Legacy MEDSearch

OCTOBER 25, 2022

EndoStim therapy is designed to restore normal esophageal function and preserve normal anatomy to avoid the typical gastrointestinal side effects of traditional anti-reflux surgery. Food and Drug Administration (FDA) granted Breakthrough Device Designation for the Company’s EndoStim System.

Food and Drug Administration 98

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Pharmaceutical Technology

APRIL 14, 2023

Madrigal Pharmaceuticals’ resmetirom for nonalcoholic steohepatitis (NASH) could be fairly priced at a higher range than Intercept Pharmaceuticals’ obeticholic acid, based on a revised evidence report published by the Institute for Clinical and Economic Review (ICER). This verdict applies to NASH patients with liver fibrosis of any stage.

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PM360

MAY 15, 2023

At the top of this year’s list is our Uber ELITE winner Tom McCourt, CEO, Ironwood Pharmaceuticals, who has left an undeniable mark within the gastrointestinal space for the past 35 years. He has worked on game-changing brands including Prilosec , Nexium , Zelnorm , and LINZESS—plus, he isn’t nearly done. and Similasan Corp.

Education 105

Education Media Marketing Sales 105

PM360

DECEMBER 14, 2022

In its latest venture into the healthcare arena, Amazon is reaching out directly to the consumer via its soon-to-be-launched Amazon Clinic , a virtual health service for patients to see licensed clinicians about common medical issues. The services are cash pay only at this point. Ayogu referred to, Amazon is also in the midst of a $3.9

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Legacy MEDSearch

JUNE 10, 2022

. “And it further showed that the discovery of the additional polyps was not predicated on physician’s experience level or practice environment,” added Brandy Crawford, VP of Clinical Affairs. Our groundbreaking five-camera endoscope platform provides an unprecedented 360° integrated view of the gastrointestinal tract.

FDA 52

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PM360

MAY 16, 2023

McCourt has been in the industry for more than 35 years with most of that time spent contributing to some of the biggest breakthroughs within the gastrointestinal (GI) space. This year that honor goes to Tom McCourt, CEO, Ironwood Pharmaceuticals. 1 GI company in the U.S.

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Media Marketing Management Pharmaceutical 52

PM360

APRIL 7, 2023

At its heart, the point of care has always revolved around the when and where patients are making decisions about their health. They can also seek care at retail health clinics associated with their local pharmacy, sign up for subscription/membership-based care such as One Medical, or download care-based apps like BetterHelp or Talkspace.

Education 98

Education Doctors Patients Physicians 98

European Pharmaceutical Review

APRIL 10, 2024

Engaging in continuous dialogue with regulatory bodies in Europe and the US helps in designing clinical trials that follow the latest safety standards and international regulations. During the development of clinical trials that use faecal-derived material, the necessity of safety is paramount.

Safety 85

Safety Patients Medical FDA 85

PM360

JUNE 16, 2023

What Patients at the Center Really Means Pharma organizations that make advocacy and patient support an absolute priority—just like clinical research—stand out in the industry. They can open doors to clinical trial recruitment programs, healthcare systems, the biotech community, local policies, payer, and market access connections.

Patients 98

Patients Pharma Education Recruitment 98

European Pharmaceutical Review

MARCH 23, 2023

In final draft guidance by the National Institute for Health and Care Excellence (NICE), single dose gene therapy Upstaza (eladocagene exuparvovec) has been recommended for patients over 18 months old with severe aromatic L-amino acid decarboxylase (AADC) deficiency. How is the gene therapy administered?

Medicine 77

Medicine Healthcare Healthcare Pharmaceutical 77

Pharmaceutical Technology

FEBRUARY 26, 2023

This is largely due to the FDA’s rigorous approach to the safety of microbiome therapeutics, which has manifested in clinical holds, resulting in delays that have dimmed the enthusiasm in the space in recent times. We lost three years,” says Dr. Susy Hota, infectious disease specialist at University Health Network, University of Toronto.

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Safety FDA Medicine Side effects 111

Pharmaceutical Technology

JUNE 30, 2022

In the wake of Russia’s invasion of Ukraine, sponsors are increasingly evaluating other European countries to conduct their clinical trials. Among them, the Eastern European nation of Georgia has emerged as a key rescue country for multinational clinical trials that were put on hold due to the war. Room to grow.

Food and Drug Administration 52

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Pharmaceutical Technology

MARCH 2, 2023

Pembrolizumab is under clinical development by Merck and currently in Phase III for Bile Duct Cancer (Cholangiocarcinoma). Attributes of the drug, company and its clinical trials play a fundamental role in drug-specific PTSR and likelihood of approval.

Patients 40

Patients FDA Prescription Retail 40