Phase 3 Study to Assess Safety and Efficacy of 177Lu-TLX250 in Advanced Relapsed or Recurrent ccRCC
PHASE3RECRUITING
Multicenter Phase 3 study of 177Lu-TLX250 in adult participants with CAIX-expressing advanced, relapsed or recurrent clear cell renal cell carcinoma (ccRCC). Part 1 will evaluate two dosing regimens to determine the recommended Phase 3 dose (RP3D). Part 2 will compare 177Lu-TLX250 with investigator's choice of monotherapy aligned with Australian standard-of-care.
Study details:
This is a randomized, open-label, multi-center 3 study evaluating the safety and efficacy of 177Lu-TLX250, a CAIX-targeting radioligand therapy, in adult participants with advanced, relapsed or recurrent clear cell renal cell carcinoma (ccRCC). The study consists of two parts:. • Part 1 (Phase 2a - Dose Optimization): Participants will be randomized to receive one of two dosing regimens of 177Lu-TLX250.
The objective of Part 1 is to determine the recommended Phase 3 dose (RP3D) for use in Part 2.
Eligibility criteria
Researchers look for people who fit a certain description, called eligibility criteria. See if you qualify.
Inclusion criteria
- be aged ≥ 18 years.
- have provided written informed consent, dated and signed by the participant prior to any study-specific procedure;
- have relapsed or recurrent, locally advanced, or metastatic RCC with histologically or cytologically confirmed diagnosis of RCC with clear cell component per American Joint Committee on Cancer Staging Manual (Edge SB et al., 2017), with or without sarcomatoid features;
- have received at least 2 and no more than 3 prior lines of systemic therapies for locally advanced or metastatic ccRCC including a PD-1/PD-L1 inhibitor (at least 2 administrations) and a VEGF/VEGFR-targeting agent (including TKI or mAb) in sequence or in combination;
- have had radiographic disease progression occurring during or after the most recent line of therapy or intolerance to most recent line of therapy;
- have at least one measurable lesion according to RECIST, version 1.1. Lesions situated in a previously irradiated area are considered measurable if progression has been demonstrated in such lesions;
- be CAIX-positive at Screening defined as having at least 1 lesion with a tumor-lesion CAIX ratio of the maximum standardized uptake value (SUVmax) to liver mean standardized uptake value (SUVmean) ≥ 1.5 as determined by BICR of 89Zr-TLX250 PET outcomes;
- have an Eastern Cooperative Oncology Group (ECOG) Performance Status of 0 to 1;
- have recovered from the AEs related to prior lines of therapy or returned to baseline with the exception of Grade 2 neurotoxicity. Ongoing, controlled AEs, such as hypothyroidism or hypertension, are permitted;
- have adequate organ function, defined as Bone Marrow: leukocytes ≥ 3,000/µL; absolute neutrophil count ≥ 1500/µL (administration of granulocyte colony stimulating factor is not allowed within 4 weeks prior to the first administration of 177Lu-TLX250; platelets ≥ 100,000/µL (platelet transfusion is not allowed within 4 weeks prior to the first administration of 177Lu-TLX250); and hemoglobin ≥ 9g/dL (red blood cell transfusion is not allowed within 2 weeks prior to the first administration of 177Lu-TLX250). Liver Function: total bilirubin ≤ 1.5 × the upper limit of normal (ULN). For patients with known Gilbert's Syndrome ≤ 3 × ULN is permitted; and alanine aminotransferase (ALT) and aspartate aminotransferase (AST) ≤ 2.5 × ULN or ≤ 5.0 × ULN for participants with liver metastases. Renal Function: creatinine clearance ≥ 40 mL/min as measured by Cockroft-Gault formula or directly calculated by 24h urine; have negative pregnancy test for women of childbearing potential (serum);
Exclusion criteria
- have any of the following: visceral metastatic lesions that are ≥ 1 cm that have a CAIX TLR < 1; lytic bone metastatic lesions with a soft tissue component of at least 1 cm with a TLR < 1; and/or at least one metastatic lymph node lesion with short axis ≥ 2.5 cm with a TLR <1;
- received prior 177Lu-TLX250 therapy, any other radioligand therapy, or any prior CAIX-targeting therapy;
- have any known hypersensitivity to compounds of similar chemical or biologic composition to girentuximab, DFO or DOTA linker, zirconium or lutetium, and/or any excipient in the study drug or radiographic contrast-agents;
- has received G-CSF or erythropoietin within 4 weeks prior to laboratory evaluations at Screening;
- be currently receiving or have received any radionuclide within 10 half-lives of the radionuclide prior to 89Zr-TLX250 administration;
- any type of systemic anticancer therapy within 2 weeks before the first administration of 177Lu-TLX250;
- prior radiotherapy within 2 weeks prior to the first administration of 177Lu-TLX250 (must have recovered from all radiation-related toxicities and not currently require steroid treatment); and/or prior palliative radiation (≤2 weeks of radiotherapy) within 1-week of the first administration of 177Lu-TLX250 for non-central nervous system disease; NOTE: If the investigator feels that the patient is continuing to receive some clinical benefit from standard-of-care (SOC) therapy, the patient may continue SOC therapy up until 2 weeks prior to dosing with 177Lu-TLX250.
- have known brain metastases, unless these have been treated and stabilized for at least 4 weeks prior to the first administration of 177Lu-TLX250; Note: Participants with a history of brain metastases must have either a head CT with contrast-or brain MRI performed at Screening to document stable disease prior to the first administration of 177LuTLX250.
- Have experienced any major trauma including major surgery (such as abdominal/ cardiac/thoracic surgery) within 3 weeks of administration of the first administration of 177LuTLX250;
- be pregnant or intend to become pregnant, breastfeed, or conceive a child during the study period and for at least 42 days after last administration of 89Zr-TLX250 or 6 months after last administration of 177Lu-TLX250, depending on which study drug is administered last to the respective participant;
- Note: Contraceptive use should be consistent with local regulations regarding the methods of contraception for those participating in clinical studies (see Appendix 10.4).
- be planning to breastfeed during the study period and for 28 days after last administration of 89ZrTLX250 or 75 days after last administration of 177Lu-TLX250, depending on which study drug is administered last to the respective participant;
- have active and uncontrolled infections requiring systemic therapy or other severe concurrent disease, which, in the opinion of the investigator, would place the participant at undue risk or interfere with the study;
- have a history of concurrent malignancy with a life expectancy of ≤ 2 years or requirement of systemic anti-cancer therapy or requirement of local therapy that would confound study results; however; participants with the following malignancies can be enrolled into the study: basal cell or squamous cell carcinoma of the skin; carcinoma in situ of the cervix, breast or bladder; and/or incidental histologic finding of prostate cancer;
- have a serious, non-healing wound, ulcer, or bone fracture;
- be unable to stay in the scanner bed with the arms resting out of the thoracic and abdominal fields (i.e., arms alongside the body or raised arm position) for the duration of the scan;
- have not had resolution of clinically significant toxic effects of prior systemic cancer therapy, surgery, or radiotherapy to Grade ≤1 (except for laboratory parameters specified above, Grade 2 alopecia, and/or stable Grade 2 sensory neuropathy, according to National Cancer Institute Common Terminology Criteria for Adverse Events (NCI-CTCAE) v5.0;
- have inflammatory bowel disease (e.g. Crohn's disease, ulcerative colitis, etc.);
- have a life expectancy shorter than 3 months;
- have bleeding or thrombotic disorders or subjects at risk for severe hemorrhage;
- have experienced any clinically significant bleeding, including hemoptysis or tumor bleeding within 2 weeks prior to the first administration of 177Lu-TLX250;
- has evidence of a serious active or sub-clinical infection or angina pectoris (New York Heart Association [NYHA] Class III or IV), significantly prolonged QT interval or other serious illness(es) involving the cardiac, respiratory, central nervous system, renal, hepatic or hematological organ systems, that might impair the ability to complete this study or could interfere with determination of causality of any adverse effects experienced in this study, or which require treatment that could interact with study treatment;
- have any medical or other condition that in the opinion of the investigator(s) would preclude the subject's participation in a clinical study.
