CClinicalTrials.gg
CompletedNCT00889057Updated Mar 28, 2013

Sorafenib in Relapsed High Grade Osteosarcoma

A Phase 2 interventional study of sorafenib in Osteosarcoma, sponsored by Italian Sarcoma Group. Completed at 4 sites in Italy. Open to participants aged 15 Years to 75 Years. Per ClinicalTrials.gov, last updated 2013-03-28.

Sponsored by Italian Sarcoma Group · Phase 2, Interventional, and Treatment

Phase
Phase 2
Study type
Interventional
Enrollment
35
Allocation
Not applicable
Ages
15 Years to 75 Years
Sex
All
01

Study summary

Aim of this exploratory phase II study is to assess the clinical activity of sorafenib as single agent, in terms of percentage of patients with high grade advanced osteosarcoma free from progression following 4 months of therapy

02

Conditions studied

  • Osteosarcoma

Browse trials for

Keywords

  • osteosarcoma
  • sorafenib
  • target therapy
03

In context

Osteosarcoma

437 studies on the registry are indexed under Osteosarcoma; 116 are open to participants now.

This study's enrollment of 35 is below the median of 42 across 325 interventional studies indexed under Osteosarcoma.

Browse Osteosarcoma studies →

Lead sponsor

Italian Sarcoma Group is the lead sponsor of 31 studies on the registry; 11 are open to participants now.

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

04

Who can participate

Ages eligible
15 Years to 75 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • histologically documented and not surgically resectable or metastatic high-grade osteosarcoma which progressed after first or second line treatments for relapsing disease.
  • measurable disease as defined by having at least one lesion that can be accurately measured by means of CT or MRI.
  • ECOG PS of 0, 1 and an estimated life expectancy of at least 3 months. ECOG P.S. 2 is acceptable provided that it depends solely on orthopedic problems
  • Age ≥15 years.
  • Adequate bone marrow, liver and renal function
  • Written informed consent

Exclusion criteria

Exclusion Criteria:

  • Dementia or significantly altered mental status that would prohibit the understanding or rendering of informed consent and compliance with the requirements of this protocol.
  • Coexisting malignancies, except for basal or epithelial cell carcinoma of the skin or other solid tumors curatively treated with no evidence of disease for ≥3 years.
  • History of cardiac disease: congestive heart failure >NYHA class 2; active CAD (MI more than 6 months prior to study entry is allowed); cardiac arrhythmias requiring anti-arrhythmic therapy (beta blockers or digoxin are permitted) or uncontrolled hypertension.
  • History of HIV infection or chronic hepatitis B or C.
  • Active clinically serious infections (> grade 2 NCI-CTC version 3.0)
  • Symptomatic metastatic brain or meningeal tumors (unless the patient is > 6 months from definitive therapy, has a negative imaging study within 4 weeks of study entry and is clinically stable with respect to the tumor at the time of study entry)
  • Patients with seizure disorders requiring medication (such as steroids or anti-epileptics)
  • Pregnant or breast-feeding patients. Women of childbearing potential must have a negative pregnancy test performed within 7 days of the start of treatment. Both men and women enrolled in this trial must use adequate barrier birth control measures during the course of the trial and two weeks after the completion of trial.
  • Patients with evidence or history of bleeding diathesis
  • Patients undergoing renal dialysis
  • Patients unable to swallow oral medications
05

Study design

Phase
Phase 2
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
35 participants (actual)

Study arms

  • Experimental
    sorafenib

    Drug: sorafenib

Interventions

  • Drugsorafenib

    400 mg bid until progression or inacceptable toxicity

06

What researchers measure

Primary outcomes

  1. Tumor assessment through radiologic evaluation.

    Time frame: every 8 weeks

07

Study locations

4 sites
  • I.R.C.C. - Unit of Medical Oncology
    Candiolo, Torino 10060, Italy
  • Istituti Ortopedici Rizzoli - Unit of Chemotherapy of Muscoloskeletal Tumors
    Bologna, 40136, Italy
  • Istituto Nazionale Tumori - Unit of Medical Oncology
    Milano, 20133, Italy
  • Ospedale Infantile Regina Margherita - Unit of Paediatric Oncoematology
    Torino, 10126, Italy
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Mar 28, 2013, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT00889057
Lead sponsor
Italian Sarcoma Group
Responsible party
Prof. Massimo Aglietta (Professor, Italian Sarcoma Group) — Principal investigator
First posted
Apr 28, 2009
Start date
Jan 2008
Primary completion
Dec 2010
Completion
Jun 2011
Last update
Mar 28, 2013

Study contacts

Massimo Aglietta, MD
study chair · I.R.C.C - FPO Candiolo
Giovanni Grignani, MD
principal investigator · I.R.C.C. - FPO Candiolo
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Mar 2013. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion