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Clinical Trials associated with DEG-6498 / Not yet recruitingPhase 1IIT A First in Human Phase 1 Open-Label, Multicenter, Dose Escalation and Expansion Study of DEG6498 in Patients With Solid Tumors
/ Not yet recruitingPhase 1 A First in Human Phase 1 Open-Label, Multicenter, Dose Escalation and Expansion Study of DEG6498 in Patients With Solid Tumors
The goal of this first in human, Phase 1, multi-center, open-label, and 2-part study is to learn whether DEG6498 is safe and tolerable in participants with advanced solid tumors. It will also learn about DEG6498 pharmacokinetics (PK) profile and potential antitumor activity. The main questions it aims to answer are:
* what is an appropriate dose to be given to participants?
* are the side effects of treatment manageable?
Participants who are treated in this study will receive DEG6498 orally once a day and be closely monitored by the treating physicians.
/ Not yet recruitingPhase 1 DEG6498 在实体瘤患者中的首次人体 I 期开放标签、多中心、剂量递增及扩展研究
[Translation] First-in-human, open-label, multicenter, dose-escalation and expansion study of DEG6498 in patients with solid tumors.
评价DEG6498口服给药的安全性/耐受性, 确定DEG6498单药的最大耐受剂量(MTD) 和/或推荐 II 期剂量(RP2D).
[Translation] Evaluate the safety/tolerability of oral DEG6498, and determine the maximum tolerated dose (MTD) and/or recommended phase II dose (RP2D) of DEG6498 monotherapy.
100 Clinical Results associated with DEG-6498
100 Translational Medicine associated with DEG-6498
100 Patents (Medical) associated with DEG-6498
100 Deals associated with DEG-6498