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Completed

NCT Number: NCT01163097

Study to Characterize the Effect of Heparin on Palifermin Activity

The purpose of this study is to evaluate the effect of a continuous intravenous infusion of unfractionated heparin on the multiple-dose pharmacodynamics of palifermin in healthy adult subjects.

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Key information

Conditions

Oral Mucositis Mouth Diseases Stomatitis Stomatognathic Diseases

Age range

18 year–45 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 1

Primary location

New Orleans Center for Clinical Research (NOCCR)

Knoxville, Tennessee, 37920, United States

About this study

The planned study is designed to characterize the impact of heparin on the biologic activity of palifermin and assess the impact of the combination of palifermin and heparin on tolerability. Approximately forty-three (43) eligible healthy adult men and oophorectomized or postmenopausal women between 18-45 years of age will be assigned to one of three treatment groups where treatment group A will receive a daily dose of palifermin 40 µg/kg for three consecutive days as intravenous (IV) bolus injections and continuous heparin IV infusion, treatment B will receive a daily dose of palifermin 40 µg/kg for three consecutive days as IV bolus injections and treatment C will be a control group without any treatment administered. The subjects will be randomized in a 20:15:8 ratio (Treatment A:B:C).

The study consists of a up to 21-days screening period, a 5-days treatment period and a up to 45-days follow-up period.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Healthy men or postmenopausal or oophorectomized women.
  • Subjects should have a Body Mass Index between 19 and 30 inclusive.
  • A negative screen for drug abuse, tobacco use and alcohol breath test.
  • Subjects should be willing to be resident in the research facility for up to 6 nights and return to the research facility for scheduled study and follow-up procedures.
  • Men must agree for the duration of the study to use an appropriate method of birth control

Exclusion criteria

  • History or evidence of clinically significant disorder, condition or disease that would pose a risk to subject safety or interfere with the study evaluation, procedures, or completion.
  • History or evidence of any oral mucosal disease that may affect mucosal keratinocyte proliferation.
  • Evidence or history of thrombocytopenia, heparin-induced thrombocytopenia or other contraindications to heparin (e.g. recent surgeries).
  • Known hypersensitivity to heparin or topical or injectable local anesthetic.
  • Known allergies to Escherichia coli-derived products or allergies to palifermin or its excipients.
  • Use of medications (except vitamins, hormonal replacement therapy and topical medications) within 10 days of admission to research facility.
  • Blood donation within 8 weeks prior to dosing of investigational drug.
  • History of hypertension, clinically significant bleeding, gastrointestinal ulcers, arteriovenous malformation (AVM), aneurysm, or other vascular malformation.
  • History of coagulopathy, bleeding disorders or abnormal platelet counts.
  • History of malignancy of any type, other than surgically excised non-melanoma skin cancers or in situ cervical cancer.
  • For males, past history of epididymitis.
  • Known alcohol abuse or use of illicit drugs within 12 months prior to admission to the research facility.
  • History of smoking or using smokeless tobacco within the past year before admission to the research facility.
  • Any other condition that might reduce the chance of obtaining data (eg, known poor compliance) required by the protocol or that might compromise the ability to give informed consent.
  • Previous participation in a palifermin study.

Treatment and study plan

Palifermin

Drug

40 µg/kg IV bolus injections for three consecutive days

Heparin

Drug

Heparin continuous IV infusion

Primary outcomes

  1. Ratio to Baseline of Epithelial Cell Proliferation as Assessed by Ki67 Staining of Buccal Mucosal Tissue.

    Time frame: Day 4

    This outcome is a measure of the palifermin effect on the buccal mucosal cells. Ki67 is a measure of proliferation of cells in the buccal mucosa. This measure assess the number of cells per millimeter (mm) before and after palifermin treatment.

  2. Incidence of Grade 2 or Higher Specific Skin-related Adverse Events.

    Time frame: Day 45

    Incidence of grade 2 or higher specific skin-related treatment emergent adverse events following palifermin administration was calculated for subjects in treatment groups A and B. Incidence was calculated by treatment as number of subjects with grade 2 or higher specific skin-related AEs divided by the total number of subjects.

    The Common Terminology Criteria for Adverse Events (CTCAE v3.0) for Dermatology/Skin was used to determine the toxicity grade for a skin-related adverse event. (http://ctep.cancer.gov/protocolDevelopment/electronic_applications/docs/ctcaev3.pdf)

  3. Ratio to Baseline of Amylase

    Time frame: Day 5

    Ratio to baseline amylase at Day 5 was calculated as Day 5 amylase divided by baseline amylase.

  4. Ratio to Baseline of Lipase.

    Time frame: Day 5

    Ratio to baseline lipase at Day 5 was calculated as Day 5 lipase divided by baseline lipase.

  5. Ratio to Baseline of Protein/Creatinine

    Time frame: Day 4

    Protein/creatinine ratio is the urinary protein (mg) divided by the urinary creatinine (g) result.

    Ratio to baseline protein/creatinine ratio was calculated as protein/creatinine ratio at specified day divided by baseline protein/creatinine ratio.

Secondary outcomes

  1. Palifermin Pharmacokinetic (PK) Parameters: Clearance (CL)

    Time frame: Day 1

    Blood samples for palifermin PK was collected pre-dose on Days 1 and 3 of the treatment period; 2, 5, 15 and 30 minutes; and 1, 2, 4, 6, 12, 18 and 24 hours after the Day 1 and Day 3 dose of palifermin.

    Descriptive PK parameters for palifermin CL for subjects assigned to Treatment A and Treatment B was determined by linear/log trapezoidal method. Parameters was calculated from individual subject serum concentration-time data using actual subject blood collection times. Serum concentrations reported below the lower limit of quantification (LLOQ) was treated as zero.

  2. Palifermin PK Parameters: CL

    Time frame: Day 3

    Blood samples for palifermin PK was collected pre-dose on Days 1 and 3 of the treatment period; 2, 5, 15 and 30 minutes; and 1, 2, 4, 6, 12, 18 and 24 hours after the Day 1 and Day 3 dose of palifermin.

    Descriptive PK parameters for palifermin CL for subjects assigned to Treatment A and Treatment B was determined by linear/log trapezoidal method. Parameters was calculated from individual subject serum concentration-time data using actual subject blood collection times. Serum concentrations reported below the lower limit of quantification (LLOQ) was treated as zero.

  3. Palifermin PK Parameters: Area Under the Serum Curve (AUC) (0-24)

    Time frame: Day 1

    Blood samples for palifermin PK was collected pre-dose on Days 1 and 3 of the treatment period; 2, 5, 15 and 30 minutes; and 1, 2, 4, 6, 12, 18 and 24 hours after the Day 1 and Day 3 dose of palifermin.

    Descriptive pharmacokinetic parameters for palifermin AUC(0-24) was determined by linear/log trapezoidal method. Parameters was calculated from individual subject serum concentration-time data using actual subject blood collection times. Serum concentrations reported below the lower limit of quantification (LLOQ) was deleted from calculation.

  4. Palifermin PK Parameters: AUC (0-24)

    Time frame: Day 3

    Blood samples for palifermin PK was collected pre-dose on Days 1 and 3 of the treatment period; 2, 5, 15 and 30 minutes; and 1, 2, 4, 6, 12, 18 and 24 hours after the Day 1 and Day 3 dose of palifermin.

    Descriptive pharmacokinetic parameters for palifermin AUC(0-24) was determined by linear/log trapezoidal method. Parameters was calculated from individual subject serum concentration-time data using actual subject blood collection times. Serum concentrations reported below the lower limit of quantification (LLOQ) was deleted from calculation.

  5. Palifermin PK Parameters: Estimated Concentration at Time 0 (C0)

    Time frame: Day 1

    Blood samples for palifermin PK was collected pre-dose on Days 1 and 3 of the treatment period; 2, 5, 15 and 30 minutes; and 1, 2, 4, 6, 12, 18 and 24 hours after the Day 1 and Day 3 dose of palifermin.

    Descriptive pharmacokinetic parameters for palifermin C0 was determined by linear/log trapezoidal method. Parameters was calculated from individual subject serum concentration-time data using actual subject blood collection times. Serum concentrations reported below the lower limit of quantification (LLOQ) was treated as zero.

  6. Palifermin PK Parameters: C0

    Time frame: Day 3

    Blood samples for palifermin PK was collected pre-dose on Days 1 and 3 of the treatment period; 2, 5, 15 and 30 minutes; and 1, 2, 4, 6, 12, 18 and 24 hours after the Day 1 and Day 3 dose of palifermin.

    Descriptive pharmacokinetic parameters for palifermin C0 was determined by linear/log trapezoidal method. Parameters was calculated from individual subject serum concentration-time data using actual subject blood collection times. Serum concentrations reported below the lower limit of quantification (LLOQ) was treated as zero.

