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Part A: Radiolabel Study With GW786034 Part B: Single Dose of GW786034

This study has been completed.
Sponsor:
Information provided by (Responsible Party):
GlaxoSmithKline
ClinicalTrials.gov Identifier:
NCT00478725
First received: May 24, 2007
Last updated: November 8, 2012
Last verified: November 2012
  Purpose

To study the absorption, distribution, metabolism and excretion of GW786034, and the absorption of a single IV dose of GW786034


Condition Intervention Phase
Carcinoma, Renal Cell
Cancer
Drug: GW786034, oral
Drug: GW786034, IV
Drug: GW786034, radiolabeled oral
Phase 1

Study Type: Interventional
Study Design: Allocation: Randomized
Endpoint Classification: Pharmacokinetics Study
Intervention Model: Single Group Assignment
Masking: Open Label
Primary Purpose: Treatment
Official Title: An Open-Label, Two-Part Study to Characterize the Pharmacokinetics of a Single Intravenous Dose of Pazopanib (GW786034) and the Absorption, Distribution, Metabolism and Elimination of a Single Oral [14C] Labeled Dose of Pazopanib in Subjects With Solid Tumor Malignancies

Resource links provided by NLM:


Further study details as provided by GlaxoSmithKline:

Primary Outcome Measures:
  • Part A: excretion of radioactivity [ Time Frame: over 168 hrs ]
  • Part B: Plasma pazopanib, clearance (CL) and AUC(0-t), AUC(0-8),Cmax and half-life (t1/2) pazopanib and pazopanib metabolites (GSK 1268992, GSK1268997, GSK1071306 and GW700201) [ Time Frame: over 48 hrs ]

Secondary Outcome Measures:
  • Part A: Blood and plasma total radioactivity AUC(0-t), AUC(0-8),Cmax and t1/2 [ Time Frame: over 168 hrs. ]
  • Part B: Safety parameters [ Time Frame: over 48 hrs. ]
  • Blood and plasma total radioactivity AUC(0-t), AUC(0-∞), Cmax and t1/2 following oral administration of 400 mg of [14C]-pazopanib containing approximately 70 µCi of radioactivity.
  • Samples (for use in a separate study) to characterize and quantify metabolites of pazopanib in plasma, urine and feces.
  • Blood:plasma ratio of total drug-related material (radioactivity).
  • Plasma pazopanib AUC(0-t), AUC(0-∞), Cmax, tmax following oral administration of 400 mg of [14C]-pazopanib containing 70 µCi of radioactivity.
  • Safety parameters: adverse events (AEs), vital signs, electrocardiograms (ECGs) and clinical laboratory assessments.
  • Plasma pazopanib AUC(0-24), Cmax, tmax following oral administration of 800 mg pazopanib [ Time Frame: on Day 15 of Cycle 1. ]

Enrollment: 10
Study Start Date: July 2007
Study Completion Date: July 2008
Primary Completion Date: July 2008 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
Experimental: Part A
Absorption, Distribution, Metabolism and Elimination of a Single Oral [14C] Labeled Dose of GW786034
Drug: GW786034, oral
oral, 800 mg
Other Names:
  • GW786034
  • pazopanib
Drug: GW786034, radiolabeled oral
oral, 400 mg radiolabeled
Other Names:
  • GW786034
  • pazopanib
Experimental: Part B
characterize the pharmacokinetics of a single IV dose of GW786034
Drug: GW786034, oral
oral, 800 mg
Other Names:
  • GW786034
  • pazopanib
Drug: GW786034, IV
IV, 5 mg
Other Names:
  • GW786034
  • pazopanib

  Eligibility

Ages Eligible for Study:   18 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Criteria

Inclusion criteria:

  • Subject must provide written informed consent prior to performance of study-specific procedures or assessments, and must be willing to comply with treatment and follow-up. Procedures conducted as part of the subject's routine clinical management (e.g., blood count, imaging study) and obtained prior to signing of informed consent may be utilized for screening or baseline purposes provided these procedures are conducted as specified in the protocol.
  • Has histologically or cytologically confirmed advanced solid tumor malignancy.
  • For Part A: Males, age: 30 years or greater.
  • For Part B: Males or Females, age: 18 years or greater.
  • For Part A or B, males that meet the following criteria.
  • A male subject with a female partner of childbearing potential is eligible to enter and participate in this study if he:

    • Agrees to use double-barrier contraception (condom with spermicidal jelly, foam, suppository or film, or a condom and his partner uses a diaphragm with spermicide), OR
    • Agrees to complete abstinence from sexual intercourse for 14 days before exposure to investigational product, through the clinical trial, and for at least 21 days after the last dose of investigational product.
  • For Part B, females that meet the following criteria:
  • A female subject is eligible to enter and participate in this study if she is of:

    • Non-childbearing potential (i.e., physiologically incapable of becoming pregnant), including any female who has had:

      • A hysterectomy
      • A bilateral oophorectomy (ovariectomy)
      • A bilateral tubal ligation
      • Is post-menopausal (total cessation of menses for >/ 1 year), OR
    • Childbearing potential and has a negative serum pregnancy test within 2 weeks prior to the first dose of study treatment, preferably as close to the first dose as possible, and agrees to use adequate contraception. GSK acceptable contraceptive methods, when used consistently and in accordance with both the product label and the instructions of the physician, are as follows:

