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Completed Phase 1 Interventional

STA-5312 Administered on Alternate Weekdays Every Two Weeks to Patients With Hematologic Malignancies and Patients With Solid Tumors

ClinicalTrials.gov ID: NCT00088101

Public ClinicalTrials.gov record NCT00088101. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 1, 2026, 11:10 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

Phase I Trial of STA-5312 Administered on Alternate Weekdays Every Two Weeks to Patients With Hematological Malignancies and Patients With Solid Tumors

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The purpose of this study is to determine the safety, toxicity and patient tolerance of STA-5312 administered intravenously to patients with relapsed or refractory hematological malignancies and patients with solid tumors.

Study identification

NCT ID
NCT00088101
Recruitment status
Completed
Study type
Interventional
Phase
Phase 1
Lead sponsor
Synta Pharmaceuticals Corp.
Industry
Enrollment
42 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Feb 2004 (Type not available)
Primary completion
Not listed
Completion
Dec 2004 (Type not available)
Last update posted
Dec 4, 2008

2004

United States locations

U.S. sites
8
U.S. states
7
U.S. cities
8
Facility City State ZIP Site status
Wilshire Oncology Medical Group Pomona California 91767 —
Baptist Cancer Institute Jacksonville Florida 32207 —
University of Chicago Chicago Illinois 60637 —
Tufts New England Medical Center Boston Massachusetts 02111 —
Newark Beth Israel Medical Center Newark New Jersey — —
Carolinas HealthCare System Charlotte North Carolina 28203 —
The West Clinic Memphis Tennessee 38120 —
The Sarah Cannon Cancer Center Nashville Tennessee 37203 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00088101, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Dec 4, 2008 · Synced Oct 1, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00088101 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →