Remdesivir for COVID-19” Study Accidentally Proved Effectiveness of Hydroxychloroquine

By Leo Goldstein – Re-Blogged From WUWT

  • The use of Remdesivir for COVID-19 was authorized by the FDA based on a single RCT, conducted by NIAID with the participation of Gilead Sciences, the exclusive manufacturer of Remdesivir. A final report from this study was published on October 8, five months after the drug’s authorization.
  • The final report shows that at least 35% of the patients were treated with Hydroxychloroquine, probably with Azithromycin. The data in the final report suggests that Hydroxychloroquine, not Remdesivir, was the main factor benefitting the patients in this study.
  • Nothing in the study supports the hypothesis that Remdesivir is an effective antiviral for SARS-COV-19

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