A phase 2 trial of CK-0804 in JAK ihnibitor resistant/ suboptimal myelofibrosis
Latest Information Update: 12 Jan 2026
At a glance
- Drugs CK 0804 (Primary)
- Indications Myelofibrosis
- Focus Therapeutic Use
Most Recent Events
- 06 Jan 2026 According to a Cellenkos media release,company announced that the U.S. Food and Drug Administration (FDA) has granted Orphan Drug Designation to its investigational product, CK0804, for treatment of myelofibrosis.
- 20 Dec 2025 New trial record
- 10 Dec 2025 According to a Cellenkos media release, the company will initiate phase 2 trial of CK0804 in JAK ihnibitor resistant/ suboptimal myelofibrosis, as the responses in thrombocytopenic patients (failed or had suboptimal benefit from prior JAK inhibitor therapy) are encouraging and pave way for phase 2 trial.