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CompletedNCT00012324Updated Jun 26, 2013

Nolatrexed Dihydrochloride Compared With Doxorubicin in Treating Patients With Recurrent or Unresectable Liver Cancer

A Phase 3 interventional study of doxorubicin hydrochloride and nolatrexed dihydrochloride in Liver Cancer, sponsored by Eximias Pharmaceutical. Completed at 42 sites in 3 countries. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2013-06-26.

Sponsored by Eximias Pharmaceutical · Phase 3, Interventional, and Treatment

Phase
Phase 3
Study type
Interventional
Allocation
Randomized
Ages
18 Years and older
Sex
All
01

Study summary

RATIONALE: Drugs used in chemotherapy use different ways to stop tumor cells from dividing so they stop growing or die. It is not yet known which chemotherapy regimen is more effective for liver cancer.

PURPOSE: Randomized phase III trial to compare the effectiveness of two different chemotherapy regimens in treating patients who have recurrent or unresectable liver cancer.

Read the detailed description

OBJECTIVES:

  • Compare the overall survival in patients with unresectable or recurrent hepatocellular carcinoma treated with nolatrexed dihydrochloride vs doxorubicin.
  • Compare time to progression, time to treatment failure, and response rates in patients treated with these regimens.
  • Compare the probability of survival at 3, 6, 9, and 12 months in patients treated with these regimens.
  • Compare the safety and clinical benefit of these regimens in these patients.
  • Compare the response rates and survival of patients who have received prior therapy or no prior therapy after treatment with these two regimens.
  • Compare the rates of conversion from unresectable to resectable lesions in patients treated with these regimens.

OUTLINE: This is a randomized, open-label, multicenter study. Patients are stratified according to CLIP score (0-1 vs 2-3) and Karnofsky performance status (60-70% vs 80-100%). Patients are randomized to one of two treatment arms.

  • Arm I: Patients receive nolatrexed dihydrochloride IV continuously on days 1-5.
  • Arm II: Patients receive doxorubicin IV on day 1. Treatment continues in both arms every 3 weeks in the absence of unacceptable toxicity or disease progression.

Patients are followed every 2 months for survival.

PROJECTED ACCRUAL: Approximately 446 patients (223 per treatment arm) will be accrued for this study within 12 months.

02

Conditions studied

  • Liver Cancer

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Keywords

  • localized unresectable adult primary liver cancer
  • advanced adult primary liver cancer
  • recurrent adult primary liver cancer
  • adult primary hepatocellular carcinoma
03

In context

Liver Neoplasms

1,391 studies on the registry are indexed under Liver Neoplasms; 345 are open to participants now.

Browse Liver Neoplasms studies →

Lead sponsor

This is the only study on the registry with Eximias Pharmaceutical as lead sponsor.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Eligibility criteria

DISEASE CHARACTERISTICS:

  • Histologically or cytologically proven or presumptive diagnosis of hepatocellular carcinoma

    • Presumptive diagnosis based on rising alpha-fetoprotein (AFP) levels over 2 assessments, CT scan or MRI of liver, spiral CT scan of portal/splenic vein, and biopsy evidence of cirrhosis
    • Unresectable or recurrent disease after prior surgical resection or embolization therapy
  • Fibrolamellar histology allowed if considered surgically unresectable based on tumor size, extrahepatic involvement, or multiple lobe involvement
  • CLIP (Cancer of the Liver Italian Program) score less than 4
  • Concurrent assignment to a transplantation list allowed

PATIENT CHARACTERISTICS:

Age:

  • 18 and over

Performance status:

  • Karnofsky 60-100%

Life expectancy:

  • Not specified

Hematopoietic:

  • Absolute neutrophil count at least 1,200/mm\^3
  • Platelet count at least 80,000/mm\^3

Hepatic:

  • Bilirubin no greater than 3.0 mg/dL (except for known Gilbert's Syndrome)
  • AST no greater than 5 times upper limit of normal (ULN)
  • PT no greater than 1.5 times ULN

Renal:

  • Creatinine no greater than 2.0 mg/dL

Cardiovascular:

  • No uncontrolled hypertension within the past 3 months
  • No unstable angina, symptomatic congestive heart failure, or myocardial infarction within the past 3 months
  • No uncontrolled cardiac arrhythmia

Other:

  • Not pregnant or nursing
  • Negative pregnancy test
  • Fertile patients must use effective contraception
  • No active bacterial infections
  • HIV negative
  • No AIDS
  • No other primary malignancy except carcinoma in situ of the cervix or urinary bladder or non-melanoma skin cancer
  • No mental incapacitation or psychiatric illness that would preclude study participation
  • No other severe disease that would preclude study participation
  • Candidate for placement of a central venous access device

PRIOR CONCURRENT THERAPY:

Biologic therapy:

  • Prior biologic therapy allowed
  • No concurrent biologic therapy

Chemotherapy:

  • No prior IV doxorubicin except intraarterial administration in locoregional therapy

Endocrine therapy:

  • Prior endocrine therapy allowed
  • No concurrent endocrine therapy

Radiotherapy:

  • Prior radiotherapy allowed
  • No concurrent radiotherapy

Surgery:

  • See Disease Characteristics
  • Surgery allowed if previously unresectable lesions become resectable
  • Recovered from any prior surgery
  • No concurrent liver transplantation

Other:

  • No other concurrent investigational or marketed anticancer drugs
  • No other concurrent therapy for hepatocellular carcinoma
  • No concurrent terfenadine, astemizole, or cisapride that may not be interrupted during nolatrexed dihydrochloride administration
05

Study design

Phase
Phase 3
Primary purpose
Treatment
Allocation
Randomized
Masking
None (open label)

Interventions

  • Drugdoxorubicin hydrochloride
  • Drugnolatrexed dihydrochloride
06

What researchers measure

Primary outcomes

  1. Overall survival

Secondary outcomes

  1. Time to progression

  2. Time to treatment failure

  3. Response rate (complete response, partial response, stable disease)

  4. Survival probabilities at 3, 6, 9, and 12 months

  5. Safety

  6. Response to treatment in patients with and without prior therapy

07

Study locations

42 sites
  • Arizona Clinical Research Center, Incorporated
    Tucson, Arizona 85715, United States
  • Arkansas Cancer Research Center at University of Arkansas for Medical Sciences
    Little Rock, Arkansas 72205, United States
  • Tower Cancer Research Foundation
    Beverly Hills, California 90211, United States
  • Scripps Cancer Center at Scripps Clinic
    La Jolla, California 92037, United States
  • David and Donna Long Center for Cancer Treatment at Sharp Grossmont Hospital
    La Mesa, California 91942, United States
  • Veterans Affairs Medical Center - Long Beach
    Long Beach, California 90822, United States
  • California Pacific Medical Center - Pacific Campus
    San Francisco, California 94115, United States
  • Olive View - UCLA Medical Center Foundation
    Sylmar, California 91342, United States
  • California Hematology/Oncology Medical Group
    Torrance, California 90505, United States
  • Helen F. Graham Cancer Center
    Newark, Delaware 19713, United States
  • Lombardi Cancer Center at Georgetown University Medical Center
    Washington, District of Columbia 20007, United States
  • Florida Cancer Institute - Bayonet Point
    Hudson, Florida 34667, United States
  • University of Miami Sylvester Comprehensive Cancer Center
    Miami, Florida 33136, United States
  • Oncology-Hematology Group of South Florida, P.A.
    Miami, Florida 33176, United States
  • Ocala Research Institute, Incorporated
    Ocala, Florida 34480, United States
  • Cancer Research Center of Hawaii
    Honolulu, Hawaii 96813, United States
  • Robert H. Lurie Comprehensive Cancer Center at Northwestern University
    Chicago, Illinois 60611, United States
  • University of Illinois at Chicago Cancer Center
    Chicago, Illinois 60612, United States
  • Holden Comprehensive Cancer Center at University of Iowa
    Iowa City, Iowa 52242-1009, United States
  • Louisiana Oncology Associates - Lafayette
    Lafayette, Louisiana 70506, United States
  • Stanley S. Scott Cancer Center at Louisiana State University Medical Center - New Orleans
    New Orleans, Louisiana 70112, United States
  • Alvin and Lois Lapidus Cancer Institute at Sinai Hospital
    Baltimore, Maryland 21215, United States
  • University of Minnesota Cancer Center
    Minneapolis, Minnesota 55455, United States
  • Saint Louis University Cancer Center
    Saint Louis, Missouri 63110, United States
  • Siteman Cancer Center at Barnes-Jewish Hospital
    Saint Louis, Missouri 63110, United States
  • UNMC Eppley Cancer Center at the University of Nebraska Medical Center
    Omaha, Nebraska 68198-7680, United States
  • Hackensack University Medical Center
    Hackensack, New Jersey 07601, United States
  • Veterans Affairs Medical Center - Albuquerque
    Albuquerque, New Mexico 87108, United States
  • Albert Einstein Cancer Center at Albert Einstein College of Medicine
    Bronx, New York 10467, United States
  • New York Weill Cornell Cancer Center at Cornell University
    New York, New York 10021, United States
  • Herbert Irving Comprehensive Cancer Center at Columbia University
    New York, New York 10032, United States
  • SUNY Upstate Medical University Hospital
    Syracuse, New York 13210, United States
  • New York Medical College
    Valhalla, New York 10595, United States
  • Cleveland Clinic Taussig Cancer Center
    Cleveland, Ohio 44111, United States
  • Albert Einstein Cancer Center
    Philadelphia, Pennsylvania 19141, United States
  • Cancer Centers of the Carolinas - Eastside
    Greenville, South Carolina 29615, United States
  • Medical City Dallas Hospital
    Dallas, Texas 75230, United States
  • Joe Arrington Cancer Research and Treatment Center
    Lubbock, Texas 79410-1894, United States
  • St. Boniface General Hospital
    Winnipeg, Manitoba R2H 2A6, Canada
  • Ottawa Hospital Regional Cancer Centre - General Campus
    Ottawa, Ontario K1H 8L6, Canada
  • Princess Margaret Hospital
    Toronto, Ontario M5G 2M9, Canada
  • Fundacion de Investagacion De Diego
    Santurce, 00909, Puerto Rico
08

References and documents

Publications

  • Gish RG, Porta C, Lazar L, Ruff P, Feld R, Croitoru A, Feun L, Jeziorski K, Leighton J, Gallo J, Kennealey GT. Phase III randomized controlled trial comparing the survival of patients with unresectable hepatocellular carcinoma treated with nolatrexed or doxorubicin. J Clin Oncol. 2007 Jul 20;25(21):3069-75. doi: 10.1200/JCO.2006.08.4046. PubMed 17634485 ↗
09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jun 26, 2013, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT00012324
Lead sponsor
Eximias Pharmaceutical
First posted
Jan 27, 2003
Start date
Sep 2000
Completion
Nov 2005
Last update
Jun 26, 2013

Study contacts

Gregory R. Suplick
study chair · Eximias Pharmaceutical
View the source record on ClinicalTrials.gov ↗

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