RecruitingPhase 1NCT07346846

A Study of BGM-2121 in Patients With Advanced Solid Tumors

A Phase 1 First-in-human Study of BGM-2121 in Patients With Advanced Solid Tumors


Sponsor

BioGate Precision Medicine Corp.

Enrollment

35 participants

Start Date

Mar 10, 2026

Study Type

INTERVENTIONAL

Conditions

Summary

This study is to explore the safety, tolerability, pharmacokinetics, and preliminary efficacy of BGM-2121 in adult patients with advanced solid tumors.


Eligibility

Min Age: 18 Years

Inclusion Criteria5

  • With either gender aged ≥ 18 years,
  • Has a confirmed diagnosis of advanced solid tumor(s),
  • The subject has received and failed standard-of-care anti-cancer therapy
  • Has at least one measurable lesion according to Response Evaluation Criteria in Solid Tumors (RECIST)
  • ...

Exclusion Criteria4

  • Has any ongoing toxicity from previous anti-cancer treatments
  • Has signs or symptoms of end-stage organ failure, major chronic illnesses other than cancer(s)
  • History of another primary malignancy within the last three years
  • ...

Interested in this trial?

Get notified about updates and connect with the research team.

Interventions

DRUGBGM-2121

BGM-2121 treatment


Locations(3)

National Cheng Kung University Hospital

Tainan, Taiwan

National Taiwan University Hospital

Taipei, Taiwan

Taipei Veterans General Hospital

Taipei, Taiwan

View Full Details on ClinicalTrials.gov

For the most up-to-date information, visit the official listing.

Visit

NCT07346846


Related Trials