ChiCTR1900023266: A Phase 1 Study to Assess the Safety, Tolerability, Pharmacokinetics, Pharmacodynamics, and Preliminary Efficacy of BLU-554 in Patients with Hepatocellular Carcinoma |
|
|
| Not yet recruiting | 1 | 40 | | It is anticipated that patients will receive at least 1 cycle of BLU?554(subject will take 600mg qd); no maximum treatment duration has been set. After C1, patients may continue to receive BLU?554 until precluded by toxicity, noncompliance, progressive disease, withdrawal of consent, death, or closure of the st | The Chinese People's Liberation Army 81th Hospital; West China Hospital, Sichuan University, Blueprint Medicines,Cstone | Hepatocellular carcinoma | | | | |