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A Multiple-Dose Research Study on Safety Evaluation of the GD Antrodia Camphorata in 30 Healthy Adult Subjects

A Multiple-Dose Research Study on Safety Evaluation of the GD Antrodia Camphorata in 30 Healthy Adult Subjects

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01007656
Enrollment
31
Registered
2009-11-04
Start date
2009-11-30
Completion date
2010-03-31
Last updated
2016-06-21

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Healthy

Keywords

healthy adult subjects, safety evaluation, GD Antrodia camphorata

Brief summary

* Study design is multiple-dose, open-label study * The purpose of this study is to evaluate the safety after twice daily GD Antrodia camphorata administration for 90 days in 30 healthy adult subjects. * Primary objective: The mean change from baseline in laboratory assessment after twice daily GD Antrodia camphorata administration at 90th day in 30 healthy adult subjects. * Secondary objective: The mean change from baseline in laboratory assessment after twice daily GD Antrodia camphorata administration at 10th, 20th, 30th, 45th and 60th day in 30 healthy adult subjects. * Safety Measurement: * including SGOT(AST), SGPT(ALT), albumin, glucose, creatinine, uric acid, cholesterol, TG, r-GT, alkaline phosphatase, total bilirubin, D-Bil, BUN, TP, GLO will be documented at 1st, 10th, 20th, 30th, 45th, 60th and 90th day. * vital signs (heart rate, blood pressure, and body temperature) will be documented at 1st, 10th, 20th, 30th, 45th, 60th and 90th day. * Subjects will be monitored throughout the confinement portion of the study.

Detailed description

* Study design is multiple-dose, open-label study * Antrodia camphorata has been proved to alleviate liver injury and fibrosis induced by chemical and reduces ALT and AST according to the literatures. * GD Antrodia camphorata will be marketed as dietary supplement. * The purpose of this study is to evaluate the safety after twice daily GD Antrodia camphorata administration for 90 days in 30 healthy adult subjects. * Primary objective: The mean change from baseline in laboratory assessment after twice daily GD Antrodia camphorata administration at 90th day in 30 healthy adult subjects. * Secondary objective: The mean change from baseline in laboratory assessment after twice daily GD Antrodia camphorata administration at 10th, 20th, 30th, 45th and 60th day in 30 healthy adult subjects. * Study design is multiple-dose, open-label study * The study site is Pingtung Christian Hospital Ruiguang Branch. * Safety Measurement: * including SGOT(AST), SGPT(ALT), albumin, glucose, creatinine, uric acid, cholesterol, TG, r-GT, alkaline phosphatase, total bilirubin, D-Bil, BUN, TP, GLO will be documented at 1st, 10th, 20th, 30th, 45th, 60th and 90th day. * vital signs (heart rate, blood pressure, and body temperature) will be documented at 1st, 10th, 20th, 30th, 45th, 60th and 90th day. * Subjects will be monitored throughout the confinement portion of the study.

Interventions

DIETARY_SUPPLEMENTGD Antrodia camphorata

Three 500mg capsules per oral dose, twice daily with an interval of 12 hours for 90 days

Sponsors

Golden Biotechnology Corporation
Lead SponsorINDUSTRY

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
20 Years to 40 Years
Healthy volunteers
Yes

Inclusion criteria

* Healthy adult, aged between 20 to 40 years old * Physically and mentally healthy subjects as confirmed by an interview, medical history, clinical examination, laboratory tests, chest X-ray and electrocardiogram * The normal range of the body mass index should between 18.5 and 24.9; body mass equals \[weight(Kg)\]/\[height(m)\]2 * Normal laboratory determinations results (within normal range or considered not clinically significant by the investigator) including: SGOT (AST), SGPT (ALT), albumin, glucose, creatinine, uric acid, cholesterol, TG, γ-GT, alkaline phosphatase, total bilirubin, D-Bil, BUN, TP, GLO, HBsAg and Anti-HCV. * Normal hematology results (within normal range or considered not clinically significant by the investigator) including: hemoglobin, hematocrit, WBC count with differential, RBC count and platelet count. * Normal urinalysis results (within normal range or considered not clinically significant by the investigator) including: glucose, protein, RBC, WBC, epith, casts and bacteria. * Female subject who is using adequate contraception since last menstruation and no plan for conception during the study * Female subject who is non-lactating * Female subject who has negative pregnancy test (urine) within 14 days prior to the study * Informed consent form signed

Exclusion criteria

* A recent history of drug or alcohol abuse * Medical history of allergic asthma or sensitivity to analogous product * A clinically significant illness within the past 4 weeks. * Evidence of any clinical significant renal, cardiovascular, hepatic, hematopoetic, neurological, pulmonary or gastrointestinal pathology within the past 4 weeks. * Ongoing peptic ulcer and constipation. * Planed vaccination during the time course of the study. * Participation of any clinical investigation during the last 60 days. * Regular use of any medication during the last 4 weeks. * Single use of any medication during the last one week. * Blood donation of more than 500 mL within the past 12 weeks. * Individuals are judged by the investigators or co-investigator to be undesirable as subjects.

