Your analogies are procedurally illustrative, but but not at all predictive, and therefore not useful here. Obviously, the chances of an MAA positive opinion at this stage are unrelated to the chances of receiving a concealed carry permit or a random job offer at their similar stages.
"I do not think Anavex will apply in June, or even at all without an additional trial."
The company didn't approach the EMA just for giggles, obviously. They intend to "apply", ie submit an MAA, in around June. Nothing foreseeable will stop that. You'd have to explain why the company possibly would not. (Note: There are optional pre-submission meetings with the CHMP, but they are merely to ensure the MAA is prepared correctly, not to pre-evaluate it.)
What causes Rett syndrome? Almost all cases of Rett syndrome are caused by a mutation (a change in the DNA) in the MECP2 gene, which is found on the X chromosome (one of the sex chromosomes).
The MECP2 gene contains instructions for producing a particular protein (MeCP2), which is needed for brain development. The gene abnormality prevents nerve cells in the brain from working properly.
There's usually no family history of Rett syndrome, which means it's not passed on from one generation to the next. Almost all cases (over 99%) are spontaneous, with the mutation occurring randomly.
The MECP2 gene provides instructions for making a protein called MeCP2. This protein helps regulate gene activity (expression) by modifying chromatin, the complex of DNA and protein that packages DNA into chromosomes. The MeCP2 protein is present in cells throughout the body, although it is particularly abundant in brain cells.
In the brain, the MeCP2 protein is important for the function of several types of cells, including nerve cells (neurons). The protein likely plays a role in maintaining connections (synapses) between neurons, where cell-to-cell communication occurs. Many of the genes that are known to be regulated by the MeCP2 protein play a role in normal brain function, particularly the maintenance of synapses.
Researchers believe that the MeCP2 protein may also be involved in processing molecules called messenger RNA (mRNA), which serve as genetic blueprints for making proteins. By cutting and rearranging mRNA molecules in different ways, the MeCP2 protein controls the production of different versions of certain proteins. This process is known as alternative splicing. In the brain, the alternative splicing of proteins is critical for normal communication between neurons and may also be necessary for the function of other types of brain cells.
So screwing around with patients mRNA with a vaccine may have messed up the trial, ain'a'hey?
(The last word in the above sentence is a Milwaukee/ Wisconsin colloquialism translated "Isn't it so?" or "Do you agree?"
Thanks for sharing your thoughts and CCW example. So Anavex is in the pre-submission stage after being cleared by CHMP/EMA waiver to be eligible to submit an MAA. If the 7-month clock started last December PR, the MAA submission would be after June, which coincides with when the AD OLE TLR becomes available. Maybe this OLE can be used as a second confirmation trial as indicated by CM?
The way I understand is that there is no technical reason preventing Anavex from submitting an AD MAA other than the company's judgment call on how likely the MAA get approved based on communications with EMA personnel.
From Sep-23 PR, Jin is on board with "The trial is successful in meeting the co-primary endpoints".