EMA Proposes Updating Hepatitis B Guide To Support Drugs Aiming For ‘Functional Cure’

Since the European Medicines Agency adopted its hepatitis B guideline in 2006, the treatment goal of ‘functional cure’ has evolved and changed the development landscape of agents intended for the treatment of chronic infection.

Human hand hold care liver health therapy, Liver cancer, cancer, donation liver, disease, donation, Hepatitis, cirrhosis, Hepatitis B virus, HBV, Vaccine, insurance, hospital.World hepatitis day
Nearly 300 million people globally are living with chronic hepatitis B • Source: Shutterstock

The European Medicines Agency is inviting stakeholder feedback on plans to update its hepatitis B medicines guideline to clarify the requirements for new products that aim to achieve a “functional cure,” have novel mechanisms of action and/or are intended for finite (time-limited) or combination treatment approaches.

The EMA’s proposal is outlined in a draft concept paper in which the agency explains that its current guideline...

Read the full article – start your free trial today!

Join thousands of industry professionals who rely on Pink Sheet for daily insights

  • Start your 7-day free trial
  • Explore trusted news, analysis, and insights
  • Access comprehensive global coverage
  • Enjoy instant access – no credit card required

More from Europe

New EU Filings

 

Linerixibat, GSK's treatment for cholestatic pruritus in patients with primary biliary cholangitis, is among the latest products that have been filed for review by the European Medicines Agency for potential EU marketing approval.

EMA Explores Supporting Drug Development For High Unmet Need Disorder Scleroderma

 

While treatments for scleroderma are in development, none are approved for the condition that is associated with high morbidity and mortality. The European Medicines Agency says guidance on how to design development programs for the disorder is needed.

EMA Nod For First MASH Drug Rezdiffra, Cell Therapy Zemcelpro And 11 Others

 

Madrigal Pharmaceuticals’ Rezdiffra is on track to become the first medicine approved in the EU for non-cirrhotic metabolic dysfunction-associated steatohepatitis after the European Medicines Agency recommended that it be granted conditional marketing authorization.

UK Looks To Auto-Match NHS Patients With Clinical Trials To Boost Recruitment

 
• By 

The UK government is making it easier for millions of people to participate in clinical trials and is boosting transparency around how studies are delivered across the National Health Service.

More from Geography

Recent And Upcoming FDA Advisory Committee Meetings

 
• By 

Recent and upcoming US FDA advisory committee meetings and a summary of the topics covered.

EMA Explores Supporting Drug Development For High Unmet Need Disorder Scleroderma

 

While treatments for scleroderma are in development, none are approved for the condition that is associated with high morbidity and mortality. The European Medicines Agency says guidance on how to design development programs for the disorder is needed.

EMA Nod For First MASH Drug Rezdiffra, Cell Therapy Zemcelpro And 11 Others

 

Madrigal Pharmaceuticals’ Rezdiffra is on track to become the first medicine approved in the EU for non-cirrhotic metabolic dysfunction-associated steatohepatitis after the European Medicines Agency recommended that it be granted conditional marketing authorization.