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
- PHASE3
Study ID
NCT07197580
Intervention or treatment
RADIATION: 177Lu-TLX250
Conditions
- ccRCC
- Renal Cell Carcinoma (Kidney Cancer)
- Renal Cell Carcinoma (RCC)
- Renal Cell Cancer Metastatic
- Renal Cell Cancer, Recurrent
- Clear Cell Renal Cell Cancer (ccRCC)
You may be eligible to participate in this trial based on your search. Check eligibility by answering some questions.
Research sites nearby
Closest Location:
Austin Health
Select from list below to view details:
Austin Health
Heidelberg, Victoria, Australia
Melbourne Theranostic Innovation Centre (MTIC)
Melbourne N., Victoria, Australia
GenesisCare, Fiona Stanley Hospital (Murdoch)
Murdoch, Washington, Australia
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Who is running the clinical trial?
TP(PL
Telix Pharmaceuticals (Innovations) Pty Limited
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: 1887MBq 177Lu-girentuximab tetraxetan
| Radiation: 177Lu-TLX250 |
EXPERIMENTAL: 1258 MBq 177Lu-girentuximab tetraxetan
| Radiation: 177Lu-TLX250 |
What is the study measuring?
Primary Outcome
| Measure | Description | Time Frame |
|---|---|---|
| Dose Optimization -safety and tolerability | Part 1 of the study is being done to identify the best dose to use for Part 2 of the study. Assessing adverse events of special interest (AESIs), incidence and severity of treatment-emergent adverse events (TEAEs) and frequency, severity according to National Cancer Institute Common Terminology Criteria for Adverse Events (NCI CTCAE) V5.0, seriousness, and relationship of study treatment will be assessed. Laboratory abnormalities will be assessed according to the NCI CTCAE V5.0. | Through study completion, an average of 1.5 years |
| Efficacy- median mPFS | Primary objective for Part 2 of the study and secondary objective for Part 1. Monitoring disease progression according to Response Evaluation Criteria in Solid Tumors, version 1.1 (RECIST 1.1). | Through study completion, an average of 2 years |
Secondary Outcome
| Measure | Description | Time Frame |
|---|---|---|
| Monitoring OS (Overall Survival) | Time from the date of randomization to death from any cause | Through study completion, an average of 2 years |
| Monitoring ORR (Objective Response Rate) | Proportion of participants achieving confirmed objective response rate (ORR), i.e., complete response (CR) or partial response (PR) per Response Evaluation Criteria in Solid Tumors, version 1.1 (RECIST 1.1) as assessed by a blinded independent central review (BICR) | Through study completion, an average of 2 years |
| Monitoring DoR (Duration of Response) | Time from the first documentation of objective response, i.e., complete response (CR) or partial response (PR) to the first documentation of disease progression or death due to any cause as assessed by blinded independent central review (BICR) | Through study completion, an average of 2 years |
| Monitoring DCR (Disease control Rate) | The proportion of participants achieving confirmed objective response, i.e., complete response (CR), partial response (PR), or stable disease (SD) per Response Evaluation Criteria in Solid Tumors, version 1.1 (RECIST 1.1) as assessed by blinded independent central review (BICR) | Through study completion, an average of 2 years |
| Evaluate blood radioactive PK parameter- Cmax (maximum plasma concentration) | Gamma-counting blood radioactivity will be used to derive this pharmacokinetics parameter | Treatment period (4 months) |
| Evaluate blood radioactive PK parameter- AUCinf (area under blood concentration time curve from zero to infinity) | Gamma-counting blood radioactivity will be used to derive this pharmacokinetics parameter. | During Treatment (4 months) |
| Evaluate blood radioactive PK parameter- t1/2 (Terminal half-life) | Gamma-counting blood radioactivity will be used to derive this pharmacokinetics parameter. | During Treatment (4 months) |
| Evaluate blood radioactive PK parameter- CL (Clearance) | Gamma-counting blood radioactivity will be used to derive this pharmacokinetics parameter. | During Treatment (4 months) |
| Tumor and Organ-specific 177Lu-TLX250 absorbed radiation values | Images-radiation values for tumor and lesions will be measured and analyzed after first and second administration of 177Lu-TLX250. | During Treatment (4 months) |
