A Study of BGB-B455 in Adults With Advanced or Metastatic Solid Tumors
The goal of this clinical trial is to learn if BGB-B455 can treat advanced or metastatic solid tumors expressing claudin 6 (CLDN6), a protein that is found on some tumors. The main questions it aims to answer are: * What is the recommended dosing for BGB-B455? * What medical problems do participants have when taking BGB-B455? The study has two parts: * Phase 1a: dose escalation and safety expansion * Phase 1b: dose expansion.
Study details:
Claudin proteins are cell proteins that can play an important role in how cancer starts and progresses. Because of its preferential expression in tumors compared to normal tissues, CLDN6 is an ideal tumor antigen to target for treatment. BGB-B455 is a bispecific antibody (BsAbs) that targets CLDN6 on tumor cells and the CD3 receptor on T cells, which may provide a CLDN6-dependent antitumor immune response in a more tolerable manner without undue systemic toxicity.
This new study will check how safe and helpful this potential anticancer drug is. In addition, this study will explore the recommended dosing level for BGB-B455. This drug will be tested by itself or in combination with investigator-selected chemotherapy in participants with selected solid tumors expressing the CLDN6 protein.
This study is an open label study, meaning that both you and your study doctor will know what study drug/treatment you are given. This study has two parts:. * Phase 1a consists of a dose escalation part where increasing amounts of the study treatment are given to different dose cohorts, and a safety expansion part that will enroll additional participants at selected doses for further assessments.
* Phase 1b (dose expansion) will enroll participants at the best dose found in Phase 1a to see if it helps people with certain solid tumors.
Eligibility criteria
Researchers look for people who fit a certain description, called eligibility criteria. See if you qualify.
Inclusion criteria
- Histologically or cytologically confirmed advanced or metastatic, and unresectable solid tumors who have previously received standard systemic therapy for advanced or metastatic disease or for whom treatment is not available or not tolerated.
- Agreement for collection of formalin-fixed paraffin-embedded (FFPE) tumor tissue for central CLDN6 testing and other biomarker assessments.
- Tumor CLDN6 expression (CDLN6+) by central immunohistochemistry testing is required for certain cohorts.
- ≥ 1 measurable lesion as assessed by RECIST v1.1.
- Stable Eastern Cooperative Oncology Group (ECOG) Performance Status of 0 or 1.
- Adequate organ function.
Exclusion criteria
- Prior systemic anticancer therapy, including chemotherapy, immunotherapy (eg, interleukin, interferon, thymosin), targeted therapy, and antibody drug conjugates (ADCs) that are standard or investigational agents (including herbal medicine or Chinese [or other country] patent medicines, ≤ 14 days or 5 half-lives (whichever is shorter) before the first dose of study drug(s).
- Palliative radiation treatment or other locoregional therapies ≤ 14 days before the first dose of study drug(s).
- Live vaccine ≤ 28 days before the first dose of study drug(s). Vaccines for COVID-19 are allowed except for any live vaccine that may become available. Seasonal vaccines for influenza are generally inactivated vaccines and are allowed. Intranasal vaccines are live vaccines and are not allowed.
- Any major surgical procedure ≤ 28 days before the first dose of study drug(s).
- History of prior ≥ Grade 3 cytokine release syndrome (CRS).
- Participants with toxicities (because of prior anticancer therapy) that have not recovered to baseline or stabilized, except for adverse events not considered a likely safety risk (eg, alopecia, neuropathy, and specific laboratory abnormalities).
Eligibility
Age eligible for study : NA
Healthy volunteers accepted : No
Gender eligible for study: ALL
Things to know
Study dates
Study start:
Primary completion:
Study completion finish:
Study type
TREATMENT
Phase
- PHASE1
Study ID
NCT06803680
Intervention or treatment
DRUG: BGB-B455
DRUG: Chemotherapy
Conditions
- Advanced Solid Tumor
- Metastatic Solid Tumor
You may be eligible to participate in this trial based on your search. Check eligibility by answering some questions.
Research sites nearby
Closest Location:
Blacktown Cancer and Haematology Centre
Select from list below to view details:
Blacktown Cancer and Haematology Centre
Blacktown, New South Wales, Australia
Liverpool Hospital
Liverpool, New South Wales, Australia
Mater Cancer Care Centre
South Brisbane, Queensland, Australia
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Who is running the clinical trial?
