Avrobio has up-to-date its Fabry condition gene treatment R&D designs in light of the FDA’s conversion of Sanofi’s Fabrazyme to full approval. The conversion deprives Avrobio of the chance to seek accelerated approval using its current phase 2, leading the biotech to plan to pit AVR-RD-01 against Fabrazyme in a new head-to-head clinical demo.

The Food and drug administration granted accelerated approval to Fabrazyme in 2003. Eighteen years later, the Food and drug administration converted the authorization of the enzyme replacement remedy to a full, traditional approval. The Food and drug administration up to date its surrogate endpoints table in the weeks after the conversion to reflect the fact clearance of GL-3 inclusions supported full approval of Fabrazyme.

Avrobio set out what the developments mean for AVR-RD-01 on Monday. Having originally proposed an accelerated FDA registration, Avrobio has now said it "can no longer pursue an accelerated approval pathway for AVR-RD-01 with the FAB-GT demo as currently designed.”

The plan now is to run a new registration demo, as was discussed as a possibility in Avrobio’s original proposal to the Fda. Avrobio plans to start the trial, which will compare AVR-RD-01 to Fabrazyme, in mid-2022. Avrobio said the scope, size and duration of the revised regulatory plan is similar to the original proposal for accelerated approval it put to the Food and drug administration before the full approval of Fabrazyme.

As it stands, Avrobio designs to use reduction of GL-3, also known as Gb3, inclusions as the surrogate endpoint of the head-to-head clinical trial. Food and drug administration guidance states drug developers cannot assume a surrogate endpoint used in the development of one therapy will be applicable to their applications, as Avrobio noted in its statement, but the biotech "believes this recent development could potentially apply to investigational AVR-RD-01.”

If Avrobio wins approval under the new plan, it will receive a full authorization that spares it from the conditions the Food and drug administration imposes on products that come to market place via the accelerated pathway.

Avrobio is continuing to run its existing FAB-GT phase 2 demo while preparing for the new study. The biotech now designs to cap enrollment in FAB-GT at nearly 14 patients and amend the protocol to get data "on additional parameters that are recognized to be limitations of ERT.”

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