Please note that the copy function is not enabled for this field.
If you wish to
modify
existing outcomes, please copy and paste the current outcome text into the Update field.
LOGIN
CREATE ACCOUNT
LOGIN
CREATE ACCOUNT
MY TRIALS
REGISTER TRIAL
FAQs
HINTS AND TIPS
DEFINITIONS
Trial Review
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been endorsed by the ANZCTR. Before participating in a study, talk to your health care provider and refer to this
information for consumers
Download to PDF
Trial details imported from ClinicalTrials.gov
For full trial details, please see the original record at
https://clinicaltrials.gov/ct2/show/NCT05723198
Registration number
NCT05723198
Ethics application status
Date submitted
3/02/2023
Date registered
10/02/2023
Date last updated
28/05/2024
Titles & IDs
Public title
A Study of Baricitinib (LY3009104) in Children From 6 Years to Less Than 18 Years of Age With Alopecia Areata
Query!
Scientific title
A Phase 3, Double-Blind, Randomized, Placebo-Controlled Trial to Evaluate the Efficacy, Safety, and Pharmacokinetics (PK) of Baricitinib in Children From 6 Years to Less Than 18 Years of Age With Alopecia Areata
Query!
Secondary ID [1]
0
0
I4V-MC-JAIO
Query!
Secondary ID [2]
0
0
16875
Query!
Universal Trial Number (UTN)
Query!
Trial acronym
BRAVE-AA-PEDS
Query!
Linked study record
Query!
Health condition
Health condition(s) or problem(s) studied:
Areata Alopecia
0
0
Query!
Alopecia
0
0
Query!
Hypotrichosis
0
0
Query!
Hair Diseases
0
0
Query!
Skin Diseases
0
0
Query!
Pathological Conditions, Anatomical
0
0
Query!
Condition category
Condition code
Inflammatory and Immune System
0
0
0
0
Query!
Autoimmune diseases
Query!
Skin
0
0
0
0
Query!
Other skin conditions
Query!
Skin
0
0
0
0
Query!
Dermatological conditions
Query!
Public Health
0
0
0
0
Query!
Epidemiology
Query!
Intervention/exposure
Study type
Interventional
Query!
Description of intervention(s) / exposure
Treatment: Drugs - Baricitinib
Treatment: Drugs - Placebo
Experimental: Baricitinib High Dose - Participants will receive baricitinib high dose orally.
Experimental: Baricitinib Low Dose - Participants will receive baricitinib low dose orally.
Placebo Comparator: Placebo - Participants will receive placebo
Treatment: Drugs: Baricitinib
Administered orally
Treatment: Drugs: Placebo
Administered orally
Query!
Intervention code [1]
0
0
Treatment: Drugs
Query!
Comparator / control treatment
Query!
Control group
Query!
Outcomes
Primary outcome [1]
0
0
Percentage of Participants Achieving an Absolute Severity of Alopecia Tool (SALT) =20
Query!
Assessment method [1]
0
0
Query!
Timepoint [1]
0
0
Week 36
Query!
Secondary outcome [1]
0
0
Percent Change from Baseline in SALT Score
Query!
Assessment method [1]
0
0
Query!
Timepoint [1]
0
0
Baseline, Week 36
Query!
Secondary outcome [2]
0
0
Percentage of Participants Achieving At Least 90% Improvement from Baseline (SALT90)
Query!
Assessment method [2]
0
0
Query!
Timepoint [2]
0
0
Week 36
Query!
Secondary outcome [3]
0
0
Percentage of Participants Achieving an Absolute SALT =10
Query!
Assessment method [3]
0
0
Query!
Timepoint [3]
0
0
Week 36
Query!
Secondary outcome [4]
0
0
Percentage of Participants with Patient Reported Outcome (PRO) for Scalp Hair Assessment Score of 0 or 1 Among Participants 12 Years and Older with PRO for Scalp Hair Assessment Score =3 at Baseline
Query!
Assessment method [4]
0
0
Query!
Timepoint [4]
0
0
Week 36
Query!
Secondary outcome [5]
0
0
Mean Change from Baseline in SALT Score
Query!
Assessment method [5]
0
0
Query!
Timepoint [5]
0
0
Baseline, Week 36
Query!
Secondary outcome [6]
0
0
Percentage of Participants Achieving At Least 50% Improvement from Baseline (SALT50)
Query!
Assessment method [6]
0
0
Query!
Timepoint [6]
0
0
Week 36
Query!
