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Heathly SubjectsPhase 1NCT07193576

A Pharmacokinetic Study of the Food Effect on Flonoltinib Maleate Tablets

A Phase 1 study testing flunotinib in people with Heathly Subjects, run by Chengdu Zenitar Biomedical Technology Co., Ltd at 1 site in China.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

A Randomized, Open-Label, Two-Period, Two-Crossover Study to Evaluate the Effect of Food on the Pharmacokinetics of Flonoltinib Maleate Tablets in Healthy Subjects Under Fed Conditions Read more about this study

Who is it for?
Ages 18 to 45 yearsHealthy volunteers can take part
Conditions the study is for
Heathly Subjects
What is being tested?
flunotinib
Could I receive a placebo?
No, everyone receives an active treatment
How many people
24 participants
Where
1 siteChina
Study dates
4 Aug 2024to 11 Sep 2024
Phase
Phase 1
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 45 years
  • All sexes
  • Healthy volunteers accepted
  • Adult

Who may be able to join

  • 18 to 45 years old (including 18 and 45 years old), gender is not limited;
  • Male subjects weighing ≥50.0 kg, female subjects ≥45.0 kg, with body mass index (BMI) between 19.0 and 25.0 kg/m2 (including borderline values);
  • Fully understand the content of the trial, the test drug, the trial process, etc, and be able to communicate well with the researcher, willing to comply with the study regulations, participate in the trial voluntarily and sign an Inform consent.

Who cannot join

  • Those with a history of severe allergies (e.g, angioedema and anaphylaxis), allergies (Screening Consultation/Admission Consultation) Those with a history of severe allergy (e.g, angioedema and anaphylaxis), allergy (e.g, allergy to pollen, two or more medications/foods), or history of food or drug allergy or other metabolic disorders (e.g, asthma, hives, eczematous dermatitis, etc.) judged by the investigator to be clinically significant, or a known allergy to JAK inhibitors or an allergy to excipient components of the test medication;
  • Abnormal and clinically significant results of physical examination, vital signs, 12-lead electrocardiogram, laboratory tests (including routine blood, blood biochemistry, urine routine, blood pregnancy (only for women of childbearing age), infectious disease screening, antinuclear antibody, coagulation function, tuberculosis antibody, chest X-ray, abdominal ultrasound) prior to enrolment;
  • QTcF > 440 ms for males and > 460 ms for females on ECG during the screening period;
  • Those who have undergone major surgical procedures within 3 months prior to screening or plan to undergo surgery during the trial period;
  • Acute illness within 2 weeks prior to screening; clinically significant infection (e.g, upper respiratory tract infection, nasopharyngitis, urinary tract infection, etc.) within 3 months prior to screening; evidence of any infection within 7 days prior to screening; history of herpes simplex infection, or recurrent (>once) herpes zoster or disseminated herpes zoster;
  • History of any clinically serious disease or any disease or condition that, in the opinion of the investigator, may affect the outcome of the trial, including but not limited to a history of circulatory, endocrine, neurological, gastrointestinal, urinary, or haematological, immunological, psychiatric, and metabolic disorders;
  • Dysphagia or any history of gastrointestinal disorders (or gastrointestinal resection, etc.) affecting drug absorption; 8 . Those with irregular bowel movements and habitual constipation or diarrhoea;
  • 9. Those with a history of lipid metabolism defects, such as: familial hyperlipidaemia, lipoid nephropathy, or patients with acute pancreatitis accompanied by hyperlipidaemia; 10. Those with a positive combined urine multi-drug test (including morphine, methamphetamine, ketamine, methylenedioxyamphetamine, tetrahydrocannabinolic acid); 11. Those with a history of previous drug abuse or drug dependence; 12. Anyone who has been vaccinated within 8 weeks prior to screening or who plan to be vaccinated during the course of the study or within 8 weeks of administration of study drug; 13. Anyone who has donated or lost ≥400 mL of blood or received a blood transfusion within 3 months prior to screening; or anyone who has donated blood or blood components within 1 month of the planned end of the trial; 14. Those with special dietary requirements or those who are unable to comply with the uniform dietary and appropriate regulations of the study center; 15. Those who have smoked more than 3 cigarettes/day or equivalent amount of tobacco in the 3 months prior to screening; or who have consumed ≥14 units of alcohol per week (1 unit equals to 17.5mL or 14g of pure alcohol, which is approximately equal to 35mL of 50° white wine or 350mL of 5° beer); or who do not agree to abstain from smoking or drinking alcohol for the duration of the trial; or those who have a positive result from an alcohol breathalyzer test; 16. Any person who has taken any prescription drug, over-the-counter drug, any vitamin product or herbal medicine (JAK inhibitor, immunosuppressant, etc.) within 14 days prior to screening; 17. Those who have combined strong inducers of liver metabolism enzymes (e.g, omeprazole, barbiturates, carbamazepine, amiloride, pallidomycin, aminoglutethimide, phenytoin, grumet, rifampicin, sulfinpyrazone, roxithromycin, etc.) within the 4 weeks (28 days) prior to Screening, or any other history of medication use that in the judgement of the Investigator has the potential to interfere with in vivo pharmacokinetics of the test drug. Anyone who has taken any drug known to cause prolongation of the QT/QTcF interval or a drug with a risk of causing torsades de pointes (TdP) within 4 weeks (28 days) prior to Screening; or drugs with a long half-life; 18. Anyone who consumed any food or drink containing caffeine (e.g. coffee, strong tea, cola, chocolate, etc.) or food containing grapefruit juice that may have an effect on metabolising enzymes or who consumed food or drink containing alcohol within 48 h prior to the administration of the drug; 19. Those who are participating in other clinical trials and have used an investigational drug, vaccine or device within 3 months prior to the first dose; 20. Pregnant or breastfeeding women or women of childbearing age who have had unprotected sex within 14 days prior to screening; 21. The subject or his/her partner is unwilling to use non-pharmacological contraception (e.g, total abstinence, condom, IUD, ligation, etc.) for contraception during the trial period or the subject and/or his/her partner has a pregnancy plan within 3 months of the administration of the study drug; 22. The subject may not be able to complete the study for other reasons or there are other factors that, in the opinion of the investigator, make participation in the trial unsuitable.

