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Despite these improvements, even multi-hour delays can derail treatment: industry experts note that each additional day of delay reduces the likelihood a patient ever fills the prescription ( [8] )

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[ 4 , 5 , 6 ] In November 2010, the FDA approved Tesamorelin under the brand name Egrifta after Phase III clinical trials demonstrated that Tesamorelin significantly reduced visceral adipose tissue without affecting subcutaneous adipose tissue to a clinically significant extent