Hvers vegna hefur Bretland náð forskoti á "Sambandið" í bóluefnamálum? Hvernig kaupin gerast á "bóluefnaeyrinni"

Hvers vegna hefur Bretland forskot á Evrópusambandið í bóluefnamálum? 

Hvort sem litið er til bólusetninga (% af íbúafjölda), eða að ná að samþykkja bóluefni?

Það má finna býsna góða grein sem reynir að útskýra hvers vegna Bretland hefur forskot og að hluta til  "stóra AstraZeneca málið" einnig á vefsíðu Guardian.

Þarna kemur fram að Bretland hafi skrifað undir samning um afhendingu á 100 milljón skömmtum um miðjan maí á síðasta ári.

Ég hvet alla til að lesa greinina á vefsíðu Guardian, en þegar hún er lesin fæ ég á tilfinninguna að Evrópusambandið, samdi seinna, vildi borga minna, lagði fram mikið minna áhættufé til framleiðenda bóluefnis, en vilja samt sem áður hafa forgang fram yfir aðra.

En klúðrið virðist "Sambandsins" (og þeirra sem hafa hengt sig við það), vandræðin sem það er komið í virðist mest af þeirra eigin völdum, en það getur það (að sjálfsögðu) ekki viðurkennt.

 

 

When it became clear the China coronavirus outbreak might lead to a global pandemic, Oxford University’s life scientists convened a crisis meeting. It took place on Thursday 30 January last year, and if the rest of the world hadn’t yet realised the potential consequences of what was unfolding in Wuhan, they had.

...

It was there that Prof Sarah Gilbert, a vaccine researcher, told her colleagues something remarkable; she had devised a likely vaccine, repurposing technology used by her team to develop vaccines against Ebola and Mers.

...

 

In a country not known for thinking strategically about industrial policy, the UK actually had an advantage. Gilbert’s Jenner Institute, for example, was founded in 1998, when Peter Mandelson was industry secretary, and funded at first by the UK drug company GlaxoSmithKline. It was critical in ensuring the UK got ahead.

However, the prospective deal collapsed. The UK was desperate to secure enough supply for its own citizens – and at the time, ministers including the health secretary, Matt Hancock, were concerned. Not about the EU – but about the behaviour of the then-US president, Donald Trump.

“We were worried about vaccine nationalism – but the person we feared was Trump, that he would be able to pressurise a US company, and perhaps buy up the drug stocks,” said a former adviser at the Department of Health. “We never expected there would be a row with the EU”.

Enter the Anglo-Swedish firm, AstraZeneca, whose French chief executive, Pascal Soriot, was a trusted figure in political circles.

...

AstraZeneca was signed as Oxford’s partner on 30 April and signed a deal to supply 100m doses to the UK a fortnight later. Ministers were prepared to pay a few hundred million upfront, allowing the company to build its first virus manufacturing process, and the UK government to demand its citizens be vaccinated first.

“That underpinned all of it,” an industry insider said.

Building on relationships established by the Oxford scientists, the vaccine for the UK market is cultivated at sites in Oxford and at Keele, near Stoke. It is then sent to Wrexham, where it is bottled into vials before being dispatched for final tests by UK regulators and sent on to the NHS.

AstraZeneca says the headstart it had was vital.

With Brexit looming, the UK drew huge criticism for declining to join EU schemes to purchase PPE and ventilators. There was also growing pressure to join a joint EU procurement plan for vaccines, and to put aside the Brexit rhetoric.

But Brussels’ demands were eye-watering: the UK, unlike EU member states, would not be able to take part in the governance of the scheme, including the steering group or the negotiating team.

Britain would have no say in what vaccines to procure, at what price or in what quantity, and for what delivery schedule. There would be no side-deals possible.

British officials were not convinced. “We had to go it alone,” said a UK source. “There was nothing there for us”. By the time a special UK vaccine taskforce was created in April, the seeds of a successful strategy had been sown.

Run from May by the venture capitalist Kate Bingham, a no-nonsense operator, it directed government money up and down the vaccine supply chain, and helped ensure that two other vaccine candidates were manufactured in the UK – an interventionist policy not seen since before the days of Margaret Thatcher.

...

There had been concerns from the beginning of the crisis in key EU capitals that others – the US in particular – would steal a march in the hunt for a successful vaccine. But despite the anxiety, the process of organising and purchasing prospective vaccines had been slow.

There was an early initiative by the European commission president, Ursula von der Leyen, to steal away CureVac, a biotech company working on a coronavirus vaccine, from Donald Trump, with whom it was in talks. The EU offered the company €80m in financial backing. “I hope that with this support, we can have a vaccine on the market, perhaps before autumn,” Von der Leyen said at the time. CureVac is still yet to come good.