Trial locations and contacts

1 site in 1 country.

China1 site
  • Chengdu Xinhua Hospital

    Chengdu, Sichuan, 610000

Other trials in China

About this study

Official title: A Randomized, Open-Label, Two-Period, Two-Crossover Study to Evaluate the Effect of Food on the Pharmacokinetics of Flonoltinib Maleate Tablets in Healthy Subjects Under Fed Conditions

A Randomized, Open-Label, Two-Period, Two-Crossover Study to Evaluate the Effect of Food on the Pharmacokinetics of Flonoltinib Maleate Tablets in Healthy Subjects Under Fed Conditions

Read the detailed description

Primary Study Objective. To evaluate the effect of a high-fat diet on the pharmacokinetics of single-dose oral Flonoltinib Maleate tablets in healthy subjects.

Secondary Study Objectives To evaluate the safety of single-dose oral administration of Flonoltinib Maleate Tablets under Fast or Fed condition in healthy subjects.

Being tested
flunotinib
Keywords
Flonoltinib Maleate Tablet, Pharmacokinetic study, Heathly Subjects

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • flunotinibDrug

    100mg

Study groups in NCT07193576
Study groupRoleWhat they receive
A groupExperimentalSubjects received Flonoltinib Maleate: under fast condition → washout → under fed condition
Receives: Drug: flunotinib
B groupExperimentalSubjects received Flonoltinib Maleate: under fed condition → washout → under fast condition
Receives: Drug: flunotinib

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Cmax

    maximum concentration

    Measured: Day1 and Day11 Within 2hours before administration and 0.5 hours, 1 hours, 2 hours, 3 hours, 4 hours, 6 hours, 8 hours, 12hours, 24hours, 48 hours, 72 hours, 96 hours, 120hours, 144 hours after administration

  2. AUC0-t

    Area under the blood concentration-time curve from 0 o 'clock to the last measurable concentration at collection time t

