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NCT Number: NCT06921837

A First-in-Human Study Using BDC-4182 as a Single Agent in Advanced Gastric and Gastroesophageal Cancer

A first-in-human study using BDC-4182 as a single agent in gastric and gastroesophageal cancers

Recruiting

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 1 / Phase 2

Primary location

AUS Site 2, Darlinghurst, New South Wales, Australia

Loading trial locations.

About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Key Inclusion Criteria:

  • Has disease that is measurable by Response Evaluation Criteria in Solid Tumors (RECIST) v.1.1.
  • Subjects must have histologically/cytologically confirmed gastric or gastroesophageal cancer that is metastatic (Stage 4) or unresectable (Stage 3).
  • Subjects must have received at least 1-2 prior lines of locally available standard therapies or must be intolerant of standard therapies.
  • For subjects in escalation: If prior Claudin 18 IHC expression is known, the subject must have some degree of Claudin 18 expression as defined as Positive or have expression ≥ 1% of tumor cells IHC ≥ 2+. Consult with Medical Monitor as needed.
  • Adequate organ function
  • Agree to have a biopsy prior to enrollment, at acceptable risk in the judgement of the Investigator. If a biopsy is not safely accessible or clinically feasible, an adequate archival tumor sample must be submitted.

Key Exclusion Criteria:

  • Known central nervous system (CNS) metastases except for disease that is asymptomatic, clinically stable, and has not required steroids for at least 14 days before starting study treatment.
  • Cardiac disease, pulmonary disease, or hepatic disease
  • Active infection
  • History of inflammatory eye disease
  • Residual toxicity from a previous treatment
  • Any investigational agent or standard anti-cancer therapies within 28 days before starting study treatment or within 5 estimated elimination half-lives, whichever is shorter.

Treatment and study plan

BDC-4182

Drug

Immune stimulating antibody conjugate (ISAC), consisting of an anti-claudin 18.2 monoclonal antibody conjugated to a TLR 7/8 dual agonist

Primary outcomes

  1. Incidence of adverse events (AEs) and serious adverse events (SAEs) graded according to CTCAE v5.0

    Time frame: approximately 2 years

    Escalation period

  2. Incidence and nature of AEs considered by the Investigator or Sponsor to be clinically relevant, attributable to study treatment, and meeting dose-limiting toxicity (DLT) criteria

    Time frame: Up to 21 days

    Escalation period

Secondary outcomes

  1. Objective response rate (ORR) according to RECIST v. 1.1

    Time frame: approximately 4 years

    Escalation and expansion periods

  2. Duration of Response (DOR)

    Time frame: approximately 4 years

    Escalation and expansion periods

  3. Disease control rate (DCR)

    Time frame: approximately 4 years

    Escalation and expansion periods

  4. Progression-free survival (PFS)

    Time frame: approximately 4 years

    Escalation and expansion periods

  5. Best Overall Response (BOR)

    Time frame: approximately 4 years

    Escalation and expansion periods

  6. Overall survival (OS)

    Time frame: approximately 4 years

    Escalation and expansion periods

  7. PK (Cmax) of BDC-4182

    Time frame: approximately 4 years

    Escalation and expansion periods

  8. PK (Cmin) of BDC-4182

    Time frame: approximately 4 years

    Escalation and expansion periods

  9. PK (AUC0-tau) of BDC-4182

    Time frame: approximately 4 years

    Escalation and expansion periods

  10. PK (AUC0-inf) of BDC-4182

    Time frame: approximately 4 years

    Escalation and expansion periods

  11. PK (CL) of BDC-4182

    Time frame: approximately 4 years

    Escalation and expansion periods

  12. PK (Vc or Vss) of BDC-4182

    Time frame: approximately 4 years

    Escalation and expansion periods

  13. PK (Terminal half-life) of BDC-4182

    Time frame: approximately 4 years

    Escalation and expansion periods

Study contacts

Contact information is provided by the study sponsor or research team.

Bolt Biotherapeutics

CONTACT

[email protected]

+1 650 434 8640

Sponsors and collaborators

Lead sponsor

Bolt Biotherapeutics, Inc.

Industry

Registry information

Official study title

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

Important dates

Study start
2025
Primary completion
2027
Study completion
2029
First posted
Apr 10, 2025
Registry last updated
Jan 27, 2026

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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