drugset / Trial / NCT02531295

Immunologic Response to Kansui in Treated HIV+ Individuals: a Dose Escalation Study

NCT02531295 ↗

Non-randomizedSingle-groupOpen-labelBasic science

Summary

The purpose of this study is to determine the safety and bioactivity of an herbal supplement called "kansui," which contains several active ingredients such as ingenols that may have a role in helping clear HIV from the body. Kansui has been used in traditional Chinese medicine for centuries to treat various ailments such as for eliminating excess fluid in the abdomen or lungs, loosening phlegm from the chest, and relieving constipation. Based on preliminary in vitro data from our group, kansui extract powder is a potent activator of HIV transpcription in latently infected Jurkat cells. The investigators' hypothesis is that kansui extract powder prepared as tea will be safe and well-tolerated, elicit an in vivo immunologic response, and at the doses administered, increase HIV transcription in latently-infected cells among HIV-infected patients on suppressive antiretroviral therapy.

Timeline

Start
2019-05-15
Primary completion
2020-03-19
Completion
2020-03-19

Outcome

Outcome not reported

Stopped (Enrollment): “Pause on clinical trial enrollment due to grant funding cuts after COVID-19”

Drugs

EvaluationDrugModalityDoseRoute
Subject Euphorbia kansui extract powder Traditional medicine (herbal / TCM) 1 g Oral