MoxDuoTreatment for Pain
QRxPharma Refiles MoxDuo New Drug Application with the FDA
November 26, 2013 -- Sydney, Australia and Bedminster, New Jersey – QRxPharma Limited announced today that the Company resubmitted its MoxDuo New Drug Application (NDA). At a meeting in early October, the United States Food and Drug Administration (FDA) provided QRxPharma with guidance on its requirements for the NDA refiling as well as data validation documentation. “We are confident that our refiled NDA will confirm the validity of the data defining the product’s respiratory safety advantages and we are hopeful that the FDA will view them favourably in their consideration of the benefits of immediate release MoxDuo as a therapeutic option for the millions of patients who suffer from acute pain,” said Dr. John Holaday, Managing Director and Chief Executive Officer, QRxPharma. “We were encouraged by our candid dialogue with the FDA throughout this process, and will continue to liaise closely with the Agency to bring MoxDuo to market.”
The FDA previously confirmed that the Company’s Combination Rule Trial, Study 008, satisfied efficacy requirements and that there were no efficacy or safety issues identified in any of the studies submitted in the original NDA.
QRxPharma completed an audit of the more than 30 million data points for oxygen desaturation from Study 022. We believe these data demonstrate a significant respiratory safety advantage for MoxDuo over equi-analgesic doses of morphine or oxycodone. Furthermore, MoxDuo provides a lower starting dose and finer dose titration steps than acute pain opioids presently available, giving greater flexibility to physicians and patients as the need for pain relief is balanced with lower risks of side effects.
We expect the FDA to schedule an Advisory Committee meeting preceding a Prescription Drug User Fee Act (PDUFA) date six months following this submission, projected for late May, 2014.
“We will keep our shareholders informed as we receive feedback from the FDA, and assuming approval, we anticipate product launch with our US commercialisation partner, Actavis, in the second half of CY2014,” added Holaday.
The revised NDA is the basis for recommencing the regulatory approval for MoxDuo for the treatment of moderate to severe pain, a US $2.5 billion segment of the US $8 billion spent annually on prescription opioids in the US.
Posted: November 2013
- QRxPharma Issues Statement On Moxduo Advisory Committee Meeting - April 22, 2014
- QRxPharma Announces 25 May 2014 as New PDUFA Date for MoxDuo NDA - December 11, 2013
- QRxPharma Receives Complete Response Letter From FDA Regarding MoxDuo NDA - August 28, 2013
- FDA Sets 26 August 2013 As New PDUFA Date For MoxDuo NDA - March 14, 2013
- QRxPharma Resubmits MoxDuo New Drug Application to the FDA - February 28, 2013
- QRxPharma and FDA Establish Path Forward for Resubmission Of Moxduo New Drug Application - January 16, 2013
- QRxPharma Receives Complete Response Letter From FDA Regarding MoxDuo NDA - June 27, 2012
- QRxPharma Granted Target Date for FDA Action on MoxDuo IR NDA: NDA Accepted for Review; PDUFA Date Set for June 25, 2012 - November 11, 2011
- QRxPharma Completes NDA Submission for MoxDuo IR - August 26, 2011
- QRxPharma Announces NDA Filing for MoxDuo IR - July 19, 2011
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