Secondary outcome [7]
0
0
Percentage of Participants Achieving At Least 75% Improvement from Baseline (SALT75)
Query!
Assessment method [7]
0
0
Query!
Timepoint [7]
0
0
Week 36
Query!
Secondary outcome [8]
0
0
Percentage of Participants Achieving At Least 100% Improvement from Baseline (SALT100)
Query!
Assessment method [8]
0
0
Query!
Timepoint [8]
0
0
Week 36
Query!
Secondary outcome [9]
0
0
Percentage of Participants Achieving Clinician-Reported Outcome (ClinRO) Measure for Eyebrow (EB) Hair Loss 0 or 1 Among Participants with CLinRO Measure for EB Hair Loss =2 at Baseline
Query!
Assessment method [9]
0
0
Query!
Timepoint [9]
0
0
Week 36
Query!
Secondary outcome [10]
0
0
Percentage of Participants Achieving ClinRO Measure for Eyelash (EL) Hair Loss 0 or 1 Among Participants with CLinRO Measure for EL Hair Loss =2 at Baseline
Query!
Assessment method [10]
0
0
Query!
Timepoint [10]
0
0
Week 36
Query!
Secondary outcome [11]
0
0
Percentage of Participants Achieving PRO Measure for EB 0 or 1 (Among Participants 12 Years or Older with PRO Measure for EB =2 at Baseline)
Query!
Assessment method [11]
0
0
Query!
Timepoint [11]
0
0
Week 36
Query!
Secondary outcome [12]
0
0
Percentage of Participants Achieving PRO Measure for EL 0 or 1 (Among Participants 12 Years or Older with PRO Measure for EL =2 at Baseline)
Query!
Assessment method [12]
0
0
Query!
Timepoint [12]
0
0
Week 36
Query!
Secondary outcome [13]
0
0
Mean Change from Baseline in Hospital Anxiety Depression Scale (HADS)
Query!
Assessment method [13]
0
0
The HADS is a participant-rated instrument used to assess both anxiety and depression and is available in a pediatric self-report for participants =12 years old. This instrument consists of 14 item questionnaires, each item is rated on a 4-point scale. Scores for each domain (anxiety and depression) can range from 0 to 21, with higher scores indicating greater anxiety or depression.
Query!
Timepoint [13]
0
0
Week 36
Query!
Secondary outcome [14]
0
0
Mean Change from Baseline in Patient-Reported Outcome Measurement Information System (PROMIS) Anxiety Score
Query!
Assessment method [14]
0
0
The PROMIS Anxiety Short Form (8 questions, 8a v2.0) is available in a pediatric self-report (ages 8 to <18 years) and for parents/caregivers serving as proxy reporters for their children (youth ages =5 years). Both pediatric self-report and proxy-report versions assess anxiety "in the past seven days". Response options range from 1 = Never; 2 = Rarely; 3 = Sometimes; 4 = Often; to 5 = Almost always. Total raw scores are converted to T-Scores with higher scores representing greater anxiety.
Query!
Timepoint [14]
0
0
Baseline, Week 36
Query!
Secondary outcome [15]
0
0
Mean Change from Baseline in PROMIS Depression Score
Query!
Assessment method [15]
0
0
The PROMIS Depression Short Form (8a v2.0 and 6a v2.0) is available in a pediatric self-report (ages 8 to <18 years) and for parents/caregivers serving as proxy reporters for their children (youth ages =5 years). Both pediatric self-report and proxy-report versions assess depression "in the past seven days." Response options range from 1 = Never; 2 = Rarely; 3 = Sometimes; 4 = Often; to 5 = Almost always. Total raw scores are converted to T-Scores with higher scores representing greater depression.
Query!
Timepoint [15]
0
0
Baseline, Week 36
Query!
Secondary outcome [16]
0
0
Mean Change from Baseline in PROMIS Peer Relationship Score
Query!
Assessment method [16]
0
0
The PROMIS Peer Relationships Short Form planned to be used in the study measures 2 aspects of social functioning, friendship quality and peer acceptance, and is available in a pediatric self-report (ages 8 to <18 years) and for parents/caregivers serving as proxy reporters for their children (youth ages 5 to <8 years).
Query!
Timepoint [16]
0
0
Baseline, Week 36
Query!
Secondary outcome [17]
0
0
Mean Change from Baseline in Family Dermatology Life Quality Index (FDLQI)
Query!
