Suzhou Zelgen Biopharmaceuticals Co.,Ltd
PART 1: 1. To explore the safety of ZG005 in combination with Gecacitinib in patients with relapsed or refractory lymphoma. 2. To determine the recommended Phase II dosing regimen for relapsed or refractory lymphoma. PART 2: To evaluate the efficacy of ZG005 in combination with Gecacitinib in patients with relapsed or refractory lymphoma.
Lymphoma
ZG005 for Injection
Gecacitinib Hydrochloride Tablets
PHASE1
PHASE2
Study Type : | INTERVENTIONAL |
Estimated Enrollment : | 60 participants |
Masking : | NONE |
Primary Purpose : | TREATMENT |
Official Title : | A Multicenter, Open-Label, Dose-Escalation and Dose-Expansion Phase I/II Study of ZG005 in Combination With Gecacitinib in Patients With Relapsed or Refractory Lymphoma |
Actual Study Start Date : | 2025-05 |
Estimated Primary Completion Date : | 2027-04 |
Estimated Study Completion Date : | 2027-05 |
Information not available for Arms and Intervention/treatment
Ages Eligible for Study: | 18 Years |
Sexes Eligible for Study: | ALL |
Accepts Healthy Volunteers: |
Want to participate in this study, select a site at your convenience, send yourself email to get contact details and prescreening steps.
Not yet recruiting
The First Affiliated Hospital, Zhejiang University School of Medicine
Hangzhou, Zhejiang, China,