TQB2916 Injection Combined With Chemotherapy or Penpulimab Injection in the Treatment of Solid Tumors

Phase 2

Not yet recruiting

• Conditions: Soft Tissue Sarcoma; Melanoma
• Interventions: Drug: TQB2916 injection+penpulimab injection; Drug: TQB2916 injection + doxorubicin hydrochloride for injection

• Registration Number: NCT06500091
• Lead Sponsor: Chia Tai Tianqing Pharmaceutical Group Co., Ltd.

Brief Summary

This project is a clinical trial on the efficacy and safety of TQB2916 injection combined with chemotherapy or penpulimab injection in solid tumors. This project is divided into two cohorts. Cohort 1 aims to explore the safety and efficacy of specific subtypes of soft tissue sarcoma in subjects; Cohort 2 aims to explore safety and efficacy in subjects with undifferentiated pleomorphic sarcoma and melanoma. A total of 54 subjects are planned to be enrolled in this project.

Detailed Description

Not available

Study Timeline

• Status Verified: 2023-10
• Study Start: 2024-07
• Study First Submitted: 2024-07-08
• Study First Submitted QC: 2024-07-08
• Last Update Submitted: 2024-07-08
• Study First Posted: 2024-07-15
• Last Update Posted: 2024-07-15
• Primary Completion: 2026-06
• Study Completion: 2026-12

Recruitment & Eligibility

• Status: NOT_YET_RECRUITING
• Sex: All
• Target Recruitment: 54

Inclusion Criteria

1. The subjects voluntarily joined this study, signed an informed consent form, and had good compliance.
2. Age: 18-75 years old; Eastern Cooperative Oncology Group Performance Status (ECOG PS) score: 0-1 points; The expected survival period exceeds 3 months.
3. Patients with locally advanced or unresponsive relapsed/metastatic soft tissue sarcoma and melanoma diagnosed by pathology and unable or refused surgery. Cohort 1contains the following subtypes: "dedifferentiated liposarcoma, highly differentiated liposarcoma with dedifferentiated components, leiomyosarcoma (excluding uterine leiomyosarcoma)", and cohort 2 contains undifferentiated pleomorphic sarcoma and melanoma.
4. Cohort 1: No previous history of failure of anthracycline-based chemotherapy. Cohort 2: Previously treated with standard of care.
5. Cohort 2: Previously treated.
6. According to RECIST 1.1 standard, it is confirmed that there is at least one measurable lesion.
7. The main organs are functioning well.
8. Female participants of childbearing age should agree to use contraceptive measures during the study period and within 6 months after the end of the study; Within 7 days prior to enrollment, the serum pregnancy test was negative and must be a non lactating subject; Male participants should agree to use contraceptive measures during the study period and within 6 months after the end of the study period.

Exclusion Criteria

1. Concomitant diseases and medical history:

   1. Has experienced or currently suffers from other malignant tumors within 5 years.

   2. Unresolved toxic reactions above CommonTerminology Criteria for Adverse Events level 1 caused by any previous treatment;

   3. The research treatment began with significant surgical treatment, open biopsy, or obvious traumatic injury;

   4. Long term unhealed wounds or fractures;

   5. Arterial/venous thrombotic events that have occurred within 6 months and affect current normal function;

   6. Individuals with a history of psychiatric drug abuse who are unable to quit or have mental disorders;

   7. Individuals who have previously undergone splenectomy or received splenic radiotherapy within 3 months prior to enrollment;

   8. Currently present with congenital hemorrhagic or coagulation diseases, or currently undergoing treatment with warfarin;

   9. Subjects with any severe and/or uncontrolled diseases, including:

      • Blood pressure control is still not ideal after dual drug treatment;
      • Suffering from ≥ grade 2 myocardial ischemia or myocardial infarction, arrhythmia; ≥ Grade 2 unstable angina pectoris;
      • Active or uncontrolled severe infection or unexplained fever>38.5 °C;
      • Cirrhosis and active hepatitis *;
      • Active syphilis patients;
      • Renal failure requiring hemodialysis or peritoneal dialysis;
      • Have a history of immunodeficiency;
      • Poor control of diabetes;
      • Urinary routine indicates urine protein ≥++;
      • Individuals with epilepsy who require treatment;
      • Weight<40 kg and BMI<18.5 kg/m2, or weight loss of ≥ 10% within 3 months.

2. Tumor related symptoms and treatment:

   1. Has received surgery, chemotherapy, radiation therapy, or other anti-cancer therapies before the start of the research treatment;
   2. Before the start of the study treatment, he received the treatment of traditional Chinese patent medicines and simple preparations with anti-tumor indications specified in the National MedicalProducts Administration (NMPA) approved drug directions;
   3. Cohort 1: Previously used doxorubicin exceeding 200mg/m2;
   4. Cohort 2: Undifferentiated multidirectional sarcoma that has previously received more than 2 types of anti vascular tyrosine kinase inhibitors (TKIs), or has previously received relevant immunotherapy drugs;
   5. Previously received antibodies or fusion proteins targeting CD40;
   6. Imaging shows that the tumor invades large blood vessels or has unclear boundaries with large blood vessels, or the researcher determines that the tumor is highly likely to invade important blood vessels and cause fatal massive bleeding during subsequent studies;
   7. Uncontrollable pleural effusion, pericardial effusion, or ascites that still require repeated drainage;
   8. Severe bone damage caused by tumor bone metastasis may occur in the presence or after enrollment;
   9. Uncontrollable pain related to tumor bone metastasis;
   10. There was central nervous system metastasis before enrollment.

3. Research and treatment related:

   1. History of live attenuated vaccine administration before the start of research treatment or planned live attenuated vaccine administration during the study period;
   2. There is a clear bleeding tendency or clinically significant bleeding symptoms before the first use of medication;
   3. Individuals who have experienced severe hypersensitivity reactions after using monoclonal antibodies, or who are allergic to known components of the investigational drug;
   4. Active autoimmune diseases that require systemic treatment have occurred within 2 years prior to the start of the research treatment.
   5. Diagnosed with immunodeficiency or undergoing systemic glucocorticoid therapy or any other form of immunosuppressive therapy.

4. Participated in clinical trials of other anti-tumor drugs within the first 4 weeks of grouping.

5. According to the researcher's judgment, there are individuals with accompanying diseases that seriously endanger the safety of the subjects or affect the completion of the study, or individuals who are deemed unsuitable for enrollment due to other reasons.

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
TQB2916 injection+penpulimab injection	TQB2916 injection+penpulimab injection	TQB2916 injection+penpulimab injection , 21 days as a treatment cycle.
TQB2916 injection + doxorubicin hydrochloride for injection	TQB2916 injection + doxorubicin hydrochloride for injection	TQB2916 injection + doxorubicin hydrochloride for injection, 21 days as a treatment cycle.

Primary Outcome Measures

Name	Time	Method
Overall response rate (ORR)	Up to 48 weeks	Objective response rate refers to the percentage of complete response (CR) or partial response (PR) subjects determined by the investigator based on Response Evaluation Criteria in Solid Tumors (RECIST) 1.1 or modified RECIST 1.1 for immune based therapeutics(guidelines for response criteria for use in trials testing Immunotherapeutics（iRECIST)) (CR and PR) under iRECIST criteria can occur after imaging disease progression).
Progression-Free Survival (PFS)	Up to 48 weeks	PFS will be defined as median number of months from the date of randomization until the first documented sign of disease progression or death due to any causes, whichever occurs first.

Secondary Outcome Measures

Name	Time	Method
Overall survival (OS)	Up to 2 years	Overall survival defined as the time from enrollment to death from any cause.
Duration of Response (DOR)	Up to 48 weeks	DOR will be defined as median number of months from date of first documented objective response until first documented sign of disease progression or death due to any causes.

Trial Locations

Locations (11)

Henan Cancer Hospital Affiliated Cancer Hospital of Zhengzhou University; 🇨🇳 Zhengzhou, Henan, China

Cancer Hospital Chinese Academy of Medical Science; 🇨🇳 BeiJing, Beijing, China

Beijing Cancer Hospital; 🇨🇳 Beijing, Beijing, China

Hunan Cancer Hospital; 🇨🇳 Changsha, Hunan, China

Jilin Cancer Hospital; 🇨🇳 Changchun, Jilin, China

Cancer Hospital Affiliated to Shandong First Medical University; 🇨🇳 Jinan, Shandong, China

Shanxi Cancer Hospital; 🇨🇳 Taiyuan, Shanxi, China

Fudan University Shanghai Cancer Center; 🇨🇳 Shanghai, Shanghai, China

Tianjin Medical University Cancer Institute and Hospital; 🇨🇳 Tianjin, Tianjin, China

Xinjiang Medical University Affiliated Cancer Hospital; 🇨🇳 Ürümqi, Xinjiang, China

Zhe Jiang Cancer Hospital; 🇨🇳 Hangzhou, Zhejiang, China