An Open-Label Study of QD Oral Administration of Tivozanib (AV-951) in Subjects With Non-Small Cell Lung Cancer (NSCLC)

NCT ID: NCT00826878

Last Updated: 2012-06-28

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE1
• Total Enrollment: 17 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2009-01-31
• Study Completion Date: 2011-05-31

Brief Summary

This is a standard Phase 1b and 2a, multi-center, study design that will examine the safety, tolerability, and maximum tolerated dose of tivozanib (AV-951) with this dosing schedule, as well as overall response rate of tivozanib (AV-951) administration in NSCLC.

Detailed Description

The Phase 2a portion of the study was not conducted

Conditions

Carcinoma, Non-Small-Cell Lung

Study Design

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

Study Groups

Tivozanib (AV-951)

Group Type: EXPERIMENTAL

Tivozanib (AV-951)

Intervention Type: DRUG

Subjects will receive 1.0 or 1.5 mg tivozanib (AV-951) once daily continuously beginning on Day 1 for 4 weeks. One cycle will be defined as 4 weeks of treatment. Cycles will be repeated every 4 weeks in the absence of disease progression or unacceptable toxicity.

Minimum of 8 weeks (2 consecutive dosing cycles), if tolerated.

Interventions

Tivozanib (AV-951)

Subjects will receive 1.0 or 1.5 mg tivozanib (AV-951) once daily continuously beginning on Day 1 for 4 weeks. One cycle will be defined as 4 weeks of treatment. Cycles will be repeated every 4 weeks in the absence of disease progression or unacceptable toxicity.

Minimum of 8 weeks (2 consecutive dosing cycles), if tolerated.

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

1. Age 18 years or older, of either sex and of any race.

2. Histologically or cytologically confirmed NSCL.

3. Stage IIIB (with malignant pleural effusion) or stage IV or recurrent disease.

4. Subjects that have recurred or progressed following standard therapy or failed standard therapy; or subjects that are not candidates for or unwilling to undergo standard therapy.

5. Disease that is currently not amenable to curative surgical intervention, due to either non-resectability of the tumor or medical contraindications.

6. Prior VEGF directed therapy

7. Prior chemotherapy

8. At least 4 weeks since prior immunotherapy (eg, IL-2, IFN, etc.) or biological therapy (eg, MABs) prior to the first dose of study drug.

9. At least 1 week since prior treatment with warfarin, acenocoumarol, fenprocoumon, or similar agents.

10. At least 4 weeks since prior systemic hormonal therapy.

11. At least 2 weeks since prior use of herbal preparations/supplements.

12. At least 2 weeks since prior treatment with CYP3A4 inducers or inhibitors.

13. At least 2 weeks since prior radiotherapy to ≤25% of bone marrow, or at least 4 weeks since prior radiotherapy to > 25% of bone marrow.

14. Measurable or evaluable disease; subjects enrolled in the Phase 2a study must have measurable disease by RECIST criteria.

15. ECOG performance 0-1 and life expectancy ≥ 3 months.

16. Ability to give written informed consent.

Exclusion Criteria

1. Subjects with central lung lesions involving major blood vessels.

2. Primary CNS malignancies or symptomatic CNS metastases; subjects with previously treated brain metastasis will be allowed if the brain metastasis have been stable without steroid treatment for at least 3 months following prior treatment (radiotherapy or surgery).

3. Hematologic malignancies (including leukemia in any form, lymphoma, and multiple myeloma).

4. Hematologic abnormalities:

5. Serum chemistry abnormalities:

6. Significant cardiovascular disease

7. Subjects with delayed healing of wounds, active gastric ulcers, or unhealed bone fractures.

8. Serious/active infection or infection requiring parenteral antibiotics.

9. Inadequate recovery from any prior surgical procedure or major surgical procedure within 6 weeks prior to administration of first dose of study drug.

10. Inability to comply with protocol requirements.

11. History of ≥ Grade 2 hemoptysis within 6 months prior to administration of first dose of study drug; ongoing bleeding (hemoptysis, hematemesis, hematochezia or melena) or history of clinically significant bleeding within 6 months prior to administration of first dose of study drug.

12. Cerebrovascular accident within 12 months prior to administration of first dose of study drug, or peripheral vascular disease with claudication on walking less than 1 block.

13. Deep venous thrombosis or pulmonary embolus within 6 months prior to administration of first dose of study drug.

14. Subjects with a "currently active" second primary malignancy other than non-melanoma skin cancers or nonmetastatic prostate cancer. Subjects are not considered to have a "currently active" malignancy if they have completed anti-cancer therapy and have been disease free for >2 years.

15. If female, pregnant or lactating.

16. No childbearing potential or the use of effective contraception by all fertile male and female subjects during the study and for 30 days after the last dose of study drug. All subjects must agree to use a highly effective method of contraception (including their partner).

17. Known concomitant genetic or acquired immune suppression disease such as HIV.

18. Inadequate recovery from prior antineoplastic therapy.

19. Life-threatening illness or organ system dysfunction compromising safety evaluation.

20. Psychiatric disorder, altered mental status precluding informed consent or necessary testing.

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

Sponsors

AVEO Pharmaceuticals, Inc.

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Jaroslaw Jac, M.D.

Role: STUDY_DIRECTOR

AVEO Pharmaceuticals, Inc.

Jimmy Hwang, MD

Role: PRINCIPAL_INVESTIGATOR

Georgetown University

Chao Huang, MD

Role: PRINCIPAL_INVESTIGATOR

University of Kansas

Naiyer Rizvi, MD

Role: PRINCIPAL_INVESTIGATOR

Memorial Sloan Kettering Cancer Center

Locations

Georgetown University

Washington D.C., District of Columbia, United States

Kansas University Medical Center

Kansas City, Kansas, United States

Memorial Sloan-Kettering

New York, New York, United States

Countries

United States

Other Identifiers

AV-951-08-105

Identifier Type: -

Identifier Source: org_study_id