A Clinical Trial Evaluating Injection of TQB6411 in Subjects With Advanced Malignant Tumors

NCT07043751
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Phase
Phase 1
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Recruitment status
Recruiting
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Participants
216
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Lead sponsor
Chia Tai Tianqing Pharmaceutical Group Nanjing Shunxin Pharmaceutical Co., Ltd.
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Start date
2025-07-15
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Number of sites
19
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Summary
TQB6411 for injection is an antibody-conjugated drug (ADC) targeting EGFR/c-Met. After injecting blood intravenously, the antibody part of this product binds to the surface of EGFR and c-Met on tumor cells to block the activation of EGFR and c-Met signaling pathways. The ADC is enzymatically transported to the lysosome. The linker releases toxins after enzyme cleavage, resulting in DNA damage and cell death. TQB6411 for injection is intended for the treatment of advanced malignant tumors.
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Short title
A Clinical Trial Evaluating Injection of TQB6411 in Subjects With Advanced Malignant Tumors
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Official title
A Phase I Clinical Trial Evaluating the Tolerance, Pharmacokinetics and Preliminary Efficacy of Injection TQB6411 in Subjects With Advanced Malignant Tumors
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Control arm
Open label
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Registry reports results
No
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Listing at source
Listed
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Recruitment status
Recruiting
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Phase
Phase 1
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Study type
Interventional
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Completion date
2028-06-01
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First posted
2025-06-29
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Registry last updated
2026-01-21
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Primary completion date
2027-12-01
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Start date
2025-07-15
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Participants
216
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Participant count basis
Estimated
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Planned participants
216
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Protocol amendments
0
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Number of sites
19
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Registry sponsor category
Industry
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Lead sponsor
Chia Tai Tianqing Pharmaceutical Group Nanjing Shunxin Pharmaceutical Co., Ltd.
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Source registry
ClinicalTrials.gov
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Registry ID
NCT07043751
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ClinicalTrials.gov ID
NCT07043751
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Registry record
Open registry record
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Allocation
Not applicable
Model
Single group
Purpose
Treatment
Masking
No masking
Sources for study design
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  1. Dose-limiting toxicity

    Timeframe: Up to24 months

    Dosage-limiting toxicity refers to any of the following events that researchers and sponsors believe to be related to the treatment of TQB6411 for injection (including positively related, likely related, and possible related) (except for special instructions, the degree of adverse events is evaluated in accordance with National Cancer Institute (NCI) Common Terminology Criteria (CTC) for Adverse Events (AE) v5.0.

  2. Maximum Tolerated Dose

    Timeframe: Up to24 months

    Defined as the highest dose in less than 33% of subjects with dose-limiting toxicity (DLT).

  3. Phase II recommended dose

    Timeframe: Up to24 months

    The recommended dose for subsequent phase II studies will be determined based on Maximum Tolerated Dose (MTD), Pharmacokinetics (PK), preliminary efficacy and safety.

  4. Rate and severity of adverse events

    Timeframe: Up to24 months

    Rate and severity of adverse events

  1. Peak drug concentration (Cmax)

    Timeframe: Within 14 days after administration

    It refers to the highest blood drug concentration achieved after administration of TQB6411 for injection.

  2. Area under the concentration-time curve from time zero to the last measurable concentration time t (AUC0-t)

    Timeframe: Within 14 days after administration

    Area under the concentration-time curve from time zero to the last measurable concentration time t (AUC0-t).

  3. Area under the concentration-time curve from time zero extrapolated to infinity (AUC0-∞)

    Timeframe: Within 14 days after administration

    Area under the concentration-time curve from time zero extrapolated to infinity (AUC0-∞).

  4. Peak time (Tmax)

    Timeframe: Within 14 days after administration

    It refers to the time when the maximum blood drug concentration is reached after administration of TQB6411 for injection.

  5. Overall response rate (ORR)

    Timeframe: Up to 24 months

    Proportion of subjects with best response as Partial relief (PR), Complete Response (CR).

  6. Disease Control Rate (DCR)

    Timeframe: Up to 24 months

    Proportion of subjects with best response as Complete Response (CR), Partial relief (PR), Stable Disease (SD).

  7. Progression-free survival (PFS)

    Timeframe: Up to 24 months

    The time between the first dose of the trial drug and the date of first definite disease progression or death (from any cause), whichever occurs first.

  8. Overall survival (OS)

    Timeframe: Up to 24 months

    Time from first dose of study drug to date of death from any cause.

  9. The incidence of antibiotic-resistant antibodies (ADA) and neutralizing antibodies (NAbs)

    Timeframe: Up to 24 months

    The incidence of antibiotic-resistant antibodies (ADA) and neutralizing antibodies (NAbs)

Sources for outcomes
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Sex
All
Age groups
Adults, Older adults
Minimum age
18 Years
Maximum age
75 Years
Healthy volunteers
No

  • The subjects voluntarily joined the study, signed an informed consent form, and had good compliance;
  • 18 years old≤age age≤75 years old (calculated based on the date of signing the informed consent form);
  • Eastern Cooperative Oncology Group (ECOG) score 0~1 point;
  • Expected survival is greater than 12 weeks;
  • According to the RECIST v1.1 standard, there is at least one evaluable tumor lesion in the dose escalation stage, and at least one measurable lesion in the dose expansion stage;
  • Laboratory examination standards that meet the program requirements (no use of hematopoietic stimulator drugs for correction within 7 days);
  • Subjects who failed or were intolerant of standard treatment;
  • Subject requirements for the dose expansion stage: advanced NSCLC; metastatic colon cancer; recurrent/metastatic esophageal squamous cell carcinoma; recurrent/metastatic nasopharyngeal carcinoma; advanced malignant solid tumor;
  • Can provide tumor tissue specimens that meet the requirements for immunohistochemical testing;
  • Women of childbearing age should agree that effective contraception must be adopted during the study period and within 6 months after the end of the study, and that the serum or urine pregnancy test will be negative within 7 days before the study enrollment; men should agree that effective contraception must be adopted within 6 months after the end of the study period;

