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

NCT ID: NCT04993729

Last Updated: 2024-08-13

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE3
• Total Enrollment: 853 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2021-07-21
• Study Completion Date: 2023-05-26

Brief Summary

The specific aim of this double blind, randomized phase III trial is to evaluate the safety and efficacy of T89 in preventing Acute Mountain Sickness (AMS) and relieving the symptoms of AMS after rapid ascent.

Detailed Description

Acute mountain sickness (AMS) is a common ailment in people venturing over 2,500 meters altitude. It is a pathological effect of high altitude on humans, caused by acute exposure to low partial pressure of oxygen at high altitude. It presents with a cluster of nonspecific symptoms including headache and one of the following: gastrointestinal symptoms, fatigue and/or weakness, dizziness/ lightheadedness or difficulty sleeping.

T89 capsule is a modernized industrialized version of a traditional Chinese herbal medicine. It is a botanical drug product for oral use. Previous clinical studies showed T89 has substantial benefits in the prevention or amelioration of symptoms associated with acute mountain sickness (AMS).This is double-blind, randomized, placebo controlled pivotal phase 3 study. After informed consent is obtained, eligible subjects will be randomized to one of the 3 study groups (T89 high dose, T89 low dose and placebo control). The study drug will be given orally for 5 days (2 days at sea level and 3 days at high altitude). The clinical assessment of Lake Louise Scoring System (LLSS), blood oxygen saturation, the exercise tolerance, blood pressure and heart rate will be performed at sea level and altitude. A total of 846 subjects will be enrolled with 282 subjects in each treatment arm, and a minimum of 756 subjects are expected to complete the study.

Conditions

Acute Mountain Sickness (AMS)

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: QUADRUPLE

Study Groups

T89 low-dose group

Subjects in this group will take three T89 capsules and one Placebo capsule each time by oral administration three times daily for 5 days.

Group Type: EXPERIMENTAL

T89 capsule

Intervention Type: DRUG

T89 capsule (trade name Dantonic®) is a botanical drug containing 75mg active substance which is the water extract of Danshen and Sanqi.

T89 capsules, p.o. TID.

Placebo capsule

Intervention Type: DRUG

Placebo capsules, p.o. TID.

T89 high-dose group

Subjects in this group will take four T89 capsules each time by oral administration three times daily for 5 days.

Group Type: EXPERIMENTAL

T89 capsule

Intervention Type: DRUG

T89 capsule (trade name Dantonic®) is a botanical drug containing 75mg active substance which is the water extract of Danshen and Sanqi.

T89 capsules, p.o. TID.

Placebo group

Placebo capsule does not contain any amount of active substance. Subjects in this group will take four placebo capsules each time by oral administration three times daily for 5 days.

Group Type: PLACEBO_COMPARATOR

Placebo capsule

Intervention Type: DRUG

Placebo capsules, p.o. TID.

Interventions

T89 capsule

T89 capsule (trade name Dantonic®) is a botanical drug containing 75mg active substance which is the water extract of Danshen and Sanqi.

T89 capsules, p.o. TID.

Intervention Type: DRUG

Placebo capsule

Placebo capsules, p.o. TID.

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

1. Healthy volunteers: ages 18 - 55 years old;

2. Primary residence elevation of 2,461 ft (750m) or lower;

3. Not ascending to altitude >10,000 ft within 4 months prior to screening;

4. Females of childbearing potential must have a negative pregnancy test 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;

5. Willing to participate voluntarily and sign a written informed consent.

Exclusion Criteria

1. Subjects with medical history of cardiovascular, cerebrovascular diseases or asthma; uncontrolled hypertension with SBP>140 and or DBP>90 mmHg;

2. Subjects with current and clinically significant respiratory system disease, digestive disease, liver disease, central nervous system disease, psychiatric disease, metabolic disease, renal disease, acute infection or anemia, or who test positive for COVID-19 (COVID testing will be performed, not per study requirement, but in compliance with local law or policy, and subject with known positive for COVID-19 will be excluded).

3. Total LLSS score (LLSS score) is ≥2 at any check point during screening period;

4. Blood oxygen saturation (SpO2), preferably tested on the left-hand index finger, is less than 95% at screening visits;

5. Subjects with abnormal renal or liver function with clinical significance (ALT or AST > 2×ULN, Creatinine > ULN) at screening visit;

6. Subjects with CRP > ULN at screening visit;

7. Subjects with primary (migraine, tension-type headache, and cluster headache etc.) or secondary headaches (headache related to infection, vascular disease etc.) within one month at screening;

8. Surgery or blood donation within 3 months prior to screening;

9. On treatment of any medications (including any dietary supplements) except for birth control within 14 days prior to screening and throughout the study period;

10. Smokers who had a habit of smoking during the last 4 months prior to the starting of screening;

11. Contradictive to treatment of Danshen (Radix Saliva Miltiorrhize Bge., RSM) products;

12. Women who are pregnant or lactating.

13. Substance abuse. Subjects with a recent (within the last 6 months) history of substance abuse (alcohol, marijuana, or known drug dependence). Or subjects who have a positive urine substance test at screening;

14. Participation in any other interventional clinical trial or on an investigational drug within 30 days prior to screening;

15. A family member or relative of the study site staff;

16. Any 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 at screening.

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 55 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

Tasly Pharmaceuticals, Inc.

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Henry H Sun, PhD, MD

Role: STUDY_CHAIR

Tasly Pharmaceuticals, Inc.

Locations

Hypoxia Research Lab, UCSF Parnassus Campus, S-256

San Francisco, California, United States

Affiliated Hospital of Chengdu University of TCM

Chengdu, Sichuan, China

Tibet Autonomous Region People's Hospital

Lhasa, Tibet, China

Countries

United States; China

Other Identifiers

T89-31-AMS

Identifier Type: -

Identifier Source: org_study_id