A Study of D3L-001 as Monotherapy in Subjects With HER2-Positive Advanced Solid Tumors
- Registration Number
- NCT05957536
- Lead Sponsor
- D3 Bio (Wuxi) Co., Ltd
- Brief Summary
This first-in-human (FIH) study, multi-center, open-label, dose escalation and dose expansion Phase I study to evaluate the safety, tolerability, pharmacokinetics (PK), pharmacodynamics (PD), immunogenicity, and preliminary anti-tumor activity of D3L-001 in subjects with HER2-positive advanced solid tumors.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- RECRUITING
- Sex
- All
- Target Recruitment
- 110
Inclusion Criteria
- Subject must have documented HER2 positivity (determined by immunohistochemistry [IHC], in situ hybridization [ISH], Next Generation Sequencing [NGS] or other analysis techniques as appropriate).
- Subject must have Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1.
- Subject must have left ventricular ejection fraction (LVEF) ≥50% by either echocardiography (ECHO) or multiple-gated acquisition (MUGA) within the screening period.
- Subject must have adequate organ and marrow function within the screening period.
Exclusion Criteria
- Subject has any prior treatment with anti-CD47 or SIRPα agent.
- Subject has major surgery or radiotherapy, immunostimulatory agents, investigational agents, or any other anticancer treatment including chemotherapy, targeted therapy, biologics that is not completed 28 days before first dose of study medication.
- Subject has immunosuppressive medication that is not completed 14 days before the first dose of study medication.
- Subject has uncontrolled intercurrent illness that would limit compliance with study requirements, substantially increase risk of incurring AEs, or compromise the ability of the subject to give written informed consent.
- Subject has unresolved treatment-related toxicities from previous anticancer therapy of NCI CTCAE Grade ≥2 (with exception of vitiligo or alopecia).
- Judgment by the Investigator that the subject should not participate in the study if the subject is unlikely to comply with study procedures, restrictions, and requirements.
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- SEQUENTIAL
- Arm && Interventions
Group Intervention Description D3L-001 D3L-001 Part 1 Dose Escalation in subjects with HER2-positive advanced solid tumors * Cohort 1 (starting dose) * Cohort 2 * Cohort 3 * Cohort 4 * Cohort 5 Part 2 Dose Expansion * Cohort A for subjects with HER2-positive advanced breast cancer * Cohort B for subjects with HER2-positive advanced gastric cancer/gastroesophageal junction cancer
- Primary Outcome Measures
Name Time Method Number of Participants With Adverse Events (AEs) Screening until Safety Follow Up visit (30 days after the last dose) Maximum Tolerated Dose based on Dose-Limiting Toxicities (DLTs) At the end of Cycle 1 (each cycle is 21 days).
- Secondary Outcome Measures
Name Time Method D3L-001 half-life (t1/2) First dose up to 6 months D3L-001 minimum serum concentration (Ctrough) First dose up to 6 months D3L-001 maximum observed plasma concentration (Cmax) First dose up to 6 months Incidence of anti-drug antibodies (ADA) to D3L-001 First dose up to 6 months Disease control rate (DCR) as Determined by the Investigator According to Response Evaluation Criteria in Solid Tumors, Version 1.1 Until disease progression or end of treatment (up to approximately 24 months) D3L-001 area under the concentration-time curve (AUC) First dose up to 6 months D3L-001 time to maximum plasma concentration (tmax) First dose up to 6 months Objective response rate (ORR) as Determined by the Investigator According to Response Evaluation Criteria in Solid Tumors, Version 1.1 (RECIST v1.1) Until disease progression or end of treatment (up to approximately 24 months) Progression-free survival (PFS) as determined by the investigator according to Response Evaluation Criteria in Solid Tumors, Version 1.1 (RECIST v1.1) Until disease progression or end of treatment (up to approximately 24 months) Duration of Response (DOR) as Determined by the Investigator According to Response Evaluation Criteria in Solid Tumors, Version 1.1 (RECIST v1.1) Until disease progression or end of treatment (up to approximately 24 months) Pre- and post-dose levels of CD47 receptor occupancy in particular cell types from peripheral blood First dose up to 6 months
Trial Locations
- Locations (1)
D3 Bio Investigative Site
🇨🇳Hangzhou, Zhejiang, China