Intra-Cellular says higher dose of ITI-007 can be effective to treat schizophrenia
The company carried out the trial at 12 sites in the US with 450 patients randomized to receive either ITI-007 60 mg or 40 mg or placebo once
Daiichi Sankyo and Merck & Co (MSD) have voluntarily withdrawn their biologics license application (BLA) for ifinatamab deruxtecan, aimed at treating adult patients with extensive-stage small cell lung cancer (ES-SCLC) following disease progression after platinum-based chemotherapy.
Andexanet alfa, a U.S. Food and Drug Administration (FDA)-designated breakthrough therapy, is a recombinant protein specifically designed to reverse the anticoagulant activity of Factor Xa inhibitors. Portola is