      • An intrauterine device (IUD) with a documented failure rate of less than 1% per year.
      • Vasectomized partner who is sterile prior to the female subject's entry and is the sole sexual partner for that female.
      • Complete abstinence from sexual intercourse for 14 days before exposure to investigational product, through the clinical trial, and for at least 21 days after the last dose of investigational product.
      • Double-barrier contraception (condom with spermicidal jelly, foam suppository, or film; diaphragm with spermicide; or male condom and diaphragm with spermicide).
  • Note: Oral contraceptives are not considered reliable due to potential drug-drug interaction.
  • Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1.
  • Body weight >/ 50 kg.
  • Adequate organ systems function as defined in Table 1.
  • Ability to swallow and retain oral medication.

Exclusion criteria:

  • History or clinical evidence of central nervous system (CNS) metastases or leptomeningeal carcinomatosis, except for individuals who have previously treated CNS metastases, are asymptomatic, and have had no requirement for steroids or anti-seizure medication for 6 months prior to beginning study treatment. Screening with CNS imaging studies (CT scan or MRI) is required only if clinically indicated or if the subject has a history of CNS metastases.
  • Clinically significant gastrointestinal (GI) abnormalities including, but not limited to: malabsorption syndrome, history of resection of the stomach or small bowel, active peptic ulcer disease, inflammatory bowel disease, ulcerative colitis or other conditions that increase the risk for perforation, history of abdominal fistula, GI perforation or intra-abdominal abscess within 4 weeks prior to beginning study treatment.
  • Presence of uncontrolled infection.
  • Corrected QT interval (QTc) > 480 msec.
  • History of any one or more of the following cardiovascular conditions within the past 6 months: congestive heart failure, cardiac angioplasty or stenting, myocardial infarction, unstable angina OR symptomatic peripheral vascular disease.
  • Has poorly controlled hypertension (systolic blood pressure [SBP] >/ 140 mmHg, or diastolic blood pressure [DBP] >/ 90 mmHg).
  • Note: Initiation or adjustment of anti-hypertensive medication(s) is permitted prior to study entry. The blood pressure (BP) must be re-assessed on 2 occasions that are separated by a minimum of 24 hours. The mean SBP/DBP values from both BP assessments must be < 140/90 mmHg in order for a subject to be eligible for the study.
  • History of cerebrovascular accident or pulmonary embolism within the past 6 months.
  • History of untreated deep venous thrombosis (DVT) within the past 6 months.
  • Note: Subjects with recent DVT who have been treated with therapeutic anti-coagulating agents for at least 6 weeks are eligible.
  • Prior major surgery or trauma within the past 28 days or presence of any wound, fracture or ulcer which is not fully healed.
  • Evidence of active bleeding, bleeding diathesis or hemoptysis within 6 weeks prior to study treatment.
  • Use of prohibited medications within the timeframes specified in Section 9.2, Prohibited Medications of the protocol.
  • Use of an investigational agent, including an investigational anti-cancer agent within 28 days or 5 half-lives, whichever is longer, preceding the first dose of pazopanib.
  • Treatment with any cancer therapy (including chemotherapy, radiation therapy, immunotherapy, biologic therapy, hormonal therapy, surgery or tumor embolization) within 14 days prior to the first dose of pazopanib.
  • Note: Current treatment with leuprolide is permitted.
  • Any ongoing potentially reversible toxicity from prior anti-cancer therapy that is > Grade 1 or any toxicity from prior anti-cancer therapy that is progressing in severity.
  • Any serious and/or unstable pre-existing medical, psychiatric, or other conditions that could interfere with subject's safety, obtaining informed consent or compliance to the study, including any condition that could interfere with the accurate assessment and recovery of [14C].
  • History or presence of hepatic or renal disease or any other condition known to interfere with the absorption, distribution, metabolism or excretion of drugs
  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT00478725

Locations
United States, Minnesota
GSK Investigational Site
Minneapolis, Minnesota, United States, 55404
United States, Tennessee
GSK Investigational Site
Nashville, Tennessee, United States, 37203
Sponsors and Collaborators
GlaxoSmithKline
Investigators
Study Director: GSK Clinical Trials GlaxoSmithKline
  More Information

No publications provided by GlaxoSmithKline

Additional publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):
Responsible Party: GlaxoSmithKline
ClinicalTrials.gov Identifier: NCT00478725     History of Changes
Other Study ID Numbers: VEG10004
Study First Received: May 24, 2007
Last Updated: November 8, 2012
Health Authority: United States: Food and Drug Administration

Keywords provided by GlaxoSmithKline:
Metastatic Cancer
Advanced Cancer

Additional relevant MeSH terms:
Carcinoma, Renal Cell
Adenocarcinoma
Carcinoma
Kidney Diseases
Kidney Neoplasms
Neoplasms
Neoplasms by Histologic Type
Neoplasms by Site
Neoplasms, Glandular and Epithelial
Urogenital Neoplasms
Urologic Diseases
Urologic Neoplasms

ClinicalTrials.gov processed this record on November 27, 2014