| TAC for tumor and organ | Time Activity Curves (TAC) will be used to derive time integrated activity parameters in tumor and organ | During Treatment (4 months) |
| Tumor- and organ-specific 177Lu-TLX250 residence time | Residence time of 177Lu-TLX250 in tumor and organs will be derived and interpreted | During Treatment (4 months) |
| Identification of dose-limiting organ(s) | Absorbed dose will be compared to maximal dosimetry threshold for each organ to evaluated the dose limiting organ | During Treatment (4 months) |
| Characterize health utility as measured using the European Quality of Life 5 Dimensions 5 Level Version (EuroQoL EQ-5D-5L) | Health utility scores from the European Quality of Life 5 Dimensions 5 Level Version (EuroQoL EQ-5D-5L) questionnaire | Through study completion, an average of 2 years |
| Change from Baseline in EORTC QLQ-C30 Physical Functioning | Assessed using the EORTC QLQ-C30 questionnaire to evaluate physical functioning. | Through study completion, an average of 2 years |
| Change from Baseline in EORTC QLQ-C30 Global Health Status/HRQoL | Assessed using the EORTC QLQ-C30 questionnaire to evaluate overall health-related quality of life. | Through study completion, an average of 2 years |
| Change from Baseline in FKSI-DRS Subscale | Assessed using the FKSI-DRS (Functional Assessment of Cancer Therapy - Kidney Symptom Index) to evaluate disease-related symptoms. | Through study completion, an average of 2 years |
| Incidence and Severity of AESIs and TEAEs | Adverse events will be assessed and graded per NCI-CTCAE v5.0 criteria. | Through study completion, an average of 2 years |
| Dosing Delays Due to 177Lu-TLX250-Related TEAEs | Number of dosing delays attributed to TEAEs related to 177Lu-TLX250. | Through study completion, an average of 2 years |
| Activity Level Reductions Due to 177Lu-TLX250-Related TEAEs | Number of participants with reduced activity levels due to TEAEs related to 177Lu-TLX250. | Through study completion, an average of 2 years |
| Evaluation of Immunogenicity (HACA) | Incidence of HACA positivity, overall per treatment group, and per visit (to track incidence over time) | Through study completion, an average of 2 years |
| Evaluation of HACA on PK/Biodistribution | Evaluate any correlation of incidence of HACA positivity to changes in PK/Biodistribution per treatment group | Through study completion, an average of 2 years |
| Evaluation of HACA on efficacy/safety | Evaluate any correlation of incidence of HACA positivity to changes in efficacy/safety end points per treatment group | Through study completion, an average of 2 years |
| Characterization of HACA neutralizing activity | For confirmed positive HACA samples, incidence of nAb positivity, overall per treatment group, and per visit (to track incidence over time), as applicable | Through study completion, an average of 2 years |
| Evaluation of nAb on PK/Biodistribution | Evaluate any correlation of incidence of nAb positivity to changes in PK/Biodistribution per treatment group | Through study completion, an average of 2 years |
| Evaluation of nAB on efficacy/safety | Evaluate any correlation of incidence of nAb positivity to changes in efficacy/safety end points per treatment group | Through study completion, an average of 2 years |
| Evaluate Radiation Exposure-Response parameter- normalized absorbed dose to individual organs (mGy/MBq) | Evaluate relationship between normalized absorbed dose to individual organs with DCR, ORR and incidence and severity of AESI | Through study completion, an average of 2 years |
| Evaluate Radiation Exposure-Response parameter- AUC | Evaluate relationship between AUC to individual organs with DCR, ORR and incidence and severity of AESI. | Through study completion, an average of 2 years |
| Evaluate Radiation Exposure-Response parameter- Cmax | Evaluate relationship between Cmax to individual organs with DCR, ORR and incidence and severity of AESI. | Through study completion, an average of 2 years |
| Evaluate Radiation Exposure-Response parameter- normalized absorbed dose to tumors (mGy/MBq) | Evaluate relationship between normalized absorbed dose to tumor with DCR, ORR and incidence and severity of AESI. | Through study completion, an average of 2 years |
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References
Clinical Trials Gov: Phase 3 Study to Assess Safety and Efficacy of 177Lu-TLX250 in Advanced Relapsed or Recurrent ccRCCOther trials to consider
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