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A Phase 1B Dose-escalation and Phase 2a Study of Carotuximab (TRC105) in Combination With Pazopanib in Patients With Advanced Soft Tissue Sarcoma

2020年5月11日 更新者:Tracon Pharmaceuticals Inc.

The purpose of the phase 1b portion is to evaluate safety and tolerability and determine a recommended phase 2 dose for TRC105 when added to standard dose pazopanib in patients with advanced soft tissue sarcoma. Up to 30 patients will be treated.

The purpose of the phase 2 portion is to estimate the PFS of patients with advanced soft tissue sarcoma by RECIST 1.1 and estimate ORR in a separate cohort of patients with angiosarcoma by RECIST 1.1. Up to 89 patients will be treated in phase 2, including two cohorts of up to 13 patients with angiosarcoma.

研究概览

地位

完全的

详细说明

Pazopanib is an oral inhibitor of multiple receptor tyrosine kinases, including vascular endothelial growth factor receptor VEGFR-1, VEGFR-2, and VEGFR-3 at therapeutic plasma concentrations. These receptors are implicated in pathologic angiogenesis, tumor growth, and cancer progression. Pazopanib is approved for the treatment of advanced soft tissue sarcoma, following progression on one prior systemic therapy, based on improved progression free survival. TRC105 is an antibody to CD105, an important angiogenic target on vascular endothelial cells that is distinct from VEGFR. TRC105 inhibits angiogenesis, tumor growth and metastases in preclinical models and complements the activity of bevacizumab and multi-kinase inhibitors that target the VEGFR. In a phase 1 study of advanced solid tumors, TRC105 therapy caused a global reduction in angiogenic biomarkers and reduced tumor burden at doses that were well-tolerated. In a phase 1b study, the combination of TRC105 and bevacizumab produced radiographic reductions in tumor volume in bevacizumab-refractory patients, and was well tolerated. TRC105 potentiates bevacizumab and VEGFR tyrosine kinases (VEGFR TKI) in preclinical models. By targeting a non-VEGF pathway that is upregulated following VEGF inhibition, TRC105 has the potential to complement VEGFR TKIs and could represent a major advance in cancer therapy. Together, the use of TRC105 with pazopanib may result in more effective angiogenesis inhibition and improved clinical efficacy over that seen with pazopanib alone.

研究类型

介入性

注册 (实际的)

111

阶段

  • 阶段2
  • 阶段1

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习地点

    • Alabama
      • Birmingham、Alabama、美国、35243
        • University of Alabama at Birmingham
    • California
      • Santa Monica、California、美国、90403
        • Sarcoma Oncology Center
    • Florida
      • Jacksonville、Florida、美国、32224
        • Mayo Clinic Jacksonville
    • Minnesota
      • Rochester、Minnesota、美国、55905
        • Mayo Clinic Rochester
    • New York
      • Buffalo、New York、美国、92122
        • Roswell Park Cancer Institute
      • New York、New York、美国、10029
        • Mount Sinai School of Medicine-Tisch Cancer Institute
    • North Carolina
      • Durham、North Carolina、美国、27710
        • Duke University
    • Texas
      • Dallas、Texas、美国、75230
        • Mary Crowley Cancer Research Center
    • Utah
      • Salt Lake City、Utah、美国、84112
        • University of Utah

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

12年 至 120年 (孩子、成人、年长者)

接受健康志愿者

不

有资格学习的性别

全部

描述

Inclusion Criteria:

