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Home » RMAT » Page 6

RMAT Designations Accelerate: 3 New RMATs in Two Weeks

June 25, 2018 By Cade Hildreth (CEO) Leave a Comment

3 RMATs

In the past two week, the U.S. FDA has awarded three new RMAT designations, bringing the total number of awards to 19.

The new RMAT designations were awarded to:

  • Nightstar Therapeutics: Gene therapy (NSR-REP1) for choroideremia treatment – June 14, 2018
  • Caladrius Biosciences: CD34+ cell therapy (CLBS14) for refractory angina – June 19, 2018
  • Voyager Therapeutics: Gene therapy (VY-AADC ) for Parkinson’s disease – June 22, 2018

[Read more…]

Filed Under: Cell Therapy, Stem Cell News Tagged With: RMAT

Abeona Becomes First Company to Secure Two RMATs

April 27, 2018 By Cade Hildreth (CEO) Leave a Comment

Abeona Therapeutics - Sanfilippo Syndrome TrialAbeona Therapeutics announced the U.S. FDA granted a Regenerative Medicine Advanced Therapy (RMAT) designation to ABO-102, the company’s AAV-mediated gene therapy for the treatment of Sanfilippo syndrome Type A (MPS IIIA), a rare autosomal-recessive lysosomal storage disease.

It was the 16th RMAT designation awarded by the FDA and a landmark achievement in that it makes Abeona the first company to achieve two RMAT designations.

Headquartered in Dallas, TX, Abeona (NASDAQ: ABEO) is a clinical-stage biopharmaceutical company focused on developing novel cell and gene therapies for life-threatening rare genetic diseases. Abeona’s first RMAT designation was for its EB-101 gene therapy for Epidermolysis Bullosa in January 2018. [Read more…]

Filed Under: Cell Therapy, Stem Cell News Tagged With: Abeona Therapeutics, fda, RMAT

MiMedx’s AmnioFix® Injectable Awarded 15th RMAT Designation in the U.S.

March 9, 2018 By Cade Hildreth (CEO) Leave a Comment

Mimedx RMAT

MiMedx GroupIn major news released today, MiMedx Group announced that their AmnioFix® Injectable was awarded RMAT status by the U.S. FDA. This is the third RMAT designation awarded by the FDA this year and the 15th RMAT overall since the designation was introduced by the 21st Century Cures Act. The “Regenerative Medicine Advanced Therapy” (RMAT) Designation was introduced on December 13, 2016, when Congress included several provisions in the 21st Century Cures Act, an act signed into law by the 114th United States Congress authorizing $6.3 billion in funding, the bulk of which is allocated for programs supported by the National Institutes of Health (NIH).

The 21st Century Cures Act has had a profound effect on the regenerative medicine industry, supporting expansion of this industry to 600+ companies worldwide. The act also accompanies accelerated regulatory pathways that have been introduced in several other countries worldwide, including Japan, South Korea, and the E.U.

Within the U.S., sponsors of cell and gene therapies are eligible to obtain an RMAT designation if their product is intended to treat serious or life-threatening diseases and there is preliminary clinical evidence that it could address unmet medical needs. [Read more…]

Filed Under: Cell Therapy, Press Releases, Stem Cell News Tagged With: fda, RMAT

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