Not provided
| ID | Type | Description | Link |
|---|---|---|---|
| 2017-004022-15 | EudraCT Number |
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
A study to evaluate the efficacy and safety, and pharmacokinetic (PK) profile of multiple doses of imsidolimab (ANB019) in adults with palmoplantar pustulosis (PPP)
Not provided
Not provided
Not provided
Not provided
Not provided
| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Placebo | Placebo Comparator | Participants will receive placebo administered by subcutaneous injection on Day 1 followed by monthly doses of placebo by subcutaneous injection on Days 29, 57, and 85. |
|
| imsidolimab | Experimental | Participants will receive 200 mg imsidolimab by subcutaneous injection on Day 1 followed by monthly doses of 100 mg imsidolimab by subcutaneous injection on Days 29, 57, and 85. |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Imsidolimab | Biological | Administered by subcutaneous injection once a month |
|
| Measure | Description | Time Frame |
|---|---|---|
| Change From Baseline in Palmoplantar Pustulosis Psoriasis Area Severity Index (PPPASI) | The Palmoplantar Pustulosis Area and Severity Index (PPPASI) is used to assess the severity of palmoplantar pustulosis lesions and their response to therapy. The glabrous skin of both palms and both soles are assessed for erythema, pustules, and desquamation (scaling), each on a scale from 0 (none) to 4 (very severe). The area affected of each palm and sole is scored from 0 (0%) to 6 (90-100%). Scores for the 3 characteristics of PPP are summed and adjusted for the area affected, and the scores for each palm and sole are added to calculate the total score. The PPPASI total score ranges from 0 to 72. A higher score indicates more severe disease, and a negative change from Baseline indicates improvement. | Baseline to Week 16 |
| Number of Participants With Treatment-emergent Adverse Events (TEAEs) | Clinical safety was evaluated by reporting incidence of adverse events up to week 24. TEAEs are defined as new events that occured during or after first dose of study drug or any event that worsens after first dose of study drug. A serious AE (SAE) is defined as any untoward medical occurrence that resulted in death, was life-threatening, resulted in persistent disability/incapacity, was a congenital anomaly/birth defect, or an important medical event that may jeopardize the participant or require medical or surgical intervention to prevent one of the outcomes listed above. Severity was assessed by the Investigator as mild (easily tolerated, causing minimal discomfort and not interfering with everyday activities), moderate (causes sufficient discomfort and interferes with normal everyday activities) or severe (prevents normal everyday activities). The Investigator assessed the relationship between study treatment and each AE based on clinical judgement. | From first dose of any study drug to Week 24 |
| Measure | Description | Time Frame |
|---|---|---|
| Percentage of Participants Who Achieved 50% Reduction (Improvement) From Baseline in Palmoplantar Pustulosis Psoriasis Area Severity Index Score (PPPASI 50) | The Palmoplantar Pustulosis Area and Severity Index (PPPASI) is used to assess the severity of palmoplantar pustulosis lesions and their response to therapy. The glabrous skin of both palms and both soles are assessed for erythema, pustules, and desquamation (scaling), each on a scale from 0 (none) to 4 (very severe). The area affected of each palm and sole is scored from 0 (0%) to 6 (90-100%). Scores for the 3 characteristics of PPP are summed and adjusted for the area affected, and the scores for each palm and sole are added to calculate the total score. The PPPASI total score ranges from 0 to 72. A higher score indicates more severe disease. |
Not provided
Inclusion Criteria:
Exclusion Criteria:
Other protocol-defined inclusion/exclusion criteria may apply
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Investigational Site | Birmingham | Alabama | 35233 | United States | ||
| Investigational Site |
Not provided
Not provided
Not provided
Not provided
Not provided
Participants were randomized equally to one of two treatment groups. Randomization was stratified based on the participant's history of plaque psoriasis, to ensure that the number of participants enrolled with plaque psoriasis did not exceed 50%.
Participants were enrolled in this trial at 36 sites located within North America and Europe.
