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Completed Phase 1 Interventional Results available

Study of CGC-11047 When Used in Individual Combinations With 1) Gemcitabine or 2) Docetaxel or 3) Bevacizumab or 4) Erlotinib or 5) Cisplatin or 6) 5-Flurouracil or 7) Sunitinib in Patients With Advanced Solid Tumors or Lymphoma

ClinicalTrials.gov ID: NCT00705874

Public ClinicalTrials.gov record NCT00705874. 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 22, 2026, 2:15 PM EDT

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

Official title

A Phase I Open Label, Multicenter, Dose-Escalation Study to Determine the Maximum Tolerated Dose, Dose Limiting Toxicity, Safety and Pharmacokinetics of CGC-11047 When Used in Individual Combinations With 1) Gemcitabine or 2) Docetaxel or 3) Bevacizumab or 4) Erlotinib or 5) Cisplatin or 6) 5-Flurouracil or 7) Sunitinib in Patients With Advanced Solid Tumors or Lymphoma

Brief summary

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

This study will aims to determine the maximum tolerated dose of CGC-11047 when used in individual combinations with gemcitabine, or docetaxel, or bevacizumab, or erlotinib or cisplatin or 5-flurouracil or sunitinib in one of 7 treatment arms. The dose of CGC-11047 will be escalated until the maximum tolerated dose is established.

Study identification

NCT ID
NCT00705874
Recruitment status
Completed
Study type
Interventional
Phase
Phase 1
Lead sponsor
Progen Pharmaceuticals
Industry
Enrollment
172 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
May 2006 (Type not available)
Primary completion
Aug 2011 (Actual)
Completion
Sep 2011 (Actual)
Last update posted
Jul 21, 2016

2006 – 2011

United States locations

U.S. sites
12
U.S. states
10
U.S. cities
12
Facility City State ZIP Site status
Rocky Mountain Cancer Centre Denver Colorado — —
Cancer Centres of Florida Ocoee Florida 34761 —
Central Indiana Cancer Centres Indianapolis Indiana 46219 —
Comprehensive Cancer Centres of Nevada Las Vegas Nevada 89169 —
New York Oncology Hematology PC Albany New York 12206 —
Dayton Oncology and Hematology, PA Kettering Ohio 45409 —
Cancer Centres of the Carolinas Greenville South Carolina 29605 —
Texas Oncology, PA Dallas Texas 75246 —
Tyler Cancer Centre Tyler Texas 75702 —
Virginia Oncology Associates Norfolk Virginia 23502 —
Northwest Cancer Specialists - Vancouver Cancer Centre Vancouver Washington 98684 —
North Star Lodge Cancer Centre Yakima Washington 98902 —

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 NCT00705874, 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 Jul 21, 2016 · Synced Oct 22, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00705874 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →