Study of TAK-901 in Adults With Advanced Solid Tumors or Lymphoma

NCT ID: NCT00935844

Last Updated: 2011-12-08

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE1
• Total Enrollment: 20 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2009-10-31
• Study Completion Date: 2011-11-30

Brief Summary

This study is being conducted to evaluate the safety profile and the Maximum Tolerated Dose (MTD) of TAK-901 in adult patients with advanced solid tumors or lymphoma. This study will help to identify the recommended phase 2 dose and infusion duration, and describe the pharmacokinetics of TAK-901.

Conditions

Advanced Solid Tumors; Lymphoma

Keywords

Advanced solid tumors; Lymphoma

Study Design

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

Study Groups

TAK-901 Arm

Group Type: EXPERIMENTAL

TAK-901

Intervention Type: DRUG

This study consists of three sequential parts.

Part 1: Escalating doses of TAK-901 will be administered via IV infusion over a 3-hour period on Days 1, 4, 8, 11, 15, and 18 of each 28-day cycle.

Part 2: Escalating doses of TAK-901 (starting at one-third of the dose identified as the MTD in Part 1) will be administered as a 1-hour infusion on Days 1, 4, 8, 11, 15, and 18 of each 28-day cycle.

Part 3: TAK-901 will be administered to approximately 20 patients using the dose identified as the MTD in the escalation phase. The infusion duration of TAK-901 will be determined after completion of Part 2.

Interventions

TAK-901

This study consists of three sequential parts.

Part 1: Escalating doses of TAK-901 will be administered via IV infusion over a 3-hour period on Days 1, 4, 8, 11, 15, and 18 of each 28-day cycle.

Part 2: Escalating doses of TAK-901 (starting at one-third of the dose identified as the MTD in Part 1) will be administered as a 1-hour infusion on Days 1, 4, 8, 11, 15, and 18 of each 28-day cycle.

Part 3: TAK-901 will be administered to approximately 20 patients using the dose identified as the MTD in the escalation phase. The infusion duration of TAK-901 will be determined after completion of Part 2.

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

Each patient must meet all of the following criteria to be enrolled in the study:

• ECOG performance status of < or equal to 2.
• Diagnosis of solid tumor malignancy or lymphoma for which standard treatment is no longer effective.
• Have a radiographically or clinically evaluable tumor or lymphoma.
• Measurable disease as described in the protocol.
• Suitable venous access for the study-required blood sampling.
• Female patients who are post menopausal, surgically sterile, or agree to practice 2 effective methods of contraception or abstain from heterosexual intercourse.
• Male patients who agree to practice effective barrier contraception or agree to abstain from heterosexual intercourse.
• Voluntary written consent.
• Weigh at least 45 kg.
• Recovered from the reversible effects of prior antineoplastic therapy.
• Meet clinical laboratory values during the screening period as specified in the protocol.
• Left ventricular ejection fraction (LVEF) > or equal to 50% by echocardiogram or multiple acquisition scan (MUGA).

Exclusion Criteria

• Diagnosis of primary CNS malignancy or carcinomatous meningitis.
• Patient has symptomatic brain metastasis.
• Prior bone allogeneic bone marrow or stem cell transplant.
• Prior radiotherapy involving > or equal to 30% of the hematopoietically active bone marrow, within 21 days before the start of the study drug.
• Systemic antineoplastic therapy within 28 days before the start of the study drug, except for luteinizing hormone-releasing-hormone (LHRH) agonist therapy.
• Exposure to nitrosureas or mitomycin C within 42 days before the start of the study drug.
• Treatment with monoclonal antibodies within 28 days before the start of the study drug.
• Known allergy or hypersensitivity to compounds of similar chemical composition to TAK-901 or its excipient, Captisol.
• Female patients who are lactating or who have a positive serum pregnancy test during the screening period or a positive serum pregnancy test during the screening period.
• Myocardial infarction within 6 months before enrollment.
• Evidence of current uncontrolled cardiovascular conditions, including cardiac arrhythmias, congestive heart failure, angina, or electrocardiographic evidence of acute ischemia or active conduction system abnormalities.
• Abnormalities on 12-lead electrocardiogram (ECG) as specified in the protocol.
• Infection requiring systemic anti-infective therapy within 14 days before the start of study drug.
• Known human immunodeficiency virus (HIV)positive, hepatitis B surface antigen-positive status, or known or suspected active hepatitis C infection.
• Diagnosed or treated for another malignancy within 2 years before the start of study drug or previously diagnosed with another malignancy and have any evidence of residual disease.
• Any serious medical or psychiatric illness that could, in the investigator's opinion, potentially interfere with the completion of treatment.
• Treatment with any investigational products within 28 days before the first dose of study drug.
• Systemic use of strong CYP3A inhibitors or inducers (as specified in the protocol) within 14 days before the first dose of study drug.

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

Sponsors

Millennium Pharmaceuticals, Inc.

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Medical Monitor

Role: STUDY_DIRECTOR

Millennium Pharmaceuticals, Inc.

Locations

The University of Michigan

Ann Arbor, Michigan, United States

Karmanos Cancer Center

Detroit, Michigan, United States

Fox Chase Cancer Center

Rockledge, Pennsylvania, United States

Countries

United States

Other Identifiers

C19001

Identifier Type: -

Identifier Source: org_study_id