A Study of EBC-129 in Advanced Solid Tumours

This study is testing a new drug called EBC-129, both on its own and in combination with pembrolizumab, for people with advanced solid tumors. These are cancers that have spread or cannot be removed by surgery, and for which standard treatments are no longer working or are not tolerated. The main goals are to understand the safety of EBC-129 and to find the best dose to use in future studies. The study plans to enroll 98 participants. You might be able to join if you are an adult (18 or older) with a solid tumor that has progressed and meets specific weight requirements. The study is currently recruiting, but the exact status is unclear.

Study design
This is an open-label study, meaning you and your doctors will know which treatment you are receiving. It is divided into four parts and plans to enroll 98 participants.
What's involved
You will receive EBC-129 through an IV (intravenous) infusion on Day 1 of each 21-day cycle, or multiple doses starting from Day 1 for 21-day or 28-day cycles. If you are in a combination part of the study, you will also receive pembrolizumab every 21 days.
Compensation
Not stated in the trial record.
Follow-up
You will be followed from before treatment starts until 30 days after your last dose, which is expected to be for approximately 2 years.

AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.

NCT05701527

A Study of EBC-129 in Advanced Solid Tumours

Recruiting
PHASE1Ages 18+InterventionalTreatment
EDDC (Experimental Drug Development Centre), A*STAR Research Entities
~98 participants
Updated 2026-02-05 on ClinicalTrials.gov
What's tested:EBC-129Pembrolizumab

At a glance

Recruiting sites
4 of 5 listed sites are recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Part A, Part B, Part C and Part D- Number of patients with serious adverse events (SAEs) and treatment emergent adverse events (TEAEs)
Measured over From pre-screening (≥28 days from planned date of treatment i.e. Day 1) until end of study (EOS i.e., 30 days from last dose). Approximately 2 years
+4 more outcomes measured
Advanced Solid Tumours

NCT05701527

Where you'd take part

This study runs at 5 sites. They're the same protocol — you choose where, and that choice sets who your contact draft is addressed to.

  • National Cancer Centre Singapore

    Singapore, South West, Singaporeno site contact published

    Recruiting

  • National University Hospital - Medical Oncology

    Singapore, South West, Singaporeno site contact published

    Recruiting

  • Taipei Veterans General Hospital

    Taipei, Taipei, Taiwanno site contact published

    Not yet recruiting

  • University of Colorado Hospital (UCH) - University of Colorado Cancer Center (UCCC) - Neuroendocrine Tumor Center

    Aurora, Coloradono site contact published

    Recruiting

  • UT MD Anderson Cancer Center

    Houston, Texasno site contact published

    Recruiting

Sites open and close at different times, so the status above is per site — it can differ from the study's overall status.

  • Venkateshan Srirangam Prativadibhayankara, MD · STUDY_DIRECTOR · EDDC (Experimental Drug Development Centre), A*STAR Research Entities
Venkateshan Srirangam Prativadibhayankara, MD
Email the study team

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  • Part A, Part B, Part C and Part D- Number of patients with serious adverse events (SAEs) and treatment emergent adverse events (TEAEs)From pre-screening (≥28 days from planned date of treatment i.e. Day 1) until end of study (EOS i.e., 30 days from last dose). Approximately 2 years
  • Part A, Part B and Part D- Determination of Maximum tolerated dose (MTD)Approximately 2 years
  • Part A, Part B and Part D- Determination of the Recommended Phase 2 dose (RP2D)Approximately 2 years
  • Part C- Objective response rate (ORR)Day 1 through 12 cycles (each cycle is 21 days)

    The number (%) of patients with a best overall response of complete response (CR) or partial response (PR) per RECIST v1.1 as assessed by investigator.

  • Part D- ORRDay 1 through 12 cycles (each cycle is 21 or 28 days)

    The number (%) of patients with a best overall response of CR or PR per RECIST v1.1 as assessed by investigator.