Remove p applicant Pfizer
article thumbnail

Grand Rounds September 29, 2023: Navigating the Use of Patient-Reported Outcomes in Research and Practice: The PROTEUS Consortium (Claire Snyder, PhD; Norah Crossnohere, PhD; Anne Schuster, PhD)

Rethinking Clinical Trials

The Guide is applicable to a broad range of health systems. Learn more Visit the PROTEUS Consortium Discussion Themes -Can you explain why the error bars and P values are not on some of the graphs in the presentation? In our research, we learned that patients actively do not want to see error bars and P values on graphs.

article thumbnail

Pfizer and BioNTech Initiate Phase 1/2 Study of First mRNA-based Shingles Vaccine Program

Pfizer

Pfizer and BioNTech Initiate Phase 1/2 Study of First mRNA-based Shingles Vaccine Program kimkevin Thu, 02/09/2023 - 15:05 Pfizer and BioNTech Initiate Phase 1/2 Study of First mRNA-based Shingles Vaccine Program Friday, February 10, 2023 - 06:45am Share Phase 1/2 trial will enroll up to 900 healthy U.S.

Insiders

Sign Up for our Newsletter

This site is protected by reCAPTCHA and the Google Privacy Policy and Terms of Service apply.

article thumbnail

Pfizer to Present Latest Scientific Advancements from Its Industry-Leading Portfolio at the ESMO Virtual Congress 2020

The Pharma Data

NEW YORK–(BUSINESS WIRE)– Pfizer Inc. Data to be presented include findings from the Phase 3 CROWN study of LORBRENA ® (lorlatinib)* in first-line ALK-positive non-small cell lung cancer (NSCLC), building on Pfizer’s extensive heritage in precision medicine research. Grivas P. . Ascierto P. . .

article thumbnail

Pfizer’s TALZENNA® in combination with XTANDI® receives U.S. FDA approval

The Pharma Data

Pfizer’s TALZENNA® in combination with XTANDI® receives U.S. FDA approval Pfizer (NYSE: PFE) announced that the U.S. 0.61; p<0.0001). A marketing authorization application (MAA) for the TALZENNA and XTANDI combination has been accepted for review by the European Medicines Agency. Source link: [link]

article thumbnail

Moderna’s COVID-19 Vaccine Candidate Shows Almost 95 Percent Effectiveness in Interim Analysis

XTalks

The news comes shortly after Pfizer and BioNTech’s mega announcement last week of their COVID-19 vaccine having shown 90 percent efficacy in an ongoing large-scale Phase III trial. This compared to the vaccine from Pfizer and BioNTech, which can only be refrigerated for five days. percent (p <0.0001).

article thumbnail

Unlocking the potential of synthetic DNA 

Drug Discovery World

Raquel Sanches-Kuiper , Vice President of Science and Applications at Evonetix, and Clare Whitewoods , Marketing Communications Manager at Evonetix, look at the benefits synthetic DNA brings to pharmaceutical development. Freemont, P. Their speed also allows for their potential use in personalised therapy for diseases such as cancer.

DNA 69
article thumbnail

Pfizer and BioNTech to Submit Emergency Use Authorization Request Today to the U.S. FDA for COVID-19 Vaccine

The Pharma Data

and plan to submit applications immediately to other regulatory agencies around the world. NEW YORK & MAINZ, Germany–(BUSINESS WIRE)–Friday, November 20, 2020 — Pfizer Inc. . NEW YORK & MAINZ, Germany–(BUSINESS WIRE)–Friday, November 20, 2020 — Pfizer Inc.