The U.S. Food and Drug Administration (FDA) has cleared Global Cord Blood Corporation’s (NYSE:CO) Investigational New Drug (IND) application to initiate a Phase 1b, clinical study of CK0804 as an add on therapy to ruxolitinib in patients with myelofibrosis who experience a suboptimal response to ruxolitinib.
The Phase 1b clinical trial is being launched in partnership with Incyte as part of their LIMBER initiative, will evaluate the safety of monthly doses of CK0804 as add on therapy in myelofibrosis patients who will continue treatment with ruxolitinib.
