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A Phase II Study of Imiquimod 5 % Cream for the Treatment of Hemangioma in Infancy

Primary Purpose

Hemangioma, Capillary

Status
Completed
Phase
Phase 2
Locations
Canada
Study Type
Interventional
Intervention
Imiquimod 5% cream
Sponsored by
St. Justine's Hospital
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional treatment trial for Hemangioma, Capillary focused on measuring Infantile hemangioma, Hemangioma, Hemangioma of Infancy, benign tumors of infancy, Congenital hemangioma, Capillary

Eligibility Criteria

2 Months - 12 Months (Child)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Healthy infants aged 2-12 months.
  • Superficial or mixed hemangiomas in proliferative phase (growing in size in the last 1-2 months).
  • Hemangiomas must be less than 10X10 cm and must not be ulcerated.

Exclusion Criteria:

  • Preterm infant (less than 36 weeks of gestation).
  • Ulceration of hemangioma prior to treatment.
  • Immunosuppression.
  • Hemangioma located on the eyelid or perianal region.
  • Prior treatment of the hemangioma.
  • Concomitant diseases.
  • Presence of multiple hemangiomas and/or hemangiomas that would require systemic drug treatment.
  • Potential difficulties with follow-up (patient from another town,difficult access to the hospital , etc.).
  • History of allergy to any of the components of the drug preparation.
  • Hemangiomas more than 10X 10 cm or ulcerated before the start of the treatment.

Sites / Locations

  • Sainte-Justine Hospital University Center (CHU)

Outcomes

Primary Outcome Measures

To document the efficacy of Imiquimod 5% cream in the treatment of hemangioma of infancy.

Secondary Outcome Measures

IFN and plasma drug levels, as well as clinical examinations and blood studies, will be carried out to evaluate safety of the treatment.
bFGF and VEGF will be measured in blood and urine in order to study the diagnostic and predictive value of these pro-angiogenic factors in the response of hemangiomas to the treatment with Imiquimod.

Full Information

First Posted
January 14, 2008
Last Updated
January 24, 2008
Sponsor
St. Justine's Hospital
Collaborators
Graceway Pharmaceuticals, LLC
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1. Study Identification

Unique Protocol Identification Number
NCT00601016
Brief Title
A Phase II Study of Imiquimod 5 % Cream for the Treatment of Hemangioma in Infancy
Official Title
A Phase II Study of Imiquimod 5 % Cream for the Treatment of Hemangioma in Infancy
Study Type
Interventional

2. Study Status

Record Verification Date
January 2008
Overall Recruitment Status
Completed
Study Start Date
March 2005 (undefined)
Primary Completion Date
September 2006 (Actual)
Study Completion Date
September 2006 (Actual)

3. Sponsor/Collaborators

Name of the Sponsor
St. Justine's Hospital
Collaborators
Graceway Pharmaceuticals, LLC

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Hemangiomas of infancy, the most common benign tumors of infancy, are congenital or early infancy lesions characterized by a rapid postnatal growth, with high expression of angiogenic stimulators for 9-18 months, followed by slow regression for 5-9 years. Current therapies for the hemangiomas are usually restricted to more severe forms due to the risks of adverse effects, inconvenience and cost. Nevertheless, a substantial amount of the psychological discomfort and morbidity can be caused by untreated hemangiomas, especially those in the face. Recently, Imiquimod 5% cream has emerged as a safe an effective drug for several skin conditions that benefit from modulation of the activity of the immune system, such as common warts and various forms of the skin pre-cancerous and cancerous lesions. Small case reports series have suggest that it could also be useful in hemangiomas, possibly through the inhibition of the angiogenesis by local IFN production.This is a small, open label study of 16 patients to document the efficacy of the Imiquimod 5% cream in the treatment of hemangioma of infancy (primary outcome). IFN and plasma drug levels, as well as clinical examinations and blood studies, will be carried out to evaluate safety of the treatment (secondary outcome). bFGF and VEGF will be measured in blood and urine in order to study the diagnostic and predictive value of these pro-angiogenic factors in the response of hemangiomas to the treatment with Imiquimod (secondary outcome). The study is a phase II clinical trial of a once a day application of Imiquimod 5% cream, 3 to 7 times per week for a maximum of four months. The study held at the Dermatology Clinic of Sainte-Justine Hospital, and was completed within a 20 months timeframe after IRB approval.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hemangioma, Capillary
Keywords
Infantile hemangioma, Hemangioma, Hemangioma of Infancy, benign tumors of infancy, Congenital hemangioma, Capillary

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
18 (Actual)

8. Arms, Groups, and Interventions

Intervention Type
Drug
Intervention Name(s)
Imiquimod 5% cream
Other Intervention Name(s)
Imiquimod 5% cream = Aldara, Item ID = GH-6203-0328-5, CUP-051119552409, DIN number = 02239505, Lot number -= GFK026A
Intervention Description
Imiquimod 5% cream applied topical on hemangioma once a day , 3 to 7 times a week for a maximum of 4 months.
Primary Outcome Measure Information:
Title
To document the efficacy of Imiquimod 5% cream in the treatment of hemangioma of infancy.
Time Frame
Cream is applied for 4 months. Visits occured at month 1, 2, 4, and 8.
Secondary Outcome Measure Information:
Title
IFN and plasma drug levels, as well as clinical examinations and blood studies, will be carried out to evaluate safety of the treatment.
Time Frame
4 months of treatment. Doage done at each study visits (Month 1, 2 .4 and 8).
Title
bFGF and VEGF will be measured in blood and urine in order to study the diagnostic and predictive value of these pro-angiogenic factors in the response of hemangiomas to the treatment with Imiquimod.
Time Frame
4 months of treament with a follow-up at 8 months.

