Subject recruitment
GT929 Non-hodgkin’s lymphoma
On July 24, 2023, the molecular glue degrader GT929 developed by Gluetacs was approved by Center for Drug Evaluation, NMPA to enter the phase I/IIa clinical trial. On March 6, 2024, GT929 was announced dosing of the first patient in the phase I/IIa clinical trial.
Recruitment criteria:
You may be selected for this study if you meet the following key criteria:
- Male or female,over 18 years old;
- Patients diagnosed with relapsed or refractory non-Hodgkin lymphoma (rrNHL);
- ECOG score physical status <2, expected survival >12 weeks;
- Have adequate organ function, including blood system, liver function, kidney function, coagulation function, etc.;
- Subjects of reproductive age should agree to use effective contraception from the date of signing the informed consent until 6 months after the last dosing.
Research Center:
Fudan University Shanghai Cancer Center (Director Tao Rong; Director Zhang Jian)
Sun Yat-Sen University Cancer Center(Director Cai Qingqing)
The Affiliated Hospital of Xuzhou Medical University (Director Zhu Feng)