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Trial details imported from ClinicalTrials.gov

For full trial details, please see the original record at https://clinicaltrials.gov/ct2/show/NCT06034015




Registration number
NCT06034015
Ethics application status
Date submitted
29/08/2023
Date registered
13/09/2023
Date last updated
13/09/2023

Titles & IDs
Public title
A Study to Evaluate the Safety, Tolerability and Pharmacokinetics of Single and Multiple Ascending Doses of APL-1501 Extended Release (ER) Capsules Compared to APL-1202 Immediate Release (IR) Tablets in Healthy Volunteers
Scientific title
A Phase 1, Two-Part, Open-Label Study to Evaluate the Safety, Tolerability and Pharmacokinetics (PK) of Single Ascending Doses of APL-1501 Extended Release (ER) Capsules Compared to APL-1202 Immediate Release (IR) Tablets in Healthy Volunteers (Part A) and Multiple Ascending Doses of APL-1501 ER Capsules Compared to APL-1202 IR Tablets in Healthy Volunteers (Part B)
Secondary ID [1] 0 0
YHGT-PN-02
Universal Trial Number (UTN)
Trial acronym
Linked study record

Health condition
Health condition(s) or problem(s) studied:
Bladder Cancer 0 0
Condition category
Condition code
Cancer 0 0 0 0
Bladder - transitional cell cancer

Intervention/exposure
Study type
Interventional
Description of intervention(s) / exposure
Treatment: Drugs - APL-1202 and APL-1501 (Single ascending dose)
Treatment: Drugs - APL-1202 and APL-1501 (Multiple Ascending dose)

Active Comparator: Part A -

Active Comparator: Part B -


Treatment: Drugs: APL-1202 and APL-1501 (Single ascending dose)
Period 1 drug adminstration (APL-1202 IR tablet , single dose of 375mg will be administered orally on Day 1; washout period of 72 hrs; Period 2 drug administration (APL-1501 ER capsules of 764mg, 1146 mg and 1528 mg will be administered as single dose on Day 4.

Treatment: Drugs: APL-1202 and APL-1501 (Multiple Ascending dose)
Period 1 drug adminstration (APL-1202 IR of 375mg will be administered thrice a day (TID) orally from Day 1 to Day 5; washout period of 72 hrs; Period 2 drug administration (APL-1501 ER capsules of 764mg, 1146 mg and 1528 mg will be administered twice daily (BID) from Day 9 to 13.
Intervention code [1] 0 0
Treatment: Drugs
Comparator / control treatment
Control group

Outcomes
Primary outcome [1] 0 0
Adverse Events (AEs)
Timepoint [1] 0 0
Part A: upto Day 11 post dose follow up; Part B: Upto Day 20 post dose follow up
Primary outcome [2] 0 0
Serious Adverse Events (SAEs)
Timepoint [2] 0 0
Part A: upto Day 11 post dose follow up; Part B: Upto Day 20 post dose follow up
Primary outcome [3] 0 0
Treatement Emergent Adverse Events (TEAEs)
Timepoint [3] 0 0
Part A: upto Day 11 post dose follow up; Part B: Upto Day 20 post dose follow up
Secondary outcome [1] 0 0
PK parameters: area under the curve (AUC)
Timepoint [1] 0 0
up to 120 hours post dose in each treatment period
Secondary outcome [2] 0 0
PK parameters: maximum concentration (Cmax)
Timepoint [2] 0 0
up to 120 hours post dose in each treatment period
Secondary outcome [3] 0 0
PK parameters: Tmax
Timepoint [3] 0 0
up to 120 hours post dose in each treatment period
Secondary outcome [4] 0 0
PK parameters: half-life (t1/2)
Timepoint [4] 0 0
up to 120 hours post dose in each treatment period
Secondary outcome [5] 0 0
Urine PK parameters: Renal clearance (CLr)
Timepoint [5] 0 0
up to 120 hours post dose in each treatment period
Secondary outcome [6] 0 0
Urine PK parameters: Total amount of the APL-1202 excreted in urine from time t1 to t2 hours (Aet1-t2)
Timepoint [6] 0 0
up to 120 hours post dose in each treatment period
Secondary outcome [7] 0 0
PK Parameters: Apparent total plasma clearance (CL/F)
Timepoint [7] 0 0
up to 120 hours post dose in each treatment period
Secondary outcome [8] 0 0
PK Parameters: Apparent terminal volume of distribution (Vz/F)
Timepoint [8] 0 0
up to 120 hours post dose in each treatment period

Eligibility
Key inclusion criteria
1. Healthy male or female 18 to 65 years of age (inclusive at the time of informed
consent).

