Safety and Efficacy of T89 in Prevention and Treatment of Adults With Acute Mountain Sickness (AMS)

Completed · Phase 2 · Has a placebo group

Conditions studied: Acute Mountain Sickness (AMS)

In brief

Acute mountain sickness (AMS) is one of three syndromes of altitude illness. It is very common when people venture over 2500 meters altitude. This illness is mainly induced by acute exposure to low partial pressure of oxygen at high altitude that will cause a pathological effect on humans. T89 capsule is a modernized industrialized traditional Chinese herbal medicine. It is a botanical drug for oral use. In recent years, several literatures and clinical studies have showed that oral administration of T89 may provide substantial benefits in the prevention or alleviation of symptoms associated with acute mountain sickness (AMS), including nausea, vomiting, headache, dizziness, fatigue, and sleep disturbance. Such effect was also observed in a pilot clinical study recently conducted in Tibet in China. This study is a prospective, double-blind, randomized, placebo-controlled phase 2 clinical trial having three arms including T89 low-dose, T89 high-dose and a placebo controlled group. People will be screened against the inclusion/exclusion criteria after informed consent signed. Eligible subjects will be randomly assigned into one of three arms and instructed to use T89 orally twice daily for 14 days (Days 1-14) before ascending, and 5 days after ascending during the observation period (Days 15-19). The primary efficacy parameter is Lake Louise Scoring System (LLSS) which will be evaluated by subject-self and principal investigator in clinic.

Key facts

Study ID: NCT03552263
Run by: Tasly Pharmaceuticals, Inc.
People needed: 132
Starts: 2018-06-07
Expected to finish: 2019-11-10
Last updated by the study team: 2019-11-13

Who can join

Age: 18 and older, up to 55. Sex: any. Healthy volunteers: accepted.

You may qualify if…

Healthy volunteers: ages 18 - 55 years old;
Primary residence elevation of 1,000 ft or lower;
Not ascending to altitude >10,000 ft within 4 months prior to screening;
Females of childbearing potential must have a negative pregnancy test, not be breast feeding and established on a method of contraception that in the investigator's opinion is acceptable. Females must agree to remain on their established method of contraception from the time of the screening visit and throughout the study period.
Willing to participate voluntarily and to sign a written informed consent.

You may not qualify if…

Subjects with medical history of cardiovascular, cerebrovascular diseases or asthma;
Subjects with clinically significant respiratory system disease, digestive disease, mental disease, metabolic disease, acute infection or anemia;
Total LLSS self-assessment score and clinical assessment score is greater than 1 before ascending (Screening visit and Visit 1);
Blood oxygen saturation (SpO2) <95% at sea level;
Subjects with abnormal renal or liver function with clinical significance (alanine aminotransferase (ALT) or aspartate aminotransferase (AST) > 2×upper limits of normal(ULN), Creatinine> ULN);
Subjects with C reactive protein (CRP) > ULN;
Subjects with primary headache;
Surgery or blood donation within 3 months prior to screening;
On treatment of any medications (including any dietary supplements)except for birth control within 14 days prior to screening and throughout the study period;
Contradictive to treatment of Danshen (Radix Salivae Miltiorrhizae, RSM) products;
Women in pregnancy or lactation period;
Substance abuse. Subjects with a recent history (within the last 2 years) of alcoholism or known drug dependence;
Participation in any other clinical trial or on an investigational drug within 30 days prior to screening;
A family member or relative of the study site staff;
Any other condition that, in the opinion of the investigator, is likely to prevent compliance with the study protocol, interfere with the assessment, or pose a safety concern if the subject participates in the study.

Where it is running

Hypoxia Research Lab, UCSF Parnassus Campus, S-256 — San Francisco, California, United States

Full record on ClinicalTrials.gov

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