A Study of Famitinib in Patients With Advanced Colorectal Cancer

Colorectal Cancer Clinical Trial

Official title:

A Randomized, Placebo-controlled, Double-blind, Multicenter, Phase IIb Study of Famitinib as Third Line Treatment in Patients With Advanced Colorectal Cancer

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT01762293
• Other study ID #: FMTN-IIb-CRC
• Status: Completed
• Phase: Phase 2
• First received: January 4, 2013
• Last updated: April 16, 2018
• Start date: April 2012
• Est. completion date: October 2014

Study information

• Verified date: January 2013
• Source: Jiangsu HengRui Medicine Co., Ltd.
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Famitinib is a tyrosin-inhibitor agent targeting at c-Kit, VEGFR2, PDGFR, VEGFR3, Flt1 and Flt3, and it's anti-angiogenesis effect has been viewed in preclinical tests. Phase I study has shown that the toxicity is manageable.

The purpose of this study is to determine whether Famitinib can improve progression free survival compared with placebo in patients with advanced colorectal cancer who failed in previous at least two lines of chemotherapy.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 154
• Est. completion date: October 2014
• Est. primary completion date: September 2014
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 70 Years

Eligibility

Inclusion Criteria:

• Histologically or cytologic confirmed recurrent and/or metastatic CRC and previously received at least two lines of standard therapy failure(must include 5-Fu,irinotecan and oxaliplatin)

• At least one measurable lesion, larger than 10 mm in diameter by spiral CT scan(scanning layer = 5 mm )

• age = 18 and = 70

• ECOG 0-1

• Life expectancy of more than 3 months

• More than 4 weeks after operation, chemotherapy, radiotherapy, cytotoxic agents or tyrosine kinase inhibitors

• Signed and dated informed consent

• Willingness and ability to comply with scheduled visits, treatment plans, laboratory tests, and other study procedure.

Exclusion Criteria:

• Before or at the same time any, second malignancies except cured basal cell carcinoma of skin and carcinoma in-situ of uterine cervix

• Prior therapy with tyrosine kinase -inhibitor agent targeting at VEGFR, PDGFR and c-Kit(e.g sorafenib,sunitinib,regorafenib)

• Any factors that influence the usage of oral administration

• Having obvious gastrointestinal hemorrhagic tendency

• Known Spinal Cord compression or diseases of brain or pia mater by CT /MRI screening

• Organ tumor overloading

• Inadequate hepatic, renal, heart, and hematologic functions (hemoglobin = 90g/L, platelets = 100×10^9/L, neutrophils = 1.5×10^9/L, total bilirubin = 1.25×the upper limit of normal(ULN), and serum transaminase = 1.5×ULN (If liver metastases, serum transaminase= 2.5×ULN), creatinine clearance rate = 60ml/min, cholesterol = 1.5×ULN and triglyceride= 2.5 x ULN, LVEF: < 50%

• Preexisting uncontrolled hypertension defined as more than 140/90 mmHg despite using single medical therapy, more than cla ss I (NCI CTCAE 3.0 ) myocardial ischemia, arrhythmia, or cardiac insufficiency

• urinary protein= ++ or 24-hour urinary protein = 1.0 g

• Long-term untreated wounds or fractures

• Blood coagulation abnormal, having hemorrhagic tendency

• Within 1 year before the first treatment occurs artery / venous thromboembolic events, such as cerebral vascular accident (including transient ischemic attack), deep vein thrombosis and pulmonary embolism, etc.

• Application of anticoagulants or vitamin K antagonists such as warfarin, heparin or its analogues; If the prothrombin time international normalized ratio (INR) = 1.5, with the purpose of prevention, the use of small doses of warfarin (1mg orally, once daily) or low-dose aspirin (between 80mg to 100mg daily) is allowed

• Female: 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 6 months after the last dose of test article. Child bearing potential, a negative urine or serum pregnancy test result before initiating Famitinib. 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 6 months after the last dose of test article.

• Preexisting thyroid dysfunction, even using medical therapy, thyroid function cannot maintain in the normal range

• Abuse of psychiatric drugs or dysphrenia

• Less than 4 weeks from the last clinical trial

• Ascites need treatment

• Immunodeficiency: HIV positive, or other acquired immunodeficiency, congenital immunodeficiency, or organ transplantation

• Evidence of significant medical illness that in the investigator's judgment will substantially increase the risk associated with the subject's participation in and completion of the study.

Related Conditions & MeSH terms

• Colonic Neoplasms
• Colorectal Cancer
• Colorectal Cancer Metastatic
• Colorectal Cancer Recurrent
• Colorectal Neoplasms

Intervention

Drug:
• Famitinib
Famitinib 25 mg p.o. qd

Other:
• placebo
p.o. qd

Locations

Country	Name	City	State
China	Beijing Cancer Hospital, Peking University	Beijing
China	Cancer center, Sun Yet-sen University	Guangzhou	Guangdong

Sponsors (3)

Lead Sponsor	Collaborator
Jiangsu HengRui Medicine Co., Ltd.	Beijing Cancer Hospital, Sun Yat-sen University

Country where clinical trial is conducted

China, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Other	body vitals, laboratory parameters		3 years
Primary	Progression Free Survival(PFS)		3 years
Secondary	Objective response rate(ORR)		12 weeks
Secondary	Disease Control Rate(DCR)		12 weeks
Secondary	Overall Survival(OS)		3 years
Secondary	Quality of Life		42-day cycle visit until disease progress
Secondary	Number of Participants with Adverse Events as a Measure of Safety		3 years