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Clinical Trials/NCT05868174
NCT05868174
Recruiting
Phase 1

A Phase 1b Dose Escalation/Expansion Study of the Combination of 177Lu-TLX250 and Peposertib in Patients With Carbonic Anhydrase IX (CAIX)-Expressing Solid Tumors

Telix Pharmaceuticals (Innovations) Pty Limited5 sites in 1 country36 target enrollmentMay 23, 2023

Overview

Phase
Phase 1
Intervention
Not specified
Conditions
Solid Tumor, Adult
Sponsor
Telix Pharmaceuticals (Innovations) Pty Limited
Enrollment
36
Locations
5
Primary Endpoint
Safety parameter Dose Limited Toxicity (DLT)
Status
Recruiting
Last Updated
2 years ago

Overview

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.

Registry
clinicaltrials.gov
Start Date
May 23, 2023
End Date
December 2026
Last Updated
2 years ago
Study Type
Interventional
Study Design
Sequential
Sex
All

Investigators

Sponsor
Telix Pharmaceuticals (Innovations) Pty Limited
Responsible Party
Sponsor

Eligibility Criteria

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
  • 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 CYP2C
  • 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.

Outcomes

Primary Outcomes

Safety parameter Dose Limited Toxicity (DLT)

Time Frame: 42 days

Dose level toxicity evaluation using Partial Ordering Bayesian Logistic Regression Model Method (PO-BLRM)

Disease impact causing changes in Eastern Cooperative Oncology Group (ECOG) Performance scale.

Time Frame: 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 Adverse Events and Treatment-Related Adverse Events

Time Frame: 42 days

Assessment of AEs graded by the Common Terminology Criteria for Adverse Events (CTCAE) Criteria, Version 5.0

Safety parameter Laboratory Examinations

Time Frame: 42 days

Frequency of occurrence and severity of abnormal findings in safety investigations regarding Laboratory examinations

Safety parameter ECG

Time Frame: 42 days

Frequency of occurrence and severity of abnormal findings in the 12-lead ECG (ECG QT interval)

Safety parameter Vital signs

Time Frame: 42 days

Frequency of occurrence and severity of abnormal findings in safety investigations regarding the vital signs

Secondary Outcomes

  • Immunogenicity by formation of ADA(HACA) in blood(84 days)
  • Tumor objective response rate (ORR)(Every 3 months ± 2 weeks for 12 months after the last 177Lu-TLX250 administration)
  • Overall Survival (OS)(Every 3 months ± 2 weeks for 24 months after the last 177Lu-TLX250 administration)
  • Progression-free survival (PFS)(Every 3 months ± 2 weeks for 12 months after the last 177Lu-TLX250 administration)

Study Sites (5)

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