CI

At a glance

ClinicalIndex Comparison Record
Phase 1Completed· 9 enrolled
Drug / intervention
Anti-Transforming Growth Factor-beta (GC 1008)drug
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT00923169
NCT00923169Phase 1Completed

A Phase 1 Study of the Safety and Efficacy of GC1008: A Human Anti-Transforming Growth Factor-Beta (TGFBeta) Monoclonal Antibody in Patients With Advanced Renal Cell Carcinoma or Malignant Melanoma

National Cancer Institute (NCI)·interventional·Posted Jun 18, 2009·Updated Oct 29, 2019

In Brief

A Phase 1 clinical trial evaluating Anti-Transforming Growth Factor-beta (GC 1008) for Renal Cell Carcinoma. Completed, enrolled 9 participants across 1 site.

Detailed Summary

Background: * GC1008 is a genetically engineered antibody designed to block the activity of transforming growth factor-beta (TGF-beta). Although TGF-beta has some normal and beneficial effects in the body, it is often over-produced in malignant melanoma tumors, and it can help the melanoma grow and spread. * Part 1 of this study enrolled 22 subjects with malignant melanoma or kidney cancer to determine the highest safe dose of GC1008, which was found to be 15 mg/kg. * Three of 22 patients with malignant melanoma in Part 1 of the study developed skin problems, but it is not known if these problems were related to the administration of GC1008. Objectives: -To determine the frequency of adverse skin side effects of GC1008 in patients with malignant melanoma. Eligibility: -Patients 18 years of age and older with malignant melanoma for whom previous treatment was not successful. Design: * GC1008 is given intravenously (through a vein) at a dose of 15 mg/kg or 10 mg/kg for four doses on study days 0, 28, 42 and 56 (one treatment cycle). Patients whose cancer responds to GC1008 may receive one or two additional treatment cycles of four doses given every two weeks. * Physical exam and vital signs on study days 1, 14, 28, 42, 56, 84 and 140. * Vitals signs on study days 0, 14, 28, 42, 56, 84 and 140. * Frequent blood sample collections for routine safety tests, measurement of blood levels of GC1008, analysis for antibodies against GC1008 and for research studies. * CT or MRI scan, bone scan and PET CT scan before treatment and on study day 84 and 140. * Biopsy of apparently normal skin before treatment and again on day 84. * Review of medicines and well being on study days 0, 14, 28, 42, 56, 84, 112 and 140. * Follow-up visits every 3 months for up 2 years for patients who have not received additional treatment for their cancer. Evaluations include physical exam, CT or MRI scan, PET CT scan, blood tests and possibly tumor biopsies.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesUnited States
Collaborators--

Timeline

Phase 1CompletedFinished
2006200720082009201020112012201320142015201620172018201920202021202220232024202520262027
First PostedJun 18, 2009
Enrollment StartJul 9, 2006
Primary CompletionJan 20, 2010
TodayJul 2, 2026
Enrollment to primary: 3.5 yearsPosted 17.0 years ago

Interventions

Anti-Transforming Growth Factor-beta (GC 1008)drug