US regulator to recruit 50 new gene and cell therapy clinical reviewers

pharmafile | January 16, 2019 | News story | Research and Development FDA, cell therapy, gene therapy, regulation 

FDA Commissioner Scott Gottlieb has said that the agency hopes to recruit 50 additional clinical reviewers for the group that oversees the clinical investigation, development and review of cell and gene products.

The expansion is preparation for an anticipated influx of investigational new drug (IND) applications for active cell-based or directly administered gene therapies in coming years.

“The FDA is witnessing a surge of cell and gene therapy products entering early development, evidenced by a large upswing in the number of investigational new drug (IND) applications. Based on this activity, we anticipate that the number of product approvals for cell and gene therapies will grow in the coming years, reflecting significant scientific advancement and the clinical promise of these new innovations,” Gottlieb said in a joint statement with Peter Marks director of the FDA’s Center for Biologics Evaluation and Research.

There are currently 800 active cell-based or directly administered gene therapy investigational new drug (IND) applications on file while the FDA anticipates an additional 200 INDs per year by 2020.

“By 2025, we predict that the FDA will be approving 10 to 20 cell and gene therapy products a year based on an assessment of the current pipeline and the clinical success rates of these products,” the statement said.

The FDA also revealed that it intends to unveil additional new policy guidance and other progress made in its drug development framework this year which includes gene therapy guidance: “Gene therapy products now have the potential to cure intractable diseases, and fundamentally alter the trajectory of many other vexing illnesses. To advance these opportunities, the FDA plans to introduce additional new policy guidance and other advances in our drug development framework in 2019.”

The guidance will allow individual researchers the ability to “pool their clinical data after following a common manufacturing protocol, and thereby develop a more robust data set for purposes of gaining a Biologics Licensing Agreement (BLA).” It is hoped that the new guidance will assist small sponsors in navigating the review process.

“We believe these cell-based and gene therapy technologies hold tremendous promise for addressing some of the most intractable diseases,” the joint statement said, “but with their novelty, also comes new uncertainties and some unique, theoretical risks. Our efforts are aimed at helping innovators proactively address these potential risks, while we outline a modern and efficient pathway for the continued development of these innovations.”

Louis Goss

Related Content

FDA approves first oral antiviral to treat adult patients with COVID-19

The US Food and Drug Administration (FDA) has announced that it has approved the oral …

ZOLL remedē System receives FDA approval for sleep apnoea treatment

ZOLL Medical Corporation has announced that it has received approval from the US Food and …

Artivion receives FDA PMA approval of PerClot; transfers designation to Baxter

US cardiac and vascular surgery company Artivion has announced that the US Food and Drug …

Latest content