Clinical Trial · NCT06237491

The Safety and Dosimetry Study of 177Lu-LNC1003 Injection

Overview

This proposal is a phase I, open-label study of a 3-Dose Regimen of Escalating Doses of 177Lu-LNC1003 Injection in patients with PSMA-positive mCRPC. In the clinical development, we aim to demonstrate the following: 1. Determination of the therapeutic dose(s) to be used in the expansion phase. 2. Demonstration of the safety and tolerability of 177Lu-LNC1003 at therapeutic doses. The treatment regimen will consist of a single-dose intravenous administration of 177Lu-LNC1003 Injection per 6-week cycle, for a total of 2 cycles. The dose per cycle will be fixed for each patient and will be escalated in 3 different dose levels

Sponsor

Yantai LNC Biotechnology Singapore PTE LTD

Phase

Phase 1

Contacts

A/Prof. Edmund Chiong (CONTACT)

6908 2222

ClinicalTrials.gov

NCT06237491

Drug / Compound

LNC1003

Isotope(s):

Target(s):

PSMA

Ligand Class: Small Molecules

Chelator: DOTA

Eligibility

Inclusion

Patients must have an adequate organ function, in the absence of clinical intervention within 28 days before the administration of the 177Lu-LNC1003, as defined by:Hemoglobin (Hb) \> 9.0g/dL White blood cell (WBC) count ≥ 3 x 109/L or absolute neutrophil count (ANC) \>1.5 x 109/L Platelets ≥ 100 x 109/L International normalized ratio (INR) \<1.5 for patients that are not on warfarin Prothrombin time (PTT) \< 2 x ULN Total bilirubin \<1.5 x ULN Serum albumin \>3.0 g/dL Alanine aminotransferase (ALT) \<3 x ULN, or\<5 x ULN if deemed related to liver metastases from solid tumor Aspartate aminotransferase (AST) \<3 x ULN, or\<5 x ULN if deemed related to liver metastases from solid tumor Creatinine clearance ≥ 60 mL/min (calculated using the Cockcroft-Gault formula).
Sexually active participants with female partners of childbearing potential are eligible to participate if they agree to follow 1 of the following methods of contraception consistently, starting from screening, during the study and for at least 14 weeks after the last dose of 177Lu-LNC1003 Injection:Are abstinent from penile-vaginal intercourse as their usual and preferred lifestyle (abstinent on a long-term and persistent basis) and agree to remain abstinent; Are sterilized (with the appropriate post-vasectomy documentation of the absence of sperm in the ejaculate); Agree to use a male condom and have their partner use a contraceptive method with a failure rate of \< 1% per year as described below when having penile-vaginal intercourse with a woman of childbearing potential who is not currently pregnant, and who agrees to the use of a condom by her partner.
Patients must have at least 1 measurable lesion as defined by Response Criteria in Solid Tumors (RECIST) version 1.1.
Sexually active participants with a pregnant or breastfeeding partner must agree to remain abstinent from penile vaginal intercourse; or use a male condom during each episode of penile penetration during the study.
Patients must have ≥ 1 metastatic lesion present on baseline and documented progressive mCRPC based on the Prostate Cancer Working Group 3 (PCWG3) criteria; patients must fill at least one of the following criteria:
Patients must have a castrate level of serum/plasma testosterone (\< 50 ng/dL or \< 1.7 nmol/L).
Patients must have received treatment with at least one prior novel androgen receptor pathway inhibitor (such as enzalutamide, apalutamide, and/or abiraterone).
Patients must be 68Ga-PSMA-11 PET/CT scan positive.
Patients must have an Eastern Cooperative Oncology Group performance status (ECOG PS) score of 0 or 1.
Patients must have histological, pathological, and/or cytological confirmation of PC that is refractory to or has progressed following prior treatments.
Objective radiographic progression in soft tissue
PSA progression
Patients must have been deemed not suitable for chemotherapy, i.e., the patient refused chemotherapy or was judged unsuitable for chemotherapy by the doctor. Alternatively, patients may have been previously treated with at least one, but no more than two previous taxane regimens, or have been offered, but declined, or been ineligible for taxane-based chemotherapy. A taxane regimen is defined as a minimum exposure of 2 cycles of a taxane. If a patient has received only one taxane regimen, the patient is eligible if: a. The patient\'s physician deems him unsuitable to receive a second taxane regimen (e.g., frailty assessed by geriatric or health status evaluation, intolerance, etc.).
New bone lesions
Participants must agree to refrain from donating sperm starting from Screening, during the study and for at least 14 weeks after the last dose of 177Lu-LNC1003 Injection.
All other toxicity parameters, except for alopecia, must be NCI-CTCAE v.5.0 Grade 0 or 1.
Patients must have the ability to understand and comply with all protocol requirements.

Exclusion

Transfusion for the sole purpose of making a subject eligible for study inclusion
Clinically significant abnormalities on electrocardiogram (ECG) at screening including QTcF \> 470 ms, and subjects who cannot tolerate high volume load.
History of allergic reactions attributed to compounds of similar chemical or biologic composition to 177Lu-LNC1003 as assessed from medical records
Prior external beam radiation therapy involving \> 25% of the bone marrow
Unmanageable urinary incontinence including physical outflow obstructions rendering the administration of 177Lu-LNC1003 unsafe.
Life expectancy \< 6 months as assessed by the treating physician
Unable to comply with relevant contact precautions post 177Lu-LNC1003 treatment.
Active and clinically significant bacterial, fungal, or viral infections, including hepatitis B (HBV), hepatitis C (HCV), know human immunodeficiency virus (HIV), or acquired immunodeficiency syndrome (AIDS)-related illness (patients with treated HIV and hepatitis B or C could be included)
A superscan; i.e., very high ratio of bone to background uptake due to high osteoblastic activity, as seen in the baseline Tc-99m diphosphonate bone scan.
Uncontrolled diabetes mellitus as defined by a HbA1c \> 9%
Other serious illness(es) involving the cardiac, respiratory, CNS, renal, hepatic or hematological organ systems which might preclude completion of this study or interfere with determination of causality of any adverse effects experienced in this study
Previous treatment with any of the following within 6 months before enrollment: Strontium-89, Samarium-153, Rhenium-186, Rhenium-188, Radium-223, hemi-body irradiation, 177Lu-PSMA-617 (Pluvicto) and any investigational beta-emitting radiotherapeutics.
Any other condition, assessed by the investigator, that may increase the risk associated with study participation, interfere with the study interpretation, or in any other way make the subject unsuitable for participation in the study.
Any systemic anti-cancer therapy (e.g. PSMA-targeted radioligand therapy, chemotherapy, immunotherapy or biological therapy \[including monoclonal antibodies\]) within 28 days prior to day of enrollment
Any investigational agents within 28 days of enrollment
Other concurrent cytotoxic chemotherapy, immunotherapy, radioligand therapy, or investigational therapy
Participants who have not fully recovered from major surgery or significant traumatic injury prior to the first dose of study drug or expects to have major surgery during the study period or within 3 months after the last dose of study drug