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NCT05366478RecruitingPhase 1

A Clinical Study of LM103 Injection in the Treatment of Advanced Solid Tumors

A Single-Arm, Open-Label, Exploratory Study to Evaluate Safety and Efficacy of LM103 Injection in the Treatment of Advanced Solid Tumors

Source: ClinicalTrials.gov · Last updated 2 Aug 2022 · Not updated for over 12 months - ask the site whether it is still open

Brief summary (registry, in English)

This is a single-arm, open-label, exploratory study to evaluate safety and efficacy of LM103 Injection in patients with advanced solid tumors. The purpose of this study is to evaluate the safety and tolerability, antitumor activity and immunoreactivity.

Status (registry)
Recruiting
Phase (registry)
Phase 1
Study type
Interventional
Enrollment
15 (estimated)
First submitted
5 May 2022
Start date
30 May 2022
Primary completion date
30 May 2024
Lead sponsor
Suzhou BlueHorse Therapeutics Co., Ltd.
NCT number
NCT05366478

What you commit to

  • Study type: Interventional · Phase 1
  • Planned participants: 15
  • From 30 May 2022 to the primary completion date, 30 May 2024
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Suffering from active or previous autoimmune diseases ;
  • Requires systemic steroid therapy;

Other illness

  • Severe liver and kidney dysfunction, severe heart disease, coagulation dysfunction, and hematopoietic dysfunction;
  • Combined with severe infection or persistent infection and cannot be effectively controlled;
  • Positive for hepatitis B surface antigen (HBsAg) or hepatitis B core antibody (HbcAb); positive for hepatitis C virus (HCV) antibody; positive for human immunodeficiency virus (HIV) antibody; positive for syphilis;

Other

  • Central nervous system metastasis and/or cancerous meningitis;
  • With uncontrolled pleural effusion, pericardial effusion or ascites requiring repeated drainage;

Who the study is looking for

  • AJCC (V8) stage III or IV melanoma, non-small cell lung cancer, cervical cancer and other solid tumors (confirmed by histology) for which existing treatment is ineffective or without standard treatment;
  • The patient has residual lesions that can be used for surgical resection (\>1.5cm3) or biopsy (\>1.5cm3) and measurable after resection for TIL collection and efficacy evaluation;
  • Laboratory inspection index requirements:
    • Blood routine: lymphocyte ratio \> 20%; neutrophil count \> 1.0 × 10\^9/L; white blood cells \> 3.0 × 10\^9/L; platelets \> 100 × 10\^9/L; hemoglobin \> 80 g/ L;
    • Liver function: alanine aminotransferase (ALT) and aspartate aminotransferase (AST) ≤ upper limit of normal x 2.5, if there is liver metastasis ≤ upper limit of normal x 5; alkaline phosphatase (ALP) ≤ upper limit of normal x 2.5; total gallbladder Red pigment (TBIL)≤normal upper limit×1.5;
    • Renal function: urea ≤ upper limit of normal × 1.5; creatinine (Cr) ≤ upper limit of normal × 1.5;
  • Left ventricular ejection fraction (LVEF) ≥ 50%;
  • ECOG physical condition is 0 or 1;
  • The expected survival time is more than 3 months;

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Tianjin Beichen Hospital
Coordinator of this site? Confirm its status
TianjinChinaRecruiting

Related publications

This page is information, not medical advice. Discuss any trial with your doctor.