Study of TKI 258 in Combination With Xeloda and Oxaliplatin in Advanced Colorectal and Gastric Cancer

NCT ID: NCT02720926

Last Updated: 2016-03-28

Basic Information

• Recruitment Status: TERMINATED
• Clinical Phase: PHASE1
• Total Enrollment: 3 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2011-09-30
• Study Completion Date: 2012-01-31

Brief Summary

Standard "3+3" dose escalation design of TKI258/XELOX in advanced gastric/gastro-oesophageal and colorectal cancer.

Detailed Description

This is a "3+3" dose escalation design with 4 pre-defined TKI258 dose levels (200mg, 300mg, 400mg and 500mg daily with 5 days on and 2 days off schedule) in combination with a fixed standard dose of XELOX (Capecitabine and Oxaliplatin) to establish the recommended phase 2 dose.

Conditions

Colorectal Cancer; Gastric Cancer

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

TKI258 combined with Xeloda/Oxaliplatin

TKI258 200 mg once a day (OD) 5 days on/2 days off Capecitabine (Xeloda) 2000 mg/m2 bid d1-14 Oxaliplatin 130mg/m2 d1 q21days

Group Type: EXPERIMENTAL

Xeloda,

Intervention Type: DRUG

Capecitabine (xeloda): 2000mg/m2, twice a day on Day 1-14;

Oxaliplatin

Intervention Type: DRUG

Oxaliplatin: 130mg/m2 day 1 every 21days

TKI258

Intervention Type: DRUG

4 dose levels of TKI258: 200mg, 300mg, 400mg, 500mg once daily, 5days on and 2 days off;

Interventions

Xeloda,

Capecitabine (xeloda): 2000mg/m2, twice a day on Day 1-14;

Intervention Type: DRUG

Oxaliplatin

Oxaliplatin: 130mg/m2 day 1 every 21days

Intervention Type: DRUG

TKI258

4 dose levels of TKI258: 200mg, 300mg, 400mg, 500mg once daily, 5days on and 2 days off;

Intervention Type: DRUG

Other Intervention Names

capecitabine

Eligibility Criteria

Inclusion Criteria

1. Patients must have histologically confirmed gastric, gastro-oesophageal or colorectal adenocarcinoma.

2. The gastric or gastro-oesophageal cancer must be locally advanced unresectable or metastatic. Colorectal cancer must be metastatic and for which subsequent resection of all metastatic disease is assessed not to be feasible.

3. Age >18 years.

4. Eastern Cooperative Oncology Group (ECOG) performance status <2 (Karnofsky >60%, see Appendix A).

5. Life expectancy of greater than 3 months

6. Patients must have normal organ and marrow function as defined below:

• leukocytes >3,000/mcL
• absolute neutrophil count >1,500/microliter (mcL) TKI258/XELOX phase 1 protocol version 3.3 Dated 30 November 2011 1 3
• platelets >100,000/mcL
• total bilirubin <= 1.5 x upper limit of normal (ULN)
• aspartate aminotransferase (AST)/alanine aminotransferase (ALT) <2.5 X institutional upper limit of normal
• creatinine within normal institutional limits OR
• creatinine clearance >55 mL/min for patients with creatinine levels above institutional normal.

7. The effects of TKI258 and XELOX on the developing human fetus are unknown. For this reason, women of child-bearing potential and men must agree to use adequate contraception (hormonal or barrier method of birth control; abstinence) prior to study entry and for the duration of study participation. Should a woman become pregnant or suspect she is pregnant while participating in this study, she should inform her treating physician immediately.

8. Baseline left ventricular ejection fraction (LVEF) >= 50%

9. Ability to understand and the willingness to sign a written informed consent document.

Exclusion Criteria

1. Patients are not considered to have a "currently active" malignancy if they have TKI258/XELOX phase 1 protocol version 3.3 Dated 30 November 2011 1 4 completed therapy and are considered to have a less than 30% risk of relapse.

2. Pregnant women are excluded from this study because of the potential for teratogenic or abortifacient effects. Because there is an unknown but potential risk for adverse events in nursing infants secondary to treatment of the mother with TKI258 or XELOX, breastfeeding should be discontinued if the mother is treated with TKI258 or XELOX.

3. Patients with prior history of transient ischemia attack or cerebrovascular disease or prior history of ischemia heart disease or myocardia infarction and 2 or more risk factors: ever smoker with > 30 packs per year exposure or on medication for diabetes mellitus or hypertension or hyperlipidemia.

• Patients who are not agreeable for collection of tumor tissue for correlative studies
• Patients from whom tumor tissue for correlative studies cannot be safely obtained.

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Novartis

INDUSTRY

Sponsor Role: collaborator

National Cancer Centre, Singapore

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Iain BH Tan, Dr

Role: PRINCIPAL_INVESTIGATOR

National Cancer Centre, Singapore

Locations

National Cancer Centre singapore

Singapore, , Singapore

Countries

Singapore

Other Identifiers

NCC 10-03

Identifier Type: -

Identifier Source: org_study_id