Avita Medical Release: Initial Pre-Emergency Use Authorization Submission Made To U.S. FDA For Use Of ReCell In A Mass Casualty Scenario
NEW YORK, May 10, 2017 /PRNewswire/ -- Avita Medical Limited (ASX:AVH; OTCQX:AVMXY), a regenerative medicine company focused on the treatment of wounds and skin defects, has received notification of the initial FDA review of the Pre-EUA (Emergency Use Authorization) submission to allow the emergency deployment of its ReCell® device for a mass casualty event involving burn injuries.
The Biomedical Advanced Research and Development Authority (BARDA) filed the Pre-EUA submission, and the review is conducted at this pre-approval stage because, during exigent circumstances, the time available for the submission and review of an EUA request may be severely limited. For the contract with BARDA, this brings the Company closer to establishing a national strategic stockpile of vendor-managed inventory of ReCell® autologous cell harvesting devices, which once approved, will allow physicians to rapidly deliver a suspension of skin cells to various wounds, including burns. Under Avita's USD61.9m contract with BARDA, the initial order has a value of approximately USD8m, and BARDA could opt to purchase in advance of FDA market approval, which the Company is also pursuing.
BARDA informed Avita that the pre-EUA submission has been reviewed by the FDA and that the agency has no 'additional comments or questions at this time.' BARDA said that a pre-EUA submission is not an indication of the FDA's views on the product's potential to be used under an EUA, nor that the sponsor has obtained or submitted all the information necessary for FDA to review a formal request for consideration of an EUA. BARDA explained that a pre-EUA submission is a mechanism to initiate early discussions with the FDA prior to an emergency only, and does not provide an independent legal basis for distributing or dispensing unapproved products or approved products for unapproved uses.
Avita will continue to update the required documentation to the FDA via communications with BARDA on an ongoing basis regarding any new information relevant to the ReCell® device and its potential emergency use.
"Important boxes have been ticked, and it is very positive that the information supplied to date has satisfied FDA's initial review," said Avita CEO Adam Kelliher. "My team will keep supporting BARDA so that we can fulfill our contractual goal of delivering a significant number of ReCell® devices for use in the event of a U.S. emergency."
This represents another milestone for Avita Medical's support of BARDA under the terms of their contract. EUA is a provision whereby the FDA may authorize use of an investigational device when there are no adequate, approved, and available alternatives only after the Health and Human services (HHS) Secretary has made a declaration of emergency or threat justifying authorization of emergency use. The pre-EUA documentation submitted in advance of a mass casualty event allows FDA to be in position to rapidly authorize the use of the product in the event of a disaster. BARDA operates under the Department of Health and Human Services, and is charged with ensuring the US population is prepared should there be a mass casualty event caused by chemical, biological or nuclear action.
Avita says its program to get a U.S. Pre-Market Approval (PMA) from the FDA is on track, with all data collected from its pivotal clinical trial involving seven leading U.S. burns centers. The Company says it expects to submit its PMA application in mid-2017, with an anticipated FDA decision mid-2018. The FDA has approved ReCell® for cases of Compassionate Use, where it is needed for life-saving events, and has granted Continued Access to the device for those medical professionals who participated in the clinical trial.
ABOUT RECELL® AND RES
ReCell® is Avita Medical's unique proprietary technology that enables a clinician to rapidly create, at point of care in approximately 30 minutes, Regenerative Epithelial Suspension (RES) using a small sample of the patient's skin. RES is an autologous suspension comprising the cells necessary to regenerate natural, healthy skin. RES has a broad range of applications and can be used to restart healing in unresponsive wounds, to repair burns using less donor skin, yet with improved functional and aesthetic outcomes, and to restore pigmentation and improve cosmesis of damaged skin.
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FOR FURTHER INFORMATION:
Avita Medical Ltd
Chief Executive Officer
Phone: +44 020 8947 9804
Avita Medical Ltd
Chief Financial Officer
Phone: + 1 (661) 367-9170
Phone: +61 (0)3 9620 3333
Mobile: +61 (0)407 162 530
Phone +1 (415) 513-1282
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SOURCE Avita Medical