Efficacy and Safety of CIP-Isotretinoin in Patients With Severe Recalcitrant Nodular Acne
Primary Purpose
Severe Nodular Acne
Status
Completed
Phase
Phase 3
Locations
International
Study Type
Interventional
Intervention
CIP-Isotretinoin
Isotretinoin
Sponsored by
About this trial
This is an interventional treatment trial for Severe Nodular Acne focused on measuring isotretinoin, dermatology, skin
Eligibility Criteria
Inclusion Criteria:
- Severe recalcitrant nodular acne, which in the opinion of the investigator is compatible with isotretinoin treatment.
- Ten (10) or more nodular lesions (facial and/or truncal).
- Treatment-naïve patients without any prior exposure to systemic isotretinoin or other retinoids.
- Age between 12 and 54 years.
- Weight between 40 and 110 kg.
- Negative serum human chorionic gonadotropin (hCG) pregnancy test consistent with a non-pregnant state (females only).
- No significant disease or clinically significant finding in a physical examination.
- No clinically significant abnormal laboratory value.
- No clinically significant abnormal vital sign measurement.
- Patients presenting with stable and controlled diabetes mellitus (Types I and II) may be included in the study. However, patients should not have had a hospitalization for any diabetes related complications in the last 12 months, and must be on stable medication for the preceding 6 months. To be included in the study, the patients should have Hemoglobin-A1c values ≤ 6.5% at screening and in the test done 3 - 4 months previously.
- Patients with previously diagnosed Polycystic Ovarian Syndrome (PCOS) may be included in the study if in the opinion of the investigator they do not have any other clinically significant abnormality (e.g. metabolic syndrome or elevated lipids).
Exclusion Criteria:
Female patients will be excluded from the study if they:
- Are pregnant;
- Are at high risk for becoming pregnant or likely to become pregnant during treatment;
- Will be breast-feeding or considering breast feeding during the course of the study.
- Known history or presence of any clinically significant unstable medical condition(s) which in the opinion of the investigator could pose a risk for the safety of the patient including any previous history of gastrointestinal disease.
- Patients with any skin disease or other condition that might interfere with the evaluation of recalcitrant nodular acne.
- Patients will be interviewed using the SCID-CT current and lifetime modules for Major Depression, Mania, and Psychosis. Patients with a lifetime history of psychosis will be excluded. Patients with a history of major depressive, manic, hypomanic or mixed episodes will not be excluded unless they have had an episode during the preceding year.
- Patients with any past or current psychotic symptoms.
- Patients reporting any suicidal behaviour (including attempts, interrupted attempts, aborted attempts, or other preparatory behaviours), within the past year, or serious suicidal ideation in the past year, will be excluded from study participation.
- A lifetime history of wishing to be dead, non-specific active suicidal thoughts or active suicidal ideation without intent to act will not result in exclusion.
- Known history or suspected carcinoma.
- Known history of liver or kidney disorders (hepatic and renal insufficiency).
- Known history or current pseudotumor cerebri (benign intracranial hypertension).
- Patients with HLA-B27 related disease, rheumatoid arthritis, rickets or other vitamin D depletion disease or phosphate metabolic disease, severe scoliosis > 15 Cobb angle, history of back surgery/injuries, ongoing use of anticonvulsants known to affect bone metabolism and other genetic or acquired rheumatologic and joint diseases.
- All pediatric patients with serum 25-hydroxyvitamin D levels < 20 ng/mL.
- Patients with hearing disorders who in the opinion of the investigator would not be able to participate in audiometric testing for the study.
- Hypersensitivity or idiosyncratic reaction to isotretinoin, Vitamin A and/or any other drug substances with similar activity.
- Allergy to soy beans, soy bean oil or any other ingredients in the study medications.
- On a special diet within four weeks prior to drug administration (e.g., liquid, protein, raw food diet).
- Difficulty consuming two (2) meals a day to sustain weight and health.
Sites / Locations
- Total Skin & Beauty Dermatology Center
- Burke Pharmaceutical Research
- Center for Dermatology Clinical Research
- Dermatology Research Associates
- Dermatology Specialists
- Skin Surgery Medical Group, Inc.
- Horizons Clinical Research Center
- North Florida Dermatology Associates, PA
- Ameriderm Research
- Park Avenue Dermatology
- Ameriderm Research
- Peachtree Dermatology Associates, PC
- MedaPhase Inc.
- Northwest Clinical Trials
- Northwest Clinical Trials
- Dawes Fretzin Clinical Research
- The Indiana Clinical Trials Center, PC
- The South Bend Clinic, LLP
- Dermatology and Skin Cancer Specialists / Pediaresearch, LLC
- ActivMed Practices & Research
- Great Lakes Research Group
- Hamzavi Dermatology
- Minnesota Clinical Study Center
- Skin Specialists, PC
- Comprehensive Clinical Research
- Haber Dermatology, Clinical Research Center
- Oregon Dermatology and Research Center
- Paddington Testing Company Inc.
- Radiant Research, Inc.
- Dermatology Associates of Knoxville
- Tennessee Clinical Research Center
- Arlington Center for Dermatology
- Suzanne Bruce and Associates - The Center for Skin Research
- Progressive Clinical Research
- Stephen Miller, MD, PA Dermatology
- Dermatology Research Center
- Premier Clinical Research
- Derm Research @ 888 Inc.
- Dermadvances Research
- Durondel C.P. Inc
- Newlab Clinical Research Inc.
- UltraNova Skincare
- Dermatrials Research
- The Guenther Dermatology Research Centre
- Lynderm Research Inc.
- North Bay Dermatology Centre
- Institute of Cosmetic and Laser Surgery
- K. Papp Clinical Research
- Windsor Clinical Research
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
CIP-Isotretinoin
Isotretinoin
Arm Description
Outcomes
Primary Outcome Measures
Co-primary Outcome 1: Change From Baseline in Total Nodular Lesion Count (Facial and Truncal)
The change from Baseline to Week 20 in the total number of nodular lesions was calculated as the Week 20 lesion count minus Baseline lesion count and compared using Analysis of Covariance (ANCOVA), controlling for Baseline total nodular lesion count, gender and analysis site.
The 95% CI of the adjusted least square mean difference (CIP-ISOTRETINOIN minus Isotretinoin) was also calculated using the ANCOVA model.
Pre-defined criterion for non-inferiority: upper bound of the 95% CI for the treatment difference < 4.
Co-Primary Outcome 2: Proportion of Patients Who Achieve at Least a 90% Reduction in Total Number of Nodular Lesions (Facial and Truncal).
The percentage of patients in each group who achieved ≥90% reduction in the total nodular lesion count from Baseline to Week 20 was calculated along with its 95% CI (normal approximation). A 95% 2-sided CI on the difference between treatments (CIP-ISOTRETINOIN minus Isotretinoin) was also computed.
Pre-defined criterion for non-inferiority: lower bound of the 95% CI for the treatment difference > -10.
Secondary Outcome Measures
Proportion of Patients Who Are Rated as Clear/Almost Clear on the Six-point Physicians' Global Assessment Scale (PGSA).
PGSA categories: 1 (Almost clear); 2 (Mild); 3 (Moderate); 4 (Severe); 5 (Very severe). A grade of either 0 (clear) or 1 (almost clear) on the 6-point PGSA scale within the Week 20 analysis window was considered a success.
Full Information
NCT ID
NCT00975143
First Posted
September 9, 2009
Last Updated
June 5, 2014
Sponsor
Cipher Pharmaceuticals Inc.
1. Study Identification
Unique Protocol Identification Number
NCT00975143
Brief Title
Efficacy and Safety of CIP-Isotretinoin in Patients With Severe Recalcitrant Nodular Acne
Official Title
A Double-Blind, Randomized, Phase III, Parallel Group Study Evaluating the Efficacy and Safety of CIP-Isotretinoin in Patients With Severe Recalcitrant Nodular Acne
Study Type
Interventional
2. Study Status
Record Verification Date
June 2014
Overall Recruitment Status
Completed
Study Start Date
September 2009 (undefined)
Primary Completion Date
May 2011 (Actual)
Study Completion Date
May 2011 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Cipher Pharmaceuticals Inc.
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
The purpose of this study is to compare the efficacy and safety of CIP-Isotretinoin and a marketed (generic) formulation of isotretinoin when both are administered twice daily with meals.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Severe Nodular Acne
Keywords
isotretinoin, dermatology, skin
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
925 (Actual)
8. Arms, Groups, and Interventions
Arm Title
CIP-Isotretinoin
Arm Type
Experimental
Arm Title
Isotretinoin
Arm Type
Active Comparator
Intervention Type
Drug
Intervention Name(s)
CIP-Isotretinoin
Intervention Description
0.5 mg/kg/day for 4 weeks, and 1 mg/kg/day for 16 weeks, taken orally, twice daily.
