CClinicalTrials.gg
Status unknownNCT03403452Updated Jan 18, 2018

Apatinib in the Treatment of Metastatic Colorectal Cancer

A Phase 2 interventional study of Apatinib in Colorectal Cancer, sponsored by Fudan University. Status unknown at 1 site in China. Open to participants aged 18 Years to 80 Years. Per ClinicalTrials.gov, last updated 2018-01-18.

Sponsored by Fudan University · Phase 2, Interventional, and Treatment

The sponsor has not verified this record recently (last verified Jan 2018), so the status shown — last known as Recruiting — may be out of date.
Phase
Phase 2
Study type
Interventional
Enrollment
33
Allocation
Not applicable
Ages
18 Years to 80 Years
Sex
All
01

Study summary

This is an Exploratory Clinical Trial Study on Apatinib in the Treatment of Metastatic Colorectal Cancer Who Have Progressed after Standard Second Line Therapy.

02

Conditions studied

  • Colorectal Cancer
03

Who can participate

Ages eligible
18 Years to 80 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • ≥ 18 and ≤ 80 years of age
  • Histological confirmed advanced or metastatic colorectal cancer,at least one measurable lesion, larger than 10 mm in diameter by spiral CT
  • Have failed for ≥ 2 lines of chemotherapy and/or targeted therapy
  • Life expectancy of more than 3 months
  • ECOG performance scale 0~1
  • Duration from the last therapy is more than 4 weeks for operation, radiotherapy or cytotoxic agents
  • Adequate hepatic, renal, heart, and hematologic functions (platelets > 80 ×10\^9/L, neutrophil > 1.5 × 10\^9/L, serum creatinine ≤ 1×upper limit of normal(ULN), bilirubin \< 1.5 ULN, and serum transaminase ≤ 2.0× ULN)
  • Child bearing potential, a negative urine or serum pregnancy test result before initiating apatinib, must agree and commit to the use of a reliable method of birth control for the duration of the study and for 8 weeks after the last dose of test article. Male: All subjects who are not surgically sterile or postmenopausal must agree and commit to the use of a reliable method of birth control for the duration of the study and for 8 weeks after the last dose of test article.
  • Signed and dated informed consent. Willingness and ability to comply with scheduled visits, treatment plans, laboratory tests, and other study procedure.

Exclusion criteria

Exclusion Criteria:

  • Prior VEGFR inhibitor treatment within 2 weeks
  • History of other malignancies within 5 years except cured basal cell carcinoma of skin and carcinoma in-situ of uterine cervix
  • Preexisting uncontrolled hypertension defined as more than 140/90 mmHg despite using single medical therapy
  • More than class I (NCI CTCAE 3.0 ) myocardial ischemia, arrhythmia(including QTcF:male ≥ 450 ms, female ≥ 470 ms), or cardiac insufficiency myocardial ischemia, arrhythmia, or cardiac insufficiency
  • Pregnant or lactating women
  • Before or at the same time any, second malignancies except cured basal cell carcinoma of skin and carcinoma in-situ of uterine cervix
  • URT: urine protein ≥ (++)and > 1.0 g of 24 h
  • PT, APTT, TT, Fbg abnormal, having hemorrhagic tendency or receiving the therapy of thrombolysis or anticoagulation
  • Certain possibility of gastric or intestine hemorrhage
04

Study design

Phase
Phase 2
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
33 participants (estimated)

Study arms

  • Experimental
    arm for Apatinib

    500 mg,p.o.,qd

    Drug: Apatinib

Interventions

  • DrugApatinib

    500 mg,p.o.,qd, until disease progression or intolerable toxicity or patients withdrawal of consent.

05

What researchers measure

Primary outcomes

  1. PFS(progress free survival)

    PFS was defined as the time from assignment to disease progression radiological/clinical or death due to any cause

    Time frame: From assignment of the first subject to 3 months later after the last participant is recruited

Secondary outcomes

  1. OS(overall survival)

    OS is defined as the time from date of assignment to death due to any cause

    Time frame: From assignment of the first subject until 30 death events observed, up to 2 years

  2. ORR(objective response rate)

    The percentage of subjects with total number of Complete Response (CR) + total number of Partial Response (PR)

    Time frame: From assignment of the first subject to 3 months later after the last participant is recruited

  3. DCR(disease control rate)

    DCR is defined as the percentage of subjects whose best response was not Progressive Disease (PD) according to Response Evaluation Criteria in Solid Tumors (RECIST) (= total number of Complete Response (CR) + total number of Partial Response (PR) + total number of Stable Disease (SD)

    Time frame: From assignment of the first subject to 3 months later after the last participant is recruited

06

Study locations

1 of 1 sites recruiting
  • Department of General Surgery, Zhongshan Hospital, Fudan University
    Shanghai, 200032, China
    Recruiting
07

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

08

Registry details

Key details

Study ID
NCT03403452
Lead sponsor
Fudan University
Collaborators
Jiangsu HengRui Medicine Co., Ltd.
Responsible party
Xu jianmin (Director of colorectal surgery, Fudan University) — Principal investigator
First posted
Jan 18, 2018
Start date
Jan 1, 2018
Primary completion
Jun 30, 2019 (estimated)
Completion
Dec 31, 2019 (estimated)
Last update
Jan 18, 2018

Study contacts

Jianmin Xu, PhD
Contact
xujmin@aiiyun.com
+86-13501984869

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Jan 2018. You cannot join it, but the record below documents what was studied.

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