Don't Panic! Novartis Is Still Invested In CAR-T Despite 2Q Silence

Novartis AG's CAR-T cell therapy CTL019, set to be the first in this class to achieve a US FDA filing, might not be an immediate blockbuster owing to its tricky treatment logistics, small initial indication and a lack of physician and patient exposure, but it is still a game changer in immuno-oncology, says Dr. Oz Azam, Novartis's head of cell therapies.

RedBloodCellsOnWhite_1200x675

Novartis AG's cell therapy CTL019, a CAR-T (chimeric antigen receptor T-cells) product, caused a stir last month when the big pharma neglected to include the pipeline-leading therapy on a list of its upcoming potential blockbuster drugs during its second-quarter earnings presentation. But Dr. Oz Azam, global head of cell and gene therapies at Novartis, told Scrip this was not a big deal and indeed there were a number of explanations for the medicine's exclusion.

While Azam said he couldn’t comment directly on why Novartis's senior management team did not include CTL019 on a slide...

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 Anticancer

More from Therapy Areas

PureTech’s New Spin-Off Wants Partners For Pulmonary Fibrosis Drug

 

Deupirfenidone hit its Phase II endpoint but the program remains risky and PureTech’s new Celea Therapeutics will aim to pull in extra funding for its late-stage development.

Xenon Nears Phase III Readout For Potential Epilepsy And Depression Blockbuster

 

Leading a field of rival potassium channel modulators, azetukalner will have a pivotal epilepsy readout early next year, with Phase III trials in depression and biopolar disorder also underway.

In Brief: Bayer Commits Up To $1.3bn For Kumquat’s KRAS G12D Inhibitor

 

Deal Snapshot: Bayer will take over development of the asset once Kumquat completes a Phase Ia clinical trial, but the biotech firm may opt in to share US profits and losses.