Highlights

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  string(95) "Beam Therapeutics licenses SIRION Biotech’s LentiBOOST Technology for its CAR-T pipeline"
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  string(95) "Beam Therapeutics licenses SIRION Biotech’s LentiBOOST Technology for its CAR-T pipeline"
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  string(150) "CAR-T cell therapy represents a promising and future-defining shift in cancer treatment. Beam Therapeutics is developing a new generation of CAR-T pro"
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CAR-T cell therapy represents a promising and future-defining shift in cancer treatment. Beam Therapeutics is developing a new generation of CAR-T product candidates using its proprietary base editing

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CAR-T cell therapy represents a promising and future-defining shift in cancer treatment. Beam Therapeutics is developing a new generation of CAR-T product candidates using its proprietary base editing

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The post Beam Therapeutics licenses SIRION Biotech’s LentiBOOST Technology for its CAR-T pipeline appeared first on Pharmaceutical Business review.

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Beam Therapeutics licenses SIRION Biotech’s LentiBOOST Technology for its CAR-T pip

CAR-T cell therapy represents a promising and future-defining shift in cancer treatment. Beam Therapeutics is develop

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  string(96) "Montreal Heart Institute, NYU Grossman School of Medicine collaborate on COVID-19 clinical trial"
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  string(96) "Montreal Heart Institute, NYU Grossman School of Medicine collaborate on COVID-19 clinical trial"
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  string(150) "The clinical study, dubbed COLCORONA, will assess whether colchicine will serve as an effective treatment to prevent the phenomenon of major inflammat"
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The clinical study, dubbed COLCORONA, will assess whether colchicine will serve as an effective treatment to prevent the phenomenon of major inflammatory storm present in adults suffering from

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The clinical study, dubbed COLCORONA, will assess whether colchicine will serve as an effective treatment to prevent the phenomenon of major inflammatory storm present in adults suffering from

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Montreal Heart Institute, NYU Grossman School of Medicine collaborate on COVID-19 clinical

The clinical study, dubbed COLCORONA, will assess whether colchicine will serve as an effective treatment to prevent

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  string(50) "Takeda gets EU approval for ALUNBRIG in ALK+ NSCLC"
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  string(50) "Takeda gets EU approval for ALUNBRIG in ALK+ NSCLC"
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The latest approval from the European Commission (EC) authorises ALUNBRIG to be used as a monotherapy for the treatment of adults having anaplastic lymphoma kinase-positive (ALK+) advanced non-small

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The latest approval from the European Commission (EC) authorises ALUNBRIG to be used as a monotherapy for the treatment of adults having anaplastic lymphoma kinase-positive (ALK+) advanced non-small

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The post Takeda gets EU approval for ALUNBRIG in ALK+ NSCLC appeared first on Pharmaceutical Business review.

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Takeda gets EU approval for ALUNBRIG in ALK+ NSCLC

The latest approval from the European Commission (EC) authorises ALUNBRIG to be used as a monotherapy for the treatme

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  [1]=>
  string(81) "Alnylam and Dicerna form RNAi Therapeutics collaboration on alpha-1 liver disease"
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  string(81) "Alnylam and Dicerna form RNAi Therapeutics collaboration on alpha-1 liver disease"
  [2]=>
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In addition, the companies have completed a cross-license of their respective intellectual property for Alnylam’s lumasiran and Dicerna’s nedosiran investigational programs for the treatment of primary hyperoxaluria (PH).

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In addition, the companies have completed a cross-license of their respective intellectual property for Alnylam’s lumasiran and Dicerna’s nedosiran investigational programs for the treatment of primary hyperoxaluria (PH).

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The post Alnylam and Dicerna form RNAi Therapeutics collaboration on alpha-1 liver disease appeared first on Pharmaceutical Business review.

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Alnylam and Dicerna form RNAi Therapeutics collaboration on alpha-1 liver disease

In addition, the companies have completed a cross-license of their respective intellectual property for Alnylamâ€â

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  string(122) "Gilead Sciences, Second Genome announce strategic collaboration in biomarker and inflammatory bowel disease drug discovery"
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  string(122) "Gilead Sciences, Second Genome announce strategic collaboration in biomarker and inflammatory bowel disease drug discovery"
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Under the terms of the agreement, Second Genome will utilize its proprietary Microbiome Analytics Platform™ to identify novel biomarkers associated with clinical response to Gilead’s investigational medicines. This

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Under the terms of the agreement, Second Genome will utilize its proprietary Microbiome Analytics Platform™ to identify novel biomarkers associated with clinical response to Gilead’s investigational medicines. This

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The post Gilead Sciences, Second Genome announce strategic collaboration in biomarker and inflammatory bowel disease drug discovery appeared first on Pharmaceutical Business review.

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Gilead Sciences, Second Genome announce strategic collaboration in biomarker and inflammat

Under the terms of the agreement, Second Genome will utilize its proprietary Microbiome Analytics Platformâ„¢ to

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  string(56) "ASTCT, ACCC and AACI launch initiative for CAR T therapy"
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This collaboration aims to improve the evaluation process for CAR T therapy for cancer patients. It focuses on five crucial factors to ensure timely and personalised care for

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The post ASTCT, ACCC and AACI launch initiative for CAR T therapy appeared first on Pharmaceutical Business review.

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This collaboration aims to improve the evaluation process for CAR T therapy for cancer patients. It focuses on five crucial factors to ensure timely and personalised care for

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The post ASTCT, ACCC and AACI launch initiative for CAR T therapy appeared first on Pharmaceutical Business review.

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ASTCT, ACCC and AACI launch initiative for CAR T therapy

This collaboration aims to improve the evaluation process for CAR T therapy for cancer patients. It focuses on five c

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  [1]=>
  string(53) "Zokinvy gets Japanese approval for Progeria treatment"
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The approval from the Ministry of Health, Labor and Welfare (MHLW) marks a significant milestone in the treatment of the ultra-rare, fatal paediatric disease characterised by accelerated aging.

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The post Zokinvy gets Japanese approval for Progeria treatment appeared first on Pharmaceutical Business review.

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The approval from the Ministry of Health, Labor and Welfare (MHLW) marks a significant milestone in the treatment of the ultra-rare, fatal paediatric disease characterised by accelerated aging.

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The post Zokinvy gets Japanese approval for Progeria treatment appeared first on Pharmaceutical Business review.

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Zokinvy gets Japanese approval for Progeria treatment

The approval from the Ministry of Health, Labor and Welfare (MHLW) marks a significant milestone in the treatment of

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  string(49) "Kindeva Drug Delivery acquires Summit Biosciences"
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Financial terms of the deal were undisclosed. The move is set to enhance Kindeva’s drug-delivery capabilities by adding a new platform to its portfolio. Kindeva CEO Milton Boyer

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The post Kindeva Drug Delivery acquires Summit Biosciences appeared first on Pharmaceutical Business review.

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Financial terms of the deal were undisclosed. The move is set to enhance Kindeva’s drug-delivery capabilities by adding a new platform to its portfolio. Kindeva CEO Milton Boyer

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The post Kindeva Drug Delivery acquires Summit Biosciences appeared first on Pharmaceutical Business review.

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Kindeva Drug Delivery acquires Summit Biosciences

Financial terms of the deal were undisclosed. The move is set to enhance Kindeva’s drug-delivery capabilities b

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Located in Mississauga, Canada, the 3,300ft2 facility is designed for the development and scaling of monoclonal antibodies and other mammalian-based therapeutic proteins. The facility will provide a comprehensive

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Located in Mississauga, Canada, the 3,300ft2 facility is designed for the development and scaling of monoclonal antibodies and other mammalian-based therapeutic proteins. The facility will provide a comprehensive

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The post Eurofins Alphora completes Canadian biologics development facility appeared first on Pharmaceutical Business review.

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Eurofins Alphora completes Canadian biologics development facility

Located in Mississauga, Canada, the 3,300ft2 facility is designed for the development and scaling of monoclonal antib

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  [1]=>
  string(67) "US FDA updates Sanofi’s Dupixent label for atopic dermatitis"
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  string(67) "US FDA updates Sanofi’s Dupixent label for atopic dermatitis"
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This label update is based on findings from the Phase III LIBERTY-AD-HAFT trial, the first to evaluate a biologic for this patient group. Dupixent, a fully human monoclonal

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This label update is based on findings from the Phase III LIBERTY-AD-HAFT trial, the first to evaluate a biologic for this patient group. Dupixent, a fully human monoclonal

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The post US FDA updates Sanofi’s Dupixent label for atopic dermatitis appeared first on Pharmaceutical Business review.

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US FDA updates Sanofi’s Dupixent label for atopic dermatitis

This label update is based on findings from the Phase III LIBERTY-AD-HAFT trial, the first to evaluate a biologic for

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The IND clearance has been received for patients with GPC3-positive stage IIIa hepatocellular carcinoma at high risk of recurrence after surgical resection. CT011 is designed to target Glypican-3

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CARsgen’s CT011 receives IND clearance from China’s NMPA

The IND clearance has been received for patients with GPC3-positive stage IIIa hepatocellular carcinoma at high risk

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The post GENESIS and Deciphera enter distribution agreement for Ripretinib appeared first on Pharmaceutical Business review.

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GENESIS and Deciphera enter distribution agreement for Ripretinib

This agreement focuses on treating fourth-line gastrointestinal stromal tumours (GIST) in adult patients. The territo