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A Multi-center, Open-Label, Phase 1 Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Preliminary Efficacy of YK012 in Patients With Relapsed or Refractory B-Cell Non-Hodgkin Lymphoma.
- Source :
- Vaccine Weekly; 9/13/2024, p71-71, 1p
- Publication Year :
- 2024
-
Abstract
- This article provides information about a newly launched clinical trial in China for a drug called YK012, which is being tested in patients with relapsed or refractory B-cell non-Hodgkin lymphoma (B-NHL). The trial aims to evaluate the safety, tolerability, pharmacokinetics, and preliminary efficacy of YK012, and it is the first-in-human trial for this drug. The study will involve administering YK012 to patients through intravenous infusion every two weeks for a treatment cycle of four weeks. The primary outcome measures include assessing adverse events, dose-limiting toxicity, and determining the maximum tolerated dose for further clinical trials. The trial is currently recruiting participants, with a target enrollment of 48 individuals, and the primary investigator is Yuankai Shi from the Cancer Institute and Hospital, Chinese Academy of Medical Sciences. [Extracted from the article]
Details
- Language :
- English
- ISSN :
- 10742921
- Database :
- Complementary Index
- Journal :
- Vaccine Weekly
- Publication Type :
- Periodical
- Accession number :
- 179481379