Solid Tumor, Adult
Conditions
Keywords
HMPL453, solid tumor, dose escalation
Brief summary
This is a dose escalation study consisting of two stages: Dose-escalation stage (stage 1): Patients will take a single dose of HMPL-453 on Day 1 and will be followed for one week for safety observations. After one week of observation, if no safety issues occur, patients can continue multiple dosing of HMPL-453 QD (quaque die) and start on the DLT (Dose Limited Toxicity) assessment cycles. Each cycle consists of 28-days. Patients are required to draw blood samples for PK and safety analysis at specific time points during the treatment; Dose-Expansion Stage (Stage 2): This stage is to further evaluate the safety, tolerability, PD (pharmacodynamics) profile, and preliminary anti-tumor activity of HMPL-453 at the RP2D (recommended phase 2 dose) in approximately 10 patients with advanced solid tumor.
Detailed description
Dose-escalation stage (stage 1): Patients participating in the dose-escalation stage will take a single dose of HMPL-453 on Day 1 and will be followed for one week for safety observations. After one week of observation, if no safety issues occur, patients can continue multiple dosing of HMPL-453 QD and start on the DLT assessment cycles. Each cycle consists of 28-days. Patients are required to draw blood samples for PK and safety analysis at specific time points during the treatment. The 3+3 design will be employed for the dose escalation and MTD ( maximum tolerated dose) determination. To limit the number of patients being exposed to potentially ineffective doses, one patient will be enrolled and dosed in the initial dose cohort. If there are no DLT or less than grade 2 toxicities of Common Terminology Criteria for Adverse Event ( CTC AE ) occur in the first treatment cycle, then the study will be escalated to the next dose cohort. Otherwise, the trial will revert to a standard 3+3 design. Dose-Expansion Stage (Stage 2): This stage is to further evaluate the safety, tolerability, pharmacokinetics (PK) profile, and preliminary anti-tumor activity of HMPL-453 at the RP2D in approximately 60 patients with advanced solid tumor. Patients with FGFR ( Fibroblast Growth Factor Receptor) dysregulated advanced solid tumors, including but not limited to advanced urothelial bladder cancer, advanced cholangiocarcinoma (patients with cancers of the gallbladder or ampulla of Vater are not eligible) and others solid tumors are preferred to be enrolled. Expansion stage will begin after dose-escalation stage is completed and the MTD/RP2D has been determined. Patients will receive HMPL-453 with 28-day treatment cycles until disease progression, death, intolerable toxicity, no longer benefiting from the study treatment per investigator's discretion, or withdrawal of consent, whichever comes first.
Interventions
DRUGHMPL-453
oral administrative
Sponsors
Hutchison Medipharma Limited
Study design
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE
Intervention model description
Open-label, Multi-center, Dose Escalation Study
Eligibility
Sex/Gender
ALL
Age
25 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* In the dose escalation stage, patients with locally advanced, or metastatic solid tumor who have failed, or intolerable to, standard therapies or for whom no standard therapies exist will be enrolled. * In the dose expansion stage, patients with locally advanced, or metastatic solid tumor and FGFR dysregulation who have failed or intolerable to standard therapies or no standard therapies exist are to be enrolled. * In the dose escalation stage: evaluable or measurable disease according to RECIST Version 1.1. In the dose expansion stage: measurable disease according to RECIST Version 1.1. * Life expectancy of at least 12 weeks. * ECOG (Eastern Cooperative Oncology Group) performance status of 0 or 1.
Exclusion criteria
* Prior or current treatment with any selective FGFR inhibitor.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Incidence of DLTs by the NCI CTCAE v4.03 | Cycle 1 (DLT assessment window 28 days) | Incidence of DLTs by the NCI CTCAE v4.03 |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| maximum plasma concentration (Cmax) | From first dose to day 56 of multiple dosing period | maximum plasma concentration (Cmax) of HMP 453 |
| time to reach maximum concentration (Tmax) | From first dose to day 56 of multiple dosing period | time to reach maximum concentration (Tmax) of HMP 453 |
| terminal half-life (t1/2) | From first dose to day 56 of multiple dosing period | terminal half-life (t1/2) of HMP-453 |
| area under the concentration-time curve (AUC0-t) | From first dose to day 56 of multiple dosing period | area under the concentration-time curve (AUC0-t) of HMP453 |
| apparent clearance (CL/F) | From first dose to day 56 of multiple dosing period | apparent clearance (CL/F) of HMP 453 |
| Incidence of AEs and clinically significant laboratory abnormalities | From first dose to 30 days after last dose of study treatment | incidence of any AEs associated to treatment |
| Objective response rate (ORR) | Every 8 weeks while being treated with HMPL-453 (expected average of 16 weeks) | per RECIST |
| Duration of response (DoR) | Every 8 weeks while being treated with HMPL-453 (expected average of 16 weeks) | from the date of response to progress or death |
| Disease Control Rate (DCR) | Every 8 weeks while being treated with HMPL-453 (expected average of 16 weeks) | the response rate of PR (partial response) +CR(complete response) +SD （stable disease） |
| Change in tumor size | Every 8 weeks while being treated with HMPL-453 (expected average of 16 weeks) | per RECIST to evaluate the change of target and non-target lesions |
| Progression free survival (PFS) | Every 8 weeks while being treated with HMPL-453 (expected average of 16 weeks) | Per RECIST 1.1 |
| Serum phosphate level increases | From first dose to Day 21 of the last treatment cycle | to evaluate the fluctuate level of Serum phosphate level |
Countries
China
Outcome results
None listed