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A Phase 1 First-in-human Study of BGM-2121 in Patients With Advanced Solid Tumors
This study is to explore the safety, tolerability, pharmacokinetics, and preliminary efficacy of BGM-2121 in adult patients with advanced solid tumors.
Age
18 - No limit years
Sex
ALL
Healthy Volunteers
No
National Cheng Kung University Hospital
Tainan, Taiwan
National Taiwan University Hospital
Taipei, Taiwan
Taipei Veterans General Hospital
Taipei, Taiwan
Start Date
February 1, 2026
Primary Completion Date
November 1, 2027
Completion Date
December 1, 2028
Last Updated
March 2, 2026
35
ESTIMATED participants
BGM-2121
DRUG
Lead Sponsor
BioGate Precision Medicine Corp.
NCT06898450
NCT05719558
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.
View ClinicalTrials.gov Terms and ConditionsNCT07029399