Assessment method [17]
0
0
The FDLQI is a 10-item validated questionnaire designed for adult (>16 years old) family members of participants. The questionnaire is completed by family members of the AA participants (for example, parents/caregivers) and measures the secondary impact of the participant's skin disease on family QoL. Response categories include "not at all/not relevant," "only a little," "quite a lot," and "very much," with corresponding scores of 0, 1, 2, and 3, respectively, with unanswered ("not relevant") responses scored as 0.
Query!
Timepoint [17]
0
0
Baseline, Week 36
Query!
Secondary outcome [18]
0
0
Pharmacokinetics (PK): Maximum Concentration (Cmax)
Query!
Assessment method [18]
0
0
Query!
Timepoint [18]
0
0
Baseline through Week 36
Query!
Secondary outcome [19]
0
0
PK: Area Under the Concentration Curve (AUC)
Query!
Assessment method [19]
0
0
Query!
Timepoint [19]
0
0
Baseline through Week 36
Query!
Secondary outcome [20]
0
0
Change of Immunoglobulin G (IgG) Titers
Query!
Assessment method [20]
0
0
Query!
Timepoint [20]
0
0
Pre-Vaccination to 4 Weeks and 12 Weeks Post-Vaccination
Query!
Eligibility
Key inclusion criteria
- Enrollment will be fully sequential by age group, with adolescents (12 to less than 18
years old) enrolling before children (6 to less than 12 years old).
- Have severe areata alopecia (AA) for at least 1 year
- Diagnosis for at least 1 year
- Current AA episode of at least 6 months' duration
- SALT score =50% at screening and baseline
- History of trial and failure with at least 1 available treatment (topical or other)
for AA
- History of psychological counseling related to AA
- Current episode of severe AA of less than 8 years.
- Note: Participants who have severe AA for =8 years may be enrolled if episodes of
regrowth, spontaneous or under treatment, have been observed on the affected
areas over the past 8 years.
Query!
Minimum age
6
Years
Query!
Query!
Maximum age
17
Years
Query!
Query!
Sex
Both males and females
Query!
Can healthy volunteers participate?
No
Query!
Key exclusion criteria
- Primarily "diffuse" type of AA (characterized by diffuse hair shedding).
- Are currently experiencing other forms of alopecia including, but not limited to
trichotillomania, telogen effluvium, chemotherapy-induced hair loss, or any other
concomitant conditions (for example, tinea capitis, psoriasis, lupus erythematosus, or
secondary syphilis) that would interfere with evaluations of the effect of study
medication on AA.
- Are largely or wholly incapacitated permitting little or no self-care, such as being
bedridden
- Have uncontrolled arterial hypertension
- Have had major surgery within 8 weeks prior to screening or will require major surgery
during the study
- Have a history or presence of cardiovascular, respiratory, hepatic, gastrointestinal,
endocrine, hematological, neurological, or neuropsychiatric disorders or any other
serious and/or unstable illness that, in the opinion of the investigator, could
constitute an unacceptable risk when taking IP or interfere with the interpretation of
data.
- Have a positive test for hepatitis B virus (HBV) infection
- Have hepatitis C virus (HCV) infection (positive for anti hepatitis C antibody with
confirmed presence of HCV ribonucleic acid [RNA]).
- Have evidence of human immunodeficiency virus (HIV) infection and/or positive HIV
antibodies.
Query!
Study design
Purpose of the study
Treatment
Query!
Allocation to intervention
Randomised controlled trial
Query!
Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
Query!
Methods used to generate the sequence in which subjects will be randomised (sequence generation)
Query!
Masking / blinding
Blinded (masking used)
Query!
Who is / are masked / blinded?
The people receiving the treatment/s
The people analysing the results/data
Query!
Query!
Query!
Query!
Intervention assignment
Parallel
Query!
Other design features
Query!
Phase
Phase 3
Query!
Type of endpoint/s
Query!
Statistical methods / analysis
Query!
Recruitment
Recruitment status
Recruiting
Query!
Data analysis
Query!
Reason for early stopping/withdrawal
Query!
Other reasons
Query!
Date of first participant enrolment
Anticipated
Query!
Actual
27/02/2023
Query!
Date of last participant enrolment
Anticipated
Query!
Actual
Query!
Date of last data collection
Anticipated
1/08/2029
Query!
Actual
Query!
Sample size
Target
595
Query!
Accrual to date
Query!
Final
Query!
