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Dosing Parameters for CD47 Targeting Therapies to Hematologic Malignancies
专利权人:
The Board of Trustees of the Leland Stanford Junior University
发明人:
Ravindra Majeti,Mark P. Chao,Jie Liu,Jens-Peter Volkmer,Irving L. Weissman
申请号:
US16619387
公开号:
US20200147212A1
申请日:
2018.06.21
申请国别(地区):
US
年份:
2020
代理人:
摘要:
Methods are provided herein for determining and administering optimized dosing of therapeutic anti-CD47 agents, in a schedule that provides safe escalation of dose while achieving a therapeutic level in a clinically effective period of time. The methods can comprise the steps of clearance, escalation, and maintenance. In one embodiment the dosing regimen administers an initial (i) sub-therapeutic dose of an anti-CD47 agent or (ii) a cytoreductive therapy to achieve a safe level of circulating tumor cells for subsequent treatment (clearance); escalating the dose of an anti-CD47 agent until a therapeutic dose is reached (escalation); and maintaining the therapeutic dose for a period of time sufficient to reduce tumor cells in the bone marrow of the patient (maintenance). In an alternative dosing regimen, a patient determined to have a safe level of circulating tumor cells at presentation is treated by the steps of escalation and maintenance without initial clearance.
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