Europe 1 with AFP 5:21 p.m., November 4, 2021

The American group Ventavia would have "falsified data" and "delayed in ensuring the follow-up of side effects" on a small part of the clinical trials of the Pfizer vaccine, according to the article of the "British Medical Journal". The vaccines the company tested would not have been stored at the right temperature.

A subcontractor of the pharmaceutical group Pfizer, responsible for carrying out a small part of the clinical trials of its vaccine against the Covid-19, made numerous failures during these tests, according to an article in the

British Medical Journal

which quotes a former employee.

The Texan group Ventavia, specializing in the conduct of clinical trials and commissioned last year by Pfizer to assess the effectiveness of its anti-Covid vaccine, in particular "falsified data" and "delayed in monitoring side effects, "according to this article published Tuesday.

A small part of the 44,000 people tested

Ventavia played only a small role in the trials of this vaccine, developed by Pfizer with the German BioNTech. The Texan group has conducted tests on a thousand people, while the vaccine has, in total, been evaluated on about 44,000 people around the world. These trials, demonstrating a particularly high efficacy, have led to the authorization of the vaccine in many countries, such as the United States and the countries of the European Union.

The primary source for the BMJ article is former Ventavia employee Brook Jackson, who worked there for two weeks during the Pfizer / BioNTech vaccine trials, before being fired.

Brook Jackson says he has witnessed many breaches.

Among the latter, she accuses Ventavia in particular of having, through its inconsistencies in labeling, compromised the double-blind allocation of the vaccine.

This procedure is essential for evaluating the effectiveness of a treatment compared to a placebo.

She makes sure that neither patients nor caregivers know whether it is one or the other.

Pfizer reportedly dispatched an audit of Ventavia

Brook Jackson cites other shortcomings, such as the fact that the vaccines were not stored at the right temperature, and says she informed the US health authorities, the FDA, which she said took note of her report. but did not follow up.

Contacted by AFP, the FDA refrained from commenting on this dossier but assured "its full confidence in the data which led to support the authorization of the Pfizer / BioNTech vaccine".

According to another source cited by the BMJ, this anonymous, Pfizer dispatched an audit of Ventavia, once informed of "problems" in the conduct of the tests.

Neither Pfizer nor Ventavia responded immediately to AFP's requests.