  1. Histologically confirmed unresectable soft tissue sarcoma that has progressed following treatment with chemotherapy. Prior pazopanib is allowed if the drug was not discontinued for toxicity ( Phase 1b only)
  2. Histologically confirmed metastatic soft tissue sarcoma that has progressed by RECIST following treatment with anthracycline chemotherapy. Patients may have received up to four lines of systemic therapy for metastatic disease and no more than two lines of combination treatment ( Phase 2 only)
  3. Histologically confirmed locally advanced (e.g. unresectable) or metastatic angiosarcoma that has progressed following treatment with prior systemic therapy. Progression must be documented on or following the most recent systemic therapy. Prior pazopanib is allowed if the drug was not discontinued for toxicity (Phase 2 angiosarcoma cohorts only)
  4. Measurable disease by RECIST
  5. Age of 12 years or older (patient must weigh ≥ 40 kg)
  6. ECOG performance status ≤ 1
  7. Resolution of all acute adverse events resulting from prior cancer therapies to NCI CTCAE grade ≤ 1 or baseline (except alopecia or neuropathy)
  8. Adequate organ function.
  9. Willingness and ability to consent for self to participate in study
  10. Willingness and ability to comply with scheduled visits, treatment plan, laboratory tests, and other study procedures
  11. Available archival tumor specimen of the soft tissue sarcoma that meets inclusion criterion #1, #2 or #3

Exclusion Criteria:

  1. Prior treatment with TRC105
  2. Prior treatment with a VEGFR TKI (including pazopanib) (Phase 2 only)
  3. Current treatment on another therapeutic clinical trial
  4. Receipt of systemic anticancer therapy, including investigational agents, within 28 days of starting study treatment.
  5. No major surgical procedure or significant traumatic injury within 6 weeks prior to study registration, and must have fully recovered from any such procedure; date of surgery (if applicable) or the anticipated need for a major surgical procedure within the next six months.
  6. Patients who have received wide field radiotherapy ≤ 28 days or limited field radiation for palliation < 14 days prior to cycle 1 day 1 or those patients who have not recovered adequately from side effects of such therapy
  7. Uncontrolled chronic hypertension
  8. Significant ascites or pericardial or pleural effusion
  9. History of brain involvement with cancer, spinal cord compression, or carcinomatous meningitis, or new evidence of brain or leptomeningeal disease.
  10. Angina, MI, symptomatic congestive heart failure, cerebrovascular accident, transient ischemic attack, arterial embolism, pulmonary embolism, PTCA or CABG within the past 6 months. Deep venous thrombosis within 6 months, unless the patient is anti-coagulated without the use of warfarin for at least 2 weeks. In this situation, low molecular weight heparin is preferred.
  11. Active bleeding or pathologic condition that carries a high risk of bleeding. Patients who have been uneventfully anti-coagulated with low molecular weight heparin are eligible.
  12. Thrombolytic use (except to maintain i.v. catheters) within 10 days prior to first day of study therapy
  13. Known active viral or nonviral hepatitis or cirrhosis
  14. History of hemorrhage or hemoptysis within 3 months of starting study treatment
  15. History of peptic ulcer within the past 3 months of treatment
  16. History of gastrointestinal perforation or fistula in the past 6 months, or while previously on antiangiogenic therapy, unless underlying risk has been resolved
  17. Known human immunodeficiency virus (HIV) or acquired immunodeficiency syndrome (AIDS) related illness
  18. Receipt of a strong CYP3A4 inducer within 12 days prior to cycle 1 day 1 or a strong CYP3A4 inhibitor within 7 days prior to cycle 1 day 1.
  19. Pregnancy or breastfeeding. Female patients must be surgically sterile (i.e.: hysterectomy) or be postmenopausal, or must agree to use effective contraception during the study and for 3 months following last dose of TRC105. All female patients of reproductive potential must have a negative pregnancy test (serum or urine) within 7 days prior to first dose. Male patients must be surgically sterile or must agree to use effective contraception during the study and for 3 months following last dose of TRC105. The definition of effective contraception will be based on the judgment of the Principal Investigator or a designated associate.
  20. Other severe acute or chronic medical or psychiatric condition or laboratory abnormality that may increase the risk associated with study participation or may interfere with the interpretation of study results and, in the judgment of the Investigator, would make the patient inappropriate for this study.

