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tags : Fda entities : Astellas pharma inc save search
FDA Grants Orphan Drug and Pediatric Exclusivities for CRESEMBA® (isavuconazonium sulfate) for Invasive Aspergillosis and Invasive Mucormycosis in Children
Published: 2024-03-11 (Crawled : 13:00) - prnewswire.com
ALPMY | News | $9.34 -1.11% 690K
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cresemba fda drug children grants
PADCEV® (enfortumab vedotin-ejfv) with KEYTRUDA® (pembrolizumab) Approved by FDA as the First and Only ADC Plus PD-1 to Treat Advanced Bladder Cancer
Published: 2023-12-15 (Crawled : 22:00) - prnewswire.com
PFE A | $25.42 -1.05% -0.04% 44M
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padcev fda first approved bladder cancer treat advanced plus
FDA Approves Expanded Use of CRESEMBA® (isavuconazonium sulfate) in Children with Invasive Aspergillosis and Invasive Mucormycosis
Published: 2023-12-08 (Crawled : 22:00) - biospace.com/
FNCTF | News | $11.0354 -20.84% 320
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cresemba fda children
FDA Grants Priority Review for Supplemental Biologics License Application (sBLA) of PADCEV® (enfortumab vedotin-ejfv) with KEYTRUDA® (pembrolizumab) for First-Line Treatment of Advanced Bladder Cancer
Published: 2023-11-30 (Crawled : 22:00) - prnewswire.com
ALPMF | News | $9.594 43.47% 2.2K
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padcev fda license review bladder cancer treatment application grants
Pfizer and Astellas' XTANDI® Approved by U.S. FDA in Earlier Prostate Cancer Treatment Setting
Published: 2023-11-17 (Crawled : 04:00) - prnewswire.com
ALPMF | News | $9.594 43.47% 2.2K
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xtandi fda approved cancer treatment
FDA Grants Priority Review for XTANDI® in Non-Metastatic Castration-Sensitive Prostate Cancer with High-Risk Biochemical Recurrence
Published: 2023-08-23 (Crawled : 12:00) - biospace.com/
ALPMY | News | $9.34 -1.11% 690K
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xtandi fda review cancer grants
Iveric Bio Receives U.S. FDA Approval for IZERVAY™ (avacincaptad pegol intravitreal solution), a New Treatment for Geographic Atrophy
Published: 2023-08-05 (Crawled : 04:20) - ivericbio.com
ALPMY | News | $9.34 -1.11% 690K
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ISEE | $39.95 0.38% 0.38% 0
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fda approval treatment
Astellas Announces U.S. FDA Grants Priority Review for Zolbetuximab Biologics License Application
Published: 2023-07-06 (Crawled : 06:00) - prnewswire.com
ALPMY | News | $9.34 -1.11% 690K
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fda license review application grants
Astellas' VEOZAH™ (fezolinetant) Approved by U.S. FDA for Treatment of Vasomotor Symptoms Due to Menopause
Published: 2023-05-12 (Crawled : 19:00) - prnewswire.com
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fda approved treatment
Astellas Announces Hold Lifted by FDA on FORTIS Clinical Trial of AT845 Investigational Treatment for Adult Patients with Late-Onset Pompe Disease
Published: 2023-01-20 (Crawled : 07:00) - prnewswire.com
ALPMF | News | $9.594 43.47% 2.2K
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at845 treatment fda disease lifted trial
Seagen, Astellas and Merck Announce FDA Acceptance of sBLAs for PADCEV® with KEYTRUDA® for the First-Line Treatment of Certain Patients With Locally Advanced or Metastatic Urothelial Cancer
Published: 2022-12-20 (Crawled : 12:20) - biospace.com/
ALPMY | News | $9.34 -1.11% 690K
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MRK | $125.37 0.25% 0.1% 6.1M
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padcev treatment fda cancer
Astellas, Seagen and Merck Announce FDA Acceptance of Supplemental Biologics License Applications for PADCEV® (enfortumab vedotin-ejfv) with KEYTRUDA® (pembrolizumab) for the First-Line Treatment of Certain Patients With Locally Advanced or Metastatic Urothelial Cancer
Published: 2022-12-20 (Crawled : 12:00) - prnewswire.com
ALPMY | News | $9.34 -1.11% 690K
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padcev treatment fda license cancer
U.S. FDA Accepts Astellas' New Drug Application for Fezolinetant
Published: 2022-08-18 (Crawled : 07:00) - prnewswire.com
ALPMF | News | $9.594 43.47% 2.2K
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fda drug application
Astellas Announces FDA Update on the FORTIS Clinical Trial of AT845 in Adults with Late-Onset Pompe Disease
Published: 2022-06-27 (Crawled : 08:00) - biospace.com/
ALPMY | News | $9.34 -1.11% 690K
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at845 fda disease trial update
Astellas Announces FDA Update on the FORTIS Clinical Trial of AT845 in Adults with Late-Onset Pompe Disease
Published: 2022-06-26 (Crawled : 00:00) - prnewswire.com
ALPMY | News | $9.34 -1.11% 690K
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at845 fda disease trial update
Astellas Submits Fezolinetant New Drug Application to U.S. FDA
Published: 2022-06-23 (Crawled : 00:00) - prnewswire.com
ALPMF | News | $9.594 43.47% 2.2K
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fda drug application
Frequency Therapeutics Announces First Subject Dosed in FX-322 Phase 2b Acquired Sensorineural Hearing Loss (SNHL) Study and FDA Agreement on Speech Perception as Primary Endpoint
Published: 2021-10-21 (Crawled : 12:00) - biospace.com/
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fda phase 2 sensor acquired phase 2b hearing loss
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