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Safety Study Of SNX-5422 To Treat Solid Tumor Cancers And Lymphomas

Phase 1 Study Of SNX-5422 Mesylate In Adults With Refractory Solid Tumor Malignancies And Lymphomas

Status
Completed
Phases
Phase 1
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00647764
Enrollment
32
Registered
2008-04-01
Start date
2008-03-31
Completion date
2010-09-30
Last updated
2012-05-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Leukemia, Lymphoid Malignancy (Lymphoma and CLL), Lymphoma, Solid Tumor Malignancy

Brief summary

Hsp90 is a chemical in the body that is involved in promotion of cancer. SNX-5422 is an experimental drug that blocks Hsp90. It is being evaluated for safety and efficacy in patients with cancer.

Interventions

DRUGSNX-5422 Mesylate Hsp90 inhibitor

dose escalated, tablets twice a week; undetermined duration until disease progression

Sponsors

National Cancer Institute (NCI)
CollaboratorNIH
Esanex Inc.
Lead SponsorINDUSTRY

Study design

Allocation
NON_RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Solid tumors or lymphoid malignancies refractory to standard therapy * measurable disease * recovery to Grade \< 1 toxicity due to prior adverse event or chemotherapy * no chemotherapy within 4 weeks of entering study * Age \> 18 years * Karnofsy \>= 60% * Life expectancy \> 3 months * normal or adequate organ and marrow function

Exclusion criteria

* receiving other investigational agents * brain metastases * uncontrolled medical illness * HIV+ receiving combination antiretroviral therapy * significant GI disease

Design outcomes

Primary

MeasureTime frame
MTD, safety and toxicitycontinuous

Secondary

MeasureTime frame
pharmacokinetic profile of SNX-5422first cycle
tumor response measured by X-rays or scansafter every 2 cycles

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026