Clinical trial · Interventional
A Study of Food Effect on the Pharmacokinetics of Fuzuloparib Capsules in Chinese Healthy Adult Subjects
Randomized, Open, Two Cycle, Two Sequence, Cross Reference Designed Study on the Effect of Food on the Pharmacokinetics of Fuzuloparib Capsules in Chinese Healthy Adult Subjects
NCT05440006CI-TRIAL-00060747completedPhase 1ClinicalTrials.gov clinicaltrialsProvenance
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
The objective of the study is to assess the effect of food on the pharmacokinetics, and safety of Fuzuloparib Capsules in healthy subject.
Conditions
Conditions (1)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Solid Tumor | Solid Neoplasm | CURATED_BROADER | 0.80 |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Fuzuloparib | Drug | — | UNRESOLVED |
Design
Arms and outcomes
Arms (2)
- type
- EXPERIMENTAL
- label
- Fed+ Fasted
- description
- The first cycle with high-fat meal, the second cycle under fasting.
- interventionNames
- Drug: Fuzuloparib
- type
- EXPERIMENTAL
- label
- Fasted + Fed
- description
- The first cycle under fasting, the second cycle with high-fat meal.
- interventionNames
- Drug: Fuzuloparib
Primary outcomes (3)
- measure
- Maximum Plasma Concentration (Cmax)
- timeFrame
- day 1 to day 10
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
Show eligibility criteria text
Inclusion Criteria: 1. Healthy male and female subjects over 18 years; 2. Body weight ≥ 50.0 kg for men and ≥ 45.0 kg for women, and body mass index (BMI) of 19.0 to 26.0 kg /m2 (inclusive); 3. Participants should have no fertility plan from signing the informed consent until 6 months after the last dose, and take effective contraceptive measures. Exclusion Criteria: 1. Subjects with evidence of disease or major surgery; 2. History of drug allergy; 3. Treatment with other investigational drug within 3 months, use of any prescription drugs, Chinese herbal supplements within 4 weeks, and/or need to use any over-the-counter (OTC), food supplements within 2 weeks before the first dose or during the trial; 4. Subjects refuse to stop drinking xanthine-rich beverages or foods at 48 hours before the first dose until the end of the study, and subjects refuse to stop any beverage or food containing grapefruit 7 days before the first dose; 5. Those who have heavy smokers, alcoholics or drug abuse 6. Lactating female subjects or fertile female subjects 7. Those with clinically significant abnormality of physical examination, vital signs and laboratory test during the screening period.
References
Publications (0)
Data not yet available
No reference posted for this study.