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| Name | Class |
|---|---|
| Advance Biofactures Corporation | INDUSTRY |
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The purpose of this research is to evaluate the safest and most effective dose of a Food and Drug Administration (FDA) approved drug (XIAFLEX) in the treatment of lipoma (fatty tumors of varying sizes that occur commonly in the adult population). The fat in the lipoma is like normal fat except that it is enclosed in a balloon-like structure which is made of collagen (fibrous tissue). Treatment of the lipoma with an injection of XIAFLEX (a protein that breaks down collagen fibers) may dissolve the collagen/fibrous strands thereby decreasing the size of the lipoma or removing it.
Lipomas are common mesenchymal, benign, fatty tumors of varying sizes that occur in the general adult population. They usually present as painful or annoying lumps that are palpable and often visible in the subcutaneous tissue. Many subcutaneous lipomas are asymptomatic and are removed for non-medical reasons. However, they may cause the subject pain or discomfort or interfere with normal activity.
Spontaneous remission of lipomas has not been reported. A lipoma, once it presents itself, remains there for the lifetime of a person who carries it and may stay small or become larger. Alternative treatments of the lipoma are surgery or liposuction. If a large excision is performed there is the problem of having a very large scar and the accompanying issues of healing a large scar, or possible formation of a hematoma followed by consolidation of the hematoma and the remnants of a mass of scar tissue. This is often painful and more problematic than the original lipoma. liposuction also has the potential for hematoma formation followed by scar mass residual.
To avoid the complications listed above, a non-invasive method of treatment, such as enzyme mediated disassociation of adipose tissue, would be desirable. The primary aim of this study is to perform a step-wise approach in dosing to evaluate the safety and efficacy of clostridium histolyticum as a non-operative treatment for lipoma.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Dose #1 | Experimental | single injection 0.058 mg Collagenase Clostridium Histolyticum |
|
| Dose #2 | Experimental | single injection 0.15 mg Collagenase Clostridium Histolyticum |
|
| Dose #3 | Experimental | single injection 0.29 mg Collagenase Clostridium Histolyticum |
|
| Dose #4 | Experimental | single injection 0.44 mg Collagenase Clostridium Histolyticum |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Collagenase Clostridium Histolyticum | Drug | This is a dose escalation study in which subjects will sequentially receive single injections of 0.058 mg, 0.15 mg, 0.29 mg, 0.44 mg. |
|
| Measure | Description | Time Frame |
|---|---|---|
| Change in Visible Surface Area of the Lipoma | The primary efficacy outcome is the visible surface area of the lipoma measured as the longest dimension (length) times the longest dimension perpendicular to length (width). Visible surface area will be determined by caliper and will be analyzed as the percent change from baseline at the 6-month post injection visit. | Baseline and Six months post injection of study drug |
| Measure | Description | Time Frame |
|---|---|---|
| Relative Change in Volume of the Lipoma | A secondary outcome is the relative change in volume of the lipoma as determined by MRI. This outcome will be analyzed as the change from baseline to 6 months post injection. | Baseline and 6 months post injection of study drug |
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Inclusion Criteria:
Exclusion Criteria:
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| Name | Affiliation | Role |
|---|---|---|
| Zachary E Gerut, M.D. | Gerut, Zachary, M.D. | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Zachary E. Gerut, M.D. | Hewlett | New York | 11557 | United States |
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Subjects were screened and enrolled at 1 site in the United States
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| ID | Title | Description |
|---|---|---|
| FG000 | Dose #1 | single injection 0.058 mg Collagenase Clostridium Histolyticum Collagenase Clostridium Histolyticum: This is a dose escalation study in which subjects will sequentially receive single injections of 0.058 mg, 0.15 mg, 0.29 mg, 0.44 mg. |
| FG001 | Dose #2 | single injection 0.15 mg Collagenase Clostridium Histolyticum Collagenase Clostridium Histolyticum: This is a dose escalation study in which subjects will sequentially receive single injections of 0.058 mg, 0.15 mg, 0.29 mg, 0.44 mg. |
| FG002 | Dose #3 | single injection 0.29 mg Collagenase Clostridium Histolyticum Collagenase Clostridium Histolyticum: This is a dose escalation study in which subjects will sequentially receive single injections of 0.058 mg, 0.15 mg, 0.29 mg, 0.44 mg. |
| FG003 | Dose #4 | single injection 0.44 mg Collagenase Clostridium Histolyticum Collagenase Clostridium Histolyticum: This is a dose escalation study in which subjects will sequentially receive single injections of 0.058 mg, 0.15 mg, 0.29 mg, 0.44 mg. |
| Title | Milestones | Reasons Not Completed | ||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Overall Study |
|
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| ID | Title | Description |
|---|---|---|
| BG000 | Dose #1 | single injection 0.058 mg Collagenase Clostridium Histolyticum Collagenase Clostridium Histolyticum: This is a dose escalation study in which subjects will sequentially receive single injections of 0.058 mg, 0.15 mg, 0.29 mg, 0.44 mg. |
| BG001 | Dose #2 |
| Units | Counts |
|---|---|
| Participants |
|
| Title | Description | Population Description | Parameter Type | Dispersion Type | Unit of Measure | Calculate Percentage | Denominator Units Selected | Denominators | Classes |
|---|---|---|---|---|---|---|---|---|---|
| Age, Continuous | Mean |
| Type | Title | Description | Population Description | Reporting Status | Anticipated Posting Date | Parameter Type | Dispersion Type | Unit of Measure | Calculate Percentage | Time Frame | Units Analyzed | Denominator Units Selected | Arm/Group Information | Denominators | Classes | Analyses | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Primary | Change in Visible Surface Area of the Lipoma | The primary efficacy outcome is the visible surface area of the lipoma measured as the longest dimension (length) times the longest dimension perpendicular to length (width). Visible surface area will be determined by caliper and will be analyzed as the percent change from baseline at the 6-month post injection visit. | Analysis population consists of all subjects who were enrolled and received the administration of study drug. | Posted | Mean | Standard Deviation | Percent change from baseline | Baseline and Six months post injection of study drug |
|
Adverse Events were collected from Day 0 through 6 months post administration of study medication
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| ID | Title | Description | Deaths (Affected) | Deaths (At Risk) | Serious Events (Affected) | Serious Events (At Risk) | Other Events (Affected) | Other Events (At Risk) |
|---|---|---|---|---|---|---|---|---|
| EG000 | Dose #1 | single injection 0.058 mg Collagenase Clostridium Histolyticum Collagenase Clostridium Histolyticum: This is a dose escalation study in which subjects will sequentially receive single injections of 0.058 mg, 0.15 mg, 0.29 mg, 0.44 mg. |
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| Term | Organ System | Source Vocabulary | Assessment Type | Notes | Statistical Information |
|---|---|---|---|---|---|
| Bruising | General disorders | MedDRA (Unspecified) | Non-systematic Assessment | Injection site reaction |
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| Title | Organization | Phone | Extension | |
|---|---|---|---|---|
| Dr. Zachary E.Gerut | GerutZ | 516 295-2100 | Drgerut@drgerut.com |
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| ID | Term |
|---|---|
| D008067 | Lipoma |
| ID | Term |
|---|---|
| D018205 | Neoplasms, Adipose Tissue |
| D018204 | Neoplasms, Connective and Soft Tissue |
| D009370 | Neoplasms by Histologic Type |
| D009369 | Neoplasms |
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| ID | Term |
|---|---|
| D003012 | Microbial Collagenase |
