Clinical Trials Logo

Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00798889
Other study ID # A6181030
Secondary ID
Status Completed
Phase N/A
First received November 25, 2008
Last updated December 13, 2012
Start date March 2004
Est. completion date December 2011

Study information

Verified date December 2012
Source Pfizer
Contact n/a
Is FDA regulated No
Health authority United States: Food and Drug Administration
Study type Interventional

Clinical Trial Summary

The objective of this protocol is to provide SU011248 treatment for patients who have participated in a SU011248 protocol and are eligible to enter this protocol


Other known NCT identifiers
  • NCT00569725

Recruitment information / eligibility

Status Completed
Enrollment 314
Est. completion date December 2011
Est. primary completion date December 2011
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Prior SU011248 Protocol.

- Eligible to continue SU011248 treatment.

Exclusion Criteria:

- Uncontrolled CNS metastasis.

- Unfit to receive SU011248.

Study Design

Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Drug:
Sunitinib
Sunitinib dose varies according to the doses allowed in previous protocol. It is given once a day, orally with various schedules depending on the parent protocol

Locations

Country Name City State
Australia Pfizer Investigational Site East Melbourne Victoria
Australia Pfizer Investigational Site Heidelberg Victoria
Australia Pfizer Investigational Site Randwick New South Wales
Canada Pfizer Investigational Site Montreal Quebec
France Pfizer Investigational Site Villejuif Cedex
Greece Pfizer Investigational Site Thessaloniki
Italy Pfizer Investigational Site Milano
Italy Pfizer Investigational Site Milano
Netherlands Pfizer Investigational Site Nijmegen Gld
Singapore Pfizer Investigational Site Singapore
Sweden Pfizer Investigational Site Lund
Sweden Pfizer Investigational Site Stockholm
Switzerland Pfizer Investigational Site St. Gallen
United Kingdom Pfizer Investigational Site Leeds
United Kingdom Pfizer Investigational Site London
United Kingdom Pfizer Investigational Site London
United Kingdom Pfizer Investigational Site Newcastle-Upon-Tyne
United States Pfizer Investigational Site Albuquerque New Mexico
United States Pfizer Investigational Site Albuqurque New Mexico
United States Pfizer Investigational Site Ann Arbor Michigan
United States Pfizer Investigational Site Aurora Colorado
United States Pfizer Investigational Site Birmingham Alabama
United States Pfizer Investigational Site Birmingham Alabama
United States Pfizer Investigational Site Birmingham Alabama
United States Pfizer Investigational Site Boston Massachusetts
United States Pfizer Investigational Site Boston Massachusetts
United States Pfizer Investigational Site Boston Massachusetts
United States Pfizer Investigational Site Cleveland Ohio
United States Pfizer Investigational Site Dallas Texas
United States Pfizer Investigational Site Detroit Michigan
United States Pfizer Investigational Site Durham North Carolina
United States Pfizer Investigational Site Farmington Hills Michigan
United States Pfizer Investigational Site Franklin Tennessee
United States Pfizer Investigational Site Gallatin Tennessee
United States Pfizer Investigational Site Hermitage Tennessee
United States Pfizer Investigational Site Houston Texas
United States Pfizer Investigational Site Indianapolis Indiana
United States Pfizer Investigational Site Lebanon Tennessee
United States Pfizer Investigational Site Los Angeles California
United States Pfizer Investigational Site Los Angeles California
United States Pfizer Investigational Site Madison Wisconsin
United States Pfizer Investigational Site Minneapolis Minnesota
United States Pfizer Investigational Site Murfreesboro Tennessee
United States Pfizer Investigational Site Myrtle Beach South Carolina
United States Pfizer Investigational Site Nashville Tennessee
United States Pfizer Investigational Site Nashville Tennessee
United States Pfizer Investigational Site Nashville Tennessee
United States Pfizer Investigational Site Nashville Tennessee
United States Pfizer Investigational Site Nashville Tennessee
United States Pfizer Investigational Site Nashville Tennessee
United States Pfizer Investigational Site New York New York
United States Pfizer Investigational Site New York New York
United States Pfizer Investigational Site New York New York
United States Pfizer Investigational Site Philadelphia Pennsylvania
United States Pfizer Investigational Site San Francisco California
United States Pfizer Investigational Site San Francisco California
United States Pfizer Investigational Site Santa Monica, California
United States Pfizer Investigational Site Smyrna Tennessee
United States Pfizer Investigational Site St. Louis Missouri

Sponsors (1)

Lead Sponsor Collaborator
Pfizer

Countries where clinical trial is conducted

United States,  Australia,  Canada,  France,  Greece,  Italy,  Netherlands,  Singapore,  Sweden,  Switzerland,  United Kingdom, 

Outcome

Type Measure Description Time frame Safety issue
Primary Duration of Treatment Baseline up to Day 28 after last dose of study treatment Yes
See also
  Status Clinical Trial Phase
Active, not recruiting NCT00750841 - Study of the Effect of Rifampicin on the Pharmacokinetics (PK) of Multiple Doses of Cediranib in Patients With Solid Tumours Phase 1
Withdrawn NCT05419817 - Pembrolizumab With Sitravatinib in Recurrent Endometrial Cancer and Other Solid Tumors With Deficient Mismatch Repair System Phase 2
Completed NCT02828930 - A Study to Determine the Excretion Balance, Pharmacokinetics, Metabolism and Absolute Oral Bioavailability of a Single Oral Dose of [14C]-Labeled Idasanutlin and an Intravenous Tracer Dose of [13C]-Labeled Idasanutlin in a Single Cohort of Participants With Solid Tumors (Malignancies) Phase 1
Completed NCT01197170 - Hormone Receptor Positive Disease Across Solid Tumor Types: A Phase I Study of Single-Agent Hormone Blockade and Combination Approaches With Targeted Agents to Provide Synergy and Overcome Resistance Phase 1
Completed NCT03258515 - A Study to Investigate the Effect of Single Dose of AZD6094 (600 mg) on Cardiac Repolarization in Healthy Volunteers Phase 1
Terminated NCT03225105 - M3541 in Combination With Radiotherapy in Solid Tumors Phase 1
Completed NCT01497925 - Ph 1 Trial of ADI-PEG 20 Plus Docetaxel in Solid Tumors With Emphasis on Prostate Cancer and Non-Small Cell Lung Cancer Phase 1
Completed NCT01878890 - Phase I Dose Escalation Trial of Efavirenz in Solid Tumours or Non-Hodgkin Lymphoma in Therapeutic Failure. Phase 1
Active, not recruiting NCT05059522 - Continued Access Study for Participants Deriving Benefit in Pfizer-Sponsored Avelumab Parent Studies That Are Closing Phase 3
Active, not recruiting NCT03634982 - Dose Escalation of RMC-4630 Monotherapy in Relapsed/Refractory Solid Tumors Phase 1
Recruiting NCT04685226 - A Phase I/II Clinical Trial of ICP-723 in the Treatment of Advanced Solid Tumors Phase 1/Phase 2
Recruiting NCT03175224 - APL-101 Study of Subjects With NSCLC With c-Met EXON 14 Skip Mutations and c-Met Dysregulation Advanced Solid Tumors Phase 2
Recruiting NCT06036121 - A Study of ADRX-0706 in Select Advanced Solid Tumors Phase 1
Active, not recruiting NCT03258151 - Association of Genetic Polymorphisms With Docetaxel-based Chemotherapy Toxicities in Chinese Solid Tumor Patients
Completed NCT01528046 - Metformin in Children With Relapsed or Refractory Solid Tumors Phase 1
Recruiting NCT05325866 - A Study Evaluating Bemarituzumab in Solid Tumors With Fibroblast Growth Factor Receptor 2b (FGFR2b) Overexpression Phase 1/Phase 2
Recruiting NCT04557449 - Study to Test the Safety and Tolerability of PF-07220060 in Participants With Advance Solid Tumors Phase 1/Phase 2
Terminated NCT02890368 - Trial of Intratumoral Injections of TTI-621 in Subjects With Relapsed and Refractory Solid Tumors and Mycosis Fungoides Phase 1
Completed NCT02759640 - A Phase I Trial of HS-10241 in Solid Tumors Phase 1
Withdrawn NCT01940601 - Pharmacodynamics, Pharmacokinetics, Efficacy and Safety of Balugrastim in Pediatric Patients With Solid Tumors Phase 2