We’re pleased to share news from ReveraGen, the company developing Vamorolone  (previously called VBP15) a steroid alternative, that their drug has received Fast Track designation from the FDA, which will speed up the review of Vamorolone.  

Duchenne UK, Joining Jack and the Duchenne Research Fund helped fund the Phase 1 study of this potential therapy. 
The Phase 2a&b will begin recruitment in the coming months.

Alex Johnson and Emily Crossley, Co-founders of Duchenne UK said: 

"In 2014, Duchenne UK and Duchenne Research Fund invested $1million in the successful Phase 1 study of VBP15 - now called Vamorolone - a novel steroid alternative that could be a treatment for all patients with DMD.  We are delighted to share news that that it has received fast track designation status at the FDA in the US. Phase 2a and 2b trials of Vamorolone are due to start in the US and the UK this year. As part of our commitment to making sure trials happen in the UK, we are also funding the Principal Investigator running the trial in the UK, Dr Michela Guglieri along with Duchenne Research Fund, Duchenne Now, Alex’s Wish and Action Duchenne and match funding from Newcastle University. "

You can read about Duchenne UK's involvement here: www.duchenneuk.org/vbp15

Please read the press release below for more information. 

Press release:

ROCKVILLE, Maryland, March 24, 2017

ReveraGen BioPharma Inc, a privately held corporation, today announced that the U.S. Food and Drug Administration (FDA) has granted Fast Track designation for vamorolone (VBP15) for the treatment of patients with Duchenne muscular dystrophy. This designation can speed the review of efficacy and safety data for vamorolone in boys with DMD, potentially leading to more rapid regulatory approval. Vamorolone is under parallel guidance from the FDA and the European Medicines Agency (EMA).

By granting this designation, FDA acknowledges that the vamorolone program is directed towards development of a potential treatment for a serious condition, and addresses an unmet medical need.   The VISION-DMD clinical trial program for vamorolone is currently enrolling boys with DMD into clinical trials in US, Canada, Australia, Sweden, UK, and Israel (open label Phase 2a, Phase 2a extension, and Long-term extension studies). Blinded, placebo- and glucocorticoid-controlled Phase 2b trials are expected to initiate enrollment later this year.

“We are excited about this new development in our discussions with FDA”, said Eric Hoffman, Ph.D., CEO of ReveraGen. “We hope that our innovative clinical program in DMD, with extensive use of pharmacodynamic biomarkers, will lead to a rapid read-out of drug effect”.

About vamorolone

Vamorolone is an oral, once-daily formulation with multiple mechanisms of action that are thought to target multiple aspects of DMD muscle pathology. It is a potent glucocorticoid receptor agonist that shows strong anti-inflammatory activity, but without many of the safety concerns seen with other steroidal immune modulators. Vamorolone is also a mineralocorticoid receptor antagonist, and has been shown to aid dystrophic heart function in mouse models of DMD. Finally, vamorolone stabilizes plasma membranes, and may counteract the membrane instability caused by dystrophin deficiency in DMD. The vamorolone DMD clinical program is supported by the National Institutes of Health (NIAMS, NINDS) and the European Community Horizons 2020 program.

About ReveraGen BioPharma

ReveraGen is a privately held, clinical-stage pharmaceutical company with vamorolone in DMD as the lead program. The vamorolone pre-clinical and clinical programs have been carried out in collaboration with international stake holder non-profit foundations and governments, and with Actelion Pharmaceuticals through an initial milestone payment related to an option agreement for future vamorolone sales and distribution.

Media Contact:

Eric Hoffman

CEO

ericphoffman@gmail.com