Intervention Type
Drug
Intervention Name(s)
Isotretinoin
Intervention Description
0.5 mg/kg/day for 4 weeks, and 1 mg/kg/day for 16 weeks, taken orally, twice daily.
Primary Outcome Measure Information:
Title
Co-primary Outcome 1: Change From Baseline in Total Nodular Lesion Count (Facial and Truncal)
Description
The change from Baseline to Week 20 in the total number of nodular lesions was calculated as the Week 20 lesion count minus Baseline lesion count and compared using Analysis of Covariance (ANCOVA), controlling for Baseline total nodular lesion count, gender and analysis site.
The 95% CI of the adjusted least square mean difference (CIP-ISOTRETINOIN minus Isotretinoin) was also calculated using the ANCOVA model.
Pre-defined criterion for non-inferiority: upper bound of the 95% CI for the treatment difference < 4.
Time Frame
20 weeks
Title
Co-Primary Outcome 2: Proportion of Patients Who Achieve at Least a 90% Reduction in Total Number of Nodular Lesions (Facial and Truncal).
Description
The percentage of patients in each group who achieved ≥90% reduction in the total nodular lesion count from Baseline to Week 20 was calculated along with its 95% CI (normal approximation). A 95% 2-sided CI on the difference between treatments (CIP-ISOTRETINOIN minus Isotretinoin) was also computed.
Pre-defined criterion for non-inferiority: lower bound of the 95% CI for the treatment difference > -10.
Time Frame
20 weeks
Secondary Outcome Measure Information:
Title
Proportion of Patients Who Are Rated as Clear/Almost Clear on the Six-point Physicians' Global Assessment Scale (PGSA).
Description
PGSA categories: 1 (Almost clear); 2 (Mild); 3 (Moderate); 4 (Severe); 5 (Very severe). A grade of either 0 (clear) or 1 (almost clear) on the 6-point PGSA scale within the Week 20 analysis window was considered a success.
Time Frame
20 weeks
10. Eligibility
Sex
All
Minimum Age & Unit of Time
12 Years
Maximum Age & Unit of Time
54 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Severe recalcitrant nodular acne, which in the opinion of the investigator is compatible with isotretinoin treatment.
Ten (10) or more nodular lesions (facial and/or truncal).
Treatment-naïve patients without any prior exposure to systemic isotretinoin or other retinoids.
Age between 12 and 54 years.
Weight between 40 and 110 kg.
Negative serum human chorionic gonadotropin (hCG) pregnancy test consistent with a non-pregnant state (females only).
No significant disease or clinically significant finding in a physical examination.
No clinically significant abnormal laboratory value.
No clinically significant abnormal vital sign measurement.
Patients presenting with stable and controlled diabetes mellitus (Types I and II) may be included in the study. However, patients should not have had a hospitalization for any diabetes related complications in the last 12 months, and must be on stable medication for the preceding 6 months. To be included in the study, the patients should have Hemoglobin-A1c values ≤ 6.5% at screening and in the test done 3 - 4 months previously.
Patients with previously diagnosed Polycystic Ovarian Syndrome (PCOS) may be included in the study if in the opinion of the investigator they do not have any other clinically significant abnormality (e.g. metabolic syndrome or elevated lipids).
Exclusion Criteria:
Female patients will be excluded from the study if they:
Are pregnant;
Are at high risk for becoming pregnant or likely to become pregnant during treatment;
Will be breast-feeding or considering breast feeding during the course of the study.
Known history or presence of any clinically significant unstable medical condition(s) which in the opinion of the investigator could pose a risk for the safety of the patient including any previous history of gastrointestinal disease.
Patients with any skin disease or other condition that might interfere with the evaluation of recalcitrant nodular acne.
Patients will be interviewed using the SCID-CT current and lifetime modules for Major Depression, Mania, and Psychosis. Patients with a lifetime history of psychosis will be excluded. Patients with a history of major depressive, manic, hypomanic or mixed episodes will not be excluded unless they have had an episode during the preceding year.
Patients with any past or current psychotic symptoms.
Patients reporting any suicidal behaviour (including attempts, interrupted attempts, aborted attempts, or other preparatory behaviours), within the past year, or serious suicidal ideation in the past year, will be excluded from study participation.
A lifetime history of wishing to be dead, non-specific active suicidal thoughts or active suicidal ideation without intent to act will not result in exclusion.
Known history or suspected carcinoma.
Known history of liver or kidney disorders (hepatic and renal insufficiency).
Known history or current pseudotumor cerebri (benign intracranial hypertension).
Patients with HLA-B27 related disease, rheumatoid arthritis, rickets or other vitamin D depletion disease or phosphate metabolic disease, severe scoliosis > 15 Cobb angle, history of back surgery/injuries, ongoing use of anticonvulsants known to affect bone metabolism and other genetic or acquired rheumatologic and joint diseases.
All pediatric patients with serum 25-hydroxyvitamin D levels < 20 ng/mL.
Patients with hearing disorders who in the opinion of the investigator would not be able to participate in audiometric testing for the study.
Hypersensitivity or idiosyncratic reaction to isotretinoin, Vitamin A and/or any other drug substances with similar activity.
Allergy to soy beans, soy bean oil or any other ingredients in the study medications.
On a special diet within four weeks prior to drug administration (e.g., liquid, protein, raw food diet).
Difficulty consuming two (2) meals a day to sustain weight and health.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
James J. Leyden, MD
Organizational Affiliation
University of Pennsylvania
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Guy Webster, MD
Organizational Affiliation
Jefferson Medical College of Thomas Jefferson University
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Jason A. Gross, PharmD
Organizational Affiliation
Cipher Pharmaceuticals Inc.
Official's Role
Study Director
Facility Information:
Facility Name
Total Skin & Beauty Dermatology Center
City
Birmingham
State/Province
Alabama
ZIP/Postal Code
35205
Country
United States
Facility Name
Burke Pharmaceutical Research
City
Hot Springs
State/Province
Arkansas
ZIP/Postal Code
71913
Country
United States
Facility Name
Center for Dermatology Clinical Research
City
Fremont
State/Province
California
ZIP/Postal Code
94538
Country
United States
Facility Name
Dermatology Research Associates
City
Los Angeles
State/Province
California
ZIP/Postal Code
90045
Country
United States
Facility Name
Dermatology Specialists
City
Oceanside
State/Province
California
ZIP/Postal Code
92056
Country
United States
Facility Name
Skin Surgery Medical Group, Inc.
City
San Diego
State/Province
California
ZIP/Postal Code
92117
Country
United States
Facility Name
Horizons Clinical Research Center
City
Denver
State/Province
Colorado
ZIP/Postal Code
80220
Country
United States
Facility Name
North Florida Dermatology Associates, PA
City
Jacksonville
State/Province
Florida
ZIP/Postal Code
32204
Country
United States
Facility Name
Ameriderm Research
City
Jacksonville
State/Province
Florida
ZIP/Postal Code
32216
Country
United States
Facility Name
Park Avenue Dermatology
City
Orange Park
State/Province
Florida
ZIP/Postal Code
32073
Country
United States
Facility Name
Ameriderm Research
City
Ormond Beach
State/Province
Florida
ZIP/Postal Code
32174
Country
United States
Facility Name
Peachtree Dermatology Associates, PC
City
Atlanta
State/Province
Georgia
ZIP/Postal Code
30327
Country
United States
Facility Name
MedaPhase Inc.
City
Newnan
State/Province
Georgia
ZIP/Postal Code
30263
Country
United States
Facility Name
Northwest Clinical Trials
City
Boise
State/Province
Idaho
ZIP/Postal Code
83704
Country
United States
Facility Name
Northwest Clinical Trials
City
Nampa
State/Province
Idaho
ZIP/Postal Code
83687
Country
United States
Facility Name
Dawes Fretzin Clinical Research
City
Indianapolis
State/Province
Indiana
ZIP/Postal Code
46256
Country
United States
Facility Name
The Indiana Clinical Trials Center, PC
City
Plainfield
State/Province
Indiana
ZIP/Postal Code
46168
Country
United States
Facility Name
The South Bend Clinic, LLP
City
South Bend
State/Province
Indiana
ZIP/Postal Code
46617
Country
United States
Facility Name
Dermatology and Skin Cancer Specialists / Pediaresearch, LLC
City
Owensboro
State/Province
Kentucky
ZIP/Postal Code
42303
Country
United States
Facility Name
ActivMed Practices & Research
City
Haverhill
State/Province
Massachusetts
ZIP/Postal Code
01830
Country
United States
Facility Name
Great Lakes Research Group
City
Bay City
State/Province
Michigan
ZIP/Postal Code
48706
Country
United States
Facility Name
Hamzavi Dermatology
City
Fort Gratiot
State/Province
Michigan
ZIP/Postal Code
48059
Country
United States
Facility Name
Minnesota Clinical Study Center
City
Fridley
State/Province
Minnesota
ZIP/Postal Code
55432
Country
United States
Facility Name
Skin Specialists, PC
City
Omaha
State/Province
Nebraska
ZIP/Postal Code
68144
Country
United States
Facility Name
Comprehensive Clinical Research
City
Berlin
State/Province
New Jersey
ZIP/Postal Code
08009
Country
United States
Facility Name
Haber Dermatology, Clinical Research Center
City
South Euclid
State/Province
Ohio
ZIP/Postal Code
44118
Country
United States
Facility Name
Oregon Dermatology and Research Center
City
Portland
State/Province
Oregon
ZIP/Postal Code
97210
Country
United States
Facility Name
Paddington Testing Company Inc.
