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Trump heads for 'Alligator Alcatraz' migrant detention center
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Russia ramps up drone strikes on Ukraine in June: AFP analysis
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Japan had hottest June on record: weather agency
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Thailand's PM suspended by Constitutional Court
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Saudi's Al Hilal knock Man City out of Club World Cup in huge shock
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Online memorial for children dead in Hiroshima, Nagasaki
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US Senate in final push to pass Trump spending bill
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Asian stocks rise on trade deal hopes, Tokyo hit by tariff warning
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Bangladeshis cling to protest dreams a year after revolution
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Djokovic, Sinner enter Wimbledon fray
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European security tops Denmark's EU presidency priorities
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France expecting peak temperatures as heatwave hits Europe
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Germany eye return to women's football summit at Euro 2025
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'Every day I see land disappear': Suriname's battle to keep sea at bay
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England feel pressure to perform at Euros as stars pull out
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Clashes in Istanbul over alleged 'Prophet Mohammed' cartoon
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India face 'last-minute' Bumrah call as they bid to level England series
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CS Group Announces Strategic MOU Between CS Interpharm and Gulf Center Group for Customized Manufacturing Collaboration

US drug regulator postpones meeting on infant Covid vaccines
The US Food and Drug Administration (FDA) on Friday announced it was pushing back a meeting scheduled for next week where a panel of experts would have decided whether to endorse the Pfizer-BioNTech Covid vaccine for infants.
The meeting would have evaluated whether two doses of the shot should be authorized for children aged six months through four years, even though clinical trials are still evaluating whether three shots are needed.
Interim results in fact had shown that a low dose of three micrograms given across this age group to stave off side effects did not elicit an immune response comparable to older age groups given a higher dose.
"Given that the study is advancing at a rapid pace, the companies will wait for the three-dose data as Pfizer and BioNTech continue to believe it may provide a higher level of protection in this age group," the US and German firms said in a statement.
"We will provide an update on timing for the advisory committee meeting once we receive additional data on a third dose in this age group from the company’s ongoing clinical trial and have an opportunity to complete an updated evaluation," added the FDA.
L.Mason--AMWN