Tests valsartan liquid medicine in children with high blood pressure
Tests valsartan liquid against a placebo in children and teens with high blood pressure.
Plain-language title generated from the registry record
Registry title: A Phase III Clinical Study of Valsartan Oral Solution for the Treatment of Hypertension in Children and Adolescents
Key facts
- Where
- Linyi, ChinaSee the site
- Phase
- Phase 3
Could this be for you?
Answer for yourself. This is not a decision: only the study team can say whether you can take part.
- Are you between 6 and 17 years old?
Source: NCT06863987, who can take part
Where in China
- Shandong New Time Pharmaceutical Co., LTDLinyi, ChinaNo longer taking part
Questions to ask the study team
- How often do I need to come in, and for how long each time?
- Are travel costs paid?
- Can I keep my own doctor?
- What happens if I want to stop?
Trial details
- Who runs it
- Shandong New Time Pharmaceutical Co., LTD
- Trial code
- NCT06863987
- Record updated
- 7 March 2025
- Original description
This study was an randomized, double-Blind, placebo-controlled, multicenter Phase II/III study.Read full original descriptionShow less
A Randomized, Multicenter, Double-Blind, Placebo-Controlled, Phase III Study to Evaluate the Efficacy and Safety of Valsartan Oral Solution in Children and Adolescent Hypertensive Patients
This study was an randomized, double-Blind, placebo-controlled, multicenter Phase II/III study.
Inclusion: 6 years old ≤ age ≤ 17 years old, male or female; 18kg ≤ weight ≤ 160kg; Initial diagnosis of essential hypertension or previous history of essential hypertension at the V1 visit, mean seated systolic blood pressure (MSSBP) and/or mean seated diastolic blood pressure (MSDBP) before the first administration of medication (at the V2 visit) at least in the 95th percentile for the same age, sex, and height (with reference to the "Chinese Guidelines for the Prevention and Control of Hypertension, Revised Edition 2018" for Chinese children aged 3-17 years for each year of age, height corresponding blood pressure standard) and meets the criteria for hypertension medication; Vital organ function meets the following requirements:; Blood routine: hemoglobin ≥ 90 g/L, platelet count ≥ 100 × 109 /L, serum potassium ≤ 5.3 mmol/L; Liver function: ALT and AST ≤ 3 × ULN, total bilirubin level (TBIL) ≤ 2 × ULN; Renal function: glomerular filtration rate ≥ 30 mL/min/1.73 m2 (see Appendix 1 for calculation formula); The legal guardian and/or the person himself/herself voluntarily signed the informed consent form.
Exclusion: those with confirmed or previous hypertensive emergencies, hypertensive sub-emergencies; Medication adherence <80% and/or >120% during the placebo washout period at the V2 visit; those with a prior history of biliary cirrhosis and cholestasis; persons with a prior history of organ transplantation; patients with known active gastritis, duodenal ulcer or gastric ulcer or gastrointestinal/rectal bleeding within 3 months prior to the first dose; Patients with a history of clinically significant drug/food allergy (within 6 months prior to first dose) or history of atopic allergic disease (e.g., asthma, etc.) or known allergy to valsartan and its excipients or other angiotensin II receptor antagonists (ARBs) and/or angiotensin converting enzyme inhibitors (ACEIs); Persons who have been treated with any other clinical trial drug/device within 1 month prior to the first dose or within 5 half-lives of the trial drug, whichever is shorter; Patients with secondary hypertension; Patients with diabetes mellitus judged uncontrollable by the investigator; Persons who are infectious disease screen positive for hepatitis B surface antigen and/or core antibody and test positive for HBV-DNA, hepatitis C virus antibody positive and test positive for RNA, HIV positive, or syphilis spirochete antibody positive; Females with a history of menstruation who have had a positive pregnancy test; Persons with associated electrolyte disturbances (e.g., severe hyponatremia); Those who may not be able to complete the study for other reasons or those who, in the opinion of the investigator, are not suitable for inclusion.