Highlights

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  string(54) "Japan’s Takeda buys PvP Biologics in $330m deal"
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  string(54) "Japan’s Takeda buys PvP Biologics in $330m deal"
  [2]=>
  string(150) "PvP Biologics has been acquired following the conclusion of Phase 1 proof-of-mechanism study of investigational medicine TAK-062 (Kuma062), which is b"
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  string(150) "PvP Biologics has been acquired following the conclusion of Phase 1 proof-of-mechanism study of investigational medicine TAK-062 (Kuma062), which is b"
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PvP Biologics has been acquired following the conclusion of Phase 1 proof-of-mechanism study of investigational medicine TAK-062 (Kuma062), which is being developed to treat uncontrolled celiac disease. The

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The post Japan’s Takeda buys PvP Biologics in $330m deal appeared first on Pharmaceutical Business review.

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PvP Biologics has been acquired following the conclusion of Phase 1 proof-of-mechanism study of investigational medicine TAK-062 (Kuma062), which is being developed to treat uncontrolled celiac disease. The

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The post Japan’s Takeda buys PvP Biologics in $330m deal appeared first on Pharmaceutical Business review.

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Japan’s Takeda buys PvP Biologics in $330m deal

PvP Biologics has been acquired following the conclusion of Phase 1 proof-of-mechanism study of investigational medic

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  string(67) "Novartis, DNDi to jointly develop LXE408 for visceral leishmaniasis"
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  string(67) "Novartis, DNDi to jointly develop LXE408 for visceral leishmaniasis"
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  string(150) "LXE408 was discovered at Novartis with the financial backing of the Wellcome Trust. According to Novartis, more than a billion people across the world"
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  string(150) "LXE408 was discovered at Novartis with the financial backing of the Wellcome Trust. According to Novartis, more than a billion people across the world"
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LXE408 was discovered at Novartis with the financial backing of the Wellcome Trust. According to Novartis, more than a billion people across the world are at risk of

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The post Novartis, DNDi to jointly develop LXE408 for visceral leishmaniasis appeared first on Pharmaceutical Business review.

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LXE408 was discovered at Novartis with the financial backing of the Wellcome Trust. According to Novartis, more than a billion people across the world are at risk of

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The post Novartis, DNDi to jointly develop LXE408 for visceral leishmaniasis appeared first on Pharmaceutical Business review.

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Novartis, DNDi to jointly develop LXE408 for visceral leishmaniasis

LXE408 was discovered at Novartis with the financial backing of the Wellcome Trust. According to Novartis, more than

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  string(45) "AstraZeneca divests global rights to Movantik"
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Movantik is a peripherally acting mu-opioid receptor antagonist (PAMORA) indicated for the treatment of opioid-induced constipation (OIC). Ruud Dobber, Executive Vice President, BioPharmaceuticals Business Unit, said: “This divestment

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The post AstraZeneca divests global rights to Movantik appeared first on Pharmaceutical Business review.

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Movantik is a peripherally acting mu-opioid receptor antagonist (PAMORA) indicated for the treatment of opioid-induced constipation (OIC). Ruud Dobber, Executive Vice President, BioPharmaceuticals Business Unit, said: “This divestment

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The post AstraZeneca divests global rights to Movantik appeared first on Pharmaceutical Business review.

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AstraZeneca divests global rights to Movantik

Movantik is a peripherally acting mu-opioid receptor antagonist (PAMORA) indicated for the treatment of opioid-induce

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  string(84) "Lysogene receives FDA fast track designation for LYS-SAF302 gene therapy in MPS IIIA"
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  string(84) "Lysogene receives FDA fast track designation for LYS-SAF302 gene therapy in MPS IIIA"
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  string(150) "LYS-SAF302, a second-generation gene therapy, is designed to deliver a functional copy of the SGSH (N-sulfoglucosamine sulfohydrolase) gene to the bra"
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LYS-SAF302, a second-generation gene therapy, is designed to deliver a functional copy of the SGSH (N-sulfoglucosamine sulfohydrolase) gene to the brain through a one-time direct-to-CNS administration, and is

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The post Lysogene receives FDA fast track designation for LYS-SAF302 gene therapy in MPS IIIA appeared first on Pharmaceutical Business review.