10. Eligibility

Sex
All
Minimum Age & Unit of Time
2 Months
Maximum Age & Unit of Time
12 Months
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Healthy infants aged 2-12 months. Superficial or mixed hemangiomas in proliferative phase (growing in size in the last 1-2 months). Hemangiomas must be less than 10X10 cm and must not be ulcerated. Exclusion Criteria: Preterm infant (less than 36 weeks of gestation). Ulceration of hemangioma prior to treatment. Immunosuppression. Hemangioma located on the eyelid or perianal region. Prior treatment of the hemangioma. Concomitant diseases. Presence of multiple hemangiomas and/or hemangiomas that would require systemic drug treatment. Potential difficulties with follow-up (patient from another town,difficult access to the hospital , etc.). History of allergy to any of the components of the drug preparation. Hemangiomas more than 10X 10 cm or ulcerated before the start of the treatment.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Catherine McCuaig, M.D.
Organizational Affiliation
St. Justine's Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Sainte-Justine Hospital University Center (CHU)
City
Montreal
State/Province
Quebec
ZIP/Postal Code
H3T 1C5
Country
Canada

12. IPD Sharing Statement

Citations:
Citation
Bruckner, A.L. and I.J. Frieden, Hemangiomas of infancy. J Am Acad Dermatol, 2003. 48(4): p. 477-93; quiz 494-6. 2. Dinehart, S.M., J. Kincannon, and R. Geronemus, Hemangiomas: evaluation and treatment. Dermatol Surg, 2001. 27(5): p. 475-85. 3. Jacobs, A.H. and R.G. Walton, The incidence of birthmarks in the neonate. Pediatrics, 1976. 58(2): p. 218-22. 4. Margileth, A.M. and M. Museles, Cutaneous hemangiomas in children. Diagnosis and conservative management. Jama, 1965. 194(5): p. 523-6. 5. Powell, T.G., et al., Epidemiology of strawberry haemangioma in low birthweight infants. Br J Dermatol, 1987. 116(5): p. 635-41. 6. Burton, B.K., et al., An increased incidence of haemangiomas in infants born following chorionic villus sampling (CVS). Prenat Diagn, 1995. 15(3): p. 209-14. 7. Martinez, M.I., et al., Infantile hemangioma: clinical resolution with 5% imiquimod cream. Arch Dermatol, 2002. 138(7): p. 881-4; discussion 884. 8. Gampper, T.J. and R.F. Morgan, Vascular anomalies: hemangiomas. Plast Reconstr Surg, 2002. 110(2): p. 572-85; quiz 586; discussion 587-8. 9. Ceisler, E.J., L. Santos, and F. Blei, Periocular hemangiomas: what every physician should know. Pediatr Dermatol, 2004. 21(1): p. 1-9. 10. Dadras, S.S., et al., Infantile hemangiomas are arrested in an early developmental vascular differentiation state. Mod Pathol, 2004. 17(9): p. 1068-79. 11. Oliver, G. and M. Detmar, The rediscovery of the lymphatic system: old and new insights into the development and biological function of the lymphatic vasculature. Genes Dev, 2002. 16(7): p. 773-83. 12. Vikkula, M., et al., Molecular basis of vascular anomalies. Trends Cardiovasc Med, 1998. 8(7): p. 281-92. 13. Cohen, M.M., Jr., Vasculogenesis, angiogenesis, hemangiomas, and vascular malformations. Am J Med Genet, 2002. 108(4): p. 265-74. 14. Chang, J., et al., Proliferative hemangiomas: analysis of cytokine gene expression and angiogenesis. Plast Reconstr Surg, 1999. 103(1): p. 1-9; discussion 10. 15. Takahashi, K., et al., Cellular markers that distinguish the phases of hemangioma during infancy and childhood. J Clin Invest, 1994. 93(6): p. 2357-64. 16. Bielenberg, D.R., et al., Progressive growth of infantile cutaneous hemangiomas is directly correlated with hyperplasia and angiogenesis of adjacent epidermis and inversely correlated with expression of the endogenous angiogenesis inhibitor, IFN-beta. Int J Oncol, 1999. 14(3): p. 401-8. 17. Ritter, M.R., et al., Insulin-like growth factor 2 and potential regulators of hemangioma growth and involution identified by large-scale expression analysis. Proc Natl Acad Sci U S A, 2002. 99(11): p. 7455-60. 18. Isik, F.F., et al., Monocyte chemoattractant protein-1 mRNA expression in hemangiomas and vascular malformations. J Surg Res, 1996. 61(1): p. 71-6. 19. Dosquet, C., et al., [Importance of bFGF (
Results Reference
background
PubMed Identifier
19419474
Citation
McCuaig CC, Dubois J, Powell J, Belleville C, David M, Rousseau E, Gendron R, Jafarian F, Auger I. A phase II, open-label study of the efficacy and safety of imiquimod in the treatment of superficial and mixed infantile hemangioma. Pediatr Dermatol. 2009 Mar-Apr;26(2):203-12. doi: 10.1111/j.1525-1470.2008.00857.x.
Results Reference
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A Phase II Study of Imiquimod 5 % Cream for the Treatment of Hemangioma in Infancy

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