Recruitment in Australia
Recruitment state(s)
NSW,QLD,VIC
Query!
Recruitment hospital [1]
0
0
Skin and Cancer Foundation Australia - Darlinghurst Clinic - Darlinghurst
Query!
Recruitment hospital [2]
0
0
Royal North Shore Hospital - St Leonards
Query!
Recruitment hospital [3]
0
0
Veracity Clinical Research Pty Ltd - Woolloongabba
Query!
Recruitment hospital [4]
0
0
Sinclair Dermatology - Melbourne
Query!
Recruitment hospital [5]
0
0
Institute for Skin, Health, and Immunity - Mitcham
Query!
Recruitment postcode(s) [1]
0
0
02010 - Darlinghurst
Query!
Recruitment postcode(s) [2]
0
0
2065 - St Leonards
Query!
Recruitment postcode(s) [3]
0
0
4102 - Woolloongabba
Query!
Recruitment postcode(s) [4]
0
0
3002 - Melbourne
Query!
Recruitment postcode(s) [5]
0
0
3132 - Mitcham
Query!
Recruitment outside Australia
Country [1]
0
0
United States of America
Query!
State/province [1]
0
0
Alabama
Query!
Country [2]
0
0
United States of America
Query!
State/province [2]
0
0
Arizona
Query!
Country [3]
0
0
United States of America
Query!
State/province [3]
0
0
California
Query!
Country [4]
0
0
United States of America
Query!
State/province [4]
0
0
Connecticut
Query!
Country [5]
0
0
United States of America
Query!
State/province [5]
0
0
Florida
Query!
Country [6]
0
0
United States of America
Query!
State/province [6]
0
0
Georgia
Query!
Country [7]
0
0
United States of America
Query!
State/province [7]
0
0
Illinois
Query!
Country [8]
0
0
United States of America
Query!
State/province [8]
0
0
Indiana
Query!
Country [9]
0
0
United States of America
Query!
State/province [9]
0
0
Maryland
Query!
Country [10]
0
0
United States of America
Query!
State/province [10]
0
0
Michigan
Query!
Country [11]
0
0
United States of America
Query!
State/province [11]
0
0
Minnesota
Query!
Country [12]
0
0
United States of America
Query!
State/province [12]
0
0
Missouri
Query!
Country [13]
0
0
United States of America
Query!
State/province [13]
0
0
Nebraska
Query!
Country [14]
0
0
United States of America
Query!
State/province [14]
0
0
New York
Query!
Country [15]
0
0
United States of America
Query!
State/province [15]
0
0
North Carolina
Query!
Country [16]
0
0
United States of America
Query!
State/province [16]
0
0
Ohio
Query!
Country [17]
0
0
United States of America
Query!
State/province [17]
0
0
Oklahoma
Query!
Country [18]
0
0
United States of America
Query!
State/province [18]
0
0
Oregon
Query!
Country [19]
0
0
United States of America
Query!
State/province [19]
0
0
Pennsylvania
Query!
Country [20]
0
0
United States of America
Query!
State/province [20]
0
0
South Carolina
Query!
Country [21]
0
0
United States of America
Query!
State/province [21]
0
0
Tennessee
Query!
Country [22]
0
0
United States of America
Query!
State/province [22]
0
0
Texas
Query!
Country [23]
0
0
United States of America
Query!
State/province [23]
0
0
Utah
Query!
Country [24]
0
0
United States of America
Query!
State/province [24]
0
0
Virginia
Query!
Country [25]
0
0
United States of America
Query!
State/province [25]
0
0
Wisconsin
Query!
Country [26]
0
0
Argentina
Query!
State/province [26]
0
0
Buenos Aires
Query!
Country [27]
0
0
Argentina
Query!
State/province [27]
0
0
Buenos Air
Query!
Country [28]
0
0
Argentina
Query!
State/province [28]
0
0
Provincia De Tucuman
Query!
Country [29]
0
0
Argentina
Query!
State/province [29]
0
0
Tucumán
Query!
Country [30]
0
0
Canada
Query!
State/province [30]
0
0
Alberta
Query!
Country [31]
0
0
Canada
Query!
State/province [31]
0
0
British Columbia
Query!
Country [32]
0
0
Canada
Query!
State/province [32]
0
0
Manitoba
Query!
Country [33]
0
0
Canada
Query!
State/province [33]
0
0
Ontario
Query!
Country [34]
0
0
France
Query!
State/province [34]
0
0
Brest CEDEX 2
Query!
