If anyone directly associated with Cytodyn gets the raw data then it's no longer a blinded study. The DSMC acts as a firewall to keep the blinding in place. The FDA is very preferential to blinded studies because companies and doctors can't modify things mid-trial to sway the outcome.

We received the COVID-10 raw data directly because the study was at an end so there was no worry about influencing the trial results, therefore no DSMC necessary.