  7. Palifermin PK Parameters: Apparent Volume of Distribution at Steady State (Vss)

    Time frame: Day 1

    Blood samples for palifermin PK was collected pre-dose on Days 1 and 3 of the treatment period; 2, 5, 15 and 30 minutes; and 1, 2, 4, 6, 12, 18 and 24 hours after the Day 1 and Day 3 dose of palifermin (Treatment A and Treatment B only).

    Descriptive pharmacokinetic parameters for palifermin Vss was determined by linear/log trapezoidal method. Parameters was calculated from individual subject serum concentration-time data using actual subject blood collection times. Serum concentrations reported below the lower limit of quantification (LLOQ) was treated as zero.

  8. Palifermin PK Parameters: Vss

    Time frame: Day 3

    Blood samples for palifermin PK was collected pre-dose on Days 1 and 3 of the treatment period; 2, 5, 15 and 30 minutes; and 1, 2, 4, 6, 12, 18 and 24 hours after the Day 1 and Day 3 dose of palifermin (Treatment A and Treatment B only).

    Descriptive pharmacokinetic parameters for palifermin Vss was determined by linear/log trapezoidal method. Parameters was calculated from individual subject serum concentration-time data using actual subject blood collection times. Serum concentrations reported below the lower limit of quantification (LLOQ) was treated as zero.

  9. Subject Incidence of Treatment-emergent Adverse Event

    Time frame: Day 45

    Adverse events (AE) was considered treatment emergent if the AE started after the time of heparin titration (Treatment A), palifermin dosing on Day 1 (Treatment B), or set zero point (Treatment C).

  10. Subject Incidence of Proteinuria

    Time frame: Day 4

    Protein/creatinine ratio is the urinary protein (mg) divided by the urinary creatinine (g) result at the specified time point.

    Incidence of proteinuria defined as urinary protein/creatinine ratio exceeding 200 mg/g was calculated at Day 4 and overall at any time point. Incidence was calculated by treatment as number of subjects with proteinuria divided by the total number of subjects.

  11. Ratio to Baseline of Protein/Creatinine

    Time frame: Day 1

    Protein/creatinine ratio is the urinary protein (mg) divided by the urinary creatinine (g) result.

    Ratio to baseline protein/creatinine ratio was calculated as protein/creatinine ratio at specified day divided by baseline protein/creatinine ratio.

  12. Ratio to Baseline of Protein/Creatinine

    Time frame: Day 2

    Protein/creatinine ratio is the urinary protein (mg) divided by the urinary creatinine (g) result.

    Ratio to baseline protein/creatinine ratio was calculated as protein/creatinine ratio at specified day divided by baseline protein/creatinine ratio.

  13. Ratio to Baseline of Protein/Creatinine

    Time frame: Day 3

    Protein/creatinine ratio is the urinary protein (mg) divided by the urinary creatinine (g) result.

    Ratio to baseline protein/creatinine ratio was calculated as protein/creatinine ratio at specified day divided by baseline protein/creatinine ratio.

  14. Ratio to Baseline of Albumin/Creatinine

    Time frame: Day 1

    The albumin/creatinine ratio is the urinary albumin (mg) divided by the urinary creatinine (g) result at the specified time point.

    Ratio to baseline was calculated as albumin/creatinine ratio at specified day divided by baseline albumin/creatinine ratio.

  15. Ratio to Baseline of Albumin/Creatinine

    Time frame: Day 2

    The albumin/creatinine ratio is the urinary albumin (mg) divided by the urinary creatinine (g) result at the specified time point.

    Ratio to baseline was calculated as albumin/creatinine ratio at specified day divided by baseline albumin/creatinine ratio.

  16. Ratio to Baseline of Albumin/Creatinine

    Time frame: Day 3

    The albumin/creatinine ratio is the urinary albumin (mg) divided by the urinary creatinine (g) result at the specified time point.

    Ratio to baseline was calculated as albumin/creatinine ratio at specified day divided by baseline albumin/creatinine ratio.

  17. Ratio to Baseline of Albumin/Creatinine

    Time frame: Day 4

    The albumin/creatinine ratio is the urinary albumin (mg) divided by the urinary creatinine (g) result at the specified time point.

    Ratio to baseline was calculated as albumin/creatinine ratio at specified day divided by baseline albumin/creatinine ratio.

Sponsors and collaborators

Lead sponsor

Swedish Orphan Biovitrum

Industry

Registry information

Official study title

An Open-label, Randomized, Parallel-Design Study to Characterize the Effect of Heparin on Palifermin Activity in Healthy Adult Subjects

Important dates

Study start
2010
Primary completion
2011
Study completion
2011
First posted
Jul 15, 2010
Registry last updated
Nov 6, 2014

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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