Highlights

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  [1]=>
  string(92) "BioCryst begins proof of concept trial in PNH patients with oral Factor D inhibitor, BCX9930"
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  string(92) "BioCryst begins proof of concept trial in PNH patients with oral Factor D inhibitor, BCX9930"
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  string(150) "BCX9930 is an oral Factor D inhibitor discovered and developed by BioCryst for the treatment of complement-mediated diseases. The company expects to r"
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  string(150) "BCX9930 is an oral Factor D inhibitor discovered and developed by BioCryst for the treatment of complement-mediated diseases. The company expects to r"
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BCX9930 is an oral Factor D inhibitor discovered and developed by BioCryst for the treatment of complement-mediated diseases. The company expects to report data from the proof of

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BCX9930 is an oral Factor D inhibitor discovered and developed by BioCryst for the treatment of complement-mediated diseases. The company expects to report data from the proof of

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The post BioCryst begins proof of concept trial in PNH patients with oral Factor D inhibitor, BCX9930 appeared first on Pharmaceutical Business review.

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BioCryst begins proof of concept trial in PNH patients with oral Factor D inhibitor, BCX99

BCX9930 is an oral Factor D inhibitor discovered and developed by BioCryst for the treatment of complement-mediated d

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  [1]=>
  string(92) "Urovant Sciences announces US FDA acceptance of NDA for Vibegron to treat overactive bladder"
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  string(92) "Urovant Sciences announces US FDA acceptance of NDA for Vibegron to treat overactive bladder"
  [2]=>
  string(150) "The NDA has been assigned a Prescription Drug User Fee Act (PDUFA) goal date of December 26, 2020. In addition, the FDA has communicated that they are"
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  string(150) "The NDA has been assigned a Prescription Drug User Fee Act (PDUFA) goal date of December 26, 2020. In addition, the FDA has communicated that they are"
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The NDA has been assigned a Prescription Drug User Fee Act (PDUFA) goal date of December 26, 2020. In addition, the FDA has communicated that they are not

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The NDA has been assigned a Prescription Drug User Fee Act (PDUFA) goal date of December 26, 2020. In addition, the FDA has communicated that they are not

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The post Urovant Sciences announces US FDA acceptance of NDA for Vibegron to treat overactive bladder appeared first on Pharmaceutical Business review.

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Urovant Sciences announces US FDA acceptance of NDA for Vibegron to treat overactive bladd

The NDA has been assigned a Prescription Drug User Fee Act (PDUFA) goal date of December 26, 2020. In addition, the F

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  [1]=>
  string(67) "Zydus secures DCGI approval for Saroglitazar to treat liver disease"
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  string(67) "Zydus secures DCGI approval for Saroglitazar to treat liver disease"
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  string(150) "NASH, a progressive disease of the liver, commences with fat accumulation in the liver and may lead to cirrhosis and liver failure. Saroglitazar is cl"
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  string(150) "NASH, a progressive disease of the liver, commences with fat accumulation in the liver and may lead to cirrhosis and liver failure. Saroglitazar is cl"
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NASH, a progressive disease of the liver, commences with fat accumulation in the liver and may lead to cirrhosis and liver failure. Saroglitazar is claimed to be the

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NASH, a progressive disease of the liver, commences with fat accumulation in the liver and may lead to cirrhosis and liver failure. Saroglitazar is claimed to be the

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The post Zydus secures DCGI approval for Saroglitazar to treat liver disease appeared first on Pharmaceutical Business review.

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Zydus secures DCGI approval for Saroglitazar to treat liver disease

NASH, a progressive disease of the liver, commences with fat accumulation in the liver and may lead to cirrhosis and

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  [1]=>
  string(59) "Amunix raises $73m in Series A financing led by Omega Funds"
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  string(59) "Amunix raises $73m in Series A financing led by Omega Funds"
  [2]=>
  string(150) "Boston-based Omega Funds led the financing, with participation from existing investor Frazier Healthcare Partners and new investors Longitude Capital,"
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  string(150) "Boston-based Omega Funds led the financing, with participation from existing investor Frazier Healthcare Partners and new investors Longitude Capital,"
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Boston-based Omega Funds led the financing, with participation from existing investor Frazier Healthcare Partners and new investors Longitude Capital, Redmile Group, Polaris Partners, Casdin Capital, Two River, Venrock,

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Boston-based Omega Funds led the financing, with participation from existing investor Frazier Healthcare Partners and new investors Longitude Capital, Redmile Group, Polaris Partners, Casdin Capital, Two River, Venrock,

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The post Amunix raises $73m in Series A financing led by Omega Funds appeared first on Pharmaceutical Business review.

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Amunix raises $73m in Series A financing led by Omega Funds

Boston-based Omega Funds led the financing, with participation from existing investor Frazier Healthcare Partners and

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  string(4) "8127"
  [1]=>
  string(135) "Scientists from Merck and the Walter and Eliza Hall Institute of Medical Research discover novel class of candidate anti malaria agents"
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  string(135) "Scientists from Merck and the Walter and Eliza Hall Institute of Medical Research discover novel class of candidate anti malaria agents"
  [2]=>
  string(150) "Specifically, they identified novel dual inhibitors of plasmepsins IX and X (PMIX and PMX), two proteases that are essential to Plasmodium falciparum,"
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  string(150) "Specifically, they identified novel dual inhibitors of plasmepsins IX and X (PMIX and PMX), two proteases that are essential to Plasmodium falciparum,"
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Specifically, they identified novel dual inhibitors of plasmepsins IX and X (PMIX and PMX), two proteases that are essential to Plasmodium falciparum, the predominant cause of the most

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The post Scientists from Merck and the Walter and Eliza Hall Institute of Medical Research discover novel class of candidate anti malaria agents appeared first on Pharmaceutical Business review.

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Specifically, they identified novel dual inhibitors of plasmepsins IX and X (PMIX and PMX), two proteases that are essential to Plasmodium falciparum, the predominant cause of the most

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The post Scientists from Merck and the Walter and Eliza Hall Institute of Medical Research discover novel class of candidate anti malaria agents appeared first on Pharmaceutical Business review.

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Scientists from Merck and the Walter and Eliza Hall Institute of Medical Research discover

Specifically, they identified novel dual inhibitors of plasmepsins IX and X (PMIX and PMX), two proteases that are es

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  string(4) "8255"
  [1]=>
  string(75) "Bristol Myers Squibb gets FDA nod for Opdivo + Yervoy to treat liver cancer"
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  string(75) "Bristol Myers Squibb gets FDA nod for Opdivo + Yervoy to treat liver cancer"
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  string(155) "The FDA accelerated approval was based on Opdivo + Yervoy’s overall response rate and duration of response in the cohort of the phase 1/2 CheckMate "
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  string(155) "The FDA accelerated approval was based on Opdivo + Yervoy’s overall response rate and duration of response in the cohort of the phase 1/2 CheckMate "
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The FDA accelerated approval was based on Opdivo + Yervoy’s overall response rate and duration of response in the cohort of the phase 1/2 CheckMate -040 trial. Around

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The post Bristol Myers Squibb gets FDA nod for Opdivo + Yervoy to treat liver cancer appeared first on Pharmaceutical Business review.

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The FDA accelerated approval was based on Opdivo + Yervoy’s overall response rate and duration of response in the cohort of the phase 1/2 CheckMate -040 trial. Around

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The post Bristol Myers Squibb gets FDA nod for Opdivo + Yervoy to treat liver cancer appeared first on Pharmaceutical Business review.

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Bristol Myers Squibb gets FDA nod for Opdivo + Yervoy to treat liver cancer

The FDA accelerated approval was based on Opdivo + Yervoy’s overall response rate and duration of response in

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  [1]=>
  string(64) "TOURMALINE-MM2 study on NINLARO fails to deliver desired results"
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  string(64) "TOURMALINE-MM2 study on NINLARO fails to deliver desired results"
  [2]=>
  string(150) "The late-stage TOURMALINE-MM2 trial featured 705 adult patients who are newly diagnosed with multiple myeloma and are not candidates for transplant. N"
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  string(150) "The late-stage TOURMALINE-MM2 trial featured 705 adult patients who are newly diagnosed with multiple myeloma and are not candidates for transplant. N"
  [3]=>
  string(560) "

The late-stage TOURMALINE-MM2 trial featured 705 adult patients who are newly diagnosed with multiple myeloma and are not candidates for transplant. NINLARO is an oral proteasome inhibitor, which

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The post TOURMALINE-MM2 study on NINLARO fails to deliver desired results appeared first on Pharmaceutical Business review.

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The late-stage TOURMALINE-MM2 trial featured 705 adult patients who are newly diagnosed with multiple myeloma and are not candidates for transplant. NINLARO is an oral proteasome inhibitor, which

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The post TOURMALINE-MM2 study on NINLARO fails to deliver desired results appeared first on Pharmaceutical Business review.

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TOURMALINE-MM2 study on NINLARO fails to deliver desired results

The late-stage TOURMALINE-MM2 trial featured 705 adult patients who are newly diagnosed with multiple myeloma and are

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  string(4) "8257"
  ["article_id"]=>
  string(4) "8257"
  [1]=>
  string(119) "InMed Pharmaceuticals announces completed enrollment in phase 1 clinical trial of INM-755 CBN Cream in healthy subjects"
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  string(119) "InMed Pharmaceuticals announces completed enrollment in phase 1 clinical trial of INM-755 CBN Cream in healthy subjects"
  [2]=>
  string(150) "INM-755 is a CBN cream intended as a topical therapy to treat epidermolysis bullosa (EB) and potentially other dermatological diseases. InMed has cond"
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  string(150) "INM-755 is a CBN cream intended as a topical therapy to treat epidermolysis bullosa (EB) and potentially other dermatological diseases. InMed has cond"
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INM-755 is a CBN cream intended as a topical therapy to treat epidermolysis bullosa (EB) and potentially other dermatological diseases. InMed has conducted preclinical pharmacology studies that suggest

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The post InMed Pharmaceuticals announces completed enrollment in phase 1 clinical trial of INM-755 CBN Cream in healthy subjects appeared first on Pharmaceutical Business review.

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INM-755 is a CBN cream intended as a topical therapy to treat epidermolysis bullosa (EB) and potentially other dermatological diseases. InMed has conducted preclinical pharmacology studies that suggest

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The post InMed Pharmaceuticals announces completed enrollment in phase 1 clinical trial of INM-755 CBN Cream in healthy subjects appeared first on Pharmaceutical Business review.

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InMed Pharmaceuticals announces completed enrollment in phase 1 clinical trial of INM-755

INM-755 is a CBN cream intended as a topical therapy to treat epidermolysis bullosa (EB) and potentially other dermat

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  string(4) "8258"
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  string(4) "8258"
  [1]=>
  string(92) "Kuur Therapeutics launches to develop and commercialise off-the-shelf CAR-NKT cell therapies"
  ["article_title"]=>
  string(92) "Kuur Therapeutics launches to develop and commercialise off-the-shelf CAR-NKT cell therapies"
  [2]=>
  string(150) "IP Group, Baylor College of Medicine and Schroeder Adveq are investing to support two phase 1 studies: GINAKIT 2 (autologous CAR-NKT cells in neurobla"
  ["short_description"]=>
  string(150) "IP Group, Baylor College of Medicine and Schroeder Adveq are investing to support two phase 1 studies: GINAKIT 2 (autologous CAR-NKT cells in neurobla"
  [3]=>
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IP Group, Baylor College of Medicine and Schroeder Adveq are investing to support two phase 1 studies: GINAKIT 2 (autologous CAR-NKT cells in neuroblastoma) and ANCHOR (allogeneic CAR-NKT

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The post Kuur Therapeutics launches to develop and commercialise off-the-shelf CAR-NKT cell therapies appeared first on Pharmaceutical Business review.

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IP Group, Baylor College of Medicine and Schroeder Adveq are investing to support two phase 1 studies: GINAKIT 2 (autologous CAR-NKT cells in neuroblastoma) and ANCHOR (allogeneic CAR-NKT

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The post Kuur Therapeutics launches to develop and commercialise off-the-shelf CAR-NKT cell therapies appeared first on Pharmaceutical Business review.

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Kuur Therapeutics launches to develop and commercialise off-the-shelf CAR-NKT cell therapi

IP Group, Baylor College of Medicine and Schroeder Adveq are investing to support two phase 1 studies: GINAKIT 2 (aut

array(40) {
  [0]=>
  string(4) "8384"
  ["article_id"]=>
  string(4) "8384"
  [1]=>
  string(72) "Imfinzi delivers sustained OS benefit in final analysis of CASPIAN trial"
  ["article_title"]=>
  string(72) "Imfinzi delivers sustained OS benefit in final analysis of CASPIAN trial"
  [2]=>
  string(150) "Imfinzi gave the desired result for the company through its combination with a choice of standard-of-care (SoC) chemotherapies in the first line setti"
  ["short_description"]=>
  string(150) "Imfinzi gave the desired result for the company through its combination with a choice of standard-of-care (SoC) chemotherapies in the first line setti"
  [3]=>
  string(555) "

Imfinzi gave the desired result for the company through its combination with a choice of standard-of-care (SoC) chemotherapies in the first line setting in patients with the lung

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The post Imfinzi delivers sustained OS benefit in final analysis of CASPIAN trial appeared first on Pharmaceutical Business review.

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Imfinzi gave the desired result for the company through its combination with a choice of standard-of-care (SoC) chemotherapies in the first line setting in patients with the lung

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The post Imfinzi delivers sustained OS benefit in final analysis of CASPIAN trial appeared first on Pharmaceutical Business review.

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Imfinzi delivers sustained OS benefit in final analysis of CASPIAN trial

Imfinzi gave the desired result for the company through its combination with a choice of standard-of-care (SoC) chemo

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Merck announces top-line results from phase 3 trials evaluating Gefapixant

In these studies, the primary efficacy endpoints were met for the gefapixant 45 mg twice daily treatment arms â€