  • Have appeared or are currently suffering from other malignant tumors;
  • There are diseases that affect intravenous injection and intravenous blood collection;
  • The adverse reactions of previous treatments failed to recover to CTCAE V5.0 grade score ≤1, except for toxicity without safety risk, such as grade 2 hair loss, grade 2 peripheral nerve toxicity, grade 2 anemia, non-clinical significance and asymptomatic grade 2 laboratory abnormalities, stable hypothyroidism with hormone replacement therapy;
  • Those who have received major surgical treatment, obvious traumatic injury or major surgery during the expected study treatment within 4 weeks before the first medication (except for the surgery stipulated in the program), or have long-term uncured wounds or fractures;
  • Subjects with any bleeding or bleeding events ≥CTC AE grade 3 within 4 weeks before the first dose;
  • Arterial/venous thrombosis events occurred within 6 months before the first dose;
  • People with active viral hepatitis and poor control;
  • People infected with active syphilis who need treatment;
  • There is a history of active tuberculosis, idiopathic pulmonary fibrosis, organizing pneumonia, drug-induced pneumonia/radio-pneumonia that needs treatment, or active pneumonia with obvious clinical symptoms, and interstitial lung disease (ILD) that needs treatment, or currently associated with interstitial lung disease;
  • Those with a history of abuse of psychotropic substances and cannot quit or have mental disorders;
  • Preparing for or having previously received allogeneic bone marrow transplants or solid organ transplants;
  • Have a history of hepatic brain disease;
  • Suffering from major cardiovascular disease;
  • Severe infection that is active or uncontrollable (≥CTC AE grade 2 infection);
  • People who require hemodialysis or peritoneal dialysis if renal failure is required;
  • Have a history of immunodeficiency, including HIV-positive or other acquired, congenital immunodeficiency diseases;
  • Subjects who have poorly controlled autoimmune diseases and need to use immunosuppressive agents or systemic hormones to achieve immunosuppressive purposes and still need to continue using them within 7 days before the first dose (except for daily dose of glucocorticoid <10 mg prednisone or other therapeutic hormones);
  • People with epilepsy and need treatment;
  • Poor diabetes control [fasting blood sugar (FBG) > 10mmol/L];
  • Tumor-related symptoms and treatment: subjects who have received chemotherapy, immunotherapy, small molecule targeted drugs, etc. within 3 weeks before the first dose, or are still in the 5 half-life of the drug; within 1 week before the first dose, they have received Chinese patent medicine treatment with anti-tumor indications in the National Medical Products Administration (NMPA) approved drug instructions; imaging (CT or MRI) shows that the tumor has invaded important blood vessels or the researchers judged that the tumor is very likely to invade important blood vessels during the subsequent study and causing fatal major bleeding; if it is not controlled, pleural effusion, pericardial effusion or moderate and severe ascites that still require repeated drainage; known to suffer from spinal cord compression, meningeal metastasis/cancer meningitis, accompanied by brain metastasis symptoms or symptoms/image control time is less than 4 weeks;
  • Known allergies to research drugs or excipients;
  • Have received previous treatment for Epidermal Growth Factor Receptor (EGFR)/c-Mesenchymal-epithelial transition dual anti-ADC drugs;
  • Those who participated in and used other anti-tumor clinical trial drugs within 4 weeks before the first medication;
  • According to the researcher's judgment, there are situations that seriously endanger the safety of the subject or affect the subject's completion of the study.
Sources for eligibility
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  • Beijing Friendship Hospital, Capital Medical UniversityBeijing, ChinaNot yet recruiting
  • Dongguan People's HospitalDongguan, ChinaNot yet recruiting
  • ZhuJiang Hospital of Southern Medical UniversityGuangdong, ChinaNot yet recruiting
  • Guangdong Provincial People's HospitalGuangzhou, ChinaNot yet recruiting
  • Anyang Tumor HospitalAnyang, ChinaNot yet recruiting
  • The Henan Cancer HospitalZhengzhou, ChinaNot yet recruiting
  • The First Affiliated Hospital of Zhengzhou UniversityZhengzhou, ChinaRecruiting
  • Zhongnan Hospital Of Wuhan UniversityWuhan, ChinaNot yet recruiting
  • the Second Xiangya Hospital of Central South UniversityChangsha, ChinaNot yet recruiting
  • Jiangsu Province HospitalNanjing, ChinaNot yet recruiting
  • The First Hospital of China Medical UniversityShenyang, ChinaNot yet recruiting
  • Jining First People's HospitalJining, ChinaNot yet recruiting
  • Shanghai Jiaotong University School of Medicine, Renji HospitalShanghai, ChinaNot yet recruiting
  • Shanghai Pulmonary HospitalShanghai, ChinaNot yet recruiting
  • Fudan University Shanghai Cancer CenterShanghai, ChinaNot yet recruiting
  • Sichuan Cancer HospitalChengdu, ChinaNot yet recruiting
  • West China Hospital, Sichuan UniversityChengdu, ChinaNot yet recruiting
  • Mianyang Central HospitalMianyang, ChinaNot yet recruiting
  • Tianjin Medical University Cancer Institute & HospitalTianjin, ChinaNot yet recruiting
Sources for sites
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Related records

Drugs (1)

Lead sponsors (1)

Conditions (1)