The governments of Germany, Italy, France and the Netherlands had privately decided they could not wait on Brussels finding common agreement among the 27 on a strategy – and they spotted the potential in AstraZeneca from the start.

The four governments passed on the negotiation to the commission “for the common good”, recalled Prof Walter Ricciardi, an adviser to the Italian government on its coronavirus strategy.

“We opened the door for the commission to take over but even then it took time, even when we tried to speed up the process,” Ricciardi said. “There were some countries fully aware of the importance of the vaccine but there were others that were reluctant to put money into this without guarantees of the result. That took time and the best possible energy of the commission. They did recruit the best possible officers to do that but it was a long process”.

It was another three months before the commission finally signed the deal, behind the UK, with some serious ramifications to come.

Authorisation of any vaccines would be done through the European medicines agency, rather than national regulators, to ensure that the rollout was done across the EU in tandem. But that also proved a fateful decision.

The slower authorisation by the EMA ensured that liability for the vaccine – should it prove dangerous – could potentially be pinned on the pharmaceutical companies during contract negotiations.

But if they were maintaining solidarity and perhaps even earning some extra public confidence, they were giving up speed.

The fast-track mechanisms available to national regulators, including the UK’s medicines and healthcare regulatory authority, gave Britain another potential advantage

Nevertheless, with the announcement in early November that the German startup BioNTech had made a breakthrough in the development of a new type of vaccine to combat Covid-19, hopes remained high that the bloc was on the right path.

“It is Europe’s moment”, Von der Leyen tweeted in mid-December as she announced that between 27 and 29 December, people across the EU’s 27 member states would be vaccinated. “We protect our citizens together”, she said. But her confidence was misplaced. There were hidden frailties.

Rasmus Hansen, the chief executive of Airfinity, a data analytics company working in the life sciences sector, said the EU had failed to invest as it should have in scaling-up production plants.

The EU had spent just €1.78bn in “risk money”, cash handed to pharmaceutical companies without any guarantee of a return, compared to €1.9bn by the UK and €9bn by the US, he said. There were consequences.

The first hit to the EU strategy was the announcement by Pfizer/BioNTech, one of only two vaccine producers authorised for use in the EU at this stage – along with Moderna, with whom only a smaller order has been made – that they needed to slow down production in order to upgrade a facility in Belgium and boost output in late February.

This did not unduly upset officials initially. They had AstraZeneca, and its total of 400m doses, coming down the line. “I am not sure why this debate is there because the numbers are there, the production is ramping up,” Sandra Gallina, the commission’s chief negotiator, told MEPs on 12 January

 

“It took a wrecking ball to the national plans,” admitted one diplomat. Just 2% of the EU adult population has so far received a jab, compared with 11% in the UK.

 

Officials angrily pointed to the success of the British end of AstraZeneca’s vaccine production. “If the UK plants are working better, are we expecting the UK plants to deliver doses to us? Yes. Yes. Yes. They are part of our contract,” argued an official.

Gallina, shaken by the move, dived into the customs records to find evidence that AstraZeneca had shipped EU-produced doses to the UK – but without success.

AstraZeneca’s chief executive gave an interview with a group of European newspapers. “The UK agreement was reached in June, three months before the European one,” Soriot said.

“As you could imagine, the UK government said the supply coming out of the UK supply chain would go to the UK first. Basically, that’s how it is.”

The commission has accused AstraZeneca of a breach of contract. It has given its member states the power to block exports of vaccines, raising the spectre of Pfizer doses not being delivered to the UK. But at a meeting of EU ambassadors with commission officials earlier this week, the message was that the capitals were unimpressed.

“The commission was told to change the terms of the debate – we just want vaccines,” said one diplomatic source. “That’s all we want”.

Allar leturbreytingar eru blogghöfundar.

 

 


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Athugasemdir

1 Smámynd: Kristján G. Arngrímsson

Er þetta ekki bara gamli, góði yfirgangurinn og entitlementið í Bretum?

Kristján G. Arngrímsson, 31.1.2021 kl. 21:33

2 Smámynd: G. Tómas Gunnarsson

@Kristján, þakka þér fyrir þetta.  Það er að erfitta fyrir almening að dæma um hvað býr að baki í máli eins og þessu.

En eins og málið blasir við mér er frekar um yfirgang og frekju "Sambandsins" að ræða.

Sambandið hefur lagt minna "áhættufé" til bóluefnaframleiðendanna en Bretland (þrátt fyrir margfaldan íbúafjölda), samdi mun síðar, og lagði mun meiri áherslu á lægra verð en aðrir.

