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Acer Therapeutics, Relief Therapeutics Receive CRL From FDA For ACER-001 For UCDs

Acer Therapeutics, Relief Therapeutics Receive CRL From FDA For ACER-001 For UCDs

Pharmaceutical company Acer Therapeutics Inc. (ACER) and its collaboration partner, Relief Therapeutics Holding SA (RLFTF, RLFTY), announced Tuesday that the U.S. Food and Drug Administration (FDA) has issued a Complete Response Letter (CRL) regarding the New Drug Application (NDA) for ACER-001 (sodium phenylbutyrate) for oral suspension for the treatment of patients with urea cycle disorders (UCDs).
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