Adverum Biotechnologies announces FDA regenerative medicine advanced therapy designation granted for ixo-vec for the treatment of wet AMD

1 August 2024 -  Adverum Biotechnologies today announced that the US FDA has granted regenerative medicine advanced therapy designation for ...

Read more →

Cartesian Therapeutics receives FDA regenerative medicine advanced therapy designation for Descartes-08 for the treatment of myasthenia gravis

22 May 2024 - Cartesian Therapeutics today announced that the US FDA has granted regenerative medicine advanced therapy designation for ...

Read more →

Atsena Therapeutics receives FDA regenerative medicine advanced therapy designation for ATSN-101 gene therapy for GUCY2D associated Leber congenital amaurosis

14 November 2023 - ATSN-101 has demonstrated clinically meaningful improvements in vision at the highest dose with no drug-related serious ...

Read more →

FDA grants Direct Biologics regenerative medicine advanced therapy designation for the use of ExoFlo in COVID-19 related ARDS

12 April 2022 - Direct Biologics announced that the U.S. FDA has awarded their EV drug product ExoFlo with a regenerative ...

Read more →

Innovative regenerative medicine therapies – patient safety comes first

3 June 2021 - The U.S. FDA continues to facilitate the development and availability of innovative medical products, such as regenerative ...

Read more →

Potential risks of treatment with unapproved regenerative medicine products

22 July 2020 - Protecting patients is at the core of what we do at the U.S. Food and Drug ...

Read more →

Identifying the risks of unproven regenerative medicine therapies

17 June 2020 - In the middle of the coronavirus disease 2019 public health response, many priorities are currently competing for ...

Read more →

Framework for the regulation of regenerative medicine products

21 May 2019 - The U.S. FDA has published four final guidance documents that are part of a comprehensive policy framework ...

Read more →

Advanced therapy medicinal products and health technology assessment principles and practices for value-based and sustainable healthcarehe

1 April 2019 - Advanced therapy medicinal products are beginning to reach European markets, and questions are being asked about their ...

Read more →

FDA advances new efforts to promote development of safe and effective regenerative medicine products

15 February 2019 - Today, the FDA finalised two guidance documents regarding regenerative medicine therapies.  ...

Read more →

Hope for regenerative medicine bonanza

30 October 2018 - Regenerative medicine could be worth $6 billion in annual revenue and 6,000 new jobs for Australia ...

Read more →

Rejuvenating regenerative medicine regulation

7 February 2018 - The FDA recently made long-awaited progress toward protecting patients from interventions involving human cell- and tissue-based products ...

Read more →

Mesoblast receives FDA regenerative medicine advanced therapy designation for its cell therapy in heart failure patients with left ventricular assist devices

21 December 2017 - Mesoblast today announced that the United States FDA has granted Regenerative Medicine Advanced Therapy (RMAT) designation for ...

Read more →

Statement from FDA Commissioner on FDA’s comprehensive new policy approach to facilitating the development of innovative regenerative medicine products to improve human health

16 November 2017 - One of the most promising fields of science is the area of cell-based therapies and their ...

Read more →

FDA announces comprehensive regenerative medicine policy framework

16 November 2017 - Framework aims to spur innovation, efficient access to potentially transformative products, while ensuring safety and efficacy. ...

Read more →