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Trial details imported from ClinicalTrials.gov

For full trial details, please see the original record at https://clinicaltrials.gov/study/NCT02397005




Registration number
NCT02397005
Ethics application status
Date submitted
27/02/2015
Date registered
24/03/2015
Date last updated
24/01/2019

Titles & IDs
Public title
Study of the Tolerability and Pharmacokinetic of ZL-2102 With an Investigation of Food Effect in Healthy Male Subjects
Scientific title
Randomized, Double-blind, Placebo-controlled Study of the Tolerability and Pharmacokinetics of Ascending Single and 14-day Repeated Oral Doses of ZL-2102 With a Pilot Investigation of Food Effect in Healthy Male Subjects
Secondary ID [1] 0 0
ZL-2102-SAD/FED/MAD
Universal Trial Number (UTN)
Trial acronym
Linked study record

Health condition
Health condition(s) or problem(s) studied:
Chronic Obstructive Pulmonary Disease 0 0
Asthma 0 0
Idiopathic Pulmonary Fibrosis 0 0
Condition category
Condition code
Respiratory 0 0 0 0
Chronic obstructive pulmonary disease
Respiratory 0 0 0 0
Other respiratory disorders / diseases

Intervention/exposure
Study type
Interventional
Description of intervention(s) / exposure
Treatment: Drugs - ZL-2102

Active comparator: ZL-2102 - Planned to be administrated in an ascending manner: 5,20,60,150,300,500,750mg

Placebo comparator: Placebo - Placebo matching ZL-2102


Treatment: Drugs: ZL-2102
A selective and reversible inhibitor of Hematopoietic Prostaglandin D Synthase (HPGDS).
Intervention code [1] 0 0
Treatment: Drugs
Comparator / control treatment
Control group

Outcomes
Primary outcome [1] 0 0
Part1,ZL-2102-SAD: Safety as measured by Adverse Events
Timepoint [1] 0 0
8 days
Primary outcome [2] 0 0
Part2,ZL-2102-FED: Safety as measured by Adverse Events
Timepoint [2] 0 0
15 days
Primary outcome [3] 0 0
Part3,ZL-2102-MAD: Safety as measured by Adverse Events
Timepoint [3] 0 0
21 days
Primary outcome [4] 0 0
Peak Plasma Concentration (Cmax) of ZL-2102
Timepoint [4] 0 0
48 hours
Primary outcome [5] 0 0
Area under the plasma concentration versus time curve (AUC) of ZL-2102
Timepoint [5] 0 0
48 hours
Secondary outcome [1] 0 0
Part1,ZL-2102-SAD: Safety as measured by Physical examination, body weight, hematology, biochemistry, urinalysis, vital signs and 12-lead ECG.
Timepoint [1] 0 0
8 days
Secondary outcome [2] 0 0
Part2,ZL-2102-FED: Safety as measured by Physical examination, body weight, hematology, biochemistry, urinalysis, vital signs and 12-lead ECG.
Timepoint [2] 0 0
15 days
Secondary outcome [3] 0 0
Part3,ZL-2102-MAD: Safety as measured by Physical examination, body weight, hematology, biochemistry, urinalysis, vital signs and 12-lead ECG.
Timepoint [3] 0 0
21 days

Eligibility
Key inclusion criteria
* Male subject, between 18 and 45 years of age inclusive.
* Body weight between 50.0 and 100.0 kg inclusive, body mass index (BMI) between 18.0 and 30.0 kg/m² inclusive.
* Certified as healthy by a comprehensive clinical assessment (detailed medical history and complete physical examination).
* Normal vital signs after 5 minutes resting in a semi recumbent position.
* Normal standard 12-lead ECG after 5 minutes resting in a semi recumbent position.
* Laboratory parameters within the normal range, or considered not clinically significant by the Investigator.
* Subject returns a negative result to the Serology,Urine drug screen and alcohol breath tests.
* Having given written informed consent prior to any procedure related to the study.
* Not under any administrative or legal supervision.
* Males must agree to use adequate contraception for the duration of the study and for 3 months post completion of dosing.
* Subject agrees to the following study restrictions:

1. Subject will not consume citrus fruits and their juices for 5 days before the start of the study, and for the duration of the study.
2. Subject will not consume alcohol, tea, coffee, chocolate, quinine or caffeine-containing beverages from Day 1 and for the duration of the study.
3. Subject will note smoke or use tobacco from Day 1 and for the duration of the study.
4. Subject will avoid intensive physical activity from Day 1 and for the duration of the study.
Minimum age
18 Years
Maximum age
45 Years
Sex
Males
Can healthy volunteers participate?
Yes
Key exclusion criteria
* Any history or presence of clinically relevant cardiovascular, pulmonary, gastrointestinal, hepatic, renal, metabolic, hematological, neurological, osteo-muscular, articular, psychiatric, systemic, ocular, or infectious disease, or signs of acute illness.
* Frequent headaches and/or migraine, recurrent nausea and/or vomiting (more than twice a month).
* Blood donation, any volume, within 2 months prior to Screening.
* Symptomatic postural hypotension, whatever the decrease in blood pressure, or asymptomatic postural hypotension defined by a decrease in systolic blood pressure = 20 mmHg within 3 minutes when changing from the supine to the standing position.
* Presence or history of drug hypersensitivity, or allergic disease (excluding hay fever) diagnosed and treated by a physician.
* History or presence of drug or alcohol abuse (alcohol consumption >40 grams per day).
* Smoking more than 5 cigarettes or equivalent per day, unable to stop smoking during the study.
* Excessive consumption of beverages with xanthine bases (>4 cups or glasses per day).
* Any prescription medication within 14 days and any over the counter medication within 7 days before Screening or within 5 times the elimination half-life or Pharmacodynamic half-life of that drug whichever is longest unless approved by both the Investigator and the Medical Monitor; any vaccination within the last 28 days. If necessary, paracetamol (acetaminophen) may be administered with the approval of the Investigator.
* Any subject who, in the judgment of the Investigator, is likely to be non-compliant during the study, or unable to cooperate because of a language problem or poor mental development.
* Receipt of any investigational study drug within 30 days prior to screening.
* Any subject who is the Investigator or any sub-investigator, research assistant, pharmacist, study coordinator, or other staff thereof, directly involved in the conduct of the protocol.

Study design
Purpose of the study
Treatment
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


The people analysing the results/data
Intervention assignment
Parallel
Other design features
Phase
Phase 1
Type of endpoint/s
Statistical methods / analysis

Recruitment
Recruitment status
UNKNOWN
Data analysis
Reason for early stopping/withdrawal
Other reasons
Date of first participant enrolment
Anticipated
Actual
1/03/2015
Date of last participant enrolment
Anticipated
Actual
Date of last data collection
Anticipated
1/08/2019
Actual
Sample size
Target
Accrual to date
Final
120
Recruitment in Australia
Recruitment state(s)
Recruitment hospital [1] 0 0
Linear Clinical Research Unit - Perth
Recruitment postcode(s) [1] 0 0
- Perth

Funding & Sponsors
Primary sponsor type
Commercial sector/industry
Name
Zai Lab Pty. Ltd.
Address
Country

Ethics approval
Ethics application status

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

Contacts
Principal investigator
Name 0 0
Address 0 0
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

No information has been provided regarding IPD availability


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/NCT02397005