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Tuesday, 8 June 2021

23.02.21 ‘Held to ransom’: Pfizer plays hardball in Covid-19 vaccine negotiations with Latin American countries

Pfizer has been accused of “bullying” Latin American governments during negotiations to acquire its Covid-19 vaccine


Pfizer has been accused of “bullying” Latin American governments during negotiations to acquire its Covid-19 vaccine, and the company has asked some countries to put up sovereign assets, such as embassy buildings and military bases, as a guarantee against the cost of any future legal cases, according to an investigation by the U.K.-based Bureau of Investigative Journalism.

In the case of one Latin American country, demands made by the pharmaceutical giant led to a three-month delay in a vaccine deal being reached. For Argentina and Brazil, no national deals were agreed to at all with Pfizer. Any hold-up in countries receiving vaccines can lead to more people contracting Covid-19 and potentially dying.

Officials from Argentina and the other Latin American country, which cannot be named as it has signed a confidentiality agreement with Pfizer, said the company’s negotiators demanded more than the usual indemnity against civil claims filed by citizens who suffer serious adverse events after being inoculated. They said Pfizer also insisted the governments cover the potential costs of civil cases brought as a result of Pfizer’s own acts of negligence, fraud, or malice. In Argentina and Brazil, Pfizer asked for sovereign assets to be put up as collateral for any future legal costs.

One government health official who was present in the unnamed country’s negotiations described Pfizer’s demands as “high-level bullying” and said the government felt like it was being “held to ransom” in order to access lifesaving vaccines.

Campaigners are already warning of a “vaccine apartheid” in which rich Western countries may be inoculated years before lower-income regions. Now, legal experts have raised concerns that Pfizer’s demands amount to an abuse of power.

“Pharmaceutical companies shouldn’t be using their power to limit lifesaving vaccines in low- and middle-income countries,” said Lawrence Gostin, a law professor at Georgetown University and director of the World Health Organization’s Collaborating Center on National and Global Health Law. “[This] seems to be exactly what they’re doing.”

Protection against liability shouldn’t be used as “the sword of Damocles hanging over the heads of desperate countries with a desperate population,” he added.

Pfizer, which partnered with BioNTech, a German biotech, to make the vaccine, has been in talks with more than 100 countries and international bodies, and has supply agreements with nine countries in Latin America and the Caribbean: Chile, Colombia, Costa Rica, Dominican Republic, Ecuador, Mexico, Panama, Peru, and Uruguay. The terms of those deals are unknown.

Pfizer declined to comment on the allegations about its demands in negotiations, citing “ongoing negotiations which are private and confidential.”

The company told the Bureau in a statement: “Pfizer and BioNTech are firmly committed to working with governments and other relevant stakeholders to ensure equitable and affordable access to our COVID-19 vaccine for people around the world.” The company said that in addition to the nine Latin American countries with which it has struck supply agreements, it has “allocated doses to low- and lower-middle-income countries at a not-for-profit price, including an advance purchase agreement with COVAX to provide up to 40 million doses in 2021.” COVAX is a global initiative to pool purchasing power and ensure vaccine access for low-income countries. “We are committed to supporting efforts aimed at providing developing countries with the same access to vaccines as the rest of the world,” Pfizer said.

Most governments are offering indemnity — exemption from legal liability — to the vaccine manufacturers they are buying from. This means that a citizen who suffers an adverse event after being vaccinated can file a claim against the manufacturer and, if successful, the government would pay the compensation. In some countries people can also apply for compensation through specific structures without going to court.

This is fairly typical for vaccines administered in a pandemic. In many cases, adverse events are so rare that they do not show up in clinical trials and only become apparent once hundreds of thousands of people have received the vaccine (a 2009 H1N1 flu vaccine, for example, was eventually linked to narcolepsy). Because manufacturers have developed vaccines quickly and because they protect everyone in society, governments often agree to cover the cost of compensation.

However, the government officials from Argentina and the unnamed country who spoke to the Bureau said Pfizer’s demands went beyond those of other vaccine companies, and beyond those of COVAX, which is also requiring its member countries to indemnify manufacturers. This presents an additional burden for some countries because it means having to hire specialist lawyers, and sometimes pass complex new legislation, so manufacturers’ liabilities can be waived.

‘An extreme demand’

Pfizer asked for an additional indemnity from civil cases, meaning that the company would not be held liable for rare adverse effects or for its own acts of negligence, fraud or malice. This includes those linked to company practices — say, if Pfizer sent the wrong vaccine or made errors during manufacturing.

“Some liability protection is warranted, but certainly not for fraud, gross negligence, mismanagement, failure to follow good manufacturing practices,” said Gostin. “Companies have no right to ask for indemnity for these things.”

Mark Eccleston-Turner, a lecturer in global health law at Keele University in England, said Pfizer and other manufacturers have received government funding to research and develop the vaccines and are now pushing the potential costs of adverse effects back on to governments, including those in low- and middle-income countries. (Pfizer’s partner, BioNTech, was given $445 million by the German government to develop a vaccine and the U.S. government agreed in July to preorder 100 million doses for nearly $2 billion, before the vaccine had even entered Phase 3 trials. Pfizer expects to make sales of $15 billion worth of vaccines in 2021.)

In Eccleston-Turner’s opinion, it looks like Pfizer “is trying to eke out as much profit and minimize its risk at every juncture with this vaccine development then this vaccine rollout. Now, the vaccine development has been heavily subsidized already. So there’s very minimal risk for the manufacturer involved there.”

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The Bureau spoke to officials from two countries, who all described how meetings with Pfizer began promisingly but quickly turned sour, and reviewed a report by the Brazilian Ministry of Health.

The Argentinian Ministry of Health began negotiating with the company in June and President Alberto Fernández held a meeting with the company’s general manager for Argentina the following month. During subsequent meetings Pfizer asked to be indemnified against the cost of any future civil claims, said an official from the president’s office. Although this had never been done before, the country’s Congress passed a new law in October allowing for it. However, Pfizer was not happy with the phrasing of the legislation, according to the official, who declined to be identified because the negotiations were confidential. The government believed Pfizer should be liable for any acts of negligence or malice. Pfizer, said the official, disagreed.

The government did offer to amend the existing law to make it clear “negligence” meant problems in the distribution and delivery of the vaccines. But Pfizer was still not satisfied. It asked the government to amend the legislation through a new decree; Fernández refused.

“Argentina could compensate for the vaccine’s adverse effects, but not if Pfizer makes a mistake,” said the official, who has detailed knowledge of the negotiations. “For example, what would happen if Pfizer unintentionally interrupted the vaccine’s cold chain [of -70 Celsius during transport and storage] … and a citizen wants to sue them? It would not be fair for Argentina to pay for a Pfizer error.”

The official said talks soon became tense and complicated: “Instead of giving in on some points, Pfizer demanded more and more.” In addition to the changes sought in the new law, it asked Argentina to take out international insurance to pay for potential future cases against the company (countries were also asked by vaccine makers and the WHO to do this during the H1N1 outbreak).

In late December, Pfizer made another unexpected request: that the government put up sovereign assets — which might include federal bank reserves, embassy buildings, or military bases — as collateral.

“We offered to pay millions of doses in advance, we accepted this international insurance, but the last request was unusual: Pfizer demanded that the sovereign assets of Argentina also be part of the legal support,” the official said. “It was an extreme demand that I had only heard when the foreign debt had to be negotiated, but both in that case and in this one, we rejected it immediately.”

The failed negotiations mean Argentinian citizens, unlike those in neighboring countries, do not have access to Pfizer’s vaccine, leaving them with Russia’s Sputnik V vaccine, AstraZeneca’s vaccine, and those delivered through COVAX. The government is also negotiating to acquire vaccines from Moderna, Sinopharm, and CanSino.

“Pfizer misbehaved with Argentina,” said Ginés González Garcia, Argentina’s former minister of health. “Its intolerance with us was tremendous.”

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‘Good cop, bad cop’

The same demands were made of Brazil’s Ministry of Health, according to a ministry statement. Pfizer asked to be indemnified against all civil claims and asked the ministry to put up sovereign assets as collateral, as well as create a guarantee fund with money deposited in a foreign bank account. In January, the ministry refused these terms, describing the clauses as “abusive.”

An official from the Latin American country that cannot be named described talks unfolding similarly. This person said the government began negotiating with Pfizer in July, before the vaccine was approved. There was a perception that Pfizer’s negotiators had a “good cop, bad cop” routine, with the “bad cop” pressing the government to buy more doses.

“[At that time] there was not a single drug or vaccine in the world with this kind of technology that had been shown to be safe and effective. … You had this lady putting pressure saying: ‘Buy more, you’re going to kill people, people are going to die because of you,’” the official said.

Negotiations became fraught when the company asked for additional indemnity, for civil cases alleging Pfizer’s acts of negligence, fraud, or malice. The government had never awarded any kind of indemnity before and did not want to waive liability, but Pfizer said this was non-negotiable. Negotiations continued and eventually a deal was signed that included the additional indemnity provisions, but after a delay of three months.

As Pfizer has only 2 billion doses to sell across the world this year — apparently on a first-come, first-served basis — the official is angry about a delay that likely pushed the country further back in the queue.

One of the reasons the government wanted Pfizer’s vaccines was because the company said they could be delivered quickly. Yet in the contract, Pfizer wanted to reserve the right to modify the schedule. There was no room for negotiation. “It was take it or leave it,” said the official.

The official added: “Five years in the future when these confidentiality agreements are over, you will learn what really happened in these negotiations.”

