Advanced Renal Cell Carcinoma, Advanced Solid Tumor, Solid Tumor, Adult
Conditions
Keywords
CAIX
Brief summary
This is an open label, single-arm, multicentre dose escalation (Part 1) and dose expansion (Part 2) study to evaluate different combinations of 3 radioactive dose levels of 177Lu-TLX250 administered intravenously with 3 different doses of peposertib in patients with CAIX-expressing solid tumors.
Detailed description
Part 1 (dose escalation) will evaluate the combination of 3 different activities of 177Lu-TLX250 and 3 different dose levels of peposertib. Patients with CAIX positive solid tumors will be enrolled in a given dose/activity level in Cohorts of approximately 2-6 patients. Treatment cycles will have a fixed length of 84 days. Patients will be treated during 3 cycles, or until clinically significant progression or unacceptable toxicity. Part 2 (dose expansion) patients will be enrolled in 2 Cohorts: * Cohort A: 40 patients with metastatic or non-resectable ccRCC * Cohort B: 20 patients with CAIX-positive solid tumors (excluding RCC). Patients will be treated at the Recommended phase 2 dose of 177Lu-TLX250 in combination with peposertib at the dosing schedule of the selected Recommended phase 2 dose.
Interventions
DIAGNOSTIC_TEST89Zr-TLX250
Single IV administration followed by 89Zr-DFO-girentuximab PET/CT (or PET/MRI) scan at screening and approximately 8-10 weeks (±1 week) after Cycle 3 Day 1, as well as at the end of treatment visit (if feasible). The PET/CT should be obtained within 4-7 days after 89Zr-TLX250 administration
COMBINATION_PRODUCT177Lu-TLX250 and Peposertib
Dose escalation and de-escalation for the determination of the Maximum tolerated combination/ Recommended phase 2 dose. All subjects will receive 177Lu-TLX250 intravenously on day 1 and Peposertib BID on days 4-21 of each 84-day cycle.
Sponsors
Merck KGaA, Darmstadt, Germany
Telix Pharmaceuticals (Innovations) Pty Limited
Study design
Allocation
NA
Intervention model
SEQUENTIAL
Primary purpose
TREATMENT
Masking
NONE
Intervention model description
Dose escalation/de-escalations will be supported by the guidance given by outputs of the Bayesian model-based dose-escalation design.
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* Histologically confirmed advanced or metastatic solid tumor that has progressed on or during/after recognized standard of care therapies and are not eligible for resection, or patients that are not eligible or not consenting to recognized standard of care therapies. * At least one measurable lesion on CT/MRI according to RECIST 1.1 with corresponding 89Zr-TLX250 uptake (i.e., CAIX positive). * CAIX positivity in at least 75% of the total lesion volume (defined as 89Zr- TLX250 uptake with intensity significantly greater than normal liver \[i.e., standardized uptake value \[SUV\]max at least 1.5 times SUV of normal liver\]). * ECOG status 0 or 1. * Have adequate organ function during screening * Must have a life expectancy of at least 6 months.
Exclusion criteria
* Prior 177Lu-TLX250 or other radioligand therapy; or any prior CAIX targeting therapy. * Known hypersensitivity to compounds of similar chemical or biologic composition to peposertib, girentuximab radiolabelled by zirconium or lutetium, any excipient in the study medication or any other intravenously administered human proteins/peptides/antibodies. * Administration of any radionuclide within 10 half-lives of the radionuclide prior to signature of the ICF. * Patients who have had chemotherapy, definitive radiation, biological cancer therapy, or investigational agent/device within 28 days of first planned dose of study therapy. * Patients who had \> 2 prior lines of cytotoxic chemotherapy or had Grade 4 neutropenia or Grade 3/Grade 4 thrombocytopenia (both of a duration of at least 48 hours) during the last line of therapy. Note: This criterion may be removed in total or in part by the SRC upon review of the safety data from the initial dose level(s). * Patients who cannot discontinue concomitant medications or herbal supplements that are strong inhibitors or strong inducers of cytochrome P450 (CYP) isoenzymes CYP3A4/5, CYP2C9, and CYP2C19. Concomitant use of CYP3A4/5 substrates with a narrow therapeutic index are also excluded. * Patients who cannot discontinue concomitant H2-blockers or proton-pump inhibitors (PPIs). Patients may confer with the investigator to determine if such medications can be discontinued. These must be discontinued ≥ 5 days prior to study treatment. Patients do not need to discontinue calcium carbonate. * Patients who are receiving therapeutic doses of anticoagulation, including but not limited to low-molecular weight heparin in therapeutic dosing or platelet aggregation inhibitors. Note: This criterion may be removed by the SRC upon review of the safety data from the initial dose level(s). * Patients with ≥ 5 bone metastases and/or bulky (\> 3cm in diameter) pelvic or femoral tumors, and/or metastases/tumor in the vertebral spine involving \> 3 vertebrae. * Any severe concomitant condition which makes it undesirable for the patient to participate in the study or which could jeopardize compliance with the protocol, in the opinion of the investigator. * Presence of active and uncontrolled infections or other severe concurrent disease, which, in the opinion of the investigator, would place the patient at undue risk or interfere with the study. * Requirement of concurrent use of other anti-cancer treatments or agents other than study medications. Supportive care therapies are permitted.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Disease impact causing changes in Eastern Cooperative Oncology Group (ECOG) Performance scale. | Screening/Baseline, Day1, Day 29, D57 and End of Treatment | Quality of life ( in terms of their ability to care for themself, daily activity, and physical ability (walking, working) is to be evaluated using the ECOG Performance Scale. |
| Safety parameter Dose Limited Toxicity (DLT) | 42 days | Dose level toxicity evaluation using Partial Ordering Bayesian Logistic Regression Model Method (PO-BLRM) |
| Safety parameter Vital signs | 42 days | Frequency of occurrence and severity of abnormal findings in safety investigations regarding the vital signs |
| Safety parameter ECG | 42 days | Frequency of occurrence and severity of abnormal findings in the 12-lead ECG (ECG QT interval) |
| Safety parameter Adverse Events and Treatment-Related Adverse Events | 42 days | Assessment of AEs graded by the Common Terminology Criteria for Adverse Events (CTCAE) Criteria, Version 5.0 |
| Safety parameter Laboratory Examinations | 42 days | Frequency of occurrence and severity of abnormal findings in safety investigations regarding Laboratory examinations |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Tumor objective response rate (ORR) | Every 3 months ± 2 weeks for 12 months after the last 177Lu-TLX250 administration | Tumor response in terms of objective response rate (ORR) (solid tumor tissue response and overall radiological response \[tumor response by RECIST 1.1 and overall radiological response by RECIST 1.1\]) |
| Progression-free survival (PFS) | Every 3 months ± 2 weeks for 12 months after the last 177Lu-TLX250 administration | Progression free survival (PFS) defined as the time from enrollment to disease progression confirmed by radiology, clinical progression or death (whichever comes first) |
| Immunogenicity by formation of ADA(HACA) in blood | 84 days | This outcome will be measured by analyzing the incidence of ADA(HACA) formation in blood on day 1, day 22, Day 43, Day 57 of each cycle (each cycle is 84 days) and at the end of treatment visit. |
| Overall Survival (OS) | Every 3 months ± 2 weeks for 24 months after the last 177Lu-TLX250 administration | Overall Survival (OS), determined from enrollment , until death from any cause |
Countries
Australia
Contacts
Primary ContactMEDICAL DIRECTOR, MD
Outcome results
None listed