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GSK’s Promacta Cleared For Use With Interferon In Hep C Patients

 
• By Shirley Haley

The new indication fills an unmet need in a population of patients who have a short window to cure chronic hepatitis C infection before liver damage becomes too great for treatment, but for whom interferon-based therapy – currently their only option - is not indicated because of low platelet levels.

GlaxoSmithKline PLC’s oral thrombocytopenia therapy Promacta (eltrombopag) received FDA approval as supportive care for a population of chronic hepatitis C patients lost in the flurry of activity around new and emerging antiviral therapies: those who don’t have time to wait for interferon-free regimens to be approved but are unable to take interferon because their blood platelet count is too low.

FDA cleared Promacta for treatment of patients with chronic hepatitis C to allow the initiation and maintenance of interferon-based therapy,...

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Ocaliva: Still No Clarity On Why EU Court Opposed Revocation Of Approval

 
• By Neena Brizmohun

Advanz Pharma would have had to show that the European Commission’s decision to revoke Ocaliva’s conditional marketing approval risked causing serious and irreparable harm, according to lawyers from Van Bael & Bellis.

Final Chance To Have Your Say: Take Our Reader Survey This Week

 
• By Nielsen Hobbs

This is your final call to participate in the survey to better understand our subscribers’ content and delivery needs. The deadline is 20 September.

Shape Our Content: Take The Reader Survey

 
• By Nielsen Hobbs

We are conducting a survey to better understand our subscribers’ content and delivery needs. If there are any changes you’d like to see in coverage topics, article format, or the method in which you access the Pink Sheet – or if you love it how it is – now is the time to have your voice heard.

Brazil Pilots Digital Drug Pack Inserts

 
• By Francesca Bruce

A new pilot aims to take Brazil closer to ‘digital transformation.’

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UK MHRA: Bacteriophage Developers Wanted ‘More Clarity’ On UK Framework

 
• By Eliza Slawther

Julian Beach, interim executive director of healthcare quality and access at the UK drug regulator, the MHRA, tells the Pink Sheet how the agency is responding to increased efforts to develop bacteriophage therapies.

Respiratory Treatments Hit Hardest By HTA Terminations In England

 
• By Leela Barham

Exclusive analysis by the Pink Sheet explores how non-submissions by pharmaceutical companies to England’s health technology appraisal body are impacting the availability of medicines on the National Health Service.

New Era Begins In Korea: Policy Predictions For Biopharma

 
• By Jung Won Shin

As South Korea's new president immediately gets to work on setting initial policies, essential drug supplies, R&D incentives and AI-driven digital healthcare are among the key topics in focus.