2. In good general health, with no significant medical history and no clinically
significant abnormalities on physical examination, 12-lead ECG, vital signs and
oximetry measurements at Screening and/or before the first administration of
Investigational Products (IP), as determined by the Principal Investigator or
designee.

3. Clinical laboratory values within normal range as specified by the testing laboratory,
at Screening and/or before the first administration of IP unless deemed not clinically
significant (NCS) by the Principal Investigator or designee.

4. Body-mass index (BMI) between = 18.0 and = 32.0 kg/m2 at Screening and weight = 50 kg.

5. Current non-smoker or casual smoker who used no more than 5 cigarettes (or equivalent
quantity of any other nicotine-containing products eg, snuff, chewing tobacco, cigars,
cigarettes, pipes, e-cigarettes [Vaping] etc.) per week for 3 months prior to
Screening. Participants must abstain from smoking and abstain from using
nicotine-containing products (eg, nicotine chewing gum, nicotine plasters, or other
product used for smoking cessation) for 2 weeks prior to admission and throughout the
study period, and test negative at Screening and on Day -1 for urinary cotinine.

6. No relevant dietary restrictions.

7. Females must not be pregnant or lactating, and must use acceptable, highly effective
double contraception from Screening until 30 days after study completion, including
the Follow-up period.

8. Males must be surgically sterile (> 90 days since vasectomy with no viable sperm), or
if engaged in sexual relations with a women of child bearing potential (WOCBP), his
partner must be either surgically sterile (eg, hysterectomy, bilateral salpingectomy,
bilateral oophorectomy), or use an acceptable, highly effective contraceptive method
(see Section 7.3.3) from Screening until 90 days after study completion, including the
Follow-up period.

9. Able and willing to attend the necessary visits to the study site.

10. Able and willing to provide written informed consent after the nature of the study has
been explained and prior to the commencement of any study procedures.
Minimum age
18 Years
Maximum age
65 Years
Sex
Both males and females
Can healthy volunteers participate?
Yes
Key exclusion criteria
1. Underlying physical or psychological medical condition that, in the opinion of the PI,
would make it unlikely for the participant to comply with the protocol or complete the
study per protocol.

2. Receipt of blood products, or significant blood loss deemed to be CTCAE Grade 3 or
Grade 4 within 6 weeks prior to the first administration of IP.

3. Plasma donation within 7 days prior to the first administration of IP, or
platelet/blood donation within 4 weeks prior to the first administration of IP

4. Fever (body temperature > 38°C) or symptomatic viral or bacterial infection within 2
weeks prior to the first administration of IP.

5. Poor pill swallowing ability.

6. History of severe allergic or anaphylactic reactions, or sensitivity to the IP or its
constituents, including lactose intolerance/allergy.

7. History of malignancy, except for non-melanoma skin cancer, excised more than 1 year
prior to Screening and cervical intraepithelial neoplasia that has been successfully
cured more than 5 years prior to Screening.

8. History or presence of a condition associated with significant immunosuppression.

9. History of life-threatening infection (eg, meningitis). Severe infections within 4
weeks prior to the first administration of IP including but not limited to
hospitalisation for complications of infection, bacteraemia, or severe pneumonia.

10. Infections requiring parenteral antibiotics within 6 months prior to the first
administration of IP.

11. Vaccination with a live vaccine within 4 weeks prior to the first administration of
IP. COVID-19 or influenza can be exempted.

12. Exposure to any significantly immune suppressing drug (including experimental
therapies as part of a clinical study) within 4 months prior to the first
administration of IP or 5-half-lives, whichever is longer.

13. Positive test for hepatitis C virus antibody (HCVAb), hepatitis B virus surface
antigen (HBsAg), human Immunodeficiency virus (HIV) antibody, or COVID-19 at Screening
and Day-1.

14. History of tuberculosis (TB) or positive QuantiFERON®-TB Gold test at Screening or 2
successive indeterminate QuantiFERON-TB Gold test results.

15. Positive toxicology screening panel (urine test including qualitative identification
of barbiturates, tetrahydrocannabinol, amphetamines, benzodiazepines, opiates, cocaine
and tricyclic antidepressants), or alcohol breath test at Screening and Day-1.

