Highlights

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  string(4) "5533"
  [1]=>
  string(80) "Halozyme’s PEGPH20 pancreas cancer drug candidate fails in HALO-301 trial"
  ["article_title"]=>
  string(80) "Halozyme’s PEGPH20 pancreas cancer drug candidate fails in HALO-301 trial"
  [2]=>
  string(150) "PEGPH20 was being assessed in combination with ABRAXANE (nab-paclitaxel) and gemcitabinein in the HALO-301 study as a first-line therapy for the condi"
  ["short_description"]=>
  string(150) "PEGPH20 was being assessed in combination with ABRAXANE (nab-paclitaxel) and gemcitabinein in the HALO-301 study as a first-line therapy for the condi"
  [3]=>
  string(582) "

PEGPH20 was being assessed in combination with ABRAXANE (nab-paclitaxel) and gemcitabinein in the HALO-301 study as a first-line therapy for the condition. The late-stage trial enrolled 500 patients

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The post Halozyme’s PEGPH20 pancreas cancer drug candidate fails in HALO-301 trial appeared first on Pharmaceutical Business review.

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PEGPH20 was being assessed in combination with ABRAXANE (nab-paclitaxel) and gemcitabinein in the HALO-301 study as a first-line therapy for the condition. The late-stage trial enrolled 500 patients

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The post Halozyme’s PEGPH20 pancreas cancer drug candidate fails in HALO-301 trial appeared first on Pharmaceutical Business review.

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Halozyme’s PEGPH20 pancreas cancer drug candidate fails in HALO-301 trial

PEGPH20 was being assessed in combination with ABRAXANE (nab-paclitaxel) and gemcitabinein in the HALO-301 study as a

array(40) {
  [0]=>
  string(4) "5534"
  ["article_id"]=>
  string(4) "5534"
  [1]=>
  string(88) "RedHill Biopharma secures FDA approval for Talicia to treat H pylori infection in adults"
  ["article_title"]=>
  string(88) "RedHill Biopharma secures FDA approval for Talicia to treat H pylori infection in adults"
  [2]=>
  string(150) "RedHill said that its Talicia has been indicated for oral administration in the form of delayed-release capsules in 10mg, or 250mg or in 12.5mg dosage"
  ["short_description"]=>
  string(150) "RedHill said that its Talicia has been indicated for oral administration in the form of delayed-release capsules in 10mg, or 250mg or in 12.5mg dosage"
  [3]=>
  string(570) "

RedHill said that its Talicia has been indicated for oral administration in the form of delayed-release capsules in 10mg, or 250mg or in 12.5mg dosage. RedHill Biopharma chief

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The post RedHill Biopharma secures FDA approval for Talicia to treat H pylori infection in adults appeared first on Pharmaceutical Business review.

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RedHill said that its Talicia has been indicated for oral administration in the form of delayed-release capsules in 10mg, or 250mg or in 12.5mg dosage. RedHill Biopharma chief

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The post RedHill Biopharma secures FDA approval for Talicia to treat H pylori infection in adults appeared first on Pharmaceutical Business review.

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RedHill Biopharma secures FDA approval for Talicia to treat H pylori infection in adults

RedHill said that its Talicia has been indicated for oral administration in the form of delayed-release capsules in 1

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  string(4) "5535"
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  string(4) "5535"
  [1]=>
  string(97) "BioCryst begins phase 1 trial with BCX9250 for treatment of fibrodysplasia ossificans progressiva"
  ["article_title"]=>
  string(97) "BioCryst begins phase 1 trial with BCX9250 for treatment of fibrodysplasia ossificans progressiva"
  [2]=>
  string(150) "The Phase 1 trial will evaluate single and multiple ascending doses of oral BCX9250 in healthy volunteers. The company expects to report the results f"
  ["short_description"]=>
  string(150) "The Phase 1 trial will evaluate single and multiple ascending doses of oral BCX9250 in healthy volunteers. The company expects to report the results f"
  [3]=>
  string(633) "

The Phase 1 trial will evaluate single and multiple ascending doses of oral BCX9250 in healthy volunteers. The company expects to report the results from the trial in

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The post BioCryst begins phase 1 trial with BCX9250 for treatment of fibrodysplasia ossificans progressiva appeared first on Pharmaceutical Business review.

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The Phase 1 trial will evaluate single and multiple ascending doses of oral BCX9250 in healthy volunteers. The company expects to report the results from the trial in

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The post BioCryst begins phase 1 trial with BCX9250 for treatment of fibrodysplasia ossificans progressiva appeared first on Pharmaceutical Business review.

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BioCryst begins phase 1 trial with BCX9250 for treatment of fibrodysplasia ossificans prog

The Phase 1 trial will evaluate single and multiple ascending doses of oral BCX9250 in healthy volunteers. The compan

array(40) {
  [0]=>
  string(4) "5536"
  ["article_id"]=>
  string(4) "5536"
  [1]=>
  string(78) "Novartis’ Cosentyx delivers mixed results in EXCEED trial in active PsA"
  ["article_title"]=>
  string(78) "Novartis’ Cosentyx delivers mixed results in EXCEED trial in active PsA"
  [2]=>
  string(150) "Cosentyx, which is an inhibitor of interleukin-17A (IL-17A), could not show statistical significance for superiority in ACR 20 over the AbbVie drug in"
  ["short_description"]=>
  string(150) "Cosentyx, which is an inhibitor of interleukin-17A (IL-17A), could not show statistical significance for superiority in ACR 20 over the AbbVie drug in"
  [3]=>
  string(569) "

Cosentyx, which is an inhibitor of interleukin-17A (IL-17A), could not show statistical significance for superiority in ACR 20 over the AbbVie drug in the head-to-head late-stage trial. As

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The post Novartis’ Cosentyx delivers mixed results in EXCEED trial in active PsA appeared first on Pharmaceutical Business review.

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Cosentyx, which is an inhibitor of interleukin-17A (IL-17A), could not show statistical significance for superiority in ACR 20 over the AbbVie drug in the head-to-head late-stage trial. As

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The post Novartis’ Cosentyx delivers mixed results in EXCEED trial in active PsA appeared first on Pharmaceutical Business review.

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Novartis’ Cosentyx delivers mixed results in EXCEED trial in active PsA

Cosentyx, which is an inhibitor of interleukin-17A (IL-17A), could not show statistical significance for superiority

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  string(4) "5537"
  ["article_id"]=>
  string(4) "5537"
  [1]=>
  string(91) "Amgen enters into strategic collaboration with BeiGene to expand oncology presence in China"
  ["article_title"]=>
  string(91) "Amgen enters into strategic collaboration with BeiGene to expand oncology presence in China"
  [2]=>
  string(150) "BeiGene is a research-based, oncology-focused biotechnology company with an established and highly experienced team in China, including a 700-person c"
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  string(150) "BeiGene is a research-based, oncology-focused biotechnology company with an established and highly experienced team in China, including a 700-person c"
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  string(691) "

BeiGene is a research-based, oncology-focused biotechnology company with an established and highly experienced team in China, including a 700-person commercial organization and a 600-person clinical development organization. “This

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The post Amgen enters into strategic collaboration with BeiGene to expand oncology presence in China appeared first on Pharmaceutical Business review.

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BeiGene is a research-based, oncology-focused biotechnology company with an established and highly experienced team in China, including a 700-person commercial organization and a 600-person clinical development organization. “This

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The post Amgen enters into strategic collaboration with BeiGene to expand oncology presence in China appeared first on Pharmaceutical Business review.

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Amgen enters into strategic collaboration with BeiGene to expand oncology presence in Chin

BeiGene is a research-based, oncology-focused biotechnology company with an established and highly experienced team i

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  string(4) "5538"
  [1]=>
  string(104) "Daiichi Sankyo initiates clinical trial of DS-7300 in collaboration with Sarah Cannon Research Institute"
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  string(104) "Daiichi Sankyo initiates clinical trial of DS-7300 in collaboration with Sarah Cannon Research Institute"
  [2]=>
  string(150) "The study is the first in the strategic oncology partnership announced between Daiichi Sankyo and Sarah Cannon, designed to expedite and optimize glob"
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  string(150) "The study is the first in the strategic oncology partnership announced between Daiichi Sankyo and Sarah Cannon, designed to expedite and optimize glob"
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The study is the first in the strategic oncology partnership announced between Daiichi Sankyo and Sarah Cannon, designed to expedite and optimize global clinical development of Daiichi Sankyo’s

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The post Daiichi Sankyo initiates clinical trial of DS-7300 in collaboration with Sarah Cannon Research Institute appeared first on Pharmaceutical Business review.

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The study is the first in the strategic oncology partnership announced between Daiichi Sankyo and Sarah Cannon, designed to expedite and optimize global clinical development of Daiichi Sankyo’s

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The post Daiichi Sankyo initiates clinical trial of DS-7300 in collaboration with Sarah Cannon Research Institute appeared first on Pharmaceutical Business review.

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Daiichi Sankyo initiates clinical trial of DS-7300 in collaboration with Sarah Cannon Rese

The study is the first in the strategic oncology partnership announced between Daiichi Sankyo and Sarah Cannon, desig

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  string(4) "5539"
  ["article_id"]=>
  string(4) "5539"
  [1]=>
  string(109) "Cycle Pharmaceuticals and Catalent partner to develop treatments for rare diseases using Zydis ODT technology"
  ["article_title"]=>
  string(109) "Cycle Pharmaceuticals and Catalent partner to develop treatments for rare diseases using Zydis ODT technology"
  [2]=>
  string(157) "This agreement covers four products in rare metabolic and neurological disorders and each product will utilise Catalent’s Zydis® oral disintegratin"
  ["short_description"]=>
  string(157) "This agreement covers four products in rare metabolic and neurological disorders and each product will utilise Catalent’s Zydis® oral disintegratin"
  [3]=>
  string(713) "

This agreement covers four products in rare metabolic and neurological disorders and each product will utilise Catalent’s Zydis® oral disintegrating tablet (ODT) and Zydis Ultra® technologies. Zydis technology

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The post Cycle Pharmaceuticals and Catalent partner to develop treatments for rare diseases using Zydis ODT technology appeared first on Pharmaceutical Business review.

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This agreement covers four products in rare metabolic and neurological disorders and each product will utilise Catalent’s Zydis® oral disintegrating tablet (ODT) and Zydis Ultra® technologies. Zydis technology

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The post Cycle Pharmaceuticals and Catalent partner to develop treatments for rare diseases using Zydis ODT technology appeared first on Pharmaceutical Business review.

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Cycle Pharmaceuticals and Catalent partner to develop treatments for rare diseases using Z

This agreement covers four products in rare metabolic and neurological disorders and each product will utilise Catale

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  ["article_id"]=>
  string(4) "5697"
  [1]=>
  string(115) "Cyclica collaborates with Enamine to use REAL technology in its ligand design platform for AI-augmented drug design"
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  string(115) "Cyclica collaborates with Enamine to use REAL technology in its ligand design platform for AI-augmented drug design"
  [2]=>
  string(160) "The companies aim to empower Cyclica’s patented, evolutionary algorithm with new design options based on the 73,000 Enamine’s in-stock building bl"
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  string(160) "The companies aim to empower Cyclica’s patented, evolutionary algorithm with new design options based on the 73,000 Enamine’s in-stock building bl"
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The companies aim to empower Cyclica’s patented, evolutionary algorithm with new design options based on the 73,000 Enamine’s in-stock building blocks and 171 thoroughly validated synthesis procedures. The

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The post Cyclica collaborates with Enamine to use REAL technology in its ligand design platform for AI-augmented drug design appeared first on Pharmaceutical Business review.

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The companies aim to empower Cyclica’s patented, evolutionary algorithm with new design options based on the 73,000 Enamine’s in-stock building blocks and 171 thoroughly validated synthesis procedures. The

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The post Cyclica collaborates with Enamine to use REAL technology in its ligand design platform for AI-augmented drug design appeared first on Pharmaceutical Business review.

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Cyclica collaborates with Enamine to use REAL technology in its ligand design platform for

The companies aim to empower Cyclica’s patented, evolutionary algorithm with new design options based on the 7

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  string(4) "5698"
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  string(4) "5698"
  [1]=>
  string(80) "A2 Biotherapeutics emerges from Stealth Mode to develop tumour cell therapeutics"
  ["article_title"]=>
  string(80) "A2 Biotherapeutics emerges from Stealth Mode to develop tumour cell therapeutics"
  [2]=>
  string(150) "The company, founded in 2018 by veteran biotechnology leaders, has a unique and potentially broad solution for the central problem of cancer research "
  ["short_description"]=>
  string(150) "The company, founded in 2018 by veteran biotechnology leaders, has a unique and potentially broad solution for the central problem of cancer research "
  [3]=>
  string(616) "

The company, founded in 2018 by veteran biotechnology leaders, has a unique and potentially broad solution for the central problem of cancer research – targeted killing of tumor

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The post A2 Biotherapeutics emerges from Stealth Mode to develop tumour cell therapeutics appeared first on Pharmaceutical Business review.

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The company, founded in 2018 by veteran biotechnology leaders, has a unique and potentially broad solution for the central problem of cancer research – targeted killing of tumor

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The post A2 Biotherapeutics emerges from Stealth Mode to develop tumour cell therapeutics appeared first on Pharmaceutical Business review.

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A2 Biotherapeutics emerges from Stealth Mode to develop tumour cell therapeutics

The company, founded in 2018 by veteran biotechnology leaders, has a unique and potentially broad solution for the ce

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  string(4) "5699"
  ["article_id"]=>
  string(4) "5699"
  [1]=>
  string(66) "Sandoz secures FDA approval for pegfilgrastim biosimilar Ziextenzo"
  ["article_title"]=>
  string(66) "Sandoz secures FDA approval for pegfilgrastim biosimilar Ziextenzo"
  [2]=>
  string(150) "Ziextenzo, like its reference drug pegfilgrastim, has been indicated to reduce the chances of infection caused by low white blood cell count with a fe"
  ["short_description"]=>
  string(150) "Ziextenzo, like its reference drug pegfilgrastim, has been indicated to reduce the chances of infection caused by low white blood cell count with a fe"
  [3]=>
  string(554) "

Ziextenzo, like its reference drug pegfilgrastim, has been indicated to reduce the chances of infection caused by low white blood cell count with a fever – a condition

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The post Sandoz secures FDA approval for pegfilgrastim biosimilar Ziextenzo appeared first on Pharmaceutical Business review.

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Ziextenzo, like its reference drug pegfilgrastim, has been indicated to reduce the chances of infection caused by low white blood cell count with a fever – a condition

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The post Sandoz secures FDA approval for pegfilgrastim biosimilar Ziextenzo appeared first on Pharmaceutical Business review.

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Sandoz secures FDA approval for pegfilgrastim biosimilar Ziextenzo

Ziextenzo, like its reference drug pegfilgrastim, has been indicated to reduce the chances of infection caused by low

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The company will use the new manufacturing plant for formulation, fill, finish and secondary packaging of the TAK-003 tetravalent dengue vaccine candidate. Takeda started the initial construction activities

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The post Japan’s Takeda opens dengue vaccine manufacturing facility in Germany appeared first on Pharmaceutical Business review.

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The post Japan’s Takeda opens dengue vaccine manufacturing facility in Germany appeared first on Pharmaceutical Business review.

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Japan’s Takeda opens dengue vaccine manufacturing facility in Germany

The company will use the new manufacturing plant for formulation, fill, finish and secondary packaging of the TAK-003

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SB11, a biosimilar candidate referencing LUCENTIS (ranibizumab), is undergoing phase 3 clinical trial, while SB15, a biosimilar candidate referencing EYLEAiii (aflibercept), is in pre-clinical development. In addition, the

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The post Samsung Bioepis enters into commercialisation agreement for next-generation biosimilar candidates appeared first on Pharmaceutical Business review.

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SB11, a biosimilar candidate referencing LUCENTIS (ranibizumab), is undergoing phase 3 clinical trial, while SB15, a biosimilar candidate referencing EYLEAiii (aflibercept), is in pre-clinical development. In addition, the

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The post Samsung Bioepis enters into commercialisation agreement for next-generation biosimilar candidates appeared first on Pharmaceutical Business review.

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Samsung Bioepis enters into commercialisation agreement for next-generation biosimilar can

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