Based in the U.K., the Bureau of Investigative Journalism is an independent, not-for-profit organization. This story was produced by its Global Health desk.

https://www.statnews.com/2021/02/23/pfizer-plays-hardball-in-covid19-vaccine-negotiations-in-latin-america/

Tuesday, 1 June 2021

27.05.21 Sanofi, GSK kick off Phase Three trial for Covid-19 shot

 THU, MAY 27, 2021 - 4:50 PM

France's Sanofi and Britain's GlaxoSmithKline launched a late-stage human trial for a recombinant Covid-19 vaccine candidate on Thursday which they hope to get approved by the end of 2021. 


[PARIS] France's Sanofi and Britain's GlaxoSmithKline launched a late-stage human trial for a recombinant Covid-19 vaccine candidate on Thursday which they hope to get approved by the end of 2021.

The study initiated by Sanofi and GSK is one of the first late stage trials that combines tests for boosters and variants, as drugmakers adapt their strategies to deal with an evolving coronavirus.

The two drugmakers, which earlier this month reported positive interim results, confirmed their double-blind, placebo-controlled, Phase Three study would include more than 35,000 adults in the United States, Asia, Africa, and Latin America.

"In a two-stage approach, the study will initially investigate the efficacy of a vaccine formulation targeting the original virus, while a second stage will evaluate a second formulation targeting the B.1.351 virus," Sanofi said.

The virus lineage known as B.1.351 was first detected in South Africa.

"Recent scientific evidence shows that antibodies created against the B.1.351 variant may provide broad cross-protection against other more transmissible variants," Sanofi said.

"The design of the Phase Three, conducted across a broad diversity of geographies, also allows evaluation of the efficacy of the candidate against a variety of circulating variants," the French drugmaker added in a statement.

Sanofi also confirmed it would begin clinical studies in the coming weeks to assess the efficacy of the vaccine as a booster, regardless of what vaccine a subject may have received first.

Pending a positive Phase Three outcome, the vaccine could be approved in the fourth quarter after it was initially targeted for the first half of the year before a setback.

Sanofi and GSK were forced to restart their trial in December when the vaccine showed a low immune response in older adults as a result of a weak antigen formulation.

REUTERS

https://www.businesstimes.com.sg/consumer/sanofi-gsk-kick-off-phase-three-trial-for-covid-19-shot

01.06.21 Sinovac shot controls Covid in Brazil town after 75% covered

 TUE, JUN 01, 2021 - 11:35 AM

The vaccine developed by Sinovac Biotech Ltd. was effective in controlling Covid-19 in a mass-inoculation study in a small Brazilian town after 75 per cent of adults were covered with a second shot, preliminary numbers show. 


[SAO PAULO] The vaccine developed by Sinovac Biotech Ltd. was effective in controlling Covid-19 in a mass-inoculation study in a small Brazilian town after 75 per cent of adults were covered with a second shot, preliminary numbers show.

The study carried out by the Sao Paulo state government in the small town of Serrana - population 45,000 - may offer clues for other developing nations on how much of the public needs to be vaccinated in order to begin moving past the pandemic that continues to wreak havoc in Latin America and beyond.

While infection rates improved after first doses were administered, Covid-19 wasn't properly controlled in the town until after a second shot was given. A complete study will be published soon.

The study was led by the Butantan Institute, which produces Sinovac's so-called CoronaVac in Brazil. Almost two-thirds of Serrana's inhabitants got the vaccine between February and April with another third ineligible to receive the shot if they were under 18 years old or pregnant. About 95 per cent of the targeted adult population received the required two doses in the study.

"This is the first study of its kind in the world," Dimas Covas, Butantan's director, said at a press conference Monday. "This is primary data on the effects of vaccination in a population that will help authorities develop public policies." While neighboring cities were being hit hard by the pandemic, Serrana saw deaths fall by 95 per cent in the five weeks right after the mass-vaccination was completed. Symptomatic cases dropped by 80 per cent and hospitalizations decreased by 86 per cent.

"Now we can say that it's possible to control the pandemic with vaccines," Ricardo Palacios, research director at Butantan said, adding that Covid-19 numbers also fell for children. "This shows that it isn't necessary to vaccinate children to open schools." 

No severe side effects from the vaccine were reported and there were no Covid-related deaths among participants 14 days after the second dose was applied. The area around Serrana, some 315 kilometers (195 miles) from Sao Paulo, was overrun by the P1 variant during the study, reaffirming the jab's effectiveness against the strain first found in Brazil, Palacios said.

Sinovac's vaccine is being used widely in the developing world including Chile, Turkey, Indonesia and the Philippines.

The findings also underline the importance of people returning for a second shot. In Brazil, some 66 million vaccines have been administered, covering 21.4 per cent of the population with a single dose. About 10.5 per cent of the country is now considered to be fully inoculated, according to the Bloomberg vaccine tracker.

BLOOMBERG

https://www.businesstimes.com.sg/consumer/sinovac-shot-controls-covid-in-brazil-town-after-75-covered