| ID | Term |
|---|---|
| D017364 | Collagenases |
| D008666 | Metalloendopeptidases |
| D010450 | Endopeptidases |
| D010447 | Peptide Hydrolases |
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|
single injection 0.15 mg Collagenase Clostridium Histolyticum Collagenase Clostridium Histolyticum: This is a dose escalation study in which subjects will sequentially receive single injections of 0.058 mg, 0.15 mg, 0.29 mg, 0.44 mg. |
| BG002 | Dose #3 | single injection 0.29 mg Collagenase Clostridium Histolyticum Collagenase Clostridium Histolyticum: This is a dose escalation study in which subjects will sequentially receive single injections of 0.058 mg, 0.15 mg, 0.29 mg, 0.44 mg. |
| BG003 | Dose #4 | single injection 0.44 mg Collagenase Clostridium Histolyticum Collagenase Clostridium Histolyticum: This is a dose escalation study in which subjects will sequentially receive single injections of 0.058 mg, 0.15 mg, 0.29 mg, 0.44 mg. |
| BG004 | Total | Total of all reporting groups |
| Years |
|
| Sex: Female, Male | Count of Participants | Participants |
|
| Region of Enrollment | Number | participants |
|
| OG001 | Dose #2 | single injection 0.15 mg Collagenase Clostridium Histolyticum Collagenase Clostridium Histolyticum: This is a dose escalation study in which subjects will sequentially receive single injections of 0.058 mg, 0.15 mg, 0.29 mg, 0.44 mg. |
| OG002 | Dose #3 | single injection 0.29 mg Collagenase Clostridium Histolyticum Collagenase Clostridium Histolyticum: This is a dose escalation study in which subjects will sequentially receive single injections of 0.058 mg, 0.15 mg, 0.29 mg, 0.44 mg. |
| OG003 | Dose #4 | single injection 0.44 mg Collagenase Clostridium Histolyticum Collagenase Clostridium Histolyticum: This is a dose escalation study in which subjects will sequentially receive single injections of 0.058 mg, 0.15 mg, 0.29 mg, 0.44 mg. |
|
|
|
| Secondary | Relative Change in Volume of the Lipoma | A secondary outcome is the relative change in volume of the lipoma as determined by MRI. This outcome will be analyzed as the change from baseline to 6 months post injection. | Analysis is based on the population that consists of all subjects who are enrolled and received administration of study drug | Posted | Mean | Standard Deviation | Percent reduction from baseline | Baseline and 6 months post injection of study drug |
|
|
|
|
| 0 |
| 2 |
| 1 |
| 2 |
| EG001 | Dose #2 | single injection 0.15 mg Collagenase Clostridium Histolyticum Collagenase Clostridium Histolyticum: This is a dose escalation study in which subjects will sequentially receive single injections of 0.058 mg, 0.15 mg, 0.29 mg, 0.44 mg. | 0 | 4 | 3 | 4 |
| EG002 | Dose #3 | single injection 0.29 mg Collagenase Clostridium Histolyticum Collagenase Clostridium Histolyticum: This is a dose escalation study in which subjects will sequentially receive single injections of 0.058 mg, 0.15 mg, 0.29 mg, 0.44 mg. | 0 | 4 | 3 | 4 |
| EG003 | Dose #4 | single injection 0.44 mg Collagenase Clostridium Histolyticum Collagenase Clostridium Histolyticum: This is a dose escalation study in which subjects will sequentially receive single injections of 0.058 mg, 0.15 mg, 0.29 mg, 0.44 mg. | 0 | 4 | 4 | 4 |
|
| Pain | General disorders | MedDRA (Unspecified) | Non-systematic Assessment | Injection Site |
|
| Swelling | General disorders | MedDRA (Unspecified) | Non-systematic Assessment | Injection site |
|
| Contusion | Vascular disorders | MedDRA (Unspecified) | Non-systematic Assessment |
|
| Headache | Nervous system disorders | MedDRA (Unspecified) | Non-systematic Assessment |
|
| Nausea | Gastrointestinal disorders | MedDRA (Unspecified) | Non-systematic Assessment |
|
| Dizziness | Cardiac disorders | MedDRA (Unspecified) | Non-systematic Assessment |
|
| Sinusitis | Respiratory, thoracic and mediastinal disorders | MedDRA (Unspecified) | Non-systematic Assessment |
|
| Upper Respiratory Tract Infection | Respiratory, thoracic and mediastinal disorders | MedDRA (Unspecified) | Non-systematic Assessment |
|
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| D006867 |
| Hydrolases |
| D004798 | Enzymes |
| D045762 | Enzymes and Coenzymes |
| D045726 | Metalloproteases |