (EDS) in

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The post Jazz’s JZP-258 investigational medicine meets key end points in phase 3 narcolepsy trial appeared first on Pharmaceutical Business review.

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Jazz’s JZP-258 investigational medicine meets key end points in phase 3 narcolepsy

The phase 3 global, double-blind, placebo-controlled, randomised-withdrawal, multicentre study has assessed the effic

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  string(4) "4768"
  [1]=>
  string(142) "Amphivena closes $62m Series C financing to expand clinical development of AMV564 into solid tumors and to develop T Cell engagement portfolio"
  ["article_title"]=>
  string(142) "Amphivena closes $62m Series C financing to expand clinical development of AMV564 into solid tumors and to develop T Cell engagement portfolio"
  [2]=>
  string(150) "The round was co-led by NanoDimension and Qiming Venture Partners USA, and included new investors Clough Capital, Aju IB, Korys Merieux, Kaitai Capita"
  ["short_description"]=>
  string(150) "The round was co-led by NanoDimension and Qiming Venture Partners USA, and included new investors Clough Capital, Aju IB, Korys Merieux, Kaitai Capita"
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The round was co-led by NanoDimension and Qiming Venture Partners USA, and included new investors Clough Capital, Aju IB, Korys Merieux, Kaitai Capital, Industrial Investors, Nawton Limited and

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The post Amphivena closes $62m Series C financing to expand clinical development of AMV564 into solid tumors and to develop T Cell engagement portfolio appeared first on Pharmaceutical Business review.

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The round was co-led by NanoDimension and Qiming Venture Partners USA, and included new investors Clough Capital, Aju IB, Korys Merieux, Kaitai Capital, Industrial Investors, Nawton Limited and

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The post Amphivena closes $62m Series C financing to expand clinical development of AMV564 into solid tumors and to develop T Cell engagement portfolio appeared first on Pharmaceutical Business review.

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Amphivena closes $62m Series C financing to expand clinical development of AMV564 into sol

The round was co-led by NanoDimension and Qiming Venture Partners USA, and included new investors Clough Capital, Aju

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Aldeyra Therapeutics receives fast track designation for ADX-2191 for prevention of prolif

“Fast track designation is an important milestone for our retinal disease platform, and promising news for PVR