July 4 (Reuters) - RELIEF THERAPEUTICS HOLDING SA RLFB.S :
* RELIEF REPORTS THAT ITS U.S. COLLABORATION PARTNER HAS
ANNOUNCED
THAT THE FDA HAS DECLINED EMERGENCY USE AUTHORIZATION FOR
AVIPTADIL FOR A SUBGROUP OF PATIENTS WITH CRITICAL COVID-19 AT
IMMEDIATE RISK
* THAT ITS U.S. COLLABORATION PARTNER HAS ANNOUNCED THAT FDA
HAS
DECLINED EMERGENCY USE AUTHORIZATION FOR AVIPTADIL FOR A
SUBGROUP OF PATIENTS WITH CRITICAL COVID-19 AT IMMEDIATE RISK OF
DEATH FROM RESPIRATORY FAILURE DESPITE TREATMENT WITH APPROVED
THERAPY, INCLUDING REMDESIVIR
Source text for Eikon: ID:nEQ4r1KgTa
Further company coverage: RLFB.S
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