    Measured: Day1 and Day11 Within 2 hours before administration and 0.5 hours, 1 hours, 2 hours, 3 hours, 4 hours, 6 hours, 8 hours, 12hours, 24hours, 48 hours, 72 hours, 96 hours, 120hours, 144 hours after administration

  3. AUC0-∞

    The area under the blood drug concentration-time curve from 0 to infinity time

    Measured: Day1 and Day11 Within 2 hours before administration and 0.5 hours, 1 hours, 2 hours, 3 hours, 4 hours, 6 hours, 8 hours, 12hours, 24hours, 48 hours, 72 hours, 96 hours, 120hours, 144 hours after administration

  4. Tmax

    time to peak

    Measured: Day1 and Day11 Within 2 hours before administration and 0.5 hours, 1 hours, 2 hours, 3 hours, 4 hours, 6 hours, 8 hours, 12hours, 24hours, 48 hours, 72 hours, 96 hours, 120hours, 144 hours after administration

  5. t1/2

    Terminal phase elimination half-life

    Measured: Day1 and Day11 Within 2 hours before administration and 0.5 hours, 1 hours, 2 hours, 3 hours, 4 hours, 6 hours, 8 hours, 12hours, 24hours, 48 hours, 72 hours, 96 hours, 120hours, 144 hours after administration

  6. tlag

    retardation time

    Measured: Day1 and Day11 Within 2 hours before administration and 0.5 hours, 1 hours, 2 hours, 3 hours, 4 hours, 6 hours, 8 hours, 12hours, 24hours, 48 hours, 72 hours, 96 hours, 120hours, 144 hours after administration

  7. CL/F

    apparent clearance

    Measured: Day1 and Day11 Within 2 hours before administration and 0.5 hours, 1 hours, 2 hours, 3 hours, 4 hours, 6 hours, 8 hours, 12hours, 24hours, 48 hours, 72 hours, 96 hours, 120hours, 144 hours after administration

  8. Vd/F

    apparent volume of distribution

    Measured: Day1 and Day11 Within 2 hours before administration and 0.5 hours, 1 hours, 2 hours, 3 hours, 4 hours, 6 hours, 8 hours, 12hours, 24hours, 48 hours, 72 hours, 96 hours, 120hours, 144 hours after administration

  9. λz

    Terminal elimination rate constant

    Measured: Day1 and Day11 Within 2 hours before administration and 0.5 hours, 1 hours, 2 hours, 3 hours, 4 hours, 6 hours, 8 hours, 12hours, 24hours, 48 hours, 72 hours, 96 hours, 120hours, 144 hours after administration

  10. %AUCex

    The extrapolation percentage of AUC0--∞

    Measured: Day1 and Day11 Within 2 hours before administration and 0.5 hours, 1 hours, 2 hours, 3 hours, 4 hours, 6 hours, 8 hours, 12hours, 24hours, 48 hours, 72 hours, 96 hours, 120hours, 144 hours after administration

Secondary outcomes (26)
  1. health checkup

    General examination

    Measured: Screening period, day 17 or early withdrawal

  2. participants with abnormal vital signs

    Temperature

    Measured: Screening period,Day1to day7 and day11 to day17

  3. participants with abnormal laboratory tests results

    White blood cell count

    Measured: Screening period, Day-1 (examination results within 7 days are acceptable), Day17, or early withdrawal

  4. participants with abnormal laboratory tests results

    creatinine

    Measured: Screening period, Day-1 (examination results within 7 days are acceptable), Day17, or early withdrawal

  5. participants with abnormal laboratory tests results

    Blood pregnancy test,Only for women of childbearing age

    Measured: Screening period, Day-1 ,Day 10,Day 17 or early termination

  6. Urinary albumin creatinine ratio

    Urinary albumin creatinine ratio

    Measured: D-1, D17 or early termination

  7. ECG QT Interv

    12-lead electrocardiogram

    Measured: Screening period, Day-1 ,Day1, Day10, Day11, Day17 or early termination

  8. participants with abnormal vital signs

    blood pressure

    Measured: Screening period,Day1to day7 and day11 to day17

  9. participants with abnormal laboratory tests results

    neutrophil count

    Measured: Screening period, Day-1 (examination results within 7 days are acceptable), Day17, or early withdrawal

