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A Study to Evaluate the Effectiveness of Imiquimod 5% Cream for Basal Cell Carcinoma Recurrence

Primary Purpose

Basal Cell Carcinoma

Status
Completed
Phase
Phase 3
Locations
United States
Study Type
Interventional
Intervention
Imiquimod 5% cream
Sponsored by
Graceway Pharmaceuticals, LLC
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Basal Cell Carcinoma focused on measuring BCC curettage

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Basal cell carcinoma Exclusion Criteria: Psoriasis

Sites / Locations

Arms of the Study

Arm 1

Arm Type

Active Comparator

Arm Label

Imiquimod cream

Arm Description

Imiquimod 5% cream applied once daily 5x/week for up to 6 weeks

Outcomes

Primary Outcome Measures

Number of subjects with recurrence
Primary variable was the proportion of subjects with recurrence/persistence (R/P)of BCC at 1 year posttreatment

Secondary Outcome Measures

Cosmetic outcome of the target lesion
The cosmetic outcome of the target lesion at 1 year posttreatment was the secondary efficacy measurement. The investigator judged cosmetic outcome by using a visual analog scale (VAS) to assess the parameters of hypo- and hyperpigmentation,roughness, scarring, and overall skin health and appearance.

Full Information

First Posted
August 11, 2005
Last Updated
July 14, 2010
Sponsor
Graceway Pharmaceuticals, LLC
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1. Study Identification

Unique Protocol Identification Number
NCT00129519
Brief Title
A Study to Evaluate the Effectiveness of Imiquimod 5% Cream for Basal Cell Carcinoma Recurrence
Official Title
Open-label Study to Evaluate the Use of Imiquimod 5% Cream for Reducing Postsurgical Recurrence or Persistence of Basal Cell Carcinoma Following Excision by Curettage
Study Type
Interventional

2. Study Status

Record Verification Date
July 2010
Overall Recruitment Status
Completed
Study Start Date
January 2004 (undefined)
Primary Completion Date
January 2006 (Actual)
Study Completion Date
January 2006 (Actual)

3. Sponsor/Collaborators

Name of the Sponsor
Graceway Pharmaceuticals, LLC

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The primary objective of this study is to assess whether basal cell carcinoma (BCC) lesions surgically treated with curettage, followed by imiquimod 5% cream as postsurgical adjuvant therapy, will have an improved cure rate over the ED/C historical norm of approximately 70% at 1-year posttreatment follow-up. A secondary objective is to assess cosmetic outcome.
Detailed Description
This was an open-label, phase IIIb, multicenter, single arm, historical-controlled study. Biopsy-confirmed BCC lesions (1 per subject) were excised by curettage, with no electrodessication. Approximately 1 week later, treatment with imiquimod 5% cream was initiated. Imiquimod was applied to the target BCC once daily, 5 times per week (5x/week) for up to 6 weeks. Rest periods were allowed as needed. Subjects reported to the study center at treatment weeks 1, 2, and 6, and posttreatment at weeks 12, 26, and 52. At treatment week 6 and all posttreatment visits, the investigator clinically assessed the target site for tumor clearance and cosmetic outcome. A template made at initiation and created from clear plastic overlay aided in locating the target tumor site. If the investigator identified a lesion that had occurred or recurred at the target site, the subject was discontinued from the study and counted as a recurrence/persistence (R/P).

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Basal Cell Carcinoma
Keywords
BCC curettage

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
63 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Imiquimod cream
Arm Type
Active Comparator
Arm Description
Imiquimod 5% cream applied once daily 5x/week for up to 6 weeks
Intervention Type
Drug
Intervention Name(s)
Imiquimod 5% cream
Intervention Description
Imiquimod 5% cream applied once daily 5x/week for up to 6 weeks
Primary Outcome Measure Information:
Title
Number of subjects with recurrence
Description
Primary variable was the proportion of subjects with recurrence/persistence (R/P)of BCC at 1 year posttreatment
Time Frame
1 year posttreatment
Secondary Outcome Measure Information:
Title
Cosmetic outcome of the target lesion
Description
The cosmetic outcome of the target lesion at 1 year posttreatment was the secondary efficacy measurement. The investigator judged cosmetic outcome by using a visual analog scale (VAS) to assess the parameters of hypo- and hyperpigmentation,roughness, scarring, and overall skin health and appearance.
Time Frame
1 year posttreatment

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Basal cell carcinoma Exclusion Criteria: Psoriasis
Facility Information:
City
Grass Valley
State/Province
California
ZIP/Postal Code
95945
Country
United States
City
Loma Linda
State/Province
California
ZIP/Postal Code
92354
Country
United States
City
New York
State/Province
New York
ZIP/Postal Code
10016
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
18277458
Citation
Rigel DS, Torres AM, Ely H. Imiquimod 5% cream following curettage without electrodesiccation for basal cell carcinoma: preliminary report. J Drugs Dermatol. 2008 Jan;7(1 Suppl 1):s15-6.
Results Reference
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A Study to Evaluate the Effectiveness of Imiquimod 5% Cream for Basal Cell Carcinoma Recurrence

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