wanna see something funny? final CSR for sanofi-moderna booster+flu jab study was released on EMA CDP. 3 groups with 100 patients each, 1) mrna 1273 50 ug + sanofi, 2) sanofi only 3) moderna only. all 60+, 90%+ 2020-2021 flu jab rate, inclusion criterium 2x moderna. link didnt fit in the previous post, this is study QHD00028. so! of the six medically attended cases of covid, there were three in group 1 and three in group 3 and none in group 2😬imagine how salty bancel must have been, just imagine! mega.nz/folder/rBgl0Jy…

🚨FINAL MODERNA STUDY REPORT 🚨 uploaded on EMA CDP 30.5. 15k words with no end in sight into my pfizer CRF writeup, so im just gonna do a brief flyover of this 8500-page monstrosity. unlike AZ a few days ago, this is the pivotal phase 3 mega.nz/folder/nNAg3DZ…
page 11: yeah so because incidence rates were similar in vaxed-months-ago and vaxed-just-now, there is duration of protection. but because BOTH groups got more covid later, gotta boost 😵‍💫

the very first goddamn email: daszak says baric is working on nanoparticles, and baric is asked about sars glycoproteins he's making for a DARPA grant and they're trying to get them into bats

from march 2018

https://twitter.com/JamesCTobias/status/1775274710991011985

gonna read these closer tomorrow

ADSYMPT - covid signs and symptoms
ADAE - adverse events

these are the symptoms that can lead to a "covid illness visit" except for 7 days after each dose.

been looking at the latest pfizer puff piece. this is going to be a dump thread of links and files. both C4591031 and C4591007 are heavily represented on the EMA CDP portal. already did a thread on C4591031:

https://twitter.com/a_nineties/status/1764218513659502836

firstly, c4591031 has results on the EU CTR. results have been updated three times by now 👀 this includes substudies A-E so it's REALLY really long. c4591007 only has a protocol posted clinicaltrialsregister.eu/ctr-search/tri…

just gonna give some thoughts on the hypervax paper from a kraut healthcare worker perspective. HIM is "overall healthy (no chronic medications)", yet received regular blood draws from november 2019 onwards 🤔that's not how it works, labs come out of the budget the single most frequent measurement is creatinine with 23 measurements, next ist small haemogram (blutbild) with 20, then total protein and urea with 19 each. most likely being treated by a nephrologist or a hausarzt (gp) for kidney issues.

🚨some material i just have not gotten around to: ICAN received the first two PSURs for AstraZeneca and it's about as bad as you can imagine. icandecide.org/press-release/… the documents in question are the first two PSURs, spanning dec 2020 -june2021 and june 2021 to dec 2021 respectively. PSURs 3 &4 for 2022 were released end of december on the EMA page for vaxzevria. EMA & FDA colluded to "flood the zone" EoY 2023 😉 ema.europa.eu/en/medicines/h…

the sanofi study, Accord-RA ACT5488


to my considerable surprise, ClinPhone was also involved with aventis and therefore probably this trial as well. ichgcp.net/clinical-trial…
clinicaltrialsregister.eu/ctr-search/tri…

https://twitter.com/a_nineties/status/1757804374485553566

the pfizer study, A409125 cdn.pfizer.com/pfizercom/clin…

inmark, inc. quest diagnostics. "protocol CNTO148-ART-3001"? CD3/CD14+CD16 on that table of names.

https://twitter.com/wolsned/status/1757784445845635229

this is from the panel around 1:06. "including pfizer, astrazeneca, sanofi, GSK, and others"

what the fuck is this @Sabisteb the spike expressed by modRNA is classified as a drug? @kevin_mckernan how similar would you say the spike proteins between moderna and pfizer are? similar enough to be classified as the same protein? drugs.ncats.io/substance/BP87…
stumbled across this while looking up pidacmeran, the INN for BNT162c2, the saRNA version. the c2 entry contains a lot more data than the b2 entry😅

i've pretty much exhausted all search options i can come up with looking for this study. next step is FOI request to EMA.

https://twitter.com/a_nineties/status/1753516167396737372

-> screenshot 1

-> screenshots 2&3 phmpt.org/wp-content/upl…
phmpt.org/wp-content/upl…

i'll do a bit of a recap of the pfizer PASS reports, but i've looked at the moderna study and holy SHIT it couldn't look worse.

https://twitter.com/a_nineties/status/1750875050834575756

there are four reports and one protocol. the first one is only 8 pages due to being released before data collection begins 🙄 basically just a "we're all ready to start collecting data "😇 a year after marketing authorization..

still have to read the moderna/AZ PASS studies, currently back to grinding out phmpt document details. notice the submission date on the sidebar, only two days after Query 1, and then pfizer's answer @FluoridePoison endotoxin/integrity validation delayed beyond BLA

@FluoridePoison here's the initial document the previous one is referring to.

pfizer had to be asked repeatedly **just to set the date** by which they would have a validated endotoxin control method set up. what do regulators get for their polite reminders? a full year after EUA 😂

Post authorization studies for pfizer-biontech, moderna, and AZ. had this tab open for a few days without checking closely, this is a huge amount of data. many thanks to mr hunt, who also asked the important P1/P2 FOIAdailysceptic.org/2024/01/20/con…
drive.google.com/drive/folders/… this is the first pfizer interim report for c4591021. UK started boosting very early! also shows a clear bias as to the population surveilled by the british system. notably, i haven't seen a german data source ;) or rather i'd be surprised if there was one

guess who scraped the 89-page authorization changes into an excel file? pfizer-biontech have 567 "variations" or changes to the authorization on file, in 194 different applications, 62 of which required an EC decision. taking a deeper look after some food 🥩⚡️🥩



so first of all, they downscaled tenfold beginning of 2022. the date march 2022 is when CHMP gives the OK for the variation, not when pfizer turned it in. anyway, some quick numbers.

just a little incoherent dump thread for an article on the stonewalled DNase data





this is all from the EMA leak, specifically document "Rapporteur's Rolling Review Report Quality - COVID-19 mRNA Vaccine BioNTec"

🚨🚨FINAL STUDY REPORTS FOR C4591001/BNT162-01 ARE AVALABLE🚨🚨
C4591001:
BNT162-01:
uploaded on EMA CDP december 19&20. just saw and re-upped, will be reading these files! mega.nz/folder/LZJ31Kq…
mega.nz/folder/SR5nUAK…




@ClareCraigPath @ak_america @ICANdecide @joshg99 @Jikkyleaks @PaulaJardine @Taxed12 @redpill4me @Sabisteb final study reports for the pfizer-biontech trials C4591001 and BNT162-01 are available!

🚨🚨NEW DNAse FOIAs!🚨🚨
i just got into contact with the recipient of the original two documents in the quote tweet. he received these two new ones on 6.12.
1)
2)
@DJSpeicher @CanningPharm @JesslovesMJK @Kevin_McKernan mega.nz/file/GIolzLDZ#…
mega.nz/file/eIoSyQyS#…


*forgets quote tweet

https://twitter.com/a_nineties/status/1724544405556609506

just dumping some screenshots. this is from april 30 2021 "clinical overview"

this is from "clinical safety" may 5. i have a feeling december isn't going to be the last phmpt, it seems to me as if there's still so much material we should receive if we've gotten safety reports up to sep2021, including c4591017 study reports and its protocols.

November phmpt files are up! 249 files, and the most omportant bit: LOTS OF MODULE 3 STUFF! module 3 is CMC related coumentation.

uhh germany requested the EMA "review" azithromycin for systemic use.. @jikkyleaks what's going on here? ema.europa.eu/en/medicines/h…


@Jikkyleaks the perversion of truth is undeniable at this point. azithromycin gets a Type 31 referral before the modRNA jabs do. the german government, the EU and EMA must be rebuilt from the foundations up.