Chronic Lymphocytic Leukemia Clinical Trial

Safety and Tolerability of HSC835 in Patients With Hematological Malignancies

Summary

This study evaluated the safety and tolerability of using HSC835 in patients with hematological malignancies.

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Eligibility Criteria

Inclusion Criteria:

Patients with a diagnosis that qualifies them for a DUCBT
Absence of recent active mold infection
Adequate organ function
Availability of eligible donor material

Exclusion Criteria:

Pregnancy or breastfeeding women and women of child-bearing potential unless two acceptable forms of contraception are being used
Human immunodeficiency virus (HIV) infection
Active infection
Extensive prior chemotherapy
Prior myeloablative allotransplantation or autologous transplant.

Study is for people with:

Chronic Lymphocytic Leukemia

Phase:

Phase 1

Estimated Enrollment:

27

Study ID:

NCT01474681

Recruitment Status:

Completed

Sponsor:

Novartis Pharmaceuticals

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There is 1 Location for this study

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Novartis Investigative Site
Minneapolis Minnesota, 55455, United States

How clear is this clinincal trial information?

Study is for people with:

Chronic Lymphocytic Leukemia

Phase:

Phase 1

Estimated Enrollment:

27

Study ID:

NCT01474681

Recruitment Status:

Completed

Sponsor:


Novartis Pharmaceuticals

How clear is this clinincal trial information?

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