Methods: This open-label phase 1/2 study evaluated the safety, tolerability, and antitumor activity of INCB001158 in pts with advanced or metastatic solid tumors. In phase I, dose escalation of INCB001158 (50, 75, and 100 mg twice daily [BID]) was used to determine the recommended phase II dose (RP2D) of INCB001158 + gemcitabine/cisplatin. WebDec 17, 2024 · Median DOR for INCB001158 plus gemcitabine/cisplatin was 5.8 months; median PFS was 8.5 months. Based on these data, the researchers concluded that the addition of INCB001158 to the standard gemcitabine/cisplatin backbone was tolerable, did not result in significant additional toxicity, and demonstrated modest clinical activity in …
incb001158 - My Cancer Genome
WebMay 20, 2024 · INCB001158 Pharmacology Indication Not Available Build, train, & validate predictive machine-learning models with structured datasets. See how Contraindications & Blackbox Warnings Avoid life-threatening adverse drug events & improve clinical decision support. Learn more Pharmacodynamics Not Available Mechanism of action Not … WebJan 11, 2024 · Title: A phase I/II study of safety and efficacy of the arginase inhibitor … sims 4 cc mod the sims
Arginase Inhibitor INCB001158 as a Single Agent and in
WebMay 6, 2024 · INCB001158 Combined With Subcutaneous (SC) Daratumumab, Compared to Daratumumab SC, in Relapsed or Refractory Multiple Myeloma Sponsor Incyte Corporation (Industry) Overall Status Completed CT.gov ID NCT03837509 Collaborator (none) 15 Enrollment 29 Locations 3 Arms 30.3 Actual Duration (Months) 0.5 Patients Per Site 0 … WebINCB001158, Pembrolizumab Description This study is an open-label Phase 1/Phase 2 … WebCalithera Targeting Cancer, Differently Home rbh trust education centre