Not provided
| ID | Title | Description |
|---|---|---|
| FG000 | Placebo | Participants received placebo administered by subcutaneous injection on Day 1 followed by monthly doses on Days 29, 57, and 85. |
| FG001 | Imsidolimab | Participants received 200 mg imsidolimab by subcutaneous injection on Day 1 followed by monthly doses of 100 mg imsidolimab by subcutaneous injection on Days 29, 57, and 85. |
| Title | Milestones | Reasons Not Completed | |||||
|---|---|---|---|---|---|---|---|
| Overall Study |
|
Not provided
Not provided
| Type | Includes Protocol | Includes SAP | Includes ICF | Document Label | Document Date | Document Uploaded Date | Document File Name |
|---|---|---|---|---|---|---|---|
| Prot | Yes | No | No | Study Protocol | Oct 29, 2020 | May 4, 2022 |
Not provided
Not provided
Not provided
Not provided
Double-blind
| Placebo | Drug | Administered by subcutaneous injection once a month |
|
| Baseline to Week 16 |
| Percentage of Participants Who Achieved a Clear or Almost Clear Palmoplantar Pustulosis Investigator's Global Assessment (PPPIGA) Score at Week 16 | The Investigator rated the severity of participants' disease on the following 5-point scale:
| Week 16 |
| Phoenix |
| Arizona |
| 85032 |
| United States |
| Investigational Site | Encino | California | 91436 | United States |
| Investigational Site | Santa Monica | California | 90405 | United States |
| Investigational Site | Fort Lauderdale | Florida | 33316 | United States |
| Investigational Site | Miami | Florida | 33155 | United States |
| Investigational Site | Pembroke Pines | Florida | 33028 | United States |
| Investigational Site | Tampa | Florida | 33607 | United States |
| Investigational Site | Indianapolis | Indiana | 46250 | United States |
| Investigational Site | Plainfield | Indiana | 46168 | United States |
| Investigational Site | Overland Park | Kansas | 66215 | United States |
| Investigational Site | Ann Arbor | Michigan | 48109 | United States |
| Investigational Site | St Louis | Missouri | 63110 | United States |
| Investigational Site | St Louis | Missouri | 63117 | United States |
| Investigational Site | Wilmington | North Carolina | 28405 | United States |
| Investigational Site | Columbus | Ohio | 43230 | United States |
| Investigational Site | Norman | Oklahoma | 73071 | United States |
| Investigational Site | Portland | Oregon | 97239 | United States |
| Investigational Site | Dallas | Texas | 75230 | United States |
| Investigational Site | Surrey | British Columbia | Canada |
| Investigational Site | Greater Sudbury | Ontario | Canada |
| Investigational Site | Markham | Ontario | Canada |
| Investigational Site | Drummondville | Quebec | Canada |
| Investigational Site | Montreal | Quebec | Canada |
| Investigational Site | Bad Bentheim | 48455 | Germany |
| Investigational Site | Berlin | 10117 | Germany |
| Investigational Site | Berlin | 10789 | Germany |
| Investigational Site | Bonn | 53127 | Germany |
| Investigational Site | Hamburg | 20253 | Germany |
| Investigational Site | Hamburg | 22391 | Germany |
| Investigational Site | Schwerin | 19055 | Germany |
| Investigational Site | Gdansk | 80-546 | Poland |
| Investigational Site | Katowice | 40-611 | Poland |
| Investigational Site | Lodz | 90-265 | Poland |
| Investigational Site | Olsztyn | 10-229 | Poland |
| Investigational Site | Ostrowiec Świętokrzyski | 27-400 | Poland |
| Investigational Site | Rzeszów | 35-055 | Poland |
| Investigational Site | Szczecin | 70-332 | Poland |
| Investigational Site | Wroclaw | 50-566 | Poland |
| COMPLETED |
|
| NOT COMPLETED |
|
|
Intent-to-treat analysis set (all randomized participants)
Not provided
| ID | Title | Description |
|---|---|---|
| BG000 | Placebo | Participants received placebo administered by subcutaneous injection on Day 1 followed by monthly doses on Days 29, 57, and 85. |
| BG001 | Imsidolimab | Participants received 200 mg imsidolimab by subcutaneous injection on Day 1 followed by monthly doses of 100 mg imsidolimab by subcutaneous injection on Days 29, 57, and 85. |
| BG002 | Total | Total of all reporting groups |
| Units | Counts |
|---|---|
| Participants |
|
| Title | Description | Population Description | Parameter Type | Dispersion Type | Unit of Measure | Calculate Percentage | Denominator Units Selected | Denominators | Classes | ||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Age, Continuous | Mean | Standard Deviation | years |
| |||||||||||||||
| Sex: Female, Male | Count of Participants | Participants |
| ||||||||||||||||
| Ethnicity (NIH/OMB) | Count of Participants | Participants |
| ||||||||||||||||
| Race (NIH/OMB) | Count of Participants | Participants |
| ||||||||||||||||
| Palmoplantar Pustulosis Psoriasis Area Severity Index Score | The Palmoplantar Pustulosis Area and Severity Index (PPPASI) is used to assess the severity of palmoplantar pustulosis lesions. The glabrous skin of both palms and both soles are assessed for erythema, pustules and desquamation (scaling), each on a scale from 0 (none) to 4 (very severe). The area affected of each palm and sole is scored from 0 (0%) to 6 (90-100%). The PPPASI total score ranges from 0 to 72. A higher score indicates more severe disease. | Mean | Standard Deviation | score on a scale |
| ||||||||||||||
| History of Plaque Psoriasis | Count of Participants | Participants |
|
| 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 From Baseline in Palmoplantar Pustulosis Psoriasis Area Severity Index (PPPASI) | The Palmoplantar Pustulosis Area and Severity Index (PPPASI) is used to assess the severity of palmoplantar pustulosis lesions and their response to therapy. The glabrous skin of both palms and both soles are assessed for erythema, pustules, and desquamation (scaling), each on a scale from 0 (none) to 4 (very severe). The area affected of each palm and sole is scored from 0 (0%) to 6 (90-100%). Scores for the 3 characteristics of PPP are summed and adjusted for the area affected, and the scores for each palm and sole are added to calculate the total score. The PPPASI total score ranges from 0 to 72. A higher score indicates more severe disease, and a negative change from Baseline indicates improvement. | Intent-to-treat analysis set with available data | Posted | Least Squares Mean | Standard Error | score on a scale | Baseline to Week 16 |
|
|
|
| ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Primary | Number of Participants With Treatment-emergent Adverse Events (TEAEs) | Clinical safety was evaluated by reporting incidence of adverse events up to week 24. TEAEs are defined as new events that occured during or after first dose of study drug or any event that worsens after first dose of study drug. A serious AE (SAE) is defined as any untoward medical occurrence that resulted in death, was life-threatening, resulted in persistent disability/incapacity, was a congenital anomaly/birth defect, or an important medical event that may jeopardize the participant or require medical or surgical intervention to prevent one of the outcomes listed above. Severity was assessed by the Investigator as mild (easily tolerated, causing minimal discomfort and not interfering with everyday activities), moderate (causes sufficient discomfort and interferes with normal everyday activities) or severe (prevents normal everyday activities). The Investigator assessed the relationship between study treatment and each AE based on clinical judgement. | Safety Analysis Set (all randomized participants who received at least 1 dose of imsidolimab or placebo). | Posted | Count of Participants | Participants | From first dose of any study drug to Week 24 |
| ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Secondary | Percentage of Participants Who Achieved 50% Reduction (Improvement) From Baseline in Palmoplantar Pustulosis Psoriasis Area Severity Index Score (PPPASI 50) | The Palmoplantar Pustulosis Area and Severity Index (PPPASI) is used to assess the severity of palmoplantar pustulosis lesions and their response to therapy. The glabrous skin of both palms and both soles are assessed for erythema, pustules, and desquamation (scaling), each on a scale from 0 (none) to 4 (very severe). The area affected of each palm and sole is scored from 0 (0%) to 6 (90-100%). Scores for the 3 characteristics of PPP are summed and adjusted for the area affected, and the scores for each palm and sole are added to calculate the total score. The PPPASI total score ranges from 0 to 72. A higher score indicates more severe disease. | Intent-to-treat analysis set with available data | Posted | Number | 95% Confidence Interval | percentage of participants | Baseline to Week 16 |
| |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Secondary | Percentage of Participants Who Achieved a Clear or Almost Clear Palmoplantar Pustulosis Investigator's Global Assessment (PPPIGA) Score at Week 16 | The Investigator rated the severity of participants' disease on the following 5-point scale:
| Intent-to-treat analysis set with available data | Posted | Number | 95% Confidence Interval | percentage of participants | Week 16 |
|
From first dose of any study drug to Week 24
Not provided
Not provided
| ID | Title | Description | Deaths (Affected) | Deaths (At Risk) | Serious Events (Affected) | Serious Events (At Risk) | Other Events (Affected) | Other Events (At Risk) |
|---|---|---|---|---|---|---|---|---|
| EG000 | Placebo | Participants received placebo administered by subcutaneous injection on Day 1 followed by monthly doses on Days 29, 57, and 85. | 0 | 29 | 1 | 29 | 20 | 29 |
| EG001 | Imsidolimab | Participants received 200 mg imsidolimab by subcutaneous injection on Day 1 followed by monthly doses of 100 mg imsidolimab by subcutaneous injection on Days 29, 57, and 85. | 0 | 30 | 0 | 30 | 21 | 30 |
| Term | Organ System | Source Vocabulary | Assessment Type | Notes | Statistical Information |
|---|---|---|---|---|---|
| Abortion early | Pregnancy, puerperium and perinatal conditions | MedDRA (23.1) | Systematic Assessment |
|
| Term | Organ System | Source Vocabulary | Assessment Type | Notes | Statistical Information |
|---|---|---|---|---|---|
| Nasopharyngitis | Infections and infestations | MedDRA (23.1) | Systematic Assessment |
| |
| Pharyngitis | Infections and infestations | MedDRA (23.1) | Systematic Assessment |
| |
| COVID-19 | Infections and infestations | MedDRA (23.1) | Systematic Assessment |
| |
| Otitis externa | Infections and infestations | MedDRA (23.1) | Systematic Assessment |
| |
| Rhinitis | Infections and infestations | MedDRA (23.1) | Systematic Assessment |
| |
| Tinea pedis | Infections and infestations | MedDRA (23.1) | Systematic Assessment |
| |
| Bacterial pyelonephritis | Infections and infestations | MedDRA (23.1) | Systematic Assessment |
| |
| Bronchitis viral | Infections and infestations | MedDRA (23.1) | Systematic Assessment |
| |
| Conjunctivitis | Infections and infestations | MedDRA (23.1) | Systematic Assessment |
| |
| Folliculitis | Infections and infestations | MedDRA (23.1) | Systematic Assessment |
| |
| Gastrointestinal infection | Infections and infestations | MedDRA (23.1) | Systematic Assessment |
| |
| Impetigo | Infections and infestations | MedDRA (23.1) | Systematic Assessment |
| |
| Urinary tract infection | Infections and infestations | MedDRA (23.1) | Systematic Assessment |
| |
| Back pain | Musculoskeletal and connective tissue disorders | MedDRA (23.1) | Systematic Assessment |
| |
| Myalgia | Musculoskeletal and connective tissue disorders | MedDRA (23.1) | Systematic Assessment |
| |
| Neck pain | Musculoskeletal and connective tissue disorders | MedDRA (23.1) | Systematic Assessment |
| |
| Osteoarthritis | Musculoskeletal and connective tissue disorders | MedDRA (23.1) | Systematic Assessment |
| |
| Pain in extremity | Musculoskeletal and connective tissue disorders | MedDRA (23.1) | Systematic Assessment |
| |
| Arthralgia | Musculoskeletal and connective tissue disorders | MedDRA (23.1) | Systematic Assessment |
| |
| Spinal pain | Musculoskeletal and connective tissue disorders | MedDRA (23.1) | Systematic Assessment |
| |
| Nausea | Gastrointestinal disorders | MedDRA (23.1) | Systematic Assessment |
| |
| Dental caries | Gastrointestinal disorders | MedDRA (23.1) | Systematic Assessment |
| |
| Vomiting | Gastrointestinal disorders | MedDRA (23.1) | Systematic Assessment |
| |
| Duodenogastric reflux | Gastrointestinal disorders | MedDRA (23.1) | Systematic Assessment |
| |
| Toothache | Gastrointestinal disorders | MedDRA (23.1) | Systematic Assessment |
| |
| Alanine aminotransferase increased | Investigations | MedDRA (23.1) | Systematic Assessment |
| |
| Aspartate aminotransferase increased | Investigations | MedDRA (23.1) | Systematic Assessment |
| |
| Blood alkaline phosphatase increased | Investigations | MedDRA (23.1) | Systematic Assessment |
| |
| Blood creatine phosphokinase increased | Investigations | MedDRA (23.1) | Systematic Assessment |
