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Prothena Corporation plc: Prothena Announces Promising New Preclinical and Clinical Data from its Neurodegenerative Programs Selected for Oral Presentations at AD/PD 2021


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Robust preclinical data support the benefit of PRX005, a novel anti-tau antibody, for the potential treatment Alzheimer s disease
New pre-specified exploratory subgroup analyses and new digital biomarker data from Part 1 of the Phase 2 PASADENA study of prasinezumab in patients with early Parkinson s disease
will be featured in two separate presentations
DUBLIN, Ireland, Feb. 24, 2021 (GLOBE NEWSWIRE) Prothena Corporation plc (NASDAQ:PRTA), a late-stage clinical company with expertise in protein dysregulation and a pipeline of investigational therapeutics for rare peripheral amyloid and neurodegenerative diseases, today announced three oral presentations and participation in a live forum at The 15
th International Conference on Alzheimer s and Parkinson s Diseases (AD/PD 2021). Prothena will present new preclinical data demonstrating that targeting a novel epitope with PRX005, an anti-tau antibody, resulted in superior attributes for the potential trea ....

Gennaro Pagano , Ellen Rose , Jennifer Zibuda , Kirsteni Taylor , Philipj Dolan , Wagner Zago , Head Of Communications , Investor Relations Communications , International Conference On Alzheimer , Company On Twitter Prothenacorp , Exchange Commission , Protein Sciences , Roche Pharma Research , Translational Technology , Early Development , Group Leader , Bristol Myers Squibb , Prothena Corporation , International Conference , Bristol Myers , Chief Scientific , Microtubule Binding Region , Bispecific Antibody , Pathological Tau Progression Via Blockade , Tau Pathology , Therapeutic Strategies ,

Oral health can save people from severe COVID-19 complications: QU research finds


 20 Feb 2021 - 9:41
The Peninsula
Doha: More commonly known as gum disease, periodontitis is a severe gum infection characterised by chronic inflammation, whose patients may be at greater risk if exposed to COVID-19.
A research team spearheaded by Dr. Nadia Maarouf, Associate Consultant from Hamad Dental Center, and led by Dr. Faleh Tamimi, Professor at Qatar University’s (QU) College of Dental Medicine, has demonstrated that there may be a strong association between COVID-19 and oral health. 
While speaking on his research about patients with (periodontitis), Dr. Faleh said: “In our study, we assessed the dental records of patients that have been infected with COVID-19. We discovered that a substantial portion of the patients that suffered severe COVID-19 complications (including death) had chronic gum infections, also known as periodontal disease. Our study concludes that there is a strong association between the severity of COVID-19 and the presence of pe ....

Ad Daw Ah , Faleh Tamimi , Nadia Maarouf , Hamad Medical Corporation , Mcgill Universityw Cai , Hamad Dental Center , Complutense University , Qatar Hamad Dental Center , Mcgill University , Qatar University Dr , Qatar University , Belinda Nicolau Mcgill University , Associate Consultant , Dental Medicine , Mariano Sanz , Belinda Nicolau , Covid 19 , ஹமாத் மருத்துவ நிறுவனம் , ஹமாத் டெஂடல் மையம் , கத்தார் ஹமாத் டெஂடல் மையம் , மகில் பல்கலைக்கழகம் , கத்தார் பல்கலைக்கழகம் டாக்டர் , கத்தார் பல்கலைக்கழகம் , பெலிண்டா நீக்கொழொஉ மகில் பல்கலைக்கழகம் , இணை ஆலோசகர் , டெஂடல் மருந்து ,

DGAP-News: Immunic, Inc. Announces That Oral Treatment IMU-838 Shows Evidence of Clinical Activity in Moderate COVID-19 in Phase 2 CALVID-1 Trial


DGAP-News: Immunic, Inc. Announces That Oral Treatment IMU-838 Shows Evidence of Clinical Activity in Moderate COVID-19 in Phase 2 CALVID-1 Trial
Table: IMU-838 Shows Acceleration of Time to Clinical Improvement
High-risk patients and patients aged over 65 years experienced a more substantial treatment benefit from IMU-838 than in the general patient population:
- The 75% probability
[5] to reach clinical improvement (based on investigator assessment) was accelerated by 3.8 days in IMU-838 treated high-risk patients
[6], as compared to placebo (FAS).
- The 75% probability
[5] to reach clinical improvement (based on investigator assessment) was accelerated by 4.8 days in IMU-838 treated elderly patients (65 years or older), as compared to placebo (FAS). ....

United States , Paula Schwartz , Edna Kaplan , Jessica Breu , Andreas Muehler , Daniel Vitt , Exchange Commission , World Health Organization , Rx Communications Group , Immunic Inc , Distribution Services , Announces That Oral Treatment , Clinical Activity , Multiple Secondary Endpoints , Including Clinically Meaningful Improvements , Clinical Recovery , Clinical Improvement , Very Low Rates , Serious Complications , Hospitalized Patients With Moderate , Risk Patients , Patients Aged Over , More Substantial Treatment Effect , Anti Inflammatory Effect Observed , More Effective Reduction , C Reactive Protein ,

Jazz Pharmaceuticals Completes Submission of Supplemental New Drug Application for Xywav (calcium, magnesium, potassium, and sodium oxybates) Oral Solution for Idiopathic Hypersomnia


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DUBLIN, Feb. 16, 2021 /PRNewswire/ Jazz Pharmaceuticals plc (Nasdaq: JAZZ) today announced the completion of the rolling submission for the supplemental New Drug Application (sNDA) to the U.S. Food and Drug Administration (FDA) seeking marketing approval for Xywav (calcium, magnesium, potassium, and sodium oxybates) oral solution for the treatment of adult patients with idiopathic hypersomnia. If approved,
Xywav will be the first and only approved treatment in the U.S. for adults with idiopathic hypersomnia.
Xywav received Fast Track designation by the FDA in September 2020 for the treatment of idiopathic hypersomnia. Jazz was granted rolling submission by FDA for this sNDA in December 2020, permitting the submission of portions of the proposed application as they were completed. ....

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