Samningur kveður á um "best efforts" og mér sýnis AstraZeneca vera að gera það enda vilja þeir auðvitað selja sem mest.

En Von der Leyen, er að sögn ýmissa Þjóðverja þekkt fyrir að standa sig vel í því að "koma sökinni" annað, en margir þarlendir eru ekki mjög hrifnir af "afrekaskrá" hennar.

Mér sýnist að ýmsu leyti akkúrat það sem hún er að reyna að gera núna.

G. Tómas Gunnarsson, 31.1.2021 kl. 21:46

3 Smámynd: Kristján G. Arngrímsson

LOL! Það kemur víst fáum á óvart sem til þekkja að þú teljir líklegra að ESB sé vondi karlinn í þessu eins og öðru.

Kristján G. Arngrímsson, 1.2.2021 kl. 08:00

4 Smámynd: G. Tómas Gunnarsson

@Kristján, þakka þér fyrir þetta.  Ætli mætti þá ekki "spegla" þetta og segja að það komi líklega engum á óvart að þú takir málstað "Sambandsins"?

En það er mun heilbrigðara að velta þvi fyrir sér hvers vegna t.d. eins og kemur fram í greininni, Evrópusambandið samdi ríflega 3. mánuðum síðar við AstraZeneca (og reyndar fleiri bóluefnaframleiðendur), en Bretland, hvers vegna Bretar hafa lagt 1.9 milljarða euroa (óendurkræfa) í áhættufé til lyfjaframleiðenda, en "Sambandið" aðeins 1.7, (Bandríkin 9 milljarða euroa), þrátt fyrir að "Sambandið" sé líklega með ríflega 7. sinnum meiri íbúafjölda en Bretland?

Hvers vegna drógust viðræðurnar á langinn eftir að Framkvæmdastjórnin tók þær yfir?

Ef þú getur svarað þessum spurningum með einhverjum betri rökum en "LOLLI", þá getum við rætt málin frekar, annars er það tilgangslaust.

G. Tómas Gunnarsson, 1.2.2021 kl. 12:02

5 Smámynd: Kristján G. Arngrímsson

Ég er nú ekkert sérstaklega að taka málstað ESB, eða hvar skrifaði ég það?

Og ég á engin svör við spurningum þínum, hvað þá rök fyrir þeim svörum, enda er ég lítt að mér um málefnið. Ég reyndar er ekki alveg viss um hver afstaða þín í málinu er, þ.e. af hverju nákvæmlega þú telur að ESB sé "vondi kallinn" í þessu tiltekna máli.

Kristján G. Arngrímsson, 1.2.2021 kl. 12:16

6 Smámynd: G. Tómas Gunnarsson

@Kristján, þakka þér fyrir það.  Þegar þú skrifar: "Er þetta ekki bara gamli, góði yfirgangurinn og entitlementið í Bretum?", þá ertu (að mínu mati) ekki að taka undir með Bretum (sem eru þó ekki nema óbeinn aðili að deilunni), né AstraZeneca.

Þú gefur í skyn að einhver (Bretar) hafi farið fram með yfirgangi. Og gegn hverjum þá, eiluaðila, sem þykir hann rangindum bettum, það er.

Út frá frett the Guardian (sem nota bene er ekki þekkt fyrir að skrifa gegn "Sambandinu", eða taka málstað ríkisstjórnar Boris Johnson), finnst mér einmitt flest benda til þess að um "yfirgang og frekju" sé að ræða af hálfu Von der Leyen og Evrópusambandsins.

Það gerir "Sambandið" ekki að "vonda kallinum", en málstaður þess er ekki góður, sé tekið mið af frammistöðu Framkvæmdastjórnarinnar.

Ef þú hefur áhuga á að kynna þér málið, þannig að þú getir tjáð þig um það umfram "one linera", þá er enginn skortur af góðum greinum í Evrópskum fjölmiðlum endafarna daga.

Til dæmis þessi í Spiegel:  https://www.spiegel.de/international/europe/europe-s-vaccine-disaster-commission-president-ursula-von-der-leyen-seeking-to-duck-responsibility-a-1197547d-6219-4438-9d69-b76e64701802#ref=rss

Virkilega fróðleg grein:  Þar segir m.a.: "While others simply acted with expedience and placed huge orders, the EU – right in the middle of the worst pandemic in a century – decided to bargain like they were at the bazaar. Von der Leyen, of course, didn't lead these negotiations personally. But she is the boss, and carries the political responsibility."

En Spiegel greinin er mjög fróðleg hvet þig til að lesa hana.

G. Tómas Gunnarsson, 1.2.2021 kl. 13:12

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