AzTrials
AzTrials

Liver CancerPhase 2NCT00054262

T900607 in Treating Patients With Unresectable Liver Cancer

A Phase 2 study testing T900607 in people with Liver Cancer, run by University Hospitals Seidman Cancer Center at 1 site in United States.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
Search all trials

Trial summary

RATIONALE: Drugs used in chemotherapy use different ways to stop tumor cells from dividing so they stop growing or die. PURPOSE: Phase II trial to study the effectiveness of T900607 in treating patients who have unresectable liver cancer. Read more about this study

Who is it for?
Ages 18 years and older
Conditions the study is for
Liver Cancer
What is being tested?
T900607
How many people
Not given
Where
1 siteUnited States
Study dates
Nov 2002to Sep 2010
Phase
Phase 2
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

DISEASE CHARACTERISTICS:

  • Histologically or cytologically confirmed unresectable hepatocellular carcinoma (HCC)
  • Bidimensionally measurable disease defined as at least 1 lesion that is 1 cm or more in 2 dimensions by CT scan
  • Class A or B Child-Pugh liver classification
  • No prior CNS metastases or carcinomatous meningitis

PATIENT CHARACTERISTICS:

Age

  • 18 and over

Performance status

  • Karnofsky 70-100%

Life expectancy

  • At least 12 weeks

Hematopoietic

  • Absolute neutrophil count at least 1,500/mm^3*
  • Platelet count at least 100,000/mm^3*
  • Hemoglobin at least 8.5 g/dL* NOTE: *More than 7 days since prior blood transfusions or growth factors

Hepatic

  • Bilirubin no greater than 1.5 times upper limit of normal (ULN)
  • Albumin greater than 2.5 g/dL
  • AST and ALT no greater than 3 times ULN
  • INR no greater than 1.5 (unless receiving anticoagulants)

Renal

  • Creatinine no greater than 2 times ULN

Cardiovascular

  • LVEF at least 50%
  • No New York Heart Association class III or IV cardiac disease
  • No acute anginal symptoms

Other

  • Not pregnant or nursing
  • Negative pregnancy test
  • Fertile patients must use effective contraception during and for 3 months after study
  • No severe concurrent disease, infection, or co-morbidity that would preclude study entry
  • No other malignancy within the past 5 years except adequately treated basal cell or squamous cell skin cancer or carcinoma in situ of the cervix

PRIOR CONCURRENT THERAPY:

Biologic therapy

  • No prior immunotherapy for HCC
  • No concurrent therapeutic biological response modifier

Chemotherapy

  • No prior chemotherapy for HCC
  • No prior chemoembolization for HCC
  • No other concurrent cytotoxic chemotherapy

Endocrine therapy

  • At least 6 weeks since prior hormonal therapy (an indicator lesion must exist outside the area of therapy
  • No concurrent hormonal anticancer therapy

Radiotherapy

  • No prior radiotherapy for HCC
  • At least 6 weeks since prior radiofrequency ablation, selective internal radiation, or embolization (an indicator lesion must exist outside the area of therapy)
  • No concurrent radiotherapy (including palliative therapy)

Surgery

  • At least 6 weeks since prior surgical resection (an indicator lesion must exist outside the area of therapy)
  • Recurrence at the margin of the surgical resection is allowed
  • At least 6 weeks since prior cryosurgery
  • More than 4 weeks since other prior major surgery

Other

  • More than 4 weeks since prior investigational therapy
  • At least 6 weeks since prior intratumoral ethanol injection (an indicator lesion must exist outside the area of therapy)
  • No other concurrent investigational anticancer therapy

Trial locations and contacts

1 site in 1 country.

United States1 site
  • Ireland Cancer Center

    Cleveland, Ohio, 44106-1714

Other trials in United States

About this study

Official title: A Phase II Study Of Intravenous T900607-Sodium In Subjects With Chemotherapy-Naive Unresectable Hepatocellular Carcinoma

RATIONALE: Drugs used in chemotherapy use different ways to stop tumor cells from dividing so they stop growing or die.

PURPOSE: Phase II trial to study the effectiveness of T900607 in treating patients who have unresectable liver cancer.

Read the detailed description

OBJECTIVES:

  • Determine the complete and partial response rates of patients with chemotherapy-naïve unresectable hepatocellular carcinoma treated with T900607.
  • Determine the efficacy of this drug, in terms of duration of response and time to disease progression, in these patients.
  • Determine the pharmacokinetics of this drug in these patients.
  • Determine the safety profile of this drug in these patients.

OUTLINE: This is a multicenter study.

Patients receive T900607 IV over 1 hour once weekly. Treatment continues in the absence of disease progression or unacceptable toxicity.

Patients are followed every 3 months.

PROJECTED ACCRUAL: A total of 20-35 patients will be accrued for this study.

Conditions
Liver Cancer
Being tested
T900607
Keywords
localized unresectable adult primary liver cancer, advanced adult primary liver cancer, adult primary hepatocellular carcinoma
Medical subject headings
Liver Neoplasms, Carcinoma, Hepatocellular

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • T900607Drug

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted6 Feb 2003 (estimated)
  2. Study startNov 2002
  3. Primary completionMar 2004
  4. Study completionSep 2010

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase 2
Primary purpose
Treatment
Masking
None (open label)
IDs, dates and publications
ClinicalTrials.gov ID
NCT00054262
Sponsor's protocol ID
TULA-TULI-2202
Other IDs
CWRU-100211, CDR0000270198, TULA-T-607-004
Status last verified
Sep 2010
First submitted
5 Feb 2003
Last updated
18 Jul 2013
Results posted
No

Questions about this trial

What is this clinical trial studying?

A Phase 2 study testing T900607 in people with Liver Cancer, run by University Hospitals Seidman Cancer Center at 1 site in United States.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 18 Jul 2013. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

What does this phase mean?

Phase 2 studies give the treatment to a larger group to see whether it has the intended effect and to keep checking safety.

Not every study follows the same path, and some studies (observational studies, device studies) have no phase.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 18 Jul 2013.

Free account

Log in to keep searching

You’ve used your 3 free searches. AzTrials is free: log in or create a free account to keep searching clinical trials and save the ones you want to follow.

Create a free accountLog in