It's on the agenda this week: possibly a decision on the Oxford/AstraZeneca vaccine from EMA's (Euro drug regulator) Human Medicine Committee? Applicants will be questioned at the meeting.
Last night, I tweeted ⬆️ that the EMA (Euro drug regulator) meeting was considering the Oxford/AstraZeneca vaccine. I included a link to EMA processes, because the language on the agenda suggested there could be a problem: this is the explanation I mean in that link ....1/n
...German newspapers now reporting a claim the efficacy rate for people over 65 is only 8% & approval is indeed in question for that age group, at least (Paywalls: I can't read in full.) Rumor at this point, but a limit ...2/n bild.de/bild-plus/poli…, handelsblatt.com/politik/deutsc…
...on people >65, if that comes, would not surprise me. Here's an excerpt from my December vaccine roundup: absolutelymaybe.plos.org/2020/12/20/why… What do we know about both these issues, efficacy & safety in over 65s? ....3/n
...Here's age breakdown in Oxford paper on vaccine efficacy: <500 people aged 70+, & just over 1,400 over the age of 55. Efficacy was only analyzed for up to the age of 55: there just aren't enough people to know how this works in people over 55 ...4/n thelancet.com/journals/lance…
...Unlike some other vaccines, early phase research for this vaccine didn't include older people either. Which means there's no safety data to add, either. Because the numbers are so small in people 65+, an efficacy calculation wouldn't mean much...5/n
...Uncertainty around an estimate of vaccine efficacy in a group that could be quite a bit under 1,000 people would be huge: could fluctuate dramatically over time. For comparison, here's what I said in that post about the 2 mRNA vaccines (with thousands of older people)...6/n
...Another example: Sputnik V. Anmat, Argentina's drug regulator, originally didn't approve it for people over 60 because of lack of data. Changed recently when Sputnik V provided antibody data plus an efficacy estimate of 92% (67-98%) in 2,144 people..7/n
...One thing has changed since the report of the efficacy data though: the UK has been vaccinating a lot of elderly people using this vaccine. So although it's very short-term & mostly a single shot so far, that's considerable extra safety experience now... 8/9
...My opinion? Would I be surprised if EMA didn't approve it for people >65? No. Until US trial reports, we don't know the impact on older people. Do I believe the efficacy rate could be only 8%? Risk of an efficacy calculation in such a small group being a fluke is too high. 9/9
...PS: Dug into the MHRA report on Oxford AstraZeneca vax. Reported 1,169 people aged 65+ (don't know how many of those exactly 65) got the vax, counting all dosing regimens & studies (not just the efficacy subgroup). EMA reportedly has more recent data. assets.publishing.service.gov.uk/government/upl…
...Reuters reporting that the German Ministry of Health is implying that someone basically misunderstood something: data don't show an 8% efficacy rate.
...Handelsblatt rebutted German Ministry of Health's rebuttal of their report about efficacy of the Oxford/AstraZeneca vaccine in older people. Their sources insist no one messed up numbers. This time, not behind a paywall. handelsblatt.com/politik/deutsc… Hope EMA is clear on this & soon
...Another instalment in Oxford/AstraZeneca "he said, she said" saga. AstraZeneca chief says efficacy similar for younger/older, wide confidence intervals. Says he doesn't know the efficacy rate, but there are now 200 events (that's double the original)... repubblica.it/cronaca/2021/0…
...Also says supply problems are because 1 large Euro facility having difficulty making enough of the vaccine (Australia's CSL is too). UK facility did too early on, but that's resolved. They modified the formula (?): watch for this issue in EMA report too. (HT: @MaffewEC)
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Meanwhile, a few days ago the EMA published its EPAR (public assessment report) on the Moderna vax (HT @pajz_) ema.europa.eu/en/documents/a… It's 169 pages ...1/n
...There was "a major objection" to the US manufacturing sites, so they were withdrawn. Complete transfer for Europe to Swiss manufacturing due to conclude soon. (There have been Qs in the US about a batch there reuters.com/article/us-hea…)...2/n
...If you're interested in the chemical & biological aspects of this vaccine, there are pages for you to dig into - not an area I have any expertise in. Small amount of detail of reproductive toxicity study (in rats): no cause for concern....3/n
TGA, Australia's drug regulator, has issued a 2-year provisional approval for Tozinameran (BNT/Pfizer vaccine) from age 16, & released its 42-page assessment report tga.gov.au/auspar/auspar-… ...1/n
...One of the conditions is TGA approval of at least 20 vials from each batch before release...2/n
..Study of reproductive safety in rats has been completed & found no signs of concern related to pregnancy. This wasn't completed when the FDA reported. No data is in this report though. Otherwise it's the same data basis...3/n
For everyone else who's on ENSEMBLE-Watch - the big J&J trial for their Ad26.COV2.S vaccine - some background & context in case a press release lands soon. (On Wednesday, Stanford got the word to lock their data abc7news.com/johnson-and-va… so it is on!)...1/5
...It's a big trial - close to the size of the Pfizer trial for Tozinameran, substantially bigger than Moderna's - & the most international one. And co-primary endpoints are for moderate to severe Covid-19, including 1 at a month - which is longer than we've seen previously...2/5
...You can see the protocol for the trial here: jnj.com/coronavirus/co… (Note, it was originally for 60,000 but they got so many events it was cut back to 40)...3/5
Sputnik V news: ANMAT, Argentina's drug regulator, has now extended authorization to people 60+ & released some data this time. Here's the listing of what they've received & analyzed (but it's not published) ... 1/n argentina.gob.ar/noticias/ampli…
...The new data on people 60+ they received: in 2,144 people, vaccine efficacy of 91.8% (95% CI 67.1% -98.3%). Almost all those people had antibodies by 28 days ...2/n
...ANMAT reports there's now data for 19,866 people who received both Sputnik V injections, with no serious adverse events (SAEs) judged to be vaccine-related. There were 47 SAEs in vax group vs 23 in placebo. Safety similar for older people in small safety study. 3/3
After 10s of thousands of Brazilians participated in early trials of Covid vaccine, vaccination has at last begun there: Anvisa (drug regulator) approved Sinovac's CoronaVac & Serum Institute of India's Covishield (Oxford/AstraZeneca vaccine) ...1/n g1.globo.com/sp/sao-paulo/n…
...Before I get to the Anvisa documentation, important update on the alligator tracker: jacare-tracker.org It's tracking Brazilian as well as global vaccinations & it's now on Twitter too @jacaretracker
...Anvisa's documentation is here & includes trial data as well as manufacturing standards reports: gov.br/anvisa/pt-br/a…
CoronaVac data for the Brazilian trial only. 12,123 people in the whole trial: 64.3% female, 4.9% 60 years or older. Median age: 37 (for Pfizer: 52)...3/n
Oh my... Remembering this time 4 years ago. I was living in DC. I flew back in the night before the inauguration with my 2-yr visa freshly updated: its expiration was my personal deadline to be living back in Oz. Taxi from airport was the first clue of what was coming...
...So many barricades & security, taxi from the airport had to try many routes to get me to my apartment in the middle of DC. Lots of Trump supporters whooping it up. But there were so many women, too....
...Dragged myself, mega-jetlagged, out to the Women's March - and women were streaming everywhere. I'd been to big demonstrations before, but I never saw one as big as this...