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PPK Study Based on Quantitative Pharmacology in Patients With Pamipril
NCT05848648 · Qianfoshan Hospital
In plain English
Click the button to translate this study into plain language — what it is, who qualifies, and what participation looks like.
About this study
In recent years, the advent of poly(ADP-ribose) polymerase(PARP) inhibitors is one of the important breakthroughs in the field of tumor-targeted therapy, and its therapeutic effect on ovarian cancer is quite significant Pamiparib is a potent, selective, oral PARP 1/2 inhibitor. In preclinical models, pamiparib demonstrated PARP-DNA complex trapping, brain penetration, antitumor activity, and inhibition of PARylation.
Therefore, at least 50 patients using pamiparib will be included. Before and after treatment, the laboratory examination data ,blood concentration ,combined medication and adverse events of the patients will be collected. The population pharmacokinetic model of pamiparib was established to evaluate the correlation between pharmacokinetic parameters and adverse reactions.
Eligibility criteria
Inclusion Criteria:
1. The age of the patient is ≥ 18 years old and less than 80 years old.
2. Receive treatment with pamipalil.
3. The patient signed a written informed consent form.
Exclusion Criteria:
1. The expected survival time may be less than the treatment cycle.
2. Is being treated with other systemic trial drugs.
3. There are other factors that the researchers think are not suitable for joining the group.
Study design
Enrollment target: 50 participants
Age groups: adult, older_adult
Timeline
Starts: 2023-05-01
Estimated completion: 2026-06-01
Last updated: 2024-04-09
Primary outcomes
- • Blood drug concentration (6 months)
Sponsor
Qianfoshan Hospital · other
Contacts & investigators
ContactHuang Xin · contact · 13791120711@126.com · 13791120711
InvestigatorHuang Xin · study_director, Qianfoshan Hospital
All locations (1)
Xin HuangRecruiting
Jinan, Shandong, China