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Jazz Pharmaceuticals to Present Data Showcasing Clinical Advances Across Hematology/Oncology at ASH 2021 Annual Meeting

/PRNewswire/ Jazz Pharmaceuticals plc (Nasdaq: JAZZ) today announced that 16 new data abstracts from across its hematology/oncology development program will. ....

United States , Kristin Bhavnani , Stephana Grupp , Gregory Yanik , Meagana Jacoby , Mohamad Mohty , Daniel Rivera , Guillermo Montalban Bravo , Pierre Peterlin , Vinod Pullarkat , Andrean Flynn , Annalisa Ruggeri , Kunhwa Kim , Liposomal Cytarabine , Luke Maese , Robert Iannone , Xue Wang , Christina Rautenberg , Alex Legg , Erwinia Asparaginase , Age Group Of Treatment , Oncology Center , European Commission , Jazz Pharmaceuticals , Georgia World Congress Center , Drug Administration ,

Jazz Pharmaceuticals to Present Data Showcasing Clinical Advances Across Hematology/Oncology at ASH 2021 Annual Meeting

/PRNewswire/ Jazz Pharmaceuticals plc (Nasdaq: JAZZ) today announced that 16 new data abstracts from across its hematology/oncology development program will. ....

United States , Kristin Bhavnani , Stephana Grupp , Gregory Yanik , Meagana Jacoby , Mohamad Mohty , Daniel Rivera , Guillermo Montalban Bravo , Pierre Peterlin , Vinod Pullarkat , Andrean Flynn , Annalisa Ruggeri , Kunhwa Kim , Liposomal Cytarabine , Luke Maese , Robert Iannone , Xue Wang , Christina Rautenberg , Alex Legg , Erwinia Asparaginase , Age Group Of Treatment , Oncology Center , European Commission , Jazz Pharmaceuticals , Georgia World Congress Center , Drug Administration ,

FDA Advisory Committee Recommends Use of Investigational Drug Maribavir (TAK-620) to Treat Post-Transplant Recipients with Cytomegalovirus (CMV) Infection and Disease Refractory to Treatment With or Without Resistance

FDA Advisory Committee Recommends Use of Investigational Drug Maribavir (TAK-620) to Treat Post-Transplant Recipients with Cytomegalovirus (CMV) Infection and Disease Refractory to Treatment With or Without Resistance
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U.S. Food & Drug Administration Grants Priority Review of Maribavir for the Treatment of Post-Transplant Recipients With Cytomegalovirus Infection in Those Resistant and/or Refractory to Prior Anti-CMV Treatment

Takeda Pharmaceutical Company Limited
U.S. Food & Drug Administration Grants Priority Review of Maribavir for the Treatment of Post-Transplant Recipients With Cytomegalovirus Infection in Those Resistant and/or Refractory to Prior Anti-CMV Treat
Saturday, May 22, 2021 10:31AM IST (5:01AM GMT)

Osaka, Japan:

− If Approved, Maribavir Will Be the First and Only Treatment Indicated for Post-Transplant Cytomegalovirus (CMV) Infection in Those That Are Refractory, With or Without Resistance (R/R)
− NDA based on Phase 3 Trial of Maribavir Which Met Its Primary Endpoint of Superiority Compared to Conventional Antiviral Therapies in Transplant Recipients with R/R CMV Infection
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− The U.S. Food & Drug Administration Granted Maribavir Breakthrough Therapy Designation as a Treatment for CMV Infection in Transplant Patients Resistant or Refractory to Prior Therapy ....

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U.S. Food & Drug Administration Grants Priority Review of Maribavir for the Treatment of Post-Transplant Recipients With Cytomegalovirus Infection in Those Resistant and/or Refractory to Prior Anti-CMV Treatment - Iberonews

U.S. Food & Drug Administration Grants Priority Review of Maribavir for the Treatment of Post-Transplant Recipients With Cytomegalovirus Infection in Those Resistant and/or Refractory to Prior Anti-CMV Treatment
OSAKA, Japan (Business Wire)
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If Approved, Maribavir Will Be the First and Only Treatment Indicated for Post-Transplant Cytomegalovirus (CMV) Infection in Those That Are Refractory, With or Without Resistance (R/R)
−
NDA based on Phase 3 Trial of Maribavir Which Met Its Primary Endpoint of Superiority Compared to Conventional Antiviral Therapies in Transplant Recipients with R/R CMV Infection
1
−
The U.S. Food & Drug Administration Granted Maribavir Breakthrough Therapy Designation as a Treatment for CMV Infection in Transplant Patients Resistant or Refractory to Prior Therapy ....

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