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Brief Title: NKTR-102 Versus Irinotecan in Patients With Second-Line, Irinotecan-Naïve, KRAS Mutant, Colorectal Cancer
Official Title: A Multicenter, Open-Label, Randomized, Phase 2 Study to Evaluate the Efficacy and Safety of NKTR-102 Versus Irinotecan in Patients With Second-Line, Irinotecan-Naive, KRAS-Mutant, Metastatic Colorectal Cancer (mCRC)
Study ID: NCT00856375
Brief Summary: This study will evaluate whether NKTR-102, an investigational drug has an anti-tumor effect in patients with colorectal cancer. This study will also evaluate how the safety and anti-tumor activity of NKTR-102 compares with irinotecan, a cancer drug that is approved for use in the US for treatment of patients with certain types of colorectal cancer.
Detailed Description: NKTR-102 (Topoisomerase I Inhibitor Polymer Conjugate) is a polyethylene glycol (PEG) conjugate of irinotecan. Irinotecan is a topoisomerase I inhibitor approved worldwide. In the US, irinotecan is indicated as a component of first-line therapy in combination with 5 fluorouracil (5 FU) and leucovorin for patients with metastatic carcinoma of the colon or rectum. Irinotecan is also indicated for patients with metastatic carcinoma of the colon or rectum whose disease has recurred or progressed following initial fluorouracil-based therapy. Second-line therapy for colorectal cancer typically involves cetuximab and irinotecan. However, growing evidence indicates that cetuximab (or other EGFR inhibitors) is not appropriate therapy for patients with mutant KRAS. For these patients, irinotecan may be appropriate as a single agent, and a new therapy that could improve upon efficacy and safety would provide an important option for the treatment of advanced colorectal cancer.
Minimum Age: 18 Years
Eligible Ages: ADULT, OLDER_ADULT
Sex: ALL
Healthy Volunteers: No
Investigator Site - Peoria, Peoria, Arizona, United States
Investigator Site - Burbank, Burbank, California, United States
Investigator Site - Los Angeles, Los Angeles, California, United States
Investigator Site - Vallejo, Vallejo, California, United States
Investigator Site - Centralia, Centralia, Illinois, United States
Investigator Site - Louisville, Louisville, Kentucky, United States
Investigator Site - Detroit, Detroit, Michigan, United States
Investigator Site - Buffalo, Buffalo, New York, United States
Investigator Site - Knoxville, Knoxville, Tennessee, United States
Investigator Site - Antwerp, Antwerp, , Belgium
Investigator Site - Celle, Celle, , Germany
Investigator Site - Karlsruhe, Karlsruhe, , Germany
Investigator Site - Hyderabad, Hyderabad, Andra Pradesh, India
Investigator Site - Ahmedabad, Ahmedabad, Gujarat, India
Investigator Site - Bangalore, Bangalore, Karnatak, India
Investigator Site - Bangalore, Bangalore, Karnatak, India
Investigator Site - Kochi, Kochi, Kerata, India
Investigator Site - Mumbai, Mumbai, Maharashtra, India
Investigator Site - Kolkata, Kolkata, West Benagal, India
Investigator Site - Kolkata, Kolkata, West Bengal, India
Investigator Site - Elche, Elche, , Spain
Investigator Site - Madrid, Madrid, , Spain
Investigator Site - Aberdeen, Aberdeen, Scotland, United Kingdom
Investigator Site - Manchester, Manchester, , United Kingdom
Name: Study Director
Affiliation: Nektar Therapeutics
Role: STUDY_DIRECTOR