A Phase II Study of Imiquimod 5 % Cream for the Treatment of Hemangioma in Infancy
NCT00601016 · Status: COMPLETED · Phase: PHASE2 · Type: INTERVENTIONAL · Enrollment: 18
Last updated 2008-01-25
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.
Conditions
- Hemangioma, Capillary
Interventions
- DRUG
-
Imiquimod 5% cream
Imiquimod 5% cream applied topical on hemangioma once a day , 3 to 7 times a week for a maximum of 4 months.
Sponsors & Collaborators
-
Graceway Pharmaceuticals, LLC
collaborator INDUSTRY -
St. Justine's Hospital
lead OTHER
Principal Investigators
-
Catherine McCuaig, M.D. · St. Justine's Hospital
Study Design
- Allocation
- NA
- Purpose
- TREATMENT
- Masking
- NONE
- Model
- SINGLE_GROUP
Eligibility
- Min Age
- 2 Months
- Max Age
- 12 Months
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2005-03-31
- Primary Completion
- 2006-09-30
- Completion
- 2006-09-30
Countries
- Canada
Study Locations
More Related Trials
-
Treatment of Nodular Basal Cell Carcinoma (BCC) With Imiquimod 5% Cream After Curettage
NCT00314756 ·Status: COMPLETED ·Phase: PHASE4
-
Safety and Efficacy of Imiquimod Applied in Dose-Cycle for Actinic Keratoses
NCT00175643 ·Status: COMPLETED ·Phase: PHASE3
-
Investigating the Effect of Topical Imiquimod on Sebaceous Hyperplasia
NCT06840470 ·Status: ACTIVE_NOT_RECRUITING ·Phase: PHASE4
-
A Pilot Study of the Treatment of Facial Nodular and Nodulocystic Basal Cell Carcinoma With Double Curettage and Cautery Followed by Application of Imiquimod to the Base
NCT00463359 ·Status: UNKNOWN ·Phase: NA
-
Topical Imiquimod Compared With Surgery in Treating Patients With Basal Cell Skin Cancer
NCT00066872 ·Status: COMPLETED ·Phase: PHASE3
-
A Study to Evaluate Effectiveness of Imiquimod 5% Cream in Superficial Basal Cell Carcinoma
NCT00189241 ·Status: COMPLETED ·Phase: PHASE3
-
Topical Imiquimod in Conjunction With Nd:YAG Laser for Tattoo Removal
NCT00638651 ·Status: COMPLETED ·Phase: PHASE1
-
Tacrolimus for the Treatment of Superficial Kaposiform Hemangioendothelioma and Tufted Angioma
NCT04056962 ·Status: RECRUITING ·Phase: PHASE2
-
A Double-blind, Randomized, Single Centre, Vehicle-controlled Study to Evaluate the Safety and Tolerability of a New Topical Formulation Containing 0,09% Imiquimod (Limtop) in Healthy Subjects
NCT01567683 ·Status: COMPLETED ·Phase: PHASE1
-
Topical Imiquimod Cream in Combination With Cryotherapy for the Treatment of Actinic Keratoses
NCT00774787 ·Status: COMPLETED ·Phase: PHASE4
-
Topical 5% Imiquimod Cream for Vulvar Paget's Disease
NCT02385188 ·Status: COMPLETED ·Phase: PHASE3
-
Combination Therapy of Imiquimod 5%Cream and Cryotherapy vs Monotherapy for Common Warts:Randomized Comparative Trial.
NCT06973473 ·Status: NOT_YET_RECRUITING
-
Topical Imiquimod in Treating Patients With Recurrent Paget's Disease of the Vulva
NCT00504023 ·Status: COMPLETED ·Phase: NA
-
Imiquimod 5% Cream in the Treatment of External Genital or Perianal Warts in HIV+ Patients
NCT00761371 ·Status: COMPLETED ·Phase: PHASE4
-
Phase 3 Study of Imiquimod Creams in the Treatment of External Genital Warts
NCT00735462 ·Status: COMPLETED ·Phase: PHASE3
-
Study With a Topical Gel to Treat Common Warts in Adults
NCT00117871 ·Status: COMPLETED ·Phase: PHASE2
-
Effectiveness of Imiquimod Topical Cream in Early Stage Cutaneous T-cell Lymphoma
NCT02301494 ·Status: WITHDRAWN ·Phase: NA
-
Imiquimod 5% Cream for the Treatment of Periocular Basal Cell Carcinoma
NCT00803907 ·Status: UNKNOWN ·Phase: PHASE4
-
Topical Imiquimod Treatment of Oral Dysplasia
NCT07210775 ·Status: RECRUITING ·Phase: PHASE1/PHASE2
-
Betaglucin 0.2% Versus Imiquimod 5% in Treatment of Ano-genital Warts: Combined Results From Triple Blind Controlled Study
NCT03901690 ·Status: UNKNOWN ·Phase: PHASE3
-
Treatment of Primary Basal Cell Carcinomas of the Skin With Combination of Topical Imiquimod and Cryosurgery
NCT01212562 ·Status: COMPLETED
-
1-Year Follow up to the 1473-IMIQ Study
NCT00114023 ·Status: COMPLETED
-
A Phase 2, Baseline-Controlled Study Evaluating the Safety and Efficacy of PTX-022 (Sirolimus) Topical Gel 3.9% in the Treatment of Cutaneous Venous Malformations
NCT06653842 ·Status: ACTIVE_NOT_RECRUITING ·Phase: PHASE2
-
A Cohort Study of Hyperthermia and Imiquimod for the Treatment of Flat Warts
NCT05146895 ·Status: UNKNOWN ·Phase: NA
-
Study With a Topical Gel to Treat Common Warts in Adults
NCT00117923 ·Status: COMPLETED ·Phase: PHASE2