A complete of 30 affected individuals along with relapsed or refractory chronic lymphocytic leukemia has already been randomized within the open-label, multi-dose, single-arm, dose-escalation survey. No dose-limiting toxicity ended up being observed and the trial process ended up being improved to include a period of time extensive dosing for affected individuals responding to therapy. The phase 1 trial was created to determine the drug's overall safety, tolerability, pharmacokinetic profile and briefly anti-tumor exercise. Data coming from the trial will become featured in Q4 2012.
"We are enthusiastic about the excellent improvement of a typical MOR208 program and therefore are preparing the next steps of clinical progress in excess B-cell malignancies to immediately determine the broader commercial ability of the molecule," stated Dr. Arndt Schottelius, Chief Development Officer of MorphoSys AG. "The lengthy treatment time we have been able to combine in the phase 1 study could present us with excess statistics on preliminary anti-tumor exercise."
No comments:
Post a Comment