Highlights

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  string(77) "1st World Congress on Women’s Health Innovations and Inventions (WHII)"
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  string(77) "1st World Congress on Women’s Health Innovations and Inventions (WHII)"
  [2]=>
  string(155) "The 1st World Congress on Women’s Health Innovations and Inventions (WHII): Addressing Unmet Needs will be held on July 9-11, 2019 in Tel Aviv, Isra"
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  string(155) "The 1st World Congress on Women’s Health Innovations and Inventions (WHII): Addressing Unmet Needs will be held on July 9-11, 2019 in Tel Aviv, Isra"
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  string(533) "The 1st World Congress on Women’s Health Innovations and Inventions (WHII): Addressing Unmet Needs will be held on July 9-11, 2019 in Tel Aviv, Israel.We invite you to participate in the first Women’s Health Congress bringing technology and science together to address the unmet needs.We will discuss the unmet needs of Women’s Health with physicians, other healthcare providers, technology experts and companies involved in developing those future technologies. The Congress will explore fuel, spark…"
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  string(533) "The 1st World Congress on Women’s Health Innovations and Inventions (WHII): Addressing Unmet Needs will be held on July 9-11, 2019 in Tel Aviv, Israel.We invite you to participate in the first Women’s Health Congress bringing technology and science together to address the unmet needs.We will discuss the unmet needs of Women’s Health with physicians, other healthcare providers, technology experts and companies involved in developing those future technologies. The Congress will explore fuel, spark…"
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https://www.pharmiweb.com/event/1st-world-congress-on-women-s-health-innovations-and-inventions-whii                "
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https://www.pharmiweb.com/event/1st-world-congress-on-women-s-health-innovations-and-inventions-whii                "
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1st World Congress on Women’s Health Innovations and Inventions (WHII)

The 1st World Congress on Women’s Health Innovations and Inventions (WHII): Addressing Unmet Needs will be held o

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  [1]=>
  string(61) "Novartis multiple sclerosis product Gilenya approved in China"
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  string(61) "Novartis multiple sclerosis product Gilenya approved in China"
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  string(150) "Multiple sclerosis (MS) is categorized as rare disease in China with an estimated 30,000 MS patients in China. Gilenya is the 3rd most prescribed MS d"
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  string(150) "Multiple sclerosis (MS) is categorized as rare disease in China with an estimated 30,000 MS patients in China. Gilenya is the 3rd most prescribed MS d"
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Multiple sclerosis (MS) is categorized as rare disease in China with an estimated 30,000 MS patients in China. Gilenya is the 3rd most prescribed MS disease modifying treatment

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Multiple sclerosis (MS) is categorized as rare disease in China with an estimated 30,000 MS patients in China. Gilenya is the 3rd most prescribed MS disease modifying treatment

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The post Novartis multiple sclerosis product Gilenya approved in China appeared first on Pharmaceutical Business review.

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Novartis multiple sclerosis product Gilenya approved in China

Multiple sclerosis (MS) is categorized as rare disease in China with an estimated 30,000 MS patients in China. Gileny

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  string(4) "3710"
  [1]=>
  string(100) "Celgene gets FDA approval for Otezla to treat oral ulcers associated with Behçet’s Disease"
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  string(100) "Celgene gets FDA approval for Otezla to treat oral ulcers associated with Behçet’s Disease"
  [2]=>
  string(150) "Otezla (apremilast) 30mg is an oral small-molecule inhibitor of phosphodiesterase 4 (PDE4), particularly for cyclic adenosine monophosphate (cAMP). It"
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  string(150) "Otezla (apremilast) 30mg is an oral small-molecule inhibitor of phosphodiesterase 4 (PDE4), particularly for cyclic adenosine monophosphate (cAMP). It"
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Otezla (apremilast) 30mg is an oral small-molecule inhibitor of phosphodiesterase 4 (PDE4), particularly for cyclic adenosine monophosphate (cAMP). It is claimed to be the first and only approved

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Otezla (apremilast) 30mg is an oral small-molecule inhibitor of phosphodiesterase 4 (PDE4), particularly for cyclic adenosine monophosphate (cAMP). It is claimed to be the first and only approved

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The post Celgene gets FDA approval for Otezla to treat oral ulcers associated with Behçet’s Disease appeared first on Pharmaceutical Business review.

