Thinking of joining a study?

Register your interest

Become a volunteer?

NCT05263739 | NOT YET RECRUITING | B-cell Lymphoid Malignancies

A First-in-Human Phase I Study of ESG206 in Subjects With B-cell Lymphoid Malignancies
Sponsor:

Shanghai Escugen Biotechnology Co., Ltd

Brief Summary:

This is a first-in-human phase I, multicenter, open label, sequential-cohort, dose escalation study of ESG206. The purpose is to evaluate the clinical safety, tolerability, PK, and preliminary efficacy and to establish the MTD, if any, and RP2D(s) of ESG206 in adult subjects with B lymphoid malignancies.

Condition or disease

B-cell Lymphoid Malignancies

Intervention/treatment

ESG206

Phase

PHASE1

Detailed Description:

This is a first-in-human phase I, multicenter, open label, sequential-cohort, dose escalation study of ESG206. The study will follow a modified 3+3 dose escalation scheme. Dose escalation will continue until identification of MTD or the predicted efficacy dose in the event that a MTD is not identified due to paucity of DLTs. Toxicity including dose-limiting toxicity (DLT) observed in Cycle 1 of the first 28 days will be used to determine escalation to the next dose level as described below. Five dose levels are planned. Dose choosing will be determined by the SMC and the sponsor based on the pharmacokinetics, tolerability and preliminary antitumor activities, as well as other available data. Subjects will be monitored for safety, tolerability, and efficacy throughout the study.

Study Type : INTERVENTIONAL
Estimated Enrollment : 12 participants
Masking : NONE
Primary Purpose : TREATMENT
Official Title : A First-in-Human Phase I, Open Label, Multiple Dose, Dose Escalation Study to Investigate the Safety, Tolerability, Pharmacokinetics and Antitumor Activities of Anti-BAFFR mAb, ESG206 in Subjects With B-cell Lymphoid Malignancies
Actual Study Start Date : 2024-12
Estimated Primary Completion Date : 2026-08
Estimated Study Completion Date : 2026-12

Information not available for Arms and Intervention/treatment

Ages Eligible for Study: 18 Years
Sexes Eligible for Study: ALL
Accepts Healthy Volunteers:
Criteria
Inclusion Criteria
  • * Willing and able to provide written informed consent for the trial.
  • * Male or female and at least 18 years of age.
  • * Subjects must have a histologically confirmed (or documented), incurable B-cell hematologic malignancy that had progressed despite standard of care therapy and for which there was no alternative therapy of proven benefit or no effective standard therapy is available or tolerable.
  • * Measurable or evaluable Disease.
  • * Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1.
  • * Subject must have adequate organ function.
Exclusion Criteria
  • * Has had prior chemotherapy, targeted therapy, immunotherapy or any other agents used as systemic treatment for cancer, within 14 days before first dosing.
  • * Had major surgery within 4 weeks before first dosing.
  • * Had undergone an autologous stem cell transplant within 100 days before first dosing.
  • * Evidence of severe or uncontrolled systemic diseases (e.g., unstable or uncompensated respiratory, hepatic, or renal disease).
  • * Known immediate or delayed hypersensitivity reaction or idiosyncrasy to drugs chemically related to the investigational product or excipients.
  • * Pregnant or breastfeeding women.
  • * Unwillingness or inability to follow the procedures outlined in the protocol.
A First-in-Human Phase I Study of ESG206 in Subjects With B-cell Lymphoid Malignancies

Location Details

NCT05263739

Please Choose a site

How to Participate

Want to participate in this study, select a site at your convenience, send yourself email to get contact details and prescreening steps.

Locations

No Location Found