16. History of substance abuse or dependency or history of recreational intravenous drug
use over the last 5 years (by self-declaration).

17. Regular alcohol consumption defined as > 10 standard drinks per week (where 1 standard
drink = 360 mL of beer, 45 mL of 40% spirit or a 150 mL glass of wine) or > 4 standard
drinks on any single day. Participant is unwilling to abstain from alcohol beginning
48 hours prior to the first administration of IP and for the duration of the study.

18. Use of any IP or investigational medical device within 30 days prior to the first
administration of IP, or 5 half-lives of the product (whichever is the longest), or
participation in more than 4 investigational drug studies within 1 year prior to the
first administration of IP.

19. Use of (or anticipated use of) any prescription drugs or over-the-counter (OTC)
medication, herbal remedies, supplements or vitamins 2 weeks prior to the first
administration of IP and during the course of the study without prior approval of the
PI and Medical Monitor (MM). Simple analgesia (paracetamol, nonsteroidal
anti-inflammatory drug ) may be permitted at the discretion of the PI. The use of
hormonal contraception, oral contraceptive pills, long-acting implantable hormones,
injectable hormones, a vaginal ring, or an intrauterine device (IUD) will be
permitted.

20. Unwilling to refrain from strenuous exercise (including weightlifting) 48 hours prior
to the admission to the clinical research unit (CRU) and 48 hours prior to any
outpatient visit.

21. Significant history or clinical manifestation of any metabolic, allergic,
dermatological, hepatic, renal, haematological, pulmonary, cardiovascular,
gastrointestinal, neurological, respiratory, endocrine, ophthalmological or
psychiatric disorder, as determined by the PI or designee, if deemed clinically
relevant by PI or designee.

22. History of stomach or intestinal surgery or resection that would potentially alter
absorption and/or excretion of orally administered drugs. Uncomplicated appendectomy,
uncomplicated cholecystectomy and hernia repair will be allowed as determined by the
PI or designee.

23. Use or intent to use any medications/products/food known to alter drug absorption,
metabolism, or elimination processes, including strong inducers or inhibitors of
metabolism enzymes or transporters, including but not limited to St. John's wort,
grapefruit, and grapefruit juice, within 14 days prior to the first administration of
IP, unless deemed acceptable by the PI or designee.

24. A participant who, in the opinion of the PI or designee, should not participate in
this study

25. Anything that the PI considers would jeopardise the safety of the participant, prevent
complete participation in the study, or compromise interpretation of the study data.

26. Smoked more than 5 cigarettes per week 3 months prior to Screening.

27. Has a positive cotinine at Screening and on Day -1 and or disagreed abstinence from
the use of any tobacco products 2 weeks prior to admission to the CRU and throughout
the study period.

28. Optic nerve disease and cataracts and those with a history of related conditions

-

Study design
Purpose of the study
Treatment
Allocation to intervention
Non-randomised 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
Open (masking not used)
Who is / are masked / blinded?



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

Recruitment
Recruitment status
Not yet recruiting
Data analysis
Reason for early stopping/withdrawal
Other reasons
Date of first participant enrolment
Anticipated
9/09/2023
Actual
Date of last participant enrolment
Anticipated
Actual
Date of last data collection
Anticipated
7/02/2024
Actual
Sample size
Target
48
Accrual to date
Final
Recruitment in Australia
Recruitment state(s)
VIC
Recruitment hospital [1] 0 0
Nucleus Network Pty Ltd - Melbourne
Recruitment postcode(s) [1] 0 0
3004 - Melbourne

Funding & Sponsors
Primary sponsor type
Commercial sector/Industry
Name
Jiangsu Yahong Meditech Co., Ltd aka Asieris
Address
Country

Ethics approval
Ethics application status

Summary
Brief summary
This is an integrated Phase 1, single centre, 2-part, open-label, dose-escalation study
conducted in healthy volunteers to assess the safety, tolerability, and PK of APL-1501 ER
capsules in comparison to APL-1202 IR tablets.
Trial website
https://clinicaltrials.gov/ct2/show/NCT06034015
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
Qiuyue Qu
Address 0 0
Country 0 0
Phone 0 0
+86 021 68583863
Fax 0 0
Email 0 0
qyqu@asieris.cn
Contact person for scientific queries



Summary Results

For IPD and results data, please see https://clinicaltrials.gov/ct2/show/NCT06034015