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Thursday Jul 13 2017
By
REUTERS

Federal advisory backs Novartis' pioneering new cancer gene therapy

By
REUTERS
A sign marks a building on Novartis' campus in Cambridge, Massachusetts, US, February 28, 2017. Brian Snyder/File Photo
 

Novartis AG's pioneering new cancer drug won enthusiastic support from a federal advisory panel on Wednesday, paving the way for approval of the first US gene therapy.

The panel unanimously recommended that the Food and Drug Administration (FDA) approve tisagenlecleucel, a drug for patients ages 3 to 25 suffering from relapsed B-cell acute lymphoblastic leukaemia (ALL), the most common form of US childhood cancer.

The drug uses a new technology known as CAR-T – or chimeric antigen receptor T-cell therapy – that harnesses the body's own immune cells to recognise and attack malignant cells.

In a clinical trial, 83 percent of patients – who had relapsed or failed chemotherapy – achieved complete or partial remission three months post infusion. After one year, 79 percent of patients were still alive.

Patients with ALL who fail chemotherapy typically have only a 16-30 percent chance of survival.

"This is a potentially paradigm-changing type of benefit," said Dr. Brian Rini, a panellist and physician at Cleveland Clinic Taussig Cancer Institute.

The FDA is not obliged to follow the recommendations of its advisers but typically does so. The agency is expected to rule on the drug by the end of September.

The approval of tisagenlecleucel would have significant implications not only for Novartis but for companies developing similar treatments, including Kite Pharma Inc, Juno Therapeutics Inc, and bluebird bio Inc.

It would also advance a technique scientists have been attempting to perfect for decades and help lift the entire field of cell therapy.

"This will be a historic approval," said Brad Loncar, chief executive of Loncar Investments, which runs the Loncar Cancer Immunotherapy ETF. "As an investor, I've never seen anything like it. It's an entirely new way of treating cancer."

The product is made by extracting and isolating a patient's T cells, genetically engineering them to recognise and target cancer cells, and then infusing them back into the patient. Novartis said the entire process will take 22 days by the time it is launched.

The treatments are given just once and are expected to cost up to $500,000. Loncar said approval of tisagenlecleucel would represent an inflexion point for investors.

"Any time a new technology crosses the finish line at the FDA, it gets noticed and I think you'll see a rush of investment and see these therapies be improved over time."

More than half of patients experienced a serious complication known as cytokine release syndrome (CRS), which occurs when the body's immune system goes into overdrive. Doctors were able to manage the condition and the syndrome caused no deaths.

The FDA expressed concern that the drug could cause new malignancies over the long term. Panellists generally felt that the risk was low and said Novartis's risk mitigation proposals were adequate.

Novartis is also testing the drug in diffuse large B-cell Lymphoma, the most common form of non-Hodgkin lymphoma, as is Kite.

Novartis stock closed up 1.5 percent at $83.21 in US trading. The shares finished up 2.2 percent at 80.5 Swiss francs in Zurich before the vote was taken.

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