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Trial details imported from ClinicalTrials.gov

For full trial details, please see the original record at https://clinicaltrials.gov/study/NCT04283474




Registration number
NCT04283474
Ethics application status
Date submitted
12/02/2020
Date registered
25/02/2020

Titles & IDs
Public title
Phase 1 XG005-03 Topical Study
Scientific title
A Phase 1, Single-Blind, Placebo-Controlled, Single and Multiple Ascending Dose Study to Assess the Safety, Tolerability, and Pharmacokinetics of XG005-03 (Topical) in Healthy Subjects
Secondary ID [1] 0 0
PR-XG005-03-PK-01
Universal Trial Number (UTN)
Trial acronym
Linked study record

Health condition
Health condition(s) or problem(s) studied:
Pain 0 0
Condition category
Condition code

Intervention/exposure
Study type
Interventional
Description of intervention(s) / exposure
Treatment: Drugs - XG005-03
Treatment: Drugs - Placebo

Experimental: XG005-03 - XG005-03 in 3 dose levels

Placebo comparator: Placebo - Placebo in all cohort


Treatment: Drugs: XG005-03
3 different concentrations (1%, 5%, 10%) of XG005-03 topical formulation

Treatment: Drugs: Placebo
Placebo topical formulation
Intervention code [1] 0 0
Treatment: Drugs
Comparator / control treatment
Control group

Outcomes
Primary outcome [1] 0 0
Pharmacokinetic Analyses
Timepoint [1] 0 0
Day 1 to 4 days after last dose
Primary outcome [2] 0 0
Pharmacokinetic Analyses
Timepoint [2] 0 0
Day 1 to 4 days after last dose
Primary outcome [3] 0 0
Pharmacokinetic Analyses
Timepoint [3] 0 0
Day 1 to 4 days after last dose
Primary outcome [4] 0 0
Pharmacokinetic of XG005-03 in 1%, 5%, and 10% concentrations
Timepoint [4] 0 0
Day 1 to 4 days after last dose
Primary outcome [5] 0 0
Pharmacokinetic Analyses
Timepoint [5] 0 0
Day 1 to 4 days after last dose
Primary outcome [6] 0 0
Pharmacokinetic Analyses
Timepoint [6] 0 0
Day 1 to 4 days after last dose
Secondary outcome [1] 0 0
Safety Analyses
Timepoint [1] 0 0
treatment to follow up period, a average 20 days
Secondary outcome [2] 0 0
Safety Analyses
Timepoint [2] 0 0
treatment to follow up period, a average 20 days
Secondary outcome [3] 0 0
Safety Analyses
Timepoint [3] 0 0
treatment to follow up period, a average 20 days
Secondary outcome [4] 0 0
Safety Analyses
Timepoint [4] 0 0
treatment to follow up period, a average 20 days
Secondary outcome [5] 0 0
Safety Analyses
Timepoint [5] 0 0
treatment to follow up period, a average 20 days
Secondary outcome [6] 0 0
Safety Analyses
Timepoint [6] 0 0
treatment to follow up period, a average 20 days
Secondary outcome [7] 0 0
Safety Analyses
Timepoint [7] 0 0
treatment to follow up period, a average 20 days
Secondary outcome [8] 0 0
Safety Analyses
Timepoint [8] 0 0
treatment to follow up period, a average 20 days
Secondary outcome [9] 0 0
Safety Analyses
Timepoint [9] 0 0
treatment to follow up period, a average 20 days
Secondary outcome [10] 0 0
Safety Analyses
Timepoint [10] 0 0
treatment to follow up period, a average 20 days
Secondary outcome [11] 0 0
Safety Analyses
Timepoint [11] 0 0
treatment to follow up period, a average 20 days
Secondary outcome [12] 0 0
Safety Analyses
Timepoint [12] 0 0
treatment to follow up period, a average 20 days

Eligibility
Key inclusion criteria
1. Healthy males or females between 18 and 55 years of age
2. BMI 18.0 to 30.0 kg/m2
3. Non-pregnant, non-breastfeeding female subjects
Minimum age
18 Years
Maximum age
55 Years
Sex
Both males and females
Can healthy volunteers participate?
Yes
Key exclusion criteria
1. Unstable or severe illness
2. Skin infection or lesion
3. Subjects with scars, moles, tattoos at application site
4. Expose to excessive UV
5. Hypersensitivity or allergy to NSAID

Study design
Purpose of the study
Other
Allocation to intervention
Randomised controlled trial
Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
Methods used to generate the sequence in which subjects will be randomised (sequence generation)
Masking / blinding
Blinded (masking used)
Who is / are masked / blinded?
The people receiving the treatment/s


Intervention assignment
Other
Other design features
Phase
Phase 1
Type of endpoint/s
Statistical methods / analysis

Recruitment
Recruitment status
Completed
Data analysis
Reason for early stopping/withdrawal
Other reasons
Date of first participant enrolment
Anticipated
Actual
28/02/2020
Date of last participant enrolment
Anticipated
Actual
Date of last data collection
Anticipated
Actual
28/01/2021
Sample size
Target
Accrual to date
Final
36
Recruitment in Australia
Recruitment state(s)
SA
Recruitment hospital [1] 0 0
CMAX Clinical Research Pty Ltd - Adelaide
Recruitment postcode(s) [1] 0 0
5000 - Adelaide

Funding & Sponsors
Primary sponsor type
Commercial sector/industry
Name
Xgene Pharmaceutical Group
Address
Country

Ethics approval
Ethics application status

Summary
Brief summary
Trial website
Trial related presentations / publications
Public notes

Contacts
Principal investigator
Name 0 0
Feng Xu, PHD
Address 0 0
Xgene Pharmaceutical Group
Country 0 0
Phone 0 0
Fax 0 0
Email 0 0
Contact person for public queries
Name 0 0
Address 0 0
Country 0 0
Phone 0 0
Fax 0 0
Email 0 0
Contact person for scientific queries

Data sharing statement
Will individual participant data (IPD) for this trial be available (including data dictionaries)?
No
No/undecided IPD sharing reason/comment


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/NCT04283474