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Clinical Trials/NCT06139536
NCT06139536
Recruiting
Phase 1

A Phase 1, Multicenter, Open-label Study to Evaluate the Safety, Tolerability, Pharmacokinetics and Preliminary Efficacy of BAT4706 Injection Combined With BAT1308 Injection in Patients With Advanced Solid Tumors

Bio-Thera Solutions3 sites in 1 country210 target enrollmentMarch 6, 2024

Overview

Phase
Phase 1
Intervention
BAT4706 Injection
Conditions
Advanced Solid Tumor
Sponsor
Bio-Thera Solutions
Enrollment
210
Locations
3
Primary Endpoint
Physical examination
Status
Recruiting
Last Updated
2 years ago

Overview

Brief Summary

This is a Phase 1, Multicenter, Open-label Study to Evaluate the Safety, Tolerability, Pharmacokinetics and Preliminary Efficacy of BAT4706 Injection Combined With BAT1308 Injection in Patients With Advanced Solid Tumors.

Detailed Description

The goal of this interventional study is to evaluate the safety, tolerability, pharmacokinetics and preliminary efficacy of BAT4706 injection combined with BAT1308 injection in patients with advanced solid tumors, explore the maximum tolerable dose. The study is generally divided into two stages. In the first stage, the "3+3" dose increasing rule is proposed to explore the safety and tolerability, subject will be given BAT1308 injection and BAT4706 injection through Intravenous infusion in the first four cycles, and then maintain administration of BAT1308 monotherapy after four cycles until 18 cycles; In the second stage, based on the preliminary safety and efficacy results of the previous stage, appropriate doses and tumor types were selected for extended research, in order to further explore the safety and clinical effectiveness of BAT4706 injection and BAT1308 injection in the combined administration mode.

Registry
clinicaltrials.gov
Start Date
March 6, 2024
End Date
February 2026
Last Updated
2 years ago
Study Type
Interventional
Study Design
Sequential
Sex
All

Investigators

Sponsor
Bio-Thera Solutions
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Voluntary signing of informed consent.
  • Study population:
  • Dose increasing stage:Patients with advanced malignant solid tumors who have been pathologically confirmed, have failed to standard treatment, or are intolerant to standard treatment.
  • Dose expansion stage: Divided into 3 queues:
  • Queue A: Patient with locally advanced or metastatic non-small cell lung cancer (NSCLC) confirmed by pathology, failed to standard treatment, or are intolerant to standard treatment. And it must meet the following requirements: a) Previous PD-L1 test results have been obtained; Or b) Provide previously stored tumor tissue samples or fresh biopsy tumor lesion tissue for PD-L1 testing at the site before the first medication use;
  • Queue B: Advanced microsatellite stable (pMMR/MSS) colorectal cancer confirmed by pathology, with disease progression after receiving at least 2 standard chemotherapy regimens/lines, and no liver metastasis or resection/ablation liver metastasis.
  • Queue C: Patient with Hepatocellular carcinoma confirmed by pathology, refractory to at least 1 line of previous systemic treatment, and intolerant to this treatment.
  • An evaluable tumor focus was necessary in the dose escalation stage, and at least one measurable tumor focus in the dose expanding stage(according to RECIST 1.1 standard).
  • ECOG should be 0-1 in the dose escalation stage, and be 0-2 in the dose expanding stage.
  • The expected survival period is more than 12 weeks base on the evaluation of the investigator.

Exclusion Criteria

  • Have received any other clinical trial treatment or participated in a medical device clinical study within 4 weeks prior to the first administration of the study drug.
  • Previously failed to receive CTLA-4 monoclonal antibody treatment.
  • Received other tumor treatments within 4 weeks prior to the first administration of the study drug, such as chemotherapy, radiotherapy (palliative radiotherapy must be completed within 2 weeks prior to the first administration), targeted therapy/immunotherapy (with a minimum interval of 4 weeks or at least 5 half-lives, whichever is shorter), hormone therapy (excluding alternative therapy).
  • Prior to the first administration of the investigational drug, there were still cases of AE caused by previous anti-tumor therapy that were greater than level 1 (CTCAE5.0).
  • Having undergone major surgery (such as craniotomy, thoracotomy, or laparotomy) within 4 weeks prior to the first administration of the study drug, major surgery is defined as a level 3 or 4 surgery; Individuals with a history of organ transplant surgery.
  • Primary central nervous system tumor or symptomatic central nervous system metastasis, meningeal metastasis, or previous history of epilepsy. Excluding patients with central nervous system metastasis who are clinically asymptomatic or have symptoms but have been judged stable by investigator.
  • If other malignant tumors have been diagnosed within the past 5 years, or if previous malignant tumors have been cured for less than 5 years, the first pathological diagnosis shall prevail. Except radical skin basal cell carcinoma, skin squamous cell carcinoma or carcinoma in situ (such as breast cancer in situ, cervical carcinoma in situ).
  • Severe cardiovascular disease: Heart failure with a New York Heart Association(NYHA) rating of 2 or above, left ventricular ejection fraction (LVEF) less than 50%, unstable arrhythmia or unstable angina, uncontrollable hypertension (defined in this protocol as systolic blood pressure\>150mmHg and/or diastolic blood pressure\>100mmHg after treatment, although the optimal antihypertensive treatment is used).
  • Patients with a history of autoimmune diseases (those who undergo thyroid hormone replacement therapy to control stable hypothyroidism can be included in the group); Patients who are using immunosuppressive agents or systemic or absorbable local hormone therapy to achieve immunosuppressive effects (dosage\>10mg/day of prednisone or other therapeutic hormones) and continue to use the study drug within 2 weeks before the first administration.
  • Active infections with clinical significance that require intravenous antibiotics, including active pulmonary tuberculosis patients.

Arms & Interventions

A/ Standard 3+3 1.0mg/kg of BAT4706 with 300mg of BAT1308

Drug: BAT4706 injection, Dosage: 1.0mg/kg, Frequency: once every 3 weeks, Duration: 3 month. Drug: BAT1308 injection, Dosage: 300mg, Frequency: once every 3 weeks, Duration: 1 year.

Intervention: BAT4706 Injection

A/ Standard 3+3 1.0mg/kg of BAT4706 with 300mg of BAT1308

Drug: BAT4706 injection, Dosage: 1.0mg/kg, Frequency: once every 3 weeks, Duration: 3 month. Drug: BAT1308 injection, Dosage: 300mg, Frequency: once every 3 weeks, Duration: 1 year.

Intervention: BAT1308 Injection

B/ Standard 3+3 2.0mg/kg of BAT4706 with 300mg of BAT1308

Drug: BAT4706 injection, Dosage: 2.0mg/kg, Frequency: once every 3 weeks, Duration: 3 month. Drug: BAT1308 injection, Dosage: 300mg, Frequency: once every 3 weeks, Duration: 1 year.

Intervention: BAT4706 Injection

B/ Standard 3+3 2.0mg/kg of BAT4706 with 300mg of BAT1308

Drug: BAT4706 injection, Dosage: 2.0mg/kg, Frequency: once every 3 weeks, Duration: 3 month. Drug: BAT1308 injection, Dosage: 300mg, Frequency: once every 3 weeks, Duration: 1 year.

Intervention: BAT1308 Injection

C/ Standard 3+3 3.0mg/kg of BAT4706 with 300mg of BAT1308

Drug: BAT4706 injection, Dosage: 3.0mg/kg, Frequency: once every 3 weeks, Duration: 3 month. Drug: BAT1308 injection, Dosage: 300mg, Frequency: once every 3 weeks, Duration: 1 year.

Intervention: BAT4706 Injection

C/ Standard 3+3 3.0mg/kg of BAT4706 with 300mg of BAT1308

Drug: BAT4706 injection, Dosage: 3.0mg/kg, Frequency: once every 3 weeks, Duration: 3 month. Drug: BAT1308 injection, Dosage: 300mg, Frequency: once every 3 weeks, Duration: 1 year.

Intervention: BAT1308 Injection

D/ Standard 3+3 6.0mg/kg of BAT4706 with 300mg of BAT1308

Drug: BAT4706 injection, Dosage: 6.0mg/kg, Frequency: once every 3 weeks, Duration: 3 month. Drug: BAT1308 injection, Dosage: 300mg, Frequency: once every 3 weeks, Duration: 1 year.

Intervention: BAT4706 Injection

D/ Standard 3+3 6.0mg/kg of BAT4706 with 300mg of BAT1308

Drug: BAT4706 injection, Dosage: 6.0mg/kg, Frequency: once every 3 weeks, Duration: 3 month. Drug: BAT1308 injection, Dosage: 300mg, Frequency: once every 3 weeks, Duration: 1 year.

Intervention: BAT1308 Injection

E/ Standard 3+3 10.0mg/kg of BAT4706 with 300mg of BAT1308

Drug: BAT4706 injection, Dosage: 10mg/kg, Frequency: once every 3 weeks, Duration: 3 month. Drug: BAT1308 injection, Dosage: 300mg, Frequency: once every 3 weeks, Duration: 1 year.

Intervention: BAT4706 Injection

E/ Standard 3+3 10.0mg/kg of BAT4706 with 300mg of BAT1308

Drug: BAT4706 injection, Dosage: 10mg/kg, Frequency: once every 3 weeks, Duration: 3 month. Drug: BAT1308 injection, Dosage: 300mg, Frequency: once every 3 weeks, Duration: 1 year.

Intervention: BAT1308 Injection

Outcomes

Primary Outcomes

Physical examination

Time Frame: Through study completion, 1 year

Number of cases with abnormal physical examination results

Echocardiography

Time Frame: Through study completion, 1 year

Number of cases with abnormal echocardiography results

Adverse event

Time Frame: Through study completion, 1 year

Number of cases with all adverse medical events that occur after the subject receives the investigational drug assessed by CTCAE V5.0

Vital signs

Time Frame: Through study completion, 1 year

Number of cases with abnormal vital signs results

Dose-limiting toxicity (DLT)

Time Frame: The first administration cycle(21 days)

The following AEs related to the study drug occurred from day 1 to day 21 after administration in the first cycle: ≥grade 3 of non hematological toxicity (except for nausea, vomiting, and diarrhea that can be relieved within 3 days of supportive treatment, and those who recover within 2 hours of symptomatic treatment of infusion reactions); ≥grade 4 of Hematological toxicity(including ≥ 3 grade neutropenia with fever; however, grade 4 neutropenia requires a duration of ≥ 7 days to determine DLT);≥ grade 4 thrombocytopenia or grade 3 thrombocytopenia with bleeding.

Laboratory Examination

Time Frame: Through study completion, 1 year

Number of cases with abnormal laboratory examination results

Electrocardiogram

Time Frame: Through study completion, 1 year

Number of cases with abnormal electrocardiogram results

Secondary Outcomes

  • Best Overall Response Rate(BORR)(Through study completion, 1 year)
  • Duration of Response(DOR)(Through study completion, 1 year)
  • Overall Survival(OS)(Through study completion, 1 year)
  • Immunogenicity(Every cycle until 18 cycles (one cycle equals 3 weeks))
  • Pharmacokinetic(Every cycle until 18 cycles (one cycle equals 3 weeks))
  • Objective response rate (ORR)(Through study completion, 1 year)
  • Progression-Free Survival(PFS)(Through study completion, 1 year)

Study Sites (3)

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