Design outcomes

Primary

MeasureTime frameDescription
Serum Glutamic Oxaloacetic Transaminase (AST/SGOT)90 days
Serum Glutamic Pyruvate Transaminase (ALT/SGPT)90 days
Triglycerides (TG)90 days
Total Protein90 daysThe total protein test measures the total amount of two classes of proteins in the blood, albumin and globulin.
Uric Acid90 days
Albumin90 days
Alkaline Phosphatase90 days
Direct Bilirubin90 daysDirect bilirubin is referred to as conjugated bilirubin, which is water-soluble. It's taken up by the liver cells and conjugated to form the water-soluble bilirubin diglucuronide. It's used to diagnose and/or monitor liver diseases, such as cirrhosis, hepatitis or gallstones. If direct bilirubin is elevated more than unconjugated bilirubin, there's typically a problem associated with decreased elimination of bilirubin by the liver cells.
Total Bilirubin90 daysBilirubin is released into the blood when red blood cells break down. The liver uses bilirubin to make bile. Normally there is only a small amount of bilirubin in the blood. High levels may be caused by liver or blood problems.
BUN90 days
Cholesterol90 days
Creatinine90 days
Globulin90 days
Glucose90 days
R-glutamyl Transpeptidase (r-GT)90 days

Countries

Taiwan

Participant flow

Recruitment details

Thirty-one (31) healthy adult subjects enrolled the study. The study period was a continuous 90-day. Each subject received GD Antrodia Camphorata (as three 500 mg capsules) at 7:30 and 19:30 for continuous 90- day.

Pre-assignment details

One participant didn't continue on the trial by his own will.

Participants by arm

ArmCount
GD Antrodia Camphorata
GD Antrodia Camphorata is the extract from mycelium of the fungus Antrodia Camphorata which is an endemic species in Taiwan. According to the literatures, mycelium of Antrodia camphorata is beneficial to health. Moreover, the study product GD Antrodia Camphorata has been approved by Department of Health, Taiwan as a health supplement (approval number A00124).
31
Total31

Baseline characteristics

CharacteristicGD Antrodia Camphorata
Age, Categorical
<=18 years
0 Participants
Age, Categorical
>=65 years
0 Participants
Age, Categorical
Between 18 and 65 years
31 Participants
Albumin4.47 g/dL
STANDARD_DEVIATION 0.16
Alkaline phosphatase52.06 U/L
STANDARD_DEVIATION 13.18
BUN10.70 mg/dL
STANDARD_DEVIATION 2.53
Cholesterol169.10 mg/dL
STANDARD_DEVIATION 27.05
Creatinine0.78 mg/dL
STANDARD_DEVIATION 0.15
Direct bilirubin0.16 mg/dL
STANDARD_DEVIATION 0.06
Globulin2.41 g/dL
STANDARD_DEVIATION 0.32
Region of Enrollment
Taiwan
31 participants
r-glutamyl transpeptidase (r-GT)14.90 U/L
STANDARD_DEVIATION 6.85
Serum glutamic oxaloacetic transaminase SGOT (AST)16.74 U/L
STANDARD_DEVIATION 3.95
Serum glutamic pyruvate transaminase, SGPT (ALT)17.32 U/L
STANDARD_DEVIATION 9.03
Sex: Female, Male
Female
11 Participants
Sex: Female, Male
Male
20 Participants
Total bilirubin0.80 mg/dL
STANDARD_DEVIATION 0.28
Total protein6.88 g/dL
STANDARD_DEVIATION 0.32
Triglycerides (TG)75.19 mg/dL
STANDARD_DEVIATION 35.16
Uric acid5.79 mg/dL
STANDARD_DEVIATION 1.13

Adverse events

Event typeEG000
affected / at risk
deaths
Total, all-cause mortality
— / —
other
Total, other adverse events
0 / 31
serious
Total, serious adverse events
0 / 31

Outcome results

Primary

Albumin

Time frame: 90 days

ArmMeasureValue (MEAN)Dispersion
GD Antrodia CamphorataAlbumin4.74 g/dLStandard Deviation 0.2
Primary

Alkaline Phosphatase

Time frame: 90 days

ArmMeasureValue (MEAN)Dispersion
GD Antrodia CamphorataAlkaline Phosphatase55.81 U/LStandard Deviation 14.33
Primary

BUN

Time frame: 90 days

ArmMeasureValue (MEAN)Dispersion
GD Antrodia CamphorataBUN9.32 mg/dLStandard Deviation 2.49
Primary

Cholesterol

Time frame: 90 days

ArmMeasureValue (MEAN)Dispersion
GD Antrodia CamphorataCholesterol173.13 mg/dLStandard Deviation 28.09
Primary

Creatinine

Time frame: 90 days

ArmMeasureValue (MEAN)Dispersion
GD Antrodia CamphorataCreatinine0.84 mg/dLStandard Deviation 0.16
Primary

Direct Bilirubin

Direct bilirubin is referred to as conjugated bilirubin, which is water-soluble. It's taken up by the liver cells and conjugated to form the water-soluble bilirubin diglucuronide. It's used to diagnose and/or monitor liver diseases, such as cirrhosis, hepatitis or gallstones. If direct bilirubin is elevated more than unconjugated bilirubin, there's typically a problem associated with decreased elimination of bilirubin by the liver cells.

Time frame: 90 days

ArmMeasureValue (MEAN)Dispersion
GD Antrodia CamphorataDirect Bilirubin0.10 mg/dLStandard Deviation 0.07
Primary

Globulin

Time frame: 90 days

ArmMeasureValue (MEAN)Dispersion
GD Antrodia CamphorataGlobulin2.51 g/dLStandard Deviation 0.29
Primary

Glucose

Time frame: 90 days

ArmMeasureValue (MEAN)Dispersion
GD Antrodia CamphorataGlucose80.13 mg/dLStandard Deviation 6.13
Primary

R-glutamyl Transpeptidase (r-GT)

Time frame: 90 days

ArmMeasureValue (MEAN)Dispersion
GD Antrodia CamphorataR-glutamyl Transpeptidase (r-GT)17.42 U/LStandard Deviation 7.76
Primary

Serum Glutamic Oxaloacetic Transaminase (AST/SGOT)

Time frame: 90 days

ArmMeasureValue (MEAN)Dispersion
GD Antrodia CamphorataSerum Glutamic Oxaloacetic Transaminase (