A Clinial Trial of Lutetium [177Lu]-FAP-75 for the Treatment of Patients With Advanced Solid Tumors

Official title

A Clinical Trial on Pharmacokinetics and Radiation Dosimetry, Safety and Preliminary Efficacy Evaluation of Lutetium [177Lu]-FAP-75 for the Treatment of Patients With Advanced Solid Tumors

Overview

To explore the safety, tolerability, initial efficacy, pharmacokinetic profile and radiation dosimetry of lutetium \[177Lu\]-FAP-75 in the treatment of patients with advanced solid tumors.

Detailed description

This is a prospective, open, dose-exploring clinical study of Lutetium \[177Lu\]-FAP-75 in the treatment of patients with advanced solid tumors. The study was divided into two stages, the first stage was dose exploration study, and the second stage was case expansion study. In the first phase of this study, several dose groups were designed. Subjects may receive only one of these doses and may not receive multiple doses in the same subject. The drug was administered every 6 weeks, and the DLT observation period was 6 weeks after the first dose. Firstly, the first dose safety introduction of human body was carried out. Based on the results of the preclinical study of this product, an appropriate number of enrolled subjects in the first and second stages were selected to enter the PK and radiation dosimetry detection groups. After the end of the DLT observation period, subjects who met the criteria for continued dosing were allowed to continue to receive the investigational drug therapy for subsequent cycles. For all participants enrolled in this study, the study process included a screening period, a treatment period and a follow-up period. In the course of the trial, extended studies of other tumor species can be conducted based on new advances and results of clinical studies of similar drugs to further explore the safety, tolerability and initial effectiveness of specific tumor types.

Interventions

• Drug Lutetium [177Lu]-FAP-75
  Lutetium \[177Lu\]-FAP-75 will be administrated per dose level in which the patients are assigned.

Primary outcome measures

• Overall Response Rate(ORR) [Time frame: Up to approximately 12 months]
• Adverse events(AEs) [Time frame: From the first drug administration to within 90 days for the last drugs dose]
• Dose Limiting Toxicity(DLT) [Time frame: within 6 weeks from the first drug administration]
• Second-stage dose [Time frame: through study completion, an average of 1 year]

Secondary outcome measures (5)

• Overall survival(OS) [Time frame: Up to approximately 12 months]
• Disease Control Rate(DCR) [Time frame: Up to approximately 12 months]
• Duration of Response(DoR) [Time frame: Up to approximately 12 months]
• Progression free survival (PFS) [Time frame: From date of randomization until the date of first documented progression or date of death from any cause, whichever came first, assessed up to 12 months]
• Radiation dosimetry [Time frame: Up to 6 weeks]

Eligibility criteria

Inclusion criteria

• Voluntarily participate in the clinical trial, understand the research procedure and be able to sign the informed consent in person;
• Age 18-80 years old (including 18 and 80 years old), gender is not limited;
• ECOG score 0-1;
• The expected survival period is not less than 4 months;
• Subjects with solid tumors diagnosed histologically or cytologically at advanced stage (unresectable or metastatic) after failure of standard treatment (disease progression or intolerance) or lack of effective treatment are enrolled in this study.
• There must be at least one measurable target lesion (according to RECIST V1.1);
• Positive lesion uptake in FAP PET/CT imaging
• The level of vital organ function meets the following requirements :

• Neutrophil ≥1.5×109/L;
• Platelets ≥100×109/L;
• Hemoglobin ≥90g/L;
• Total bilirubin ≤1.5×ULN; If there is biliary obstruction or Gilbert syndrome, total bilirubin ≤3×ULN;
• ALT and AST≤3 x ULN; If liver metastasis exists, ALT and AST≤5×ULN;
• Serum albumin ≥30g/L;
• Serum creatinine ≤1.5×ULN or creatinine clearance ≥60 ml/min (calculated according to Cockcroft-Gault formula);
• INR≤1.5×ULN and APTT≤1.5×ULN (for subjects not receiving anticoagulant therapy, stable therapy dose is required for subjects receiving anticoagulant therapy).
• Women of childbearing age must undergo a blood pregnancy test within 72 hours before the first dosing, must be non-lactating.

Exclusion criteria

• Known significant weight loss (>10%) within 28 days prior to signing the informed consent.
• Prior and follow-up treatment:

• Received any radionuclide therapy or radiotherapy within 6 months before enrollment.
• Prior treatment with any FAP target nuclide.
• Received anti-tumor therapy such as surgery (except diagnostic biopsy and drainage of serosal effusion), chemotherapy, immunotherapy, and monoclonal antibodies within 4 weeks prior to admission; received anti-tumor endocrine drugs within 2 weeks; received nitrosourea or mitomycin chemotherapy within 6 weeks; eluted oral targeted therapy drugs with less than 5 half-lives or 4 weeks (whichever is shorter).
• Received any other investigational drug treatment within 4 weeks prior to enrollment.
• Any surgical procedures requiring general anesthesia and significant incisions (e.g., central venous access, percutaneous feeding tube insertion) within 6 weeks of enrollment (expected surgery).
• Combined with the following diseases:

• Patients with meningeal metastasis or diffuse central nervous system metastasis or active central nervous system metastasis who require any radiotherapy, gamma knife, surgery, or medication to control the symptoms of metastasis 1 month prior to screening are excluded. Patients with a limited number of stable central nervous system metastases could be enrolled.
• severe urinary incontinence, hydronephrosis, and severe urination dysfunction. Note: Subjects with bladder outflow tract obstruction that can be controlled with the best available standard of care are eligible for study participation.
• Co-active hepatitis B, hepatitis C.
• Known to have acquired immune deficiency syndrome (AIDS) or tested positive for HIV.
• Active syphilis infection.
• Known allergy to components of the investigatory drug or its analogues.
• Malignancies outside the target tumor species that are expected to alter life expectancy or may interfere with disease assessment within the first 5 years of enrollment. The exception is for cured malignancies with a low risk of metastasis and death, such as non-metastatic skin basal cell carcinoma or skin superficial squamous cell carcinoma.
• Serious infections occurred within 4 weeks prior to enrollment, such as severe pneumonia requiring hospitalization, bacteremia, infection complications, etc., and signs and symptoms of infection within 2 weeks prior to enrollment requiring intravenous antibiotic treatment (except for prophylactic antibiotic use).

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation

N/A

Model

Single group

Masking

Open label

Primary purpose

Treatment

Study locations

China · 1 center

• Department of Pancreatic Surgery, Fudan University Shanghai Cancer Center;Pancreatic Cance — Shanghai

Identifiers

NCT: NCT06553846 · [177Lu]-FAP-75-001

Primary sources (government registries)

• ClinicalTrials.gov (US NIH)

View this study on ClinicalTrials.gov ↗