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

A Phase 1b/2a Open-Label Study to Evaluate the Safety and Activity of Once Daily Oral Administration of Tivozanib (AV-951) in Subjects With Non-Small Cell Lung Cancer

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.

Study Overview

• Status: Completed
• Conditions: Carcinoma, Non-Small-Cell Lung
• Intervention / Treatment: Drug: Tivozanib (AV-951)

Detailed Description

The Phase 2a portion of the study was not conducted

• Study Type: Interventional
• Enrollment (Actual): 17
• Phase: Phase 1

Contacts and Locations

Study Locations

• United States
  • District of Columbia
    • Washington, District of Columbia, United States, 20007
      • Georgetown University
  • Kansas
    • Kansas City, Kansas, United States, 66160
      • Kansas University Medical Center
  • New York
    • New York, New York, United States, 10021
      • Memorial Sloan-Kettering

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 18 years and older (Adult, Older Adult)
• Accepts Healthy Volunteers: No
• Genders Eligible for Study: All

Description

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.

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Treatment
• Allocation: Non-Randomized
• Interventional Model: Single Group Assignment
• Masking: None (Open Label)

Number of Arms

1

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
Experimental: Tivozanib (AV-951)	Drug: 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.

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Time Frame
Ph1b: To determine the safety, tolerability, and MTD of tivozanib (AV-951) administered orally QD in subjects with NSCLC	4 weeks (1 cycle)
Ph2a: To determine the ORR of tivozanib (AV-951) administered orally once daily in subjects with NSCLC with no prior anti-angiogenic therapy	8 weeks (2 cycles)

Secondary Outcome Measures

Outcome Measure	Time Frame
Ph1b: To evaluate the PK of tivozanib (AV-951) administered orally QD	8 weeks (2 cycles)
Ph1b: To evaluate the preliminary antineoplastic activity of tivozanib (AV-951) administered orally QD	8 weeks (2 cycles)
Ph2a: To determine the duration of complete and partial responses and time to disease progression (TTP) for subjects treated with tivozanib (AV-951)	8 weeks (2 cycles)
Ph2a: To determine the safety and tolerability of tivozanib (AV-951) administered orally once a day	4 weeks (1 cycle)

Collaborators and Investigators

• Sponsor: AVEO Pharmaceuticals, Inc.
• Investigators: Study Director: Jaroslaw Jac, M.D., AVEO Pharmaceuticals, Inc.; Principal Investigator: Jimmy Hwang, MD, Georgetown University; Principal Investigator: Chao Huang, MD, University of Kansas

Study record dates

Study Major Dates

• Study Start: January 1, 2009
• Primary Completion (Actual): March 1, 2011
• Study Completion (Actual): May 1, 2011

Study Registration Dates

• First Submitted: January 21, 2009
• First Submitted That Met QC Criteria: January 21, 2009
• First Posted (Estimate): January 22, 2009

Study Record Updates

• Last Update Posted (Estimate): June 28, 2012
• Last Update Submitted That Met QC Criteria: June 27, 2012
• Last Verified: June 1, 2012

More Information

Terms related to this study

• Keywords: AV-951; tivozanib
• Additional Relevant MeSH Terms: Respiratory Tract Diseases; Neoplasms; Lung Diseases; Neoplasms by Site; Respiratory Tract Neoplasms; Thoracic Neoplasms; Carcinoma, Bronchogenic; Bronchial Neoplasms; Lung Neoplasms; Carcinoma, Non-Small-Cell Lung
• Other Study ID Numbers: AV-951-08-105