Phase II Clinical Study of LTC004 in Patients With Advanced Sarcoma

Trial Title: Phase II Clinical Study of LTC004 in Patients With Advanced Sarcoma

NCT ID: NCT06384248

Condition: Unresectable or Metastatic Sarcoma

Conditions: Official terms:
Sarcoma

Study type: Interventional

Study phase: Phase 1/Phase 2

Overall status: Not yet recruiting

Study design:

Allocation: Non-Randomized

Intervention model: Single Group Assignment

Primary purpose: Treatment

Masking: None (Open Label)

Intervention:

Intervention type: Drug
Intervention name: LTC004
Description: LTC004,45μg/kg,IV,Day 1,Q3W;
Arm group label: PHASE 1
Arm group label: PHASE 2

Summary: This is a phase II clinical study to evaluate the safety, tolerability and preliminary antitumor activity of LTC004 in patients with locally advanced or metastatic sarcoma；Enrollment of 10 evaluable subjects in Phase I. If ≥2 subjects experience objective remission or SD lasting >12 weeks, proceed to Phase II to enroll an additional 20 evaluable subjects to further evaluation of the safety and efficacy of LTC004

Criteria for eligibility:
Criteria:
Inclusion Criteria: 1. Aged 18 to 75 years； 2. Subjects with histologically or cytologically confirmed non-surgically treatable and failed standard therapy recommended by existing clinical standards of care or guidelines at screening (PD during treatment or PD after final treatment), or locally advanced or metastatic sarcoma that cannot tolerate standard therapy and/or for which there is currently no effective standard therapy (if recurrence or metastasis occurs during adjuvant therapy or within 6 months of completion, adjuvant therapy is considered a first-line treatment failure). Note: Embryonal rhabdomyosarcoma, follicular rhabdomyosarcoma, Ewing's sarcoma/primitive neuroectodermal tumor, gastrointestinal mesenchymal tumors, and malignant mesothelioma should be excluded. 3. At least one measurable tumor lesion based on RECIST V1.1 criteria； 4. ECOG PS ≤1； 5. Expected survival ≥12 weeks； 6. Adequate organ function； 7. Patients, both females and males, of reproductive potential must agree to use adequate contraception during and for 6 months after the last infusion of LTC004. 8. Patients who have received any chemotherapy or anti-tumor monoclonal antibody drugs within 4 weeks prior to the first dose of study drug (excluding mitomycin and nitrosoureas within 6 weeks prior to the first dose of study drug）; small molecule targeted drugs within 2 weeks prior to the first dose of study drug; Chinese medicine therapy (Chinese medicine therapy with clear anti-tumor indications in the package insert ）within 4 weeks prior to the first dose of study drug； 9. Understands and provides written informed consent and willing to follow the requirements specified in protocol. Exclusion Criteria: 1. History of severe hypersensitivity reactions to other mAbs. 2. Untreated, unstable or uncontrolled central nervous system (CNS) metastases with following exceptions:A. Clinically stable MRI scans and no progressive or uncontrolled neurologic symptoms or signs for at least 4 weeks prior to the first study treatment; 3. Patients with untreated or clinically symptomatic spinal cord compression that has not been controlled. 4. Patients with uncontrolled pleural effusion, pericardial effusion or abdominal effusion as judged by the investigator at screening; 5. Previous immunotherapy, including IL-2, IL-15, PD-1/L1 inhibitors, NK, and TCR-T cell therapy. 6. ≥2 malignant tumors within 5 years prior to first dose of drug； 7. Moderate to severe dyspnea at rest, severe primary lung disease, current need for continuous oxygen therapy, or clinically active interstitial lung disease (ILD) or pneumonia due to advanced cancer or its complications; Grade ≥3 interstitial pneumonia during prior antineoplastic therapy； 8. Presence of severe infection within 4 weeks prior to first dose of medication，Presence of active infection requiring systemic antibiotic therapy with CTCAE grade ≥2 within 2 weeks prior to first dose 9. History of serious cardiovascular disease； 10. Active hepatitis B; hepatitis C infection; syphilis infection, active tuberculosis; 11. Patients with active, or previous autoimmune disease with potential for recurrence; 12. Immunodeficiency diseases or history of such diseases, including a positive serologic test for human immunodeficiency virus (HIV) 13. Arterial/venous thrombotic events within 6 months prior to the first dose of the drug; 14. Those who received radical radiation therapy within 4 weeks prior to the first dose and those who received palliative radiation within 14 days prior to the first dose. 15. Received other unlisted clinical investigational drug or treatment within 4 weeks prior to first dose. 16. Use of live or attenuated vaccines within 4 weeks prior to the first dose, or anticipated need for live or attenuated vaccines during the study period； 17. Major surgery (other than surgery for diagnostic purposes) within 4 weeks prior to the first dose, anticipation of major surgery (other than surgery for diagnostic purposes) during the study period, or diagnostic or low-invasive surgery within 7 days prior to the first dose (excluded for puncture biopsies). 18. Tumor invasion into peripheral vital organs (e.g., aorta and trachea) or risk of esophageal-tracheal fistula or esophageal-pleural fistula; history of gastrointestinal perforation and/or fistula within 6 months prior to the first dose of the drug； 19. Adverse effects of prior antitumor therapy have not recovered to CTCAE version 5.0 grade rating ≤1； 20. Patients who have received a previous allogeneic bone marrow/hematopoietic stem cell transplant or solid organ transplant； 21. Pregnant and lactating women； 22. Subjects who in the judgment of the investigator, have a history of other serious systemic disease or are unfit to participate in this trial for any other reason (the presence of psychiatric disorders in the patient that may affect compliance with the trial, alcohol, drug or substance abuse, etc.)

Gender: All

Minimum age: 18 Years

Maximum age: 75 Years

Healthy volunteers: No

Start date: April 26, 2024

Completion date: December 28, 2025

Lead sponsor:
Agency: Letolab
Agency class: Industry

Source: Letolab

Record processing date: ClinicalTrials.gov processed this data on November 12, 2024

Source: ClinicalTrials.gov page: https://clinicaltrials.gov/ct2/show/NCT06384248