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tags : Fda    crawled date : 2021 - 09 - 09    save search

Apellis Announces Top-Line Results from Phase 3 DERBY and OAKS Studies in Geographic Atrophy (GA) and Plans to Submit NDA to FDA in the First Half of 2022
Published: 2021-09-09 (Crawled : 22:00) - biospace.com/
APLS G | $48.69 2.2% 2.16% 1.2M twitter stocktwits trandingview |
Health Technology
| | O: -0.88% H: 2.83% C: 0.94%

fda results phase 3 topline fda ide
VOR33 Granted U.S. FDA Fast Track Designation for AML
Published: 2021-09-09 (Crawled : 14:00) - biospace.com/
VOR | $1.89 3.85% 3.7% 210K twitter stocktwits trandingview |
| | O: 3.85% H: 3.03% C: -3.21%

fda fda fast track fast track granted fast track designation grant designation aml
FDA grants Jardiance® Breakthrough Therapy designation for heart failure with preserved ejection fraction
Published: 2021-09-09 (Crawled : 14:00) - biospace.com/
LLY | News | $745.69 1.96% -0.16% 2M twitter stocktwits trandingview |
Health Technology
| | O: -0.61% H: 0.29% C: -5.25%

fda heart therapy breakthrough therapy granted grant designation
FDA Grants Breakthrough Device Designation to the NovoTTF-200T™ System for Advanced Liver Cancer
Published: 2021-09-09 (Crawled : 13:00) - biospace.com/
NVCR | $12.055 1.9% 1.87% 750K twitter stocktwits trandingview |
Health Technology
| | O: 1.9% H: 3.69% C: 0.07%

fda cancer device liver granted grant designation
FDA Grants Soligenix Orphan Drug Designation for the Treatment of T-cell Lymphoma
Published: 2021-09-09 (Crawled : 12:00) - biospace.com/
SNGX | $0.4012 -1.13% -1.15% 450K twitter stocktwits trandingview |
Health Technology
| | O: 12.38% H: 4.24% C: -1.69%

treatment fda drug t-cell granted grant designation
Myovant Sciences and Pfizer Announce FDA Acceptance of Supplemental New Drug Application for MYFEMBREE® for the Management of Moderate to Severe Pain Associated With Endometriosis
Published: 2021-09-09 (Crawled : 11:00) - globenewswire.com
PFE | News 4 | $26.32 0.23% 0.0% 24M twitter stocktwits trandingview |
Health Technology
| | O: -0.09% H: 0.53% C: -0.95%
MYOV | $26.98 -0.04% 0.0% 0 twitter stocktwits trandingview |
Health Technology
| | O: -0.54% H: 1.56% C: -2.22%

new drug fda fda acceptance drug
FDA has declined Humanigen’s Emergency Use Authorization (EUA) Request for Lenzilumab in Hospitalized COVID-19 Patients
Published: 2021-09-09 (Crawled : 09:00) - biospace.com/
HGEN | $0.0361 -61.5% 120M twitter stocktwits trandingview |
Health Technology
| | O: -59.56% H: 35.35% C: 30.44%

covid fda lenzilumab merge authorized covid-19 emergency use authorization
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