A Study of BKM120 in Adult Japanese Patients With Advanced Solid Tumors

• Status: Completed
• Trial end date: 2011-10-01
• Target enrollment: 0
• Participant gender: All

Summary

In this study, BKM120 will be administered to adult patients with advanced solid tumors whose disease has progressed despite standard therapy or for whom no standard therapy exists. The trial will confirm the safety and tolerability and determine the maximum tolerated dose (MTD) of BKM120 in Japanese patients.

• Phase: Phase 1
• Accepts Healthy Volunteers?: No

Details

• Lead Sponsor: Novartis Pharmaceuticals

Criteria

Inclusion Criteria:

1. Patients with histologically confirmed, advanced unresectable solid tumors who have progressed on (or not been able to tolerate) standard therapy or for whom no standard anticancer therapy exists.

2. At least one measurable or non-measurable lesion as defined by RECIST guidelines for solid tumors.

3. Age ≥ 20 years

4. Eastern Cooperative Oncology Group Performance Status (ECOG P.S.) of ≤ 2

5. Life expectancy of ≥ 12 weeks

6. Patients must have the laboratory values

Exclusion Criteria:

1. Patients with a history of primary central nervous system tumors or brain metastases or who have signs/symptoms attribute to brain metastases and have not been assessed with radiologic imaging to rule out the presence of brain metastases

2. Prior treatment with a PI3K inhibitor

3. Patients with any peripheral neuropathy ≥ CTCAE grade 2

4. Patients with unresolved diarrhea ≥ CTCAE grade 2

5. Women of child-bearing potential who are pregnant or breast feeding. Men or women of reproductive potential not to sign informed consent for birth control. Barrier contraceptives must be used throughout the trial and six months after the end of treatment.

Other protocol-defined inclusion/exclusion criteria may apply