BeiGene
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
| Participant Group/Arm | Intervention/Treatment |
|---|---|
EXPERIMENTAL: Phase 1a: Dose Escalation and Safety Expansion
| Drug: BGB-B455 |
EXPERIMENTAL: Phase 1b: Dose Expansion
| Drug: BGB-B455, Drug: Chemotherapy |
What is the study measuring?
Primary Outcome
| Measure | Description | Time Frame |
|---|---|---|
| Phase 1a: Number of participants with adverse events (AEs) and serious adverse events (SAEs) | Number of participants with AEs and SAEs, including laboratory abnormalities, and AEs that meet protocol-defined dose-limiting toxicity (DLT) criteria or protocol-defined adverse events of special interest (AESI) criteria. | From the first dose of study drug(s) to 30 days after the last dose or initiation of a new anticancer therapy, whichever occurs first; up to approximately 7 months |
| Phase 1a: Maximum Tolerated Dose (MTD) or Maximum Administered Dose (MAD) of BGB-B455 | MTD is defined as the highest dose evaluated for which estimated toxicity rate is the closest to the target toxicity rate. MAD is defined as the highest dose administered if MTD is not reached. | Approximately 1 month |
| Phase 1a: RDFE of BGB-B455 | RDFE of BGB-B455 will be determined based upon the MTD or MAD. | Approximately 1 month |
| Phase 1b: Overall Response Rate (ORR) | ORR is defined as the percentage of participants with best overall response of complete response (CR) or partial response (PR), as determined from tumor assessments by investigator per Response Evaluation Criteria in Solid Tumors version 1.1 (RECIST v1.1). CR and PR must be confirmed by repeat assessments. | Approximately 18 months |
Secondary Outcome
| Measure | Description | Time Frame |
|---|---|---|
| Phase 1a: ORR | ORR is defined as the percentage of participants with best overall response of CR or PR, as determined from tumor assessments by investigator per RECIST v1.1. CR and PR must be confirmed by repeat assessments. | Approximately 18 months |
| Phase 1a and 1b: Duration of Response (DOR) | DOR is defined as the time from the first confirmed objective response to documented disease progression or death, whichever occurs first, as determined from tumor assessments by investigator per RECIST v1.1. | Approximately 18 months |
| Phase 1a and 1b: Disease Control Rate (DCR) | DCR is defined as the percentage of participants who achieve CR, PR, or stable disease, as determined from tumor assessments by investigator per RECIST v1.1. | Approximately 18 months |
| Phase 1a and 1b: Time to Response (TTR) | TTR is defined as the time from the date of the first administration of study drug to the first confirmed response, as determined from tumor assessments by investigator per RECIST v1.1. | Approximately 18 months |
| Phase 1a and 1b: Serum concentrations of BGB-B455 | Not Specified | Approximately 7 months |
| Phase 1a and 1b: Number of participants with anti-drug antibodies (ADAs) to BGB-B455 | Not Specified | Approximately 7 months |
| Phase 1b: Progression-Free Survival (PFS) | PFS is defined as the time from the date of the first administration of study drug to the date of the first documentation of disease progression or death, whichever occurs first, as determined from tumor assessments by investigator per RECIST v1.1. | Approximately 18 months |
| Phase 1b: Number of participants with AEs | Number of participants with AEs, including physical examinations, electrocardiograms (ECGs), and laboratory assessments as indicated. | From the first dose of study drug(s) to 30 days after the last dose or initiation of a new anticancer therapy, whichever occurs first; up to approximately 7 months |
| Phase 1a and 1b: Area under the concentration-time curve (AUC) of BGB-B455 | Not Specified | Approximately 4 months |
| Phase 1a and 1b: Maximum observed plasma concentration (Cmax) of BGB-B455 | Not Specified | Approximately 4 months |
| Phase 1a and 1b: Time to reach maximum observed plasma concentration (Tmax) of BGB-B455 | Not Specified | Approximately 4 months |
| Phase 1a and 1b: Trough Concentration (Ctrough) of BGB-B455 | Not Specified | Approximately 7 months |
| Phase 1a and 1b: Apparent clearance (CL) of BGB-B455 | Not Specified | Approximately 4 months |
| Phase 1a and 1b: Volume of distribution (Vd) of BGB-B455 | Not Specified | Approximately 4 months |
| Phase 1a and 1b: Accumulation Ratio of BGB-B455 | Not Specified | Approximately 4 months |
| Phase 1a and 1b: Terminal half-life (t1/2) of BGB-B455 | Not Specified | Approximately 4 months |
References
Clinical Trials Gov: A Study of BGB-B455 in Adults With Advanced or Metastatic Solid TumorsOther trials to consider
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