City
Philadelphia
State/Province
Pennsylvania
ZIP/Postal Code
19103
Country
United States
Facility Name
Radiant Research, Inc.
City
Greer
State/Province
South Carolina
ZIP/Postal Code
29651
Country
United States
Facility Name
Dermatology Associates of Knoxville
City
Knoxville
State/Province
Tennessee
ZIP/Postal Code
37934
Country
United States
Facility Name
Tennessee Clinical Research Center
City
Nashville
State/Province
Tennessee
ZIP/Postal Code
37215
Country
United States
Facility Name
Arlington Center for Dermatology
City
Arlington
State/Province
Texas
ZIP/Postal Code
76011
Country
United States
Facility Name
Suzanne Bruce and Associates - The Center for Skin Research
City
Houston
State/Province
Texas
ZIP/Postal Code
77056
Country
United States
Facility Name
Progressive Clinical Research
City
San Antonio
State/Province
Texas
ZIP/Postal Code
78229
Country
United States
Facility Name
Stephen Miller, MD, PA Dermatology
City
San Antonio
State/Province
Texas
ZIP/Postal Code
78229
Country
United States
Facility Name
Dermatology Research Center
City
Salt Lake City
State/Province
Utah
ZIP/Postal Code
84117
Country
United States
Facility Name
Premier Clinical Research
City
Spokane
State/Province
Washington
ZIP/Postal Code
99204
Country
United States
Facility Name
Derm Research @ 888 Inc.
City
Vancouver
State/Province
British Columbia
ZIP/Postal Code
V5Z 3Y1
Country
Canada
Facility Name
Dermadvances Research
City
Winnipeg
State/Province
Manitoba
ZIP/Postal Code
R3C 1R4
Country
Canada
Facility Name
Durondel C.P. Inc
City
Moncton
State/Province
New Brunswick
ZIP/Postal Code
E1C 8X3
Country
Canada
Facility Name
Newlab Clinical Research Inc.
City
St. John's
State/Province
Newfoundland and Labrador
ZIP/Postal Code
A1C 2H5
Country
Canada
Facility Name
UltraNova Skincare
City
Barrie
State/Province
Ontario
ZIP/Postal Code
L4M 6L2
Country
Canada
Facility Name
Dermatrials Research
City
Hamilton
State/Province
Ontario
ZIP/Postal Code
L8N 1V6
Country
Canada
Facility Name
The Guenther Dermatology Research Centre
City
London
State/Province
Ontario
ZIP/Postal Code
N6A 3H7
Country
Canada
Facility Name
Lynderm Research Inc.
City
Markham
State/Province
Ontario
ZIP/Postal Code
L3P 1A8
Country
Canada
Facility Name
North Bay Dermatology Centre
City
North Bay
State/Province
Ontario
ZIP/Postal Code
P1B 3Z7
Country
Canada
Facility Name
Institute of Cosmetic and Laser Surgery
City
Oakville
State/Province
Ontario
ZIP/Postal Code
L6J 7W5
Country
Canada
Facility Name
K. Papp Clinical Research
City
Waterloo
State/Province
Ontario
ZIP/Postal Code
N2J 1C4
Country
Canada
Facility Name
Windsor Clinical Research
City
Windsor
State/Province
Ontario
ZIP/Postal Code
N8W 5L7
Country
Canada
12. IPD Sharing Statement
Learn more about this trial
Efficacy and Safety of CIP-Isotretinoin in Patients With Severe Recalcitrant Nodular Acne
We'll reach out to this number within 24 hrs