Abstract 1010P
Background
B7H7, a novel immune checkpoint, is a promising target in solid tumors due to its overexpression and correlation with poor prognosis. HBM1020 is a first-in-class anti-B7H7 antibody designed to augment T cell anti-tumor response.
Methods
This objective of this phase 1 study is to assess the safety, pharmacokinetics (PK), and pharmacodynamics (PD) of HBM1020 in patients (pts) with advanced solid tumors. In Part 1 (dose escalation), HBM1020 was administered at dose levels between 0.3mg/kg and 30mg/kg every 3 weeks (Q3W) by intravenous infusion. Enrollment is ongoing in Part 2 (dose expansion).
Results
As of 01-April-2024, 17 pts with have received HBM1020 from 0.3mg/kg to 30 mg/kg Q3W. Median age was 62 years (34-80). All pts completed dose limiting toxicity (DLT) observation periods (21 days) and no DLT events were observed and MTD has not yet been reached. A total of 6 (35.3%) pts had a treatment related adverse event (TRAE) and all TRAEs were Grade 1-2. Eleven (64.7%) pts had reported serious adverse events (SAEs) and all SAEs were deemed unrelated to study treatment by both investigator and study sponsor. Nine (9) pts had post baseline tumor evaluation, and 6 out of 9 (66.7%) pts had stable disease (SD) as best response (including 1 pt with SD, tumor shrinkage of 25%). PK analysis of HBM1020 demonstrated a typical IgG behavior with elimination half-life of ∼two weeks in the dose range of 3 to 20 mg/kg. Drug exposure increased in a nearly dose-proportional manner. The expression of B7H7 was assessed by validated immunohistochemistry (IHC) assay for patients with available archived samples.
Conclusions
HBM1020, as a first-in-class anti-B7H7 antibody, demonstrated promising safety and tolerability profiles in patients with advanced solid tumors. Further studies are warranted to explore the therapeutic potential of HBM1020 in solid tumors.
Clinical trial identification
NCT05824663.
Editorial acknowledgement
Legal entity responsible for the study
Harbour Biomed US.
Funding
Harbour Biomed US.
Disclosure
X. Tao: Financial Interests, Personal, Full or part-time Employment: Harbour Biomed Ltd; Financial Interests, Personal, Stocks/Shares: Harbour Biomed Ltd. All authors have declared no conflicts of interest.
Resources from the same session
1003P - A first-in-human (FIH) phase I study of IPH5301, an anti-CD73 monoclonal antibody (mAb), in patients with advanced solid tumors (AST) (CHANCES, NCT05143970)
Presenter: Mathilde Beaufils
Session: Poster session 03
1004P - Phase I/II trial of ASP1570, a novel diacylglycerol kinase ζ inhibitor, in patients with advanced solid tumors
Presenter: Daniel Olson
Session: Poster session 03
1005P - Microbial ecosystem therapeutics 4 (MET4) treatment mediates a humoral response in patients treated with immune checkpoint inhibition (ICI)
Presenter: Pavlina Spiliopoulou
Session: Poster session 03
1007P - Systemic STING agonist BI 1703880 plus ezabenlimab in patients (pts) with advanced solid tumors: Initial results from a phase Ia study
Presenter: Kevin Harrington
Session: Poster session 03
1008P - Preliminary clinical PK and PD analysis of a phase I study of ZL-1218, a humanized anti-CCR8 IgG1 antibody, in patients with advanced solid tumors
Presenter: Ignacio Gil Bazo
Session: Poster session 03
1011P - Model-informed dose optimization of HFB200301, a TNFR2 agonist monoclonal antibody (mAb), in monotherapy and in combination with the anti-PD-1 mAb tislelizumab (TIS), in patients (pts) with advanced solid tumors
Presenter: Desamparados Roda Perez
Session: Poster session 03
1012P - Safety, tolerability, and efficacy of nadunolimab in combination with pembrolizumab in patients with solid tumors
Presenter: roger cohen
Session: Poster session 03
1013P - A phase I study of rivoceranib combined with nivolumab in patients with unresectable or metastatic cancer
Presenter: Neal Chawla
Session: Poster session 03
1014P - Phase Ib trial results of safety, pharmacokinetics and pharmacodynamics of TU2218, TGFβ-RI and VEGF-R2 dual inhibitor in combination with pembrolizumab in patients with advanced solid tumors
Presenter: Anthony Tolcher
Session: Poster session 03