Share
2,994 Posts.
lightbulb Created with Sketch. 1343
clock Created with Sketch. 07/07/24
16:08
Share
Originally posted by RaceOncology:
↑
A very good question. While bisantrene the molecule is out of patent, our new RC220 formulation (i.e. the drug product) is not. What we have been able to do is reformulate bisantrene so that the problem of crystallisation in the blood that caused it to be abandoned by the original developer (Lederle), has been solved.1. The old formulation is not FDA or EMA approved. Any developer of the old formulation would have to spend tens of millions dollars to bring the old formulation to market, but as soon as they brought it to market the generic drug manufacturers could start selling the own version of the old formulation and the price would immediately fall to that of a generic drug. No company will invest all the money required to develop the original formulation of bisantrene if they will face immediate generic competition.2. Even if some company is crazy enough to spend all the money required to get the old formulation of bisantrene approved, no doctors or patients are going to participate in any of the trials need for approval. You can’t run a clinical trial of a worse version of an approved drug that offers no benefit to the patient - it would be unlikely that you could even get ethics approval to run such a trial.This same priniciple applies to a different formulation of bisantrene. Unless this new formulation offered some significant clinical benefit over our RC220 formulation then it can’t be trialed and hence approved. This is exactly what happened with Abraxane which did not face any direct competition until the original formulation patents ended and the generic manufacturers could start making it.
Expand
Anyone else feel like they were mislead between 2019 and 2024 after reading this?
(20min delay)