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No longer availableNCT01473043Updated May 30, 2014

Clinical Study With Axitinib In Advanced Kidney Cancer, Who Have Failed First Line Treatment

An expanded access record providing Axitinib in Renal Cell Carcinoma, sponsored by Pfizer. No longer available at 4 sites in 2 countries. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2014-05-30.

Sponsored by Pfizer · Expanded access

Study type
Expanded access
Ages
18 Years and older
Sex
All
01

Study summary

This is a single arm study with axitinib in patients with advanced kidney cancer (clear cell variant), who have failed first line therapy. The study will recruit a maximum of 30 patients from 2 countries including Australia and Canada. Patients will be followed up for efficacy, safety and health related outcomes.

02

Conditions studied

  • Renal Cell Carcinoma

Keywords

  • Axitinib
  • metastatic renal cell carcinoma
03

In context

Carcinoma

6,741 studies on the registry are indexed under Carcinoma; 1,161 are open to participants now.

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Lead sponsor

Pfizer is the lead sponsor of 3,244 studies on the registry; 139 are open to participants now.

Of its 582 completed or terminated interventional studies of FDA-regulated products, 381 (65%) have results posted.

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

Inclusion criteria

  • Metastatic renal cell carcinoma with a component of clear cell subtype.
  • Prior first line systemic therapy
  • At least 1 measurable lesion as per Response Evaluation Criterion in Solid Tumors [RECIST 1.1].
  • Adequate hematology, liver and kidney functions
  • Eastern Cooperative Oncology Group [ECOG] performance status of 0 or 1.
  • Life expectancy of ≥12 weeks.
  • Normotensive or well controlled hypertension (less than/equal to 140/90 mm Hg.)
  • Negative pregnancy test
  • Adequate recovery time from prior systemic therapy, surgery or radiation
  • Willing and able subjects who have signed consent

Exclusion criteria

Exclusion Criteria:

  • More than one prior systemic therapy regimen
  • Major bowel-penetrating surgery \<4 weeks
  • Active gastro intestinal bleed in past 3 months
  • Active peptic ulcer disease in the past 6 months
  • Current or anticipated use of potent CYP3A4/5 inhibitors
  • Current or anticipated use of known CYP3A4/5 or CYP1A2 inducers
  • Requirement for therapeutic warfarin or high dose steroids
  • Symptomatic or untreated brain metastases
  • A serious uncontrolled medical disorder or active infection
  • Pregnant or breastfeeding females
  • History of another active malignancy
  • Dementia
05

Access details

Study type
Expanded access

Available treatment

  • DrugAxitinib

    5mg twice daily \[BD\] daily dosing until progression or prohibitive toxicity Dose titration by 2 levels upwards (7mg and 10mg) and downwards (3mg and 2mg) allowed per protocol

    Also known as: AG-013736

06

Where to request access

4 sites
  • Pfizer Investigational Site
    Douglas, Queensland 4814, Australia
  • Pfizer Investigational Site
    Hobart, Tasmania 7000, Australia
  • Pfizer Investigational Site
    Wendouree, Victoria 3355, Australia
  • Pfizer Investigational Site
    Montreal, Quebec H2X 1N8, Canada
07

References and documents

08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on May 30, 2014, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT01473043
Lead sponsor
Pfizer
Responsible party
Sponsor
First posted
Nov 17, 2011
Start date
Mar 2012
Primary completion
Mar 2014
Completion
Mar 2014
Last update
May 30, 2014

Study contacts

Pfizer CT.gov Call Center
study director · Pfizer

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Requesting access

Expanded access is arranged between your doctor and the company. Ask your care team to contact the provider listed on this record.

No contact was published for this record. The registry link below has the sponsor’s details.

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Discussion

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