Country [35]
0
0
France
Query!
State/province [35]
0
0
Marseille
Query!
Country [36]
0
0
France
Query!
State/province [36]
0
0
Nantes
Query!
Country [37]
0
0
France
Query!
State/province [37]
0
0
Nice
Query!
Country [38]
0
0
France
Query!
State/province [38]
0
0
Paris
Query!
Country [39]
0
0
France
Query!
State/province [39]
0
0
Tours Cedex
Query!
Country [40]
0
0
Germany
Query!
State/province [40]
0
0
Bayern
Query!
Country [41]
0
0
Germany
Query!
State/province [41]
0
0
Niedersachsen
Query!
Country [42]
0
0
Germany
Query!
State/province [42]
0
0
Schleswig-Holstein
Query!
Country [43]
0
0
Germany
Query!
State/province [43]
0
0
Berlin
Query!
Country [44]
0
0
Germany
Query!
State/province [44]
0
0
Dresden
Query!
Country [45]
0
0
Germany
Query!
State/province [45]
0
0
Frankfurt am Main
Query!
Country [46]
0
0
Germany
Query!
State/province [46]
0
0
Halle
Query!
Country [47]
0
0
Germany
Query!
State/province [47]
0
0
Hamburg
Query!
Country [48]
0
0
Germany
Query!
State/province [48]
0
0
Mainz
Query!
Country [49]
0
0
Germany
Query!
State/province [49]
0
0
Muenster
Query!
Country [50]
0
0
Hungary
Query!
State/province [50]
0
0
Csongrad
Query!
Country [51]
0
0
Hungary
Query!
State/province [51]
0
0
Hajdu-Bihar
Query!
Country [52]
0
0
Hungary
Query!
State/province [52]
0
0
Budapest
Query!
Country [53]
0
0
Hungary
Query!
State/province [53]
0
0
Pecs
Query!
Country [54]
0
0
Japan
Query!
State/province [54]
0
0
Fukuoka
Query!
Country [55]
0
0
Japan
Query!
State/province [55]
0
0
Miyagi
Query!
Country [56]
0
0
Japan
Query!
State/province [56]
0
0
Shizuoka
Query!
Country [57]
0
0
Japan
Query!
State/province [57]
0
0
Tokyo
Query!
Country [58]
0
0
Japan
Query!
State/province [58]
0
0
Yamaguchi
Query!
Country [59]
0
0
Japan
Query!
State/province [59]
0
0
Niigata
Query!
Country [60]
0
0
Japan
Query!
State/province [60]
0
0
Osaka
Query!
Country [61]
0
0
Korea, Republic of
Query!
State/province [61]
0
0
Chungcheongnam-do [Chungnam]
Query!
Country [62]
0
0
Korea, Republic of
Query!
State/province [62]
0
0
Geonggi-do
Query!
Country [63]
0
0
Korea, Republic of
Query!
State/province [63]
0
0
Gyeonggi-do
Query!
Country [64]
0
0
Korea, Republic of
Query!
State/province [64]
0
0
Incheon-gwangyeoksi [Incheon]
Query!
Country [65]
0
0
Korea, Republic of
Query!
State/province [65]
0
0
Jung-gu
Query!
Country [66]
0
0
Korea, Republic of
Query!
State/province [66]
0
0
Pusan-Kwangyokshi
Query!
Country [67]
0
0
Korea, Republic of
Query!
State/province [67]
0
0
Seoul, Korea
Query!
Country [68]
0
0
Korea, Republic of
Query!
State/province [68]
0
0
Seoul-teukbyeolsi [Seoul]
Query!
Country [69]
0
0
Korea, Republic of
Query!
State/province [69]
0
0
Taegu-Kwangyokshi
Query!
Country [70]
0
0
Korea, Republic of
Query!
State/province [70]
0
0
Jeonju-si
Query!
Country [71]
0
0
Korea, Republic of
Query!
State/province [71]
0
0
Seoul
Query!
Country [72]
0
0
Mexico
Query!
State/province [72]
0
0
Jalisco
Query!
Country [73]
0
0
Mexico
Query!
State/province [73]
0
0
Nuevo León
Query!
Country [74]
0
0
Mexico
Query!
State/province [74]
0
0
Chihuahua
Query!
Country [75]
0
0
Mexico
Query!
State/province [75]
0
0
Mexico City
Query!
Country [76]
0
0
Mexico
Query!
State/province [76]
0
0
Veracruz
Query!
