- CureVac lost more than half its value after its COVID-19 vaccine jab showed 47% effectiveness.
- Results were based on clinical trials conducted in Latin America and Europe on about 40,000 volunteers.
- The company attributed its results to 29 virus strains in the 10 countries where its trials took place.
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Interim analysis of data from about 40,000 volunteers showed the biotech’s jab is only 47% effective, falling short of the study’s criteria and the minimum 50% effectiveness threshold required by US regulators.
Data for the late-stage clinical trials that were conducted in Latin America and Europe was released after the US close on Wednesday. The company, backed by the Bill & Melinda Gates Foundation, attributed its disappointing results to the fact there are at least 29 COVID-19 strains circulating in the 10 countries where its trials took place.
The Gates foundation owns about 1.7% of CureVac, or 3.1 million shares, according to Bloomberg.
CureVac’s US shares are listed on the Nasdaq and plunged after hours from $94.79 at Wednesday’s close to $49.54 at Thursday’s market open.
The 47% efficacy estimate is based on 134 COVID-cases that occurred at least two weeks after the administration of the second dose, the company said in a statement.
“While we were hoping for a stronger interim outcome, we recognize that demonstrating high efficacy in this unprecedented broad diversity of variants is challenging,” CureVac CEO Franz-Werner Haas said.
CureVac said last year that it was working with Tesla on a vaccine printer, which Elon Musk reportedly called “an important product for the world.” Musk said in a tweet about the biotech in April that it “sounds like they’re a few months away from regulatory approval.” This tweet was later deleted.
The company will continue trials of its two-dose messenger RNA vaccine and expects to publish final analysis within the next few weeks.
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