FDA and Novartis back Zolgensma amid data manipulation issues

The US FDA remains confident that Zolgensma will not be pulled after allegations of data manipulation by the gene therapy manufacturer AveXis

Dan Stanton, Editorial director

August 7, 2019

2 Min Read
FDA and Novartis back Zolgensma amid data manipulation issues
Image: AdobeStock/Elnur

The US FDA remains confident that Zolgensma will not be pulled after being alerted to allegations of data manipulation by the gene therapy manufacturer AveXis.

In May 2019, Novartis company AveXis received US Food and Drug Administration (FDA) approval for its $2.1 million single-dose, one-time gene therapy Zolgensma (onasemnogene abeparvovec) to treat children less than two years of age with spinal muscular atrophy (SMA).

A month later, AveXis informed the Agency “about a data manipulation issue that impacts the accuracy of certain data from product testing performed in animals submitted in the biologics license application (BLA),” Peter Marks, director of the FDA’s Center for Biologics Evaluation and Research (CBER) wrote in a statement yesterday.

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Image: AdobeStock/Elnur

“The FDA is carefully assessing this situation and remains confident that Zolgensma should remain on the market. Out of the large amount of submitted information reviewed by the agency, our concerns at this time are limited to only a small portion of the product testing data that was contained in the marketing application.”

But while Zolgensma may not be pulled, Marks said AveXis could be subject to civil or criminal penalties because the firm became aware of the data manipulation issue and did not inform the FDA before the gene therapy won approval.

A statement issued by Novartis said AveXis immediately undertook an investigation to understand any implications and address the situation once the data issues came to light.

“Once we had interim conclusions from our investigations, we shared our findings with the FDA. As noted by the FDA, the data in question were a small portion of our overall submission and are limited to an older process no longer in use.”

The firm said: “At no time during the investigation did the findings indicate issues with product safety, efficacy or quality,” adding that it does not expect this to impact ongoing Zolgensma regulatory filings and development programs.

“AveXis is committed to taking appropriate action to prevent future incidents across its portfolio of development programs.”

Related news: ‘Zolgensma: We all know the price, but how is it made?’

About the Author

Dan Stanton

Editorial director

Journalist covering the international biopharmaceutical manufacturing and processing industries.
Founder and editor of Bioprocess Insider, a daily news offshoot of publication Bioprocess International, with expertise in the pharmaceutical and healthcare sectors, in particular, the following niches: CROs, CDMOs, M&A, IPOs, biotech, bioprocessing methods and equipment, drug delivery, regulatory affairs and business development.

From London, UK originally but currently based in Montpellier, France through a round-a-bout adventure that has seen me live and work in Leeds (UK), London, New Zealand, and China.

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