Clinical Study on the Use of Huaier Granules for the Treatment of Proteinuria Related to Bevacizu… (NCT07358520) | Clinical Trial Compass
Not Yet RecruitingPhase 4
Clinical Study on the Use of Huaier Granules for the Treatment of Proteinuria Related to Bevacizumab and Anlotinib in Lung Cancer Patients
China40 participantsStarted 2026-01-28
Plain-language summary
This study is a prospective, multicenter, parallel-controlled clinical trial designed to evaluate the therapeutic efficacy of Huaier Granules for proteinuria occurring in lung cancer patients undergoing treatment with either Bevacizumab or Anlotinib.
Who can participate
Age range18 Years
SexALL
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Inclusion Criteria:
* Age ≥18 years;
* Histopathologically confirmed diagnosis of lung cancer;
* Receiving Bevacizumab or Anlotinib treatment;
* Positive urine protein detection, with 0.15g \< 24-hour urinary protein quantification \< 3.5g;
* No treatment with Huaier Granules within one month prior to enrollment;
* Expected survival time not less than 6 months;
* Voluntary participation in this study and provision of signed informed consent.
Exclusion Criteria:
* Known allergy, contraindication, or caution to any component of Huaier Granules;
* Inability to take oral medication;
* Required or ongoing use of drugs known to potentially affect proteinuria, including but not limited to ACE inhibitors, glucocorticoids (\>3 weeks), and Chinese patent medicines (as per respective drug prescribing information);
* Proteinuria caused by underlying diseases, including but not limited to nephropathy, hypertension, urinary tract infection, systemic lupus erythematosus, multiple myeloma, etc.;
* Women who are pregnant, breastfeeding, or planning pregnancy;
* Currently participating in other clinical trials investigating drugs for treating proteinuria;
* Refusal to cooperate with follow-up;
* Any other reasons deemed by the investigator as unsuitable for participation in this study.
What they're measuring
1
16-week Efficacy Rate for Proteinuria Treatment
Timeframe: Start of treatment until 16-week follow-up