BDC-4182
DrugImmune stimulating antibody conjugate (ISAC), consisting of an anti-claudin 18.2 monoclonal antibody conjugated to a TLR 7/8 dual agonist
NCT Number: NCT06921837
A first-in-human study using BDC-4182 as a single agent in gastric and gastroesophageal cancers
Interested in participating?
Request Info18 year and older
All sexes
Interventional
Phase 1 / Phase 2
AUS Site 2, Darlinghurst, New South Wales, Australia
This is a dose escalation study designed to evaluate the safety and tolerability of BDC-4182 to establish the recommended Phase 2 dose (RP2D). Participants will be enrolled in each dose cohort until the maximum tolerated dose (MTD) is reached. Additional participants may be enrolled into backfill cohorts at dose levels that have been cleared to collect additional safety and tolerability data. Additional participants may be enrolled at the determined RP2D in an expansion portion of the study.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Key Inclusion Criteria:
Key Exclusion Criteria:
Immune stimulating antibody conjugate (ISAC), consisting of an anti-claudin 18.2 monoclonal antibody conjugated to a TLR 7/8 dual agonist
Time frame: approximately 2 years
Escalation period
Time frame: Up to 21 days
Escalation period
Time frame: approximately 4 years
Escalation and expansion periods
Time frame: approximately 4 years
Escalation and expansion periods
Time frame: approximately 4 years
Escalation and expansion periods
Time frame: approximately 4 years
Escalation and expansion periods
Time frame: approximately 4 years
Escalation and expansion periods
Time frame: approximately 4 years
Escalation and expansion periods
Time frame: approximately 4 years
Escalation and expansion periods
Time frame: approximately 4 years
Escalation and expansion periods
Time frame: approximately 4 years
Escalation and expansion periods
Time frame: approximately 4 years
Escalation and expansion periods
Time frame: approximately 4 years
Escalation and expansion periods
Time frame: approximately 4 years
Escalation and expansion periods
Time frame: approximately 4 years
Escalation and expansion periods
Contact information is provided by the study sponsor or research team.
Bolt Biotherapeutics, Inc.
Industry
A Phase 1/2, First-in-Human, Dose Escalation and Expansion Study of BDC-4182 as a Single Agent in Patients With Advanced Gastric and Gastroesophageal Cancer
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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