GSK’s gonorrhea vaccine receives fast-track designation to expedite clinical trials

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GSK’s gonorrhea vaccine receives fast-track designation to expedite clinical trials
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GSK’s gonorrhea vaccine receives fast-track designation to expedite clinical trials. Read the latest in the Clinical Pipeline by drbenjohnson

18–50 years of age. The trial includes men and women considered at risk of infection with the bacteriumin eight countries: the USA, the United Kingdom, France, Germany, Spain, Brazil, the Philippines and South Africa.

Participants are split into three groups: those who received the highest tolerated dose in the phase 1 trial; those receiving a dose below the highest tolerated dose; and those who receiving placebo. The primary outcome is local and systemic adverse events, and hematological and biochemical abnormalities. Gonorrhea cases up to 13 months after vaccination will be a closely watched secondary endpoint.

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