Country [77]
0
0
Poland
Query!
State/province [77]
0
0
Lodzkie
Query!
Country [78]
0
0
Poland
Query!
State/province [78]
0
0
Malopolskie
Query!
Country [79]
0
0
Poland
Query!
State/province [79]
0
0
Masovian
Query!
Country [80]
0
0
Poland
Query!
State/province [80]
0
0
Podkarpackie
Query!
Country [81]
0
0
Poland
Query!
State/province [81]
0
0
Pomorskie
Query!
Country [82]
0
0
Poland
Query!
State/province [82]
0
0
Bialystok
Query!
Country [83]
0
0
Poland
Query!
State/province [83]
0
0
Bydgoszcz
Query!
Country [84]
0
0
Poland
Query!
State/province [84]
0
0
Katowice
Query!
Country [85]
0
0
Poland
Query!
State/province [85]
0
0
Kielce
Query!
Country [86]
0
0
Poland
Query!
State/province [86]
0
0
Ostrowiec Swietokrzyski
Query!
Country [87]
0
0
Poland
Query!
State/province [87]
0
0
Szczecin
Query!
Country [88]
0
0
Poland
Query!
State/province [88]
0
0
Warszawa
Query!
Country [89]
0
0
Poland
Query!
State/province [89]
0
0
Wroclaw
Query!
Country [90]
0
0
Poland
Query!
State/province [90]
0
0
Slaskie
Query!
Country [91]
0
0
Spain
Query!
State/province [91]
0
0
Catalunya [Cataluña]
Query!
Country [92]
0
0
Spain
Query!
State/province [92]
0
0
Alicante
Query!
Country [93]
0
0
Spain
Query!
State/province [93]
0
0
Badalona
Query!
Country [94]
0
0
Spain
Query!
State/province [94]
0
0
Bilbao
Query!
Country [95]
0
0
Spain
Query!
State/province [95]
0
0
Madrid
Query!
Country [96]
0
0
Spain
Query!
State/province [96]
0
0
Pamplona
Query!
Country [97]
0
0
Spain
Query!
State/province [97]
0
0
Pozuelo de Alarcon
Query!
Country [98]
0
0
Spain
Query!
State/province [98]
0
0
Valencia
Query!
Country [99]
0
0
Taiwan
Query!
State/province [99]
0
0
New Taipei
Query!
Country [100]
0
0
Taiwan
Query!
State/province [100]
0
0
Taichung
Query!
Country [101]
0
0
Taiwan
Query!
State/province [101]
0
0
Tainan
Query!
Country [102]
0
0
Taiwan
Query!
State/province [102]
0
0
Taipei
Query!
Country [103]
0
0
Taiwan
Query!
State/province [103]
0
0
Taoyuan
Query!
Funding & Sponsors
Primary sponsor type
Commercial sector/Industry
Query!
Name
Eli Lilly and Company
Query!
Address
Query!
Country
Query!
Ethics approval
Ethics application status
Query!
Summary
Brief summary
The main purpose of this study is to determine the efficacy and safety of baricitinib for the
treatment of severe or very severe alopecia areata (hair loss) in children from 6 years to
less than 18 years of age.
The study is divided into 4 periods, a 5-week Screening period, a 36-week Double-Blind
Treatment Period, an approximately 2-year Long-term Extension Period, and a 4-week
Post-treatment Follow-up period.
Query!
Trial website
https://clinicaltrials.gov/ct2/show/NCT05723198
Query!
Trial related presentations / publications
Query!
Public notes
Query!
Contacts
Principal investigator
Name
0
0
Call 1-877-CTLILLY (1-877-285-4559) or 1-317-615-4559 Mon - Fri 9 AM - 5 PM Eastern time (UTC/GMT - 5 hours, EST)
Query!
Address
0
0
Eli Lilly and Company
Query!
Country
0
0
Query!
Phone
0
0
Query!
Fax
0
0
Query!
Email
0
0
Query!
Contact person for public queries
Name
0
0
There may be multiple sites in this clinical trial. 1-877-CTLILLY (1-877-285-4559) or
Query!
Address
0
0
Query!
Country
0
0
Query!
Phone
0
0
-317-615-4559
Query!
Fax
0
0
Query!
Email
0
0
[email protected]
Query!
Contact person for scientific queries
Summary Results
For IPD and results data, please see
https://clinicaltrials.gov/ct2/show/NCT05723198
Download to PDF