| |
| Blood pressure increased | Investigations | MedDRA (23.1) | Systematic Assessment |
| |
| Gamma-glutamyltransferase increased | Investigations | MedDRA (23.1) | Systematic Assessment |
| |
| Blood triglycerides increased | Investigations | MedDRA (23.1) | Systematic Assessment |
| |
| Headache | Nervous system disorders | MedDRA (23.1) | Systematic Assessment |
| |
| Nerve compression | Nervous system disorders | MedDRA (23.1) | Systematic Assessment |
| |
| Anosmia | Nervous system disorders | MedDRA (23.1) | Systematic Assessment |
| |
| Intercostal neuralgia | Nervous system disorders | MedDRA (23.1) | Systematic Assessment |
| |
| Neuralgia | Nervous system disorders | MedDRA (23.1) | Systematic Assessment |
| |
| Sciatica | Nervous system disorders | MedDRA (23.1) | Systematic Assessment |
| |
| Anxiety | Psychiatric disorders | MedDRA (23.1) | Systematic Assessment |
| |
| Panic attack | Psychiatric disorders | MedDRA (23.1) | Systematic Assessment |
| |
| Acne | Skin and subcutaneous tissue disorders | MedDRA (23.1) | Systematic Assessment |
| |
| Diffuse alopecia | Skin and subcutaneous tissue disorders | MedDRA (23.1) | Systematic Assessment |
| |
| Palmoplantar pustulosis | Skin and subcutaneous tissue disorders | MedDRA (23.1) | Systematic Assessment |
| |
| Skin lesion | Skin and subcutaneous tissue disorders | MedDRA (23.1) | Systematic Assessment |
| |
| Eczema asteatotic | Skin and subcutaneous tissue disorders | MedDRA (23.1) | Systematic Assessment |
| |
| Pustular psoriasis | Skin and subcutaneous tissue disorders | MedDRA (23.1) | Systematic Assessment |
| |
| Pyrexia | General disorders | MedDRA (23.1) | Systematic Assessment |
| |
| Fatigue | General disorders | MedDRA (23.1) | Systematic Assessment |
| |
| Peripheral swelling | General disorders | MedDRA (23.1) | Systematic Assessment |
| |
| Seasonal allergy | Immune system disorders | MedDRA (23.1) | Systematic Assessment |
| |
| Cough | Respiratory, thoracic and mediastinal disorders | MedDRA (23.1) | Systematic Assessment |
| |
| Oropharyngeal pain | Respiratory, thoracic and mediastinal disorders | MedDRA (23.1) | Systematic Assessment |
| |
| Ear discomfort | Ear and labyrinth disorders | MedDRA (23.1) | Systematic Assessment |
| |
| Vertigo | Ear and labyrinth disorders | MedDRA (23.1) | Systematic Assessment |
| |
| Hypertension | Vascular disorders | MedDRA (23.1) | Systematic Assessment |
| |
| Blepharospasm | Eye disorders | MedDRA (23.1) | Systematic Assessment |
| |
| Ligament sprain | Injury, poisoning and procedural complications | MedDRA (23.1) | Systematic Assessment |
| |
| Hypercholesterolaemia | Metabolism and nutrition disorders | MedDRA (23.1) | Systematic Assessment |
| |
| Hyperuricaemia | Metabolism and nutrition disorders | MedDRA (23.1) | Systematic Assessment |
| |
| Nephrolithiasis | Renal and urinary disorders | MedDRA (23.1) | Systematic Assessment |
| |
| Vulvovaginal pruritus | Reproductive system and breast disorders | MedDRA (23.1) | Systematic Assessment |
|
The PI may not publish trial results until after the first multi-center publication unless such publication is not published within a period that is at least 18 months but less than or equal to 24 months after trial completion. In addition, the sponsor can review results communications prior to public release and can embargo communications regarding trial results for a period that is more than 60 days but less than or equal to 180 days from the time submitted to the sponsor for review.
| Title | Organization | Phone | Extension | |
|---|---|---|---|---|
| Vanda Pharmaceuticals | Vanda Pharmaceuticals | 202-734-3400 | clinicaltrials@vandapharma.com |
| Prot_000.pdf |
| SAP | No | Yes | No | Statistical Analysis Plan | Feb 12, 2021 | May 4, 2022 | SAP_001.pdf |
| ID | Term |
|---|---|
| D011565 | Psoriasis |
| ID | Term |
|---|---|
| D017444 | Skin Diseases, Papulosquamous |
| D012871 | Skin Diseases |
| D017437 | Skin and Connective Tissue Diseases |
Not provided
Not provided
| Male |
|
| Not Hispanic or Latino |
|
| Unknown or Not Reported |
|
| Asian |
|
| Native Hawaiian or Other Pacific Islander |
|
| Black or African American |
|
| White |
|
| More than one race |
|
| Unknown or Not Reported |
|
| No |
|
| Other |
|
|
| Units | Counts |
|---|---|
| Participants |
|
|
|
|
|
|