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
- Phase
- Phase 1
- Intervention
- Lutetium [177Lu]-FAP-75
- Conditions
- Solid Tumors
- Sponsor
- Fudan University
- Enrollment
- 50
- Locations
- 1
- Primary Endpoint
- Dose Limiting Toxicity(DLT)
- Status
- Not Yet Recruiting
- Last Updated
- last year
Overview
Brief Summary
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.
Investigators
Xian-Jun Yu
Professor
Fudan University
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;
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.
Arms & Interventions
treatment group
Lutetium \[177Lu\]-FAP-75 accumulates at the tumor site, and beta rays act on surrounding tumor cells, causing tumor cell apoptosis.
Intervention: Lutetium [177Lu]-FAP-75
Outcomes
Primary Outcomes
Dose Limiting Toxicity(DLT)
Time Frame: within 6 weeks from the first drug administration
Dose Limiting Toxicity are assessed by NCI-CTCAE v5.0
Adverse events(AEs)
Time Frame: From the first drug administration to within 90 days for the last drugs dose
AEs , are assessed by NCI-CTCAE v5.0
Second-stage dose
Time Frame: through study completion, an average of 1 year
Second-stage dose is the recommend dose for the second stage of this trial which is determined by the safety profile of the first stage of this trial.
Overall Response Rate(ORR)
Time Frame: Up to approximately 12 months
Evaluated by RECIST1.1
Secondary Outcomes
- Disease Control Rate(DCR)(Up to approximately 12 months)
- Radiation dosimetry(Up to 6 weeks)
- Overall survival(OS)(Up to approximately 12 months)
- Duration of Response(DoR)(Up to approximately 12 months)
- Progression free survival (PFS)(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)