The Pharma Data

OCTOBER 22, 2020

With today’s FDA approval, and regulatory approvals or temporary authorizations in approximately 50 additional countries around the world, Veklury® (remdesivir) is one of the tools available today. ii] The ACTT-1 study sets a high bar for clinical evidence that must be considered as new data emerge.

Science 52

Science Clinical Trials Hospitals FDA Approval 52

The Pharma Data

SEPTEMBER 1, 2020

study investigator and Professor of Clinical Neurology, University of California San Francisco (UCSF) Weill Institute for Neurosciences and clinical research director, UCSF MS Center. Presentation Topic: Disease Modifying Therapies – Risk Management. Presentation Topic: Disease Modifying Therapies – Mechanism of Action.

Clinical Trials 52

Clinical Trials Treatment Trials Disease 52

PPD

AUGUST 5, 2024

Food and Drug Administration (FDA)-approved therapies for treating PAH were primarily vasodilators, designed to overcome the imbalance between vasoactive and vasodilator mediators and to restore endothelial cell function. Historically, the available drugs and U.S. None offers a cure for PAH.

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Clinical Trials Trials Clinical Research Disease 98

The Pharma Data

JULY 15, 2021

The trial investigated neoadjuvant KEYTRUDA, Merck’s anti-PD-1 therapy, plus chemotherapy followed by adjuvant KEYTRUDA as monotherapy (the KEYTRUDA regimen) compared with neoadjuvant chemotherapy followed by adjuvant placebo (the chemotherapy-placebo regimen) in patients with high-risk early-stage triple-negative breast cancer (TNBC).

Therapies 52

Therapies Treatment Trials FDA 52

The Anticancer Fund

OCTOBER 18, 2023

The authors discuss the issue of CNS penetration of the drug, which has yet to be firmly established, but suggest that there is sufficient evidence to support clinical investigation of pentamidine in human gliomas. Gauthier Bouche & Pan Pantziarka Gauthier Bouche (MD) is Director of Clinical Research at the Anticancer Fund.

Drugs 64

Drugs Clinical Trials Trials Treatment 64

Drug Target Review

AUGUST 3, 2023

Doctors and other healthcare professionals have very little time to devote to signposting patients to research, so we have to explore other ways to find participants and, crucially, keep them engaged. That needs to change. Could you provide insights into the process of developing the at-home DNA tests used by Sano?

DNA 52

DNA Clinical Trials Trials FDA Approval 52

The Pharma Data

MARCH 23, 2021

Because esophageal cancer generally has poor survival rates, new first-line therapies are urgently needed for these patients,” said Dr. Peter Enzinger, Director, Center for Esophageal and Gastric Cancer, Dana-Farber/Brigham and Women’s Cancer Center. Merck has the industry’s largest immuno-oncology clinical research program.

Treatment 52

Treatment FDA Approval FDA Therapies 52

Advarra

SEPTEMBER 30, 2022

Is the clinical research industry winning or failing at innovation? In the past decade, trials have evolved to include not just traditional drugs and medical devices, but also innovations like cell and gene therapies, wearables, and more. It probably depends on who you ask and likely full of nuance. Of course not.

Research 52

Research Clinical Research Trials FDA Approval 52

Agency IQ

OCTOBER 27, 2023

The revisions will update the existing requirements with the specifications of an international consensus standard for medical device manufacturers, ISO 13485:2016.

FDA 40

FDA Science Regulations Production 40

The Pharma Data

APRIL 27, 2022

. “There is a significant unmet need for people in the European Union living with the pain and disability caused by frequent migraines,” said Nick Lagunowich, Global President, Pfizer Internal Medicine.

Marketing 52

Marketing Treatment FDA Approval Production 52