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

  • 主要用途:治疗
  • 分配:不适用
  • 介入模型:单组作业
  • 屏蔽:无(打开标签)

武器和干预

参与者组/臂
干预/治疗
实验性的:TRC105 and Pazopanib
Weekly TRC105 in combination with standard dose pazopanib or every two week administration during cycle 1, and starting on cycle 2 day 1 and beyond, TRC105 may be administered every two weeks. This is also in combination with standard dose pazopanib.
Weekly TRC105 in combination with standard dose Pazopanib.
其他名称:
  • 志愿者
  • CD105 嵌合抗体 (TRC105)

研究衡量的是什么?

主要结果指标

结果测量
措施说明
大体时间
Number of Participants With Dose Limiting Toxicity (DLT)
大体时间:56 days
For DLT evaluation, severity (grade) was classified according to common terminology criteria for adverse events version 4.0 (CTCAE v4.0). DLTs were defined as grade 4 neutropenia persisting for ≥ 5 days, febrile neutropenia (grade 4 neutropenia with fever > 38.5 ºC both sustained over a 24 hour period), neutropenic infection (grade ≥ 3 neutropenia with grade ≥ 3 infection), anemia ≥ grade 4, grade > 4 thrombocytopenia or grade ≥ 3 thrombocytopenia and grade ≥ 3 hemorrhage, or grade 3 or 4 nonhematologic toxicity with the following exceptions: nausea, vomiting, or diarrhea for <48 hours, asymptomatic electrolyte abnormalities that are corrected to grade 1 or better in < 72 hours, or headache lasting less than 48 hours.
56 days
Progression Free Survival of Patients With Advanced Soft Tissue Sarcoma (Phase 1 and 2)
大体时间:from screening to either disease progression or death
Number of patients with progression free survival, as defined as time from screening to either first disease progression or death from any cause per RECIST version 1.1
from screening to either disease progression or death
Objective Response Rate in a Cohort of Patients With Angiosarcoma
大体时间:1.5 years
The best response according to RECIST 1.1 for each patient in the phase 2 angiosarcoma cohort with measurable disease and who received at least one dose of study drug will be listed by cohort and tumor type
1.5 years

次要结果测量

结果测量
措施说明
大体时间
Trough Concentrations of TRC105 (Phase 2)
大体时间:4, 6, 8, and 10 weeks
Trough serum TRC105 concentrations will be measured using validated ELISA methods.
4, 6, 8, and 10 weeks
Number of Patients With and Without Development of Immunogenicity Antibodies (Phase 1 and 2)
大体时间:32 months
Anti-product antibody concentrations will be measured using validated ELISA methods. Anti-product antibody concentrations will be evaluated in the context of pharmacokinetic parameters and AE profiles.
32 months
Number of Patients With and Without Expression of Endoglin on Sarcoma Tissue (Phase 1 and 2)
大体时间:12 months
Expression will be determined by immunohistochemistry for each patient who received at least one dose of TRC105
12 months
Objective Response Rate in Patients With Advanced Soft Tissue Sarcoma by RECIST 1.1
大体时间:12 months
The best response (CR, PR, SD or PD according to RECIST 1.1) for each patient (phase 1 and phase 2) with measurable disease who received at least one dose of TRC105 study drug
12 months
Progression Free Survival in a Cohort of Patients With Angiosarcoma (Phase 2)
大体时间:26 months
Time from screening to either first disease progression or death from any cause per RECIST version 1.1
26 months

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始 (实际的)

2013年12月10日

初级完成 (实际的)

2019年3月11日

研究完成 (实际的)

2019年3月11日

研究注册日期

首次提交

2013年10月23日

首先提交符合 QC 标准的

2013年10月28日

首次发布 (估计)

2013年11月3日

研究记录更新

最后更新发布 (实际的)

2020年5月20日

上次提交的符合 QC 标准的更新

2020年5月11日

最后验证

2020年5月1日

更多信息

此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.

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