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Trial details imported from ClinicalTrials.gov
For full trial details, please see the original record at
https://clinicaltrials.gov/study/NCT05352893
Registration number
NCT05352893
Ethics application status
Date submitted
25/04/2022
Date registered
29/04/2022
Titles & IDs
Public title
Study to Evaluate the Efficacy and Safety of Imsidolimab (ANB019) in the Treatment of Subjects With GPP
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Scientific title
A Phase 3, Randomized, Double-Blind, Placebo-Controlled Study to Evaluate the Efficacy and Safety of Imsidolimab (ANB019) in the Treatment of Adult Subjects With Generalized Pustular Psoriasis
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Secondary ID [1]
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ANB019-301
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Universal Trial Number (UTN)
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Trial acronym
GEMINI1
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Linked study record
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Health condition
Health condition(s) or problem(s) studied:
Generalized Pustular Psoriasis
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Condition category
Condition code
Skin
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0
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Dermatological conditions
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Skin
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0
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0
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Other skin conditions
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
Treatment: Drugs - Imsidolimab high dose
Treatment: Drugs - Imsidolimab low dose
Other interventions - Placebo
Experimental: IV high dose Imsidolimab, other name ANB019 - ANB019 Biological Humanized Monoclonal Antibody High Dose
Experimental: IV low dose Imsidolimab, other name ANB019 - ANB019 Biological Humanized Monoclonal Antibody Low Dose
Placebo comparator: IV Placebo - Placebo Solution
Treatment: Drugs: Imsidolimab high dose
intravenous
Treatment: Drugs: Imsidolimab low dose
intravenous
Other interventions: Placebo
intravenous
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Intervention code [1]
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Treatment: Drugs
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Intervention code [2]
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Other interventions
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Comparator / control treatment
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Control group
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Outcomes
Primary outcome [1]
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Proportion of subjects achieving Generalized Pustular Psoriasis Physician's Global Assessment (GPPPGA) score of 0 (clear) or 1 (almost clear)
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Assessment method [1]
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Baseline to 0 (clear) or 1 (almost clear)
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Timepoint [1]
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week 4
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Eligibility
Key inclusion criteria
-Subject has a BSA affected with pustules (excluding palms and soles) = 5%, a GPPPGA score = 3 (moderate severity), and a PRS score = 3 (moderate severity) at Day 1
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Minimum age
18
Years
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Maximum age
80
Years
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Sex
Both males and females
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Can healthy volunteers participate?
No
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Key exclusion criteria
* Subject has other form of psoriasis excluding psoriasis vulgaris
* Subject flare is so severe that patient's life is at risk
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Study design
Purpose of the study
Treatment
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Allocation to intervention
Randomised controlled trial
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Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
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Masking / blinding
Blinded (masking used)
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Who is / are masked / blinded?
The people receiving the treatment/s
The people administering the treatment/s
The people assessing the outcomes
The people analysing the results/data
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Intervention assignment
Parallel
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Other design features
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Phase
Phase 3
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Type of endpoint/s
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Statistical methods / analysis
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Recruitment
Recruitment status
Completed
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Data analysis
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Reason for early stopping/withdrawal
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Other reasons
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Date of first participant enrolment
Anticipated
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Actual
14/04/2022
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Date of last participant enrolment
Anticipated
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Actual
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Date of last data collection
Anticipated
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Actual
17/08/2023
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Sample size
Target
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Accrual to date
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Final
45
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Recruitment in Australia
Recruitment state(s)
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Recruitment hospital [1]
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Site 35-101 - Melbourne
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Recruitment hospital [2]
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Site 35102 - Sydney
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Recruitment postcode(s) [1]
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- Melbourne
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Recruitment postcode(s) [2]
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- Sydney
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Recruitment outside Australia
Country [1]
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United States of America
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State/province [1]
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Florida
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Country [2]
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United States of America
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State/province [2]
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Kentucky
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Country [3]
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United States of America
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State/province [3]
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Michigan
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United States of America
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Texas
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Country [5]
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United States of America
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Utah
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Country [6]
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Georgia
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State/province [6]
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Batumi
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Country [7]
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Georgia
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State/province [7]
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Tbilisi
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Country [8]
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Germany
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State/province [8]
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Bensheim
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Country [9]
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Germany
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State/province [9]
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Bonn
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Country [10]
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Germany
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State/province [10]
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Hanau
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Germany
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State/province [11]
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Würzburg
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Country [12]
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Korea, Republic of
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State/province [12]
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Pusan
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Korea, Republic of
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State/province [13]
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Seoul
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Country [14]
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Malaysia
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State/province [14]
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Cheras
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Malaysia
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State/province [15]
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Johor Bahru
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Malaysia
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Kota Bharu
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Country [17]
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Malaysia
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State/province [17]
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Kuala Lumpur
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Malaysia
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Muar
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Malaysia
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Putrajaya
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Morocco
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Casablanca
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Morocco
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Oujda
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Poland
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Kraków
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Ossy
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Poland
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Rzeszów
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Poland
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Wroclaw
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Poland
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Lódz
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Romania
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State/province [27]
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Bucuresti
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Romania
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Cluj-Napoca
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Romania
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Iasi
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Slovakia
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Svidník
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Spain
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Barcelona
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Spain
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Las Palmas De Gran Canaria
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Spain
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Madrid
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Spain
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Valencia
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Taiwan
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Kaohsiung
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Taiwan
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Taipei
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Bangkok
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Thailand
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Chiang Mai
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Thailand
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Khon Kaen
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Thailand
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State/province [40]
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Pathum Thani
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Country [41]
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Tunisia
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Sfax
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Tunisia
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State/province [42]
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Sousse
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Tunisia
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Tunis
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Turkey
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Ankara
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Turkey
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Antalya
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Turkey
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Istanbul
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Turkey
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State/province [47]
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Nilufer
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Funding & Sponsors
Primary sponsor type
Commercial sector/industry
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Name
AnaptysBio, Inc.
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Address
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Country
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Ethics approval
Ethics application status
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Summary
Brief summary
This is a Phase 3, multicenter, randomized, double-blind, placebo-controlled study to evaluate the efficacy and safety of imsidolimab compared with placebo in adult subjects with generalized pustular psoriasis (GPP).
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Trial website
https://clinicaltrials.gov/study/NCT05352893
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Trial related presentations / publications
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Public notes
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Contacts
Principal investigator
Name
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Bruce Randazzo, MD
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Address
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AnaptysBio, Inc.
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Country
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Phone
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Fax
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Email
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Contact person for public queries
Name
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Address
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Phone
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Fax
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Email
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Contact person for scientific queries
Data sharing statement
Will individual participant data (IPD) for this trial be available (including data dictionaries)?
No
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No/undecided IPD sharing reason/comment
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What supporting documents are/will be available?
No Supporting Document Provided
Results publications and other study-related documents
No documents have been uploaded by study researchers.
Results not provided in
https://clinicaltrials.gov/study/NCT05352893