Breast Cancer Clinical Trial

Safety of BKM120 Monotherapy in Advanced Solid Tumor Patients

Summary

This is a first-in-man, phase I clinical research study with BKM120, a potent and highly specific oral pan-class I phosphatidylinositol-3-kinase (PI3K) inhibitor. The study consists of a dose escalation part followed by a MTD expansion part.

Once the MTD has been defined, the MTD expansion part will be opened for enrollment.

View Eligibility Criteria

Eligibility Criteria

Inclusion Criteria:

All patients:

Histologically-confirmed advanced solid tumors
Progressive, recurrent unresectable disease
World Health Organization (WHO) Performance status ≤ 2
No history of primary brain tumor or brain metastases

MTD Expansion part:

Histologically-confirmed advanced solid tumors
Progressive, recurrent unresectable disease
World Health Organization (WHO) Performance status ≤ 2
No history of primary brain tumor; no brain metastases unless asymptomatic and clinically stable for ≥ 3 months
Patients with genetic or molecular alteration of the PI3K pathway

Exclusion Criteria:

Prior treatment with a PI3K inhibitor
History of or active major depressive episode, bipolar disorder, schizophrenia, or history of suicidal attempt or ideation
No clinically manifest diabetes mellitus (treated and/or with clinical signs)
No acute or chronic renal disease
No acute or chronic liver disease
No acute or chronic pancreatitis
No unresolved diarrhea
No impaired cardiac function or clinically significant cardiac diseases such as ventricular arrhythmia, congestive heart failure, uncontrolled hypertension
No acute myocardial infarction or unstable angina pectoris within the past 3 months
Not pregnant or nursing and fertile patients must use barrier contraceptives

Other protocol-defined inclusion/exclusion criteria may apply

Study is for people with:

Breast Cancer

Phase:

Phase 1

Estimated Enrollment:

107

Study ID:

NCT01068483

Recruitment Status:

Completed

Sponsor:

Novartis Pharmaceuticals

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There are 5 Locations for this study

See Locations Near You

Sarah Cannon Research Institute Dept.ofSarahCannonCancerCtr(4)
Nashville Tennessee, 37203, United States
Novartis Investigative Site
Toronto Ontario, M5G 2, Canada
Novartis Investigative Site
Rotterdam , 3015 , Netherlands
Novartis Investigative Site
Rotterdam , 3075 , Netherlands
Novartis Investigative Site
Barcelona Cataluna, 08035, Spain

How clear is this clinincal trial information?

Study is for people with:

Breast Cancer

Phase:

Phase 1

Estimated Enrollment:

107

Study ID:

NCT01068483

Recruitment Status:

Completed

Sponsor:


Novartis Pharmaceuticals

How clear is this clinincal trial information?

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