Nintedanib (BIBF 1120) vs Placebo in Refractory Metastatic Colorectal Cancer (LUME-Colon 1)

Completed · Phase 3 · Has a placebo group

Conditions studied: Colorectal Neoplasms

In brief

The objective of this Phase III study is to evaluate the efficacy of nintedanib in patients with metastatic colorectal cancer (mCRC) after failure of previous treatment with standard chemotherapy and biological agents.

Key facts

Study ID

NCT02149108

Run by

Boehringer Ingelheim

People needed

768

Starts

2014-09-25

Expected to finish

2016-08-25

Last updated by the study team

2017-07-21

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Age >= 18 years
• Signed informed consent
• Histologically or cytologically confirmed colorectal adenocarcinoma
• Metastatic or locally advanced disease not amenable to curative surgery and/or radiotherapy
• Eastern Cooperative Oncology Group (ECOG) performance status = 1
• At least one measurable lesion according to Response Evaluation Criteria In Solid Tumours (RECIST) version 1.1
• Progression on standard therapies or withdrawn from standard treatment due to unacceptable toxicity. Previous standard treatment must include all of the following:
• - fluoropyrimidine
• - oxaliplatin: Patients treated with oxaliplatin in adjuvant setting should have progressed within 6 months of completion of adjuvant therapy or they must have been treated with oxaliplatin for metastatic disease
• - irinotecan
• - bevacizumab or aflibercept
• - cetuximab or panitumumab for patients with K-Ras wt or Ras wt tumours
• - The remaining standard available therapy as recommended by investigator is best supportive care (note: previous treatment with regorafenib and TAS 102 are allowed and these agents should be administered before study if available to patient according to local standards)
• - Life expectancy of at least 12 weeks
• - Hepatic function: aspartate aminotransferase (AST)/ Alanine Amino Transferase (ALT) = 1.5 X Upper Limit of Normal (ULN) and bilirubin = ULN for patients without liver metastases. AST/ALT = 2.5 X ULN and bilirubin = ULN for patients with liver metastases. Patients with Gilbert syndrome and bilirubin < 2 X ULN and normal AST/ALT are eligible
• Coagulation parameters: International normalised ratio (INR) < 2 and partial prothrombin Time (PTT) = 2xULN

You may not qualify if…

• Previous treatment with nintedanib
• toxicity attributed to previous anticancer therapy that did not resolve to Common Terminology Criteria for Adverse Events (CTCAE) grade =1
• History of other malignancies in the last 5 years, in particular those that could interfere with interpretation of results.
• Serious concomitant disease or medical condition affecting compliance with trial requirements or which are considered relevant for the evaluation of the efficacy or safety of the trial drug,
• Significant cardiovascular diseases
• History of severe haemorrhagic or thromboembolic event in the past 12 months
• Bleeding or thrombotic disorders requiring anticoagulant therapy such as warfarin, or similar agents requiring therapeutic INR monitoring
• Gastrointestinal disorders or abnormalities that would interfere with absorption of study drug
• Patient with brain metastases that are symptomatic and/or require therapy.
• Patients of childbearing potential who are sexually active and unwilling to use a highly effective method of contraception
• Pregnancy or breast-feeding.

Where it is running

• 1199.52.0105 Boehringer Ingelheim Investigational Site — New Haven, Connecticut, United States
• 1199.52.0101 Boehringer Ingelheim Investigational Site — Plainville, Connecticut, United States
• 1199.52.0121 Boehringer Ingelheim Investigational Site — Arlington Heights, Illinois, United States
• 1199.52.0123 Boehringer Ingelheim Investigational Site — Sioux City, Iowa, United States
• 1199.52.0104 Boehringer Ingelheim Investigational Site — Topeka, Kansas, United States
• 1199.52.0114 Boehringer Ingelheim Investigational Site — New Orleans, Louisiana, United States
• 1199.52.0113 Boehringer Ingelheim Investigational Site — Detroit, Michigan, United States
• 1199.52.0125 Boehringer Ingelheim Investigational Site — Omaha, Nebraska, United States
• 1199.52.0119 Boehringer Ingelheim Investigational Site — Johnson City, New York, United States
• 1199.52.0115 Boehringer Ingelheim Investigational Site — Canton, Ohio, United States
• 1199.52.0106 Boehringer Ingelheim Investigational Site — Sylvania, Ohio, United States
• 1199.52.0102 Boehringer Ingelheim Investigational Site — Nashville, Tennessee, United States
• 1199.52.0120 Boehringer Ingelheim Investigational Site — Fort Worth, Texas, United States
• 1199.52.5404 Boehringer Ingelheim Investigational Site — Cdad. de Córdoba, Argentina
• 1199.52.5405 Boehringer Ingelheim Investigational Site — Cdad. de Córdoba, Argentina
• 1199.52.5401 Boehringer Ingelheim Investigational Site — Ciudad Autónoma de Bs As, Argentina
• 1199.52.5403 Boehringer Ingelheim Investigational Site — Ciudad Autónoma de Bs As, Argentina
• 1199.52.5406 Boehringer Ingelheim Investigational Site — Ciudad Autónoma de Bs As, Argentina
• 1199.52.6102 Boehringer Ingelheim Investigational Site — Concord, New South Wales, Australia
• 1199.52.6103 Boehringer Ingelheim Investigational Site — St Leonards, New South Wales, Australia
• 1199.52.6101 Boehringer Ingelheim Investigational Site — Wollongong, New South Wales, Australia
• 1199.52.6104 Boehringer Ingelheim Investigational Site — Heidelberg, Victoria, Australia
• 1199.52.6105 Boehringer Ingelheim Investigational Site — Nedlands, Western Australia, Australia
• 1199.52.6106 Boehringer Ingelheim Investigational Site — Perth, Western Australia, Australia
• 1199.52.0108 Boehringer Ingelheim Investigational Site — Los Angeles, California, United States

Full record on ClinicalTrials.gov

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