Inflectra To Be First Substitutable Biosimilar In Australia

Australia's Pharmaceutical Benefits Advisory Committee (PBAC) has recommended that Hospira's biosimilar infliximab product Inflectra should be listed on the Pharmaceutical Benefits Scheme. And in a highly controversial move, the PBAC has also said that Inflectra should be "a"-flagged, meaning that it can be substituted by pharmacists for the originator drug, Johnson & Johnson's Remicade.

Australia's Pharmaceutical Benefits Advisory Committee (PBAC) has recommended that Hospira's biosimilar infliximab product Inflectra should be listed on the Pharmaceutical Benefits Scheme. And in a highly controversial move, the PBAC has also said that Inflectra should be "a"-flagged, meaning that it can be substituted by pharmacists for the originator drug, Johnson & Johnson's Remicade.

The PBAC has lost no time in seeking a listing for Inflectra: the product has only just been approved by...

Read the full article – start your free trial today!

Join thousands of industry professionals who rely on Scrip 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 Alimentary/Metabolic

Regeneron Buys Tirzepatide-Like Product With Eye On Muscle-Preserving Combinations

 

Regeneron is bringing in its own GIP/GLP-1 agonist, establishing a path to develop proprietary obesity drug combinations with its internal muscle-sparing drugs.

A Short History Of MASH Deals, Culminating In GSK/Boston Pharma

 
• By 

Both high-profile failures and small investments that are yielding success so far characterize the dealmaking in MASH over the past 15 years or so.

Novo Nordisk’s CEO Forced Out After Falling Behind In GLP-1 Battle

 

Company surprises investors with Jørgensen's exit but insists its strategy will not change.

Multiple Launches Help Lilly’s Japan Growth

 
• By 

Lilly saw solid growth for its business in Japan last year on the back of several new launches and is building its obesity and Alzheimer's portfolios in the country.

More from Therapy Areas

Lyra Eyes US Filing For LYR-210 After Surprise ENLIGHTEN 2 Win

 

In a turn of fortunes, Lyra Therapeutics has reported positive Phase III results for LYR-210 in chronic rhinosinusitis, boosting hopes for US approval. The company plans to submit an NDA and pursue further trials, but its cash position is precarious.

Ascletis Plans China Submission After Positive Denifanstat Phase III Acne Results

 

Once-daily oral FASN inhibitor denifanstat meets all endpoints in a Chinese Phase III trial for moderate-to-severe acne, paving the way for a regulatory submission in China.

New Regenxbio DMD Data Support Gene Therapy Accelerated Approval

 
• By 

Regenxbio reported functional and biomarker data from an ongoing study of RGX-202, which it hopes to file for approval in Duchenne muscular dystrophy in 2026.