A Trial of ABI-010 & ABI-007 in Patients With Advanced Non-Hematologic Malignancies

NCT ID: NCT00820768

Last Updated: 2018-04-11

Basic Information

• Recruitment Status: WITHDRAWN
• Clinical Phase: PHASE1
• Study Classification: INTERVENTIONAL
• Study Start Date: 2012-04-01
• Study Completion Date: 2014-04-01

Brief Summary

To determine MTD and DLT of ABI-010 given weekly every three weeks followed by one week of rest (Cycle 1). Determine MLD and DLT in combination with ABI-007; to characterize the toxicities of ABI-010 alone and in combination with ABI-007.

Conditions

Solid Tumor

Study Design

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

Study Groups

ABI-010

Group Type: EXPERIMENTAL

ABI-010

Intervention Type: DRUG

17-AAG and ABI-007

Interventions

ABI-010

17-AAG and ABI-007

Intervention Type: DRUG

Other Intervention Names

17-AAG and ABI-007

Eligibility Criteria

Inclusion Criteria

1. Pathologically confirmed advanced solid tumor malignancy.

2. Measurable or evaluable advanced solid tumors.

3. Patients with advanced solid tumor malignancy who failed standard therapy or for whom no standard therapy exists. Patients failing standard therapy should have received no more than 3 prior chemotherapy regimens.

4. Patients must have recovered for at least 3 weeks from prior treatment regimens and have no residual toxicity > Grade 2 (with the exception of peripheral neuropathy which must have improved to ≤ Grade 1).

5. Patient should have full recovery from any reversible side effects of prior chemotherapy.

6. Patient should have full recovery for at least 4 weeks since major surgery.

7. ECOG performance status 0-2.

8. Age ≥18 years.

9. Patient must have the following blood counts at Baseline:

• WBC ≥ 3.0 x 10 cells/L.
• ANC ≥ 1.5 x 10 cells/L.
• Platelets ≥ 100 x 10 cells/L.
• Hgb ≥ 9grams/dL.

10. Patient must have the following blood chemistry levels at Baseline:

• AST (SGOT), ALT (SGPT) ≤ 1.5x upper limit of normal range (ULN);
• Total Bilirubin ≤ ULN;
• Alkaline phosphatase ≤ 2.5x ULN (unless bone metastasis is present in the absence of liver metastasis;
• Creatinine ≤ 1.5 mg/dL

11. Peripheral neuropathy Grade ≤ 1 by NCI CTCAE V3.0.

12. Female of childbearing potential with negative serum pregnancy test within 72 hours prior to the first dose of study drug.

13. Males and females with reproductive potential must agree to utilize contraception considered adequate and appropriate by the investigator (including one barrier method) for the duration of the study and for 2 months after the end of study.

14. Life expectancy ≥ 3 months.

15. Informed consent document has been obtained.

16. If obese, a patient must be treated with doses calculated using his/her actual BSA (the physician must be comfortable treating at the full BSA dose regardless of BSA).

Exclusion Criteria

1. Concurrent therapy (chemotherapy, hormonal therapy, kinase inhibitors, immunotherapy, etc) for advanced solid tumor.

2. Patients receiving known CYP450 3A4 inhibitors.

3. Bisphosphonate therapy is allowed, however, patients should be stable on their current bisphosphonate, with no change, start or stop of treatment within 4 weeks prior to enrollment.

4. Patients with known brain metastases or leptomeningeal tumor involvement should be excluded from this clinical trial.

5. Uncontrolled intercurrent illness including, but not limited to, serious ongoing or active infection, symptomatic congestive heart failure, unstable angina pectoris, cardiac arrhythmia, or psychiatric illness/ social situations that would limit compliance with study.

6. Patients with significant cardiovascular disease including congestive heart failure (New York Heart Association Class III or IV), active angina pectoris or recent myocardial infarction (within the last 6 months).

7. History of other malignancy within the last 5 years which would affect the diagnosis or assessment of advanced solid tumor excluding non-melanomatous skin cancer and cervical carcinoma.

8. Patients who have received an investigational drug within the previous 3 weeks.

9. Patient is currently enrolled in any other clinical study in which investigational procedures are performed or investigational therapies are administered. A patient may not enroll in such clinical trials while participating in this study.

10. Pregnant or nursing women.

11. Patients with history of allergy or hypersensitivity to the study drug or its excipients.

12. Patients with marked baseline prolongation of QT/QTc interval (>450 milliseconds).

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

Sponsors

Celgene

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Henry C. Pitot, MD

Role: PRINCIPAL_INVESTIGATOR

Mayo Clinic

Locations

Mayo Clinic

Rochester, Minnesota, United States

Countries

United States

Other Identifiers

CA501

Identifier Type: -

Identifier Source: org_study_id