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Friday, June 12, 2026
Get Ready for ISPOR 2026 International: Key Insights and Trends
AnalysisMay 17, 2026

Get Ready for ISPOR 2026 International: Key Insights and Trends

ISPOR 2026 International is set to be a pivotal event for pharma professionals. Join us as we explore key insights and trends to watch.

Dr. Sarah Mitchell
US Cancer Clinics Rush for Revolution Medicines' New Pancreatic Cancer Drug
AnalysisoncologyMay 17, 2026

US Cancer Clinics Rush for Revolution Medicines' New Pancreatic Cancer Drug

US cancer clinics are responding rapidly to the approval of Revolution Medicines' experimental drug for pancreatic cancer. This article explores the implications for stakeholders.

Dr. Sarah Mitchell
Political Contest in the U.K. Could Shake Up Drug Pricing
AnalysisMay 17, 2026

Political Contest in the U.K. Could Shake Up Drug Pricing

The ongoing political contest in the U.K. has significant implications for drug pricing. This article explores the potential impacts on the pharmaceutical industry.

Dr. Sarah Mitchell
Biotech Leaders Push for Pazdur Amid Takeda Layoffs
AnalysisMay 17, 2026

Biotech Leaders Push for Pazdur Amid Takeda Layoffs

Biotech leaders are rallying for Pazdur's approval while Takeda announces significant layoffs. This article explores the implications for the pharma industry.

Dr. Sarah Mitchell
CDER Chief Høeg Fired: Implications for Pharma Industry
AnalysisMay 17, 2026

CDER Chief Høeg Fired: Implications for Pharma Industry

The firing of CDER Chief Høeg from the FDA raises questions about leadership stability and its effects on the pharmaceutical industry. This article explores the implications for pharma teams and investors.

Dr. Sarah Mitchell
India's Pharma Industry Goes Global: Can It Compete with China?
AnalysisMay 17, 2026

India's Pharma Industry Goes Global: Can It Compete with China?

India's pharmaceutical sector is expanding internationally, but the question remains: can it rival China's dominance? This article explores the implications for the industry.

Dr. Sarah Mitchell
NICE Approval for Imfinzi: Implications for Stomach Cancer Treatment
Analysisstomach cancerMay 17, 2026

NICE Approval for Imfinzi: Implications for Stomach Cancer Treatment

NICE's backing of Imfinzi for stomach cancer marks a significant milestone for AstraZeneca. This article explores the implications for investors and pharma teams.

Dr. Sarah Mitchell
Amgen's 340B Program Crackdown: Implications for Pharma
AnalysisMay 17, 2026

Amgen's 340B Program Crackdown: Implications for Pharma

Amgen has intensified its efforts against perceived misuse of the 340B program. This article explores the implications for pharmaceutical companies and stakeholders.

Dr. Sarah Mitchell
Holland & Knight Health Dose: Oncology Updates from May 12, 2026
AnalysisoncologyMay 17, 2026

Holland & Knight Health Dose: Oncology Updates from May 12, 2026

This article provides a comprehensive analysis of the latest updates in oncology from the Holland & Knight Health Dose on May 12, 2026. Key insights for BD teams, investors, and analysts are highlighted.

Dr. Sarah Mitchell
Understanding the FDA: Insights on Marty Makary's Perspective
AnalysisMay 17, 2026

Understanding the FDA: Insights on Marty Makary's Perspective

This article examines Marty Makary's views on the FDA, highlighting key misunderstandings and their implications for the pharmaceutical industry.

Dr. Sarah Mitchell
NICE Backs Imfinzi for Stomach Cancer: Implications for Investors
Analysisstomach cancerMay 17, 2026

NICE Backs Imfinzi for Stomach Cancer: Implications for Investors

NICE's recent approval of Imfinzi for stomach cancer marks a significant milestone for AstraZeneca. This article explores the implications for investors and pharma teams.

Dr. Sarah Mitchell
Roche's ctDNA-Guided Approach in Bladder Cancer: A Strategic Win
Analysisbladder cancerMay 17, 2026

Roche's ctDNA-Guided Approach in Bladder Cancer: A Strategic Win

Roche's innovative ctDNA-guided approach for Tecentriq in post-surgical bladder cancer has garnered significant attention. This article explores the implications for pharmaceutical teams and investors.

Dr. Sarah Mitchell
WHO Declares Ebola Outbreak an International Emergency
AnalysisEbolaMay 17, 2026

WHO Declares Ebola Outbreak an International Emergency

The WHO has declared the Ebola outbreak an international public health emergency, prompting critical responses from the pharmaceutical sector. This article explores the implications for business and investment.

Dr. Sarah Mitchell
The Cloudy Truth About Blue Zones: An Opinion Piece
AnalysisMay 17, 2026

The Cloudy Truth About Blue Zones: An Opinion Piece

This article delves into the realities of blue zones, challenging common perceptions and exploring their implications for the pharmaceutical sector.

Dr. Sarah Mitchell
ASCO 2026 Oncology Drug Pipeline Preview
AnalysisoncologyMay 14, 2026

ASCO 2026 Oncology Drug Pipeline Preview

Get an in-depth preview of the ASCO 2026 oncology drug pipeline, focusing on key presentations from leading pharma companies and their competitive positioning.

Dr. Sarah Mitchell
FDA Approves Eli Lilly's Zepbound for Obstructive Sleep Apnea
AnalysisobesityMay 13, 2026

FDA Approves Eli Lilly's Zepbound for Obstructive Sleep Apnea

Eli Lilly's tirzepatide, branded as Zepbound, receives FDA approval for obstructive sleep apnea, marking a significant milestone in treatment options. This approval could reshape the competitive landscape and expand the GLP-1 class market.

Dr. Sarah Mitchell
BIO 2026 Preview: Companies to Watch and Key Catalysts
AnalysisMay 13, 2026

BIO 2026 Preview: Companies to Watch and Key Catalysts

Get insights into the companies to watch and key catalysts for business development teams at the BIO International Convention 2026.

Dr. Sarah Mitchell
FDA Approval for Pfizer's Breast Cancer Drug: Vepdegestrant
Analysisadvanced or metastatic HR-positive, HER2-negative breast cancerMay 4, 2026

FDA Approval for Pfizer's Breast Cancer Drug: Vepdegestrant

The FDA has granted approval for Pfizer and Arvinas' novel breast cancer drug, vepdegestrant. This marks a significant new treatment option for patients with advanced or metastatic HR-positive, HER2-negative breast cancer who have exhausted prior endocrine therapies.

Kenji Watanabe
Auvelity FDA Approval: New MDD Treatment Option
AnalysisMajor Depressive Disorder (MDD)May 3, 2026

Auvelity FDA Approval: New MDD Treatment Option

The FDA has approved Auvelity, a new oral treatment for major depressive disorder (MDD) in adults, marking a significant advancement in mental health therapeutics. Manufactured by Axsome Therapeutics, this approval offers a novel option for patients seeking relief from MDD.

Dr. Hannah O'Connor
FDA Scrutiny Post-Market Data: Impact on Pharma Investment Strategies
AnalysisMay 2, 2026

FDA Scrutiny Post-Market Data: Impact on Pharma Investment Strategies

This article examines the implications of FDA scrutiny on post-market data and its influence on pharmaceutical investment strategies and drug development.

Dr. Yuna Park