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Celgene gets FDA approval for Otezla to treat oral ulcers associated with Behçetâ€â„

Otezla (apremilast) 30mg is an oral small-molecule inhibitor of phosphodiesterase 4 (PDE4), particularly for cyclic a

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  [1]=>
  string(86) "Transgene receives MHRA approval for clinical trial of next-generation oncolytic virus"
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  string(86) "Transgene receives MHRA approval for clinical trial of next-generation oncolytic virus"
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  string(150) "TG6002 is a next-generation oncolytic virus (OV), which has multiple mechanisms of action. It has been engineered to combine the killing of cancer cel"
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  string(150) "TG6002 is a next-generation oncolytic virus (OV), which has multiple mechanisms of action. It has been engineered to combine the killing of cancer cel"
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TG6002 is a next-generation oncolytic virus (OV), which has multiple mechanisms of action. It has been engineered to combine the killing of cancer cells (oncolysis), the production of

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The post Transgene receives MHRA approval for clinical trial of next-generation oncolytic virus appeared first on Pharmaceutical Business review.

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TG6002 is a next-generation oncolytic virus (OV), which has multiple mechanisms of action. It has been engineered to combine the killing of cancer cells (oncolysis), the production of

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The post Transgene receives MHRA approval for clinical trial of next-generation oncolytic virus appeared first on Pharmaceutical Business review.

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Transgene receives MHRA approval for clinical trial of next-generation oncolytic virus

TG6002 is a next-generation oncolytic virus (OV), which has multiple mechanisms of action. It has been engineered to

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  string(90) "LifeMax receives rare pediatric disease designation for LM-030 to treat Netherton Syndrome"
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  string(90) "LifeMax receives rare pediatric disease designation for LM-030 to treat Netherton Syndrome"
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“We are very pleased to have received the rare pediatric disease designation for LM-030 which has demonstrated safety and clinical efficacy in a Phase I/II study. Netherton Syndrome

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“We are very pleased to have received the rare pediatric disease designation for LM-030 which has demonstrated safety and clinical efficacy in a Phase I/II study. Netherton Syndrome

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The post LifeMax receives rare pediatric disease designation for LM-030 to treat Netherton Syndrome appeared first on Pharmaceutical Business review.

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LifeMax receives rare pediatric disease designation for LM-030 to treat Netherton Syndrome

“We are very pleased to have received the rare pediatric disease designation for LM-030 which has demonstrated

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  [1]=>
  string(85) "Boehringer, Bridge Biotherapeutics sign licence agreement for IPF treatment candidate"
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  string(85) "Boehringer, Bridge Biotherapeutics sign licence agreement for IPF treatment candidate"
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  string(155) "The BBT-877 is Bridge Biotherapeutics’ autotaxin inhibitor being developed to treat various fibrosing interstitial lung diseases, including idiopath"
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  string(155) "The BBT-877 is Bridge Biotherapeutics’ autotaxin inhibitor being developed to treat various fibrosing interstitial lung diseases, including idiopath"
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The BBT-877 is Bridge Biotherapeutics’ autotaxin inhibitor being developed to treat various fibrosing interstitial lung diseases, including idiopathic pulmonary fibrosis (IPF). Under the deal, Bridge Biotherapeutics will secure

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The BBT-877 is Bridge Biotherapeutics’ autotaxin inhibitor being developed to treat various fibrosing interstitial lung diseases, including idiopathic pulmonary fibrosis (IPF). Under the deal, Bridge Biotherapeutics will secure

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The post Boehringer, Bridge Biotherapeutics sign licence agreement for IPF treatment candidate appeared first on Pharmaceutical Business review.

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Boehringer, Bridge Biotherapeutics sign licence agreement for IPF treatment candidate

The BBT-877 is Bridge Biotherapeutics’ autotaxin inhibitor being developed to treat various fibrosing intersti

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  string(4) "3714"
  [1]=>
  string(76) "AHF calls on Gilead to set up fund for victims harmed by its TDF-based drugs"
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  string(76) "AHF calls on Gilead to set up fund for victims harmed by its TDF-based drugs"
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  string(155) "AHF’s demand for a victim compensation fund from Gilead comes as HIV Litigation Attorneys announce its filing last Friday in Alameda County (Superio"
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  string(155) "AHF’s demand for a victim compensation fund from Gilead comes as HIV Litigation Attorneys announce its filing last Friday in Alameda County (Superio"
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AHF’s demand for a victim compensation fund from Gilead comes as HIV Litigation Attorneys announce its filing last Friday in Alameda County (Superior Court of California County of

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AHF’s demand for a victim compensation fund from Gilead comes as HIV Litigation Attorneys announce its filing last Friday in Alameda County (Superior Court of California County of

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The post AHF calls on Gilead to set up fund for victims harmed by its TDF-based drugs appeared first on Pharmaceutical Business review.

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AHF calls on Gilead to set up fund for victims harmed by its TDF-based drugs

AHF’s demand for a victim compensation fund from Gilead comes as HIV Litigation Attorneys announce its filing

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  string(4) "3715"
  [1]=>
  string(74) "PureTech acquires new clinical-stage programme LYT-100 to treat lymphedema"
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  string(74) "PureTech acquires new clinical-stage programme LYT-100 to treat lymphedema"
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  string(150) "In preclinical studies, the oral, small molecule candidate, LYT-100, demonstrated anti-fibrotic and anti-inflammatory mechanisms, and in a Phase 1 cli"
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In preclinical studies, the oral, small molecule candidate, LYT-100, demonstrated anti-fibrotic and anti-inflammatory mechanisms, and in a Phase 1 clinical trial in healthy volunteers, LYT-100 was observed to

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In preclinical studies, the oral, small molecule candidate, LYT-100, demonstrated anti-fibrotic and anti-inflammatory mechanisms, and in a Phase 1 clinical trial in healthy volunteers, LYT-100 was observed to

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The post PureTech acquires new clinical-stage programme LYT-100 to treat lymphedema appeared first on Pharmaceutical Business review.

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PureTech acquires new clinical-stage programme LYT-100 to treat lymphedema

In preclinical studies, the oral, small molecule candidate, LYT-100, demonstrated anti-fibrotic and anti-inflammatory

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  string(4) "3716"
  [1]=>
  string(69) "FDA approves Merck’s Recarbrio to treat complicated infections"
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  string(69) "FDA approves Merck’s Recarbrio to treat complicated infections"
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  string(150) "The FDA has approved Recarbrio to treat patients 18 years of age and older who have limited or no alternative treatment options for cUTI, including py"
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The FDA has approved Recarbrio to treat patients 18 years of age and older who have limited or no alternative treatment options for cUTI, including pyelonephritis, caused by

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The FDA has approved Recarbrio to treat patients 18 years of age and older who have limited or no alternative treatment options for cUTI, including pyelonephritis, caused by

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The post FDA approves Merck’s Recarbrio to treat complicated infections appeared first on Pharmaceutical Business review.

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FDA approves Merck’s Recarbrio to treat complicated infections

The FDA has approved Recarbrio to treat patients 18 years of age and older who have limited or no alternative treatme

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  string(4) "3717"
  [1]=>
  string(77) "Astellas signs licensing deal for Frequency’s regenerative drug FX-322"
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  string(77) "Astellas signs licensing deal for Frequency’s regenerative drug FX-322"
  [2]=>
  string(150) "As per the agreement terms, Astellas will undertake the development and commercialisation of FX-322 outside of the US, while Frequency will be respons"
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  string(150) "As per the agreement terms, Astellas will undertake the development and commercialisation of FX-322 outside of the US, while Frequency will be respons"
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As per the agreement terms, Astellas will undertake the development and commercialisation of FX-322 outside of the US, while Frequency will be responsible for the development and commercialisation

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As per the agreement terms, Astellas will undertake the development and commercialisation of FX-322 outside of the US, while Frequency will be responsible for the development and commercialisation

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The post Astellas signs licensing deal for Frequency’s regenerative drug FX-322 appeared first on Pharmaceutical Business review.

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Astellas signs licensing deal for Frequency’s regenerative drug FX-322

As per the agreement terms, Astellas will undertake the development and commercialisation of FX-322 outside of the US

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2nd Annual Hemophilia Drug Development Summit

Given the excitement and anticipation of increasingly more promising prophylactic treatments and gene therapies, the 2nd