  10. participants with abnormal laboratory tests results

    hemoglobin

    Measured: Screening period, Day-1 (examination results within 7 days are acceptable), Day17, or early withdrawal

  11. participants with abnormal laboratory tests results

    platelet coun

    Measured: Screening period, Day-1 (examination results within 7 days are acceptable), Day17, or early withdrawal

  12. participants with abnormal laboratory tests results

    red blood cell count

    Measured: Screening period, Day-1 (examination results within 7 days are acceptable), Day17, or early withdrawal

  13. participants with abnormal laboratory tests results

    alanine aminotransferase

    Measured: Screening period, D-1 (examination results within 7 days are acceptable), Day17, or early withdrawal

  14. participants with abnormal laboratory tests results

    aspartate aminotransferase

    Measured: Screening period, D-1 (examination results within 7 days are acceptable), Day17, or early withdrawal

  15. participants with abnormal laboratory tests results

    total bilirubin

    Measured: Screening period, Day-1 (examination results within 7 days are acceptable), Day17, or early withdrawal

  16. participants with abnormal laboratory tests results

    direct bilirubin

    Measured: Screening period, Day-1 (examination results within 7 days are acceptable), Day17, or early withdrawal

  17. participants with abnormal laboratory tests results

    γ-glutamyl transpeptidase

    Measured: Screening period, Day-1 (examination results within 7 days are acceptable), Day17, or early withdrawal

  18. participants with abnormal laboratory tests results

    Alkaline phosphatase

    Measured: Screening period, Day-1 (examination results within 7 days are acceptable), Day17, or early withdrawal

  19. participants with abnormal laboratory tests results

    triglycerides

    Measured: Screening period, Day-1 (examination results within 7 days are acceptable), Day17, or early withdrawal

  20. participants with abnormal laboratory tests results

    total cholesterol

    Measured: Screening period, Day-1 (examination results within 7 days are acceptable), Day17, or early withdrawal

  21. adverse event

    Adverse events, serious adverse events, suspected and unexpected serious adverse reactions (SUSAR), priority adverse reactions, incidence of adverse reactions

    Measured: From date of randomization until the date of completion of data collection, assessed up to 17 days or early termination

  22. participants with abnormal urinalysis

    Acidity/Alkalinity

    Measured: Screening period, Day-1 , Day17, or early withdrawal

  23. participants with abnormal urinalysis

    Red Blood Cells

    Measured: Screening period, Day-1 , Day17, or early withdrawal

  24. participants with abnormal urinalysis

    White Blood Cells

    Measured: Screening period, Day-1 , Day17, or early withdrawal

  25. participants with abnormal urinalysis

    Protein

    Measured: Screening period, Day-1 , Day17, or early withdrawal

  26. participants with abnormal urinalysis

    Glucose

    Measured: Screening period, Day-1 , Day17, or early withdrawal

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted26 Sep 2025
  2. Study start4 Aug 2024
  3. Primary completion11 Sep 2024
  4. Study completion11 Sep 2024

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase 1
Primary purpose
Other
Allocation
Randomised
Intervention model
Crossover
Masking
None (open label)
Enrolment
24 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07193576
Sponsor's protocol ID
H-FNTN-PI-FE
Status last verified
Sep 2025
First submitted
2 Apr 2025
Last updated
26 Sep 2025
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

A Phase 1 study testing flunotinib in people with Heathly Subjects, run by Chengdu Zenitar Biomedical Technology Co., Ltd at 1 site in China.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 3 inclusion and 8 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 26 Sep 2025. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in China. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

What does this phase mean?

Phase 1 studies test a treatment in a small group of people for the first time or in a new way, mainly to check safety and find the right dose.

Not every study follows the same path, and some studies (observational studies, device studies) have no phase.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Cmax (time frame: Day1 and Day11 Within 2hours before administration and 0.5 hours, 1 hours, 2 hours, 3 hours, 4 hours, 6 hours, 8 hours, 12hours, 24hours, 48 hours, 72 hours, 96 hours, 120hours, 144 hours after administration). The study lists 10 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 26 Sep 2025.

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