Tuesday, March 03, 2015 12:00:30 PM
WHY? The latest PR confirms previous PRs that HemaX protocols for a safety test that is needed to be completed before FDA approval is still under review. The protocols are under review. After they are approved we are looking at most likely 2-3 months before approval.
Let's stick to the facts of what we know. We know they've hired the Ichims and Caven and took out a loan to only cover a couple months salary. We are finally getting a steady diet of PRs with updates and seemingly good news. I don't see HemaX as the immediate factor or catalyst at the moment. HemaX right now is a future bonus as I believe NR2F6 target treatment is the key.
I will make another post with a couple quotes people may have missed that now seem to be coming to light.
Let's stick to the facts of what we know. We know they've hired the Ichims and Caven and took out a loan to only cover a couple months salary. We are finally getting a steady diet of PRs with updates and seemingly good news. I don't see HemaX as the immediate factor or catalyst at the moment. HemaX right now is a future bonus as I believe NR2F6 target treatment is the key.
I will make another post with a couple quotes people may have missed that now seem to be coming to light.
Recent RGBP News
- Regen BioPharma Update on Orphan Drug Application for HemaXellerate Will Be Presented At Emerging Growth Conference on September 24, 2025 • GlobeNewswire Inc. • 09/23/2025 12:00:00 PM
- Regen BioPharma Prepares Response For FDA Regarding Its Orphan Drug Application for HemaXellerate • GlobeNewswire Inc. • 09/16/2025 12:00:00 PM