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LYS-SAF302, a second-generation gene therapy, is designed to deliver a functional copy of the SGSH (N-sulfoglucosamine sulfohydrolase) gene to the brain through a one-time direct-to-CNS administration, and is

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The post Lysogene receives FDA fast track designation for LYS-SAF302 gene therapy in MPS IIIA appeared first on Pharmaceutical Business review.

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Lysogene receives FDA fast track designation for LYS-SAF302 gene therapy in MPS IIIA

LYS-SAF302, a second-generation gene therapy, is designed to deliver a functional copy of the SGSH (N-sulfoglucosamin

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  string(67) "Genentech, Bicycle Therapeutics sign immuno-oncology therapies deal"
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Under a strategic collaboration agreement, the companies will involve in the discovery, development and commercialisation of novel Bicycle Therapeutics-based immuno-oncology therapies. The deal allows Bicycle to explore its

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The post Genentech, Bicycle Therapeutics sign immuno-oncology therapies deal appeared first on Pharmaceutical Business review.

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Under a strategic collaboration agreement, the companies will involve in the discovery, development and commercialisation of novel Bicycle Therapeutics-based immuno-oncology therapies. The deal allows Bicycle to explore its

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The post Genentech, Bicycle Therapeutics sign immuno-oncology therapies deal appeared first on Pharmaceutical Business review.

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Genentech, Bicycle Therapeutics sign immuno-oncology therapies deal

Under a strategic collaboration agreement, the companies will involve in the discovery, development and commercialisa

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As per the supplemental New Drug Application (sNDA), the Japanese pharma company is seeking approval of ALUNBRIG for the first-line treatment of patients with anaplastic lymphoma kinase-positive (ALK+)

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The post Takeda’s ALUNBRIG gets FDA priority review for expanded indication in NSCLC appeared first on Pharmaceutical Business review.

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As per the supplemental New Drug Application (sNDA), the Japanese pharma company is seeking approval of ALUNBRIG for the first-line treatment of patients with anaplastic lymphoma kinase-positive (ALK+)

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The post Takeda’s ALUNBRIG gets FDA priority review for expanded indication in NSCLC appeared first on Pharmaceutical Business review.

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Takeda’s ALUNBRIG gets FDA priority review for expanded indication in NSCLC

As per the supplemental New Drug Application (sNDA), the Japanese pharma company is seeking approval of ALUNBRIG for

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  string(102) "TrueProfile.io and RAKMHSU sign first UAE partnership to strengthen graduates’ career potential"
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  string(102) "TrueProfile.io and RAKMHSU sign first UAE partnership to strengthen graduates’ career potential"
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  string(150) "TrueProfile.io® and Ras al Khaimah Medical and Health Sciences University (RAKMHSU) have signed the first pivotal partnership in the UAE to suppo"
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TrueProfile.io and RAKMHSU sign first UAE partnership to strengthen graduates’ care

TrueProfile.io® and Ras al Khaimah Medical and Health Sciences University (RAKMHSU) have signed the first pivotal p

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  string(83) "Janssen gets FDA breakthrough therapy status for JNJ-6372 to treat metastatic NSCLC"
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  string(83) "Janssen gets FDA breakthrough therapy status for JNJ-6372 to treat metastatic NSCLC"
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  string(150) "The designation enables to use of JNJ-6372 to treat patients with metastatic NSCLC with epidermal growth factor receptor (EGFR) Exon 20 insertion muta"
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The designation enables to use of JNJ-6372 to treat patients with metastatic NSCLC with epidermal growth factor receptor (EGFR) Exon 20 insertion mutations, whose disease has advanced on

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The designation enables to use of JNJ-6372 to treat patients with metastatic NSCLC with epidermal growth factor receptor (EGFR) Exon 20 insertion mutations, whose disease has advanced on

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The post Janssen gets FDA breakthrough therapy status for JNJ-6372 to treat metastatic NSCLC appeared first on Pharmaceutical Business review.

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Janssen gets FDA breakthrough therapy status for JNJ-6372 to treat metastatic NSCLC

The designation enables to use of JNJ-6372 to treat patients with metastatic NSCLC with epidermal growth factor recep

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  string(81) "Kala’s dry eye disease candidate KPI-121 meets objective in STRIDE 3 trial"
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  string(81) "Kala’s dry eye disease candidate KPI-121 meets objective in STRIDE 3 trial"
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  string(150) "Planned to be branded as EYSUVIS (loteprednol etabonate ophthalmic suspension) 0.25%, KPI-121 showed statistically significant results for primary and"
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Planned to be branded as EYSUVIS (loteprednol etabonate ophthalmic suspension) 0.25%, KPI-121 showed statistically significant results for primary and also key secondary endpoints in comparison to placebo in

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The post Kala’s dry eye disease candidate KPI-121 meets objective in STRIDE 3 trial appeared first on Pharmaceutical Business review.

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Planned to be branded as EYSUVIS (loteprednol etabonate ophthalmic suspension) 0.25%, KPI-121 showed statistically significant results for primary and also key secondary endpoints in comparison to placebo in

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The post Kala’s dry eye disease candidate KPI-121 meets objective in STRIDE 3 trial appeared first on Pharmaceutical Business review.

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Kala’s dry eye disease candidate KPI-121 meets objective in STRIDE 3 trial

Planned to be branded as EYSUVIS (loteprednol etabonate ophthalmic suspension) 0.25%, KPI-121 showed statistically si

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  string(149) "AbbVie receives marketing authorisation from EC to shorten MAVIRET duration for treatment-naïve genotype 3 HCV patients with compensated cirrhosis"
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  string(152) "MAVIRET was already indicated as an 8-week, pan-genotypic (GT1-6), once-daily regimen for treatment-naïve HCV patients without cirrhosis, and as an 8"
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  string(152) "MAVIRET was already indicated as an 8-week, pan-genotypic (GT1-6), once-daily regimen for treatment-naïve HCV patients without cirrhosis, and as an 8"
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MAVIRET was already indicated as an 8-week, pan-genotypic (GT1-6), once-daily regimen for treatment-naïve HCV patients without cirrhosis, and as an 8-week, once-daily regimen for treatment-naïve GT 1, 2,

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The post AbbVie receives marketing authorisation from EC to shorten MAVIRET duration for treatment-naïve genotype 3 HCV patients with compensated cirrhosis appeared first on Pharmaceutical Business review.

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MAVIRET was already indicated as an 8-week, pan-genotypic (GT1-6), once-daily regimen for treatment-naïve HCV patients without cirrhosis, and as an 8-week, once-daily regimen for treatment-naïve GT 1, 2,

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The post AbbVie receives marketing authorisation from EC to shorten MAVIRET duration for treatment-naïve genotype 3 HCV patients with compensated cirrhosis appeared first on Pharmaceutical Business review.

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AbbVie receives marketing authorisation from EC to shorten MAVIRET duration for treatment-

MAVIRET was already indicated as an 8-week, pan-genotypic (GT1-6), once-daily regimen for treatment-naïve HCV pati

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The FDA approval allows Isturisa to treat adults with Cushing’s disease who either cannot undergo pituitary gland surgery or have undergone the surgery but still suffering from the

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The post Novartis gets FDA nod for Isturisa to treat Cushing’s disease appeared first on Pharmaceutical Business review.

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Novartis gets FDA nod for Isturisa to treat Cushing’s disease

The FDA approval allows Isturisa to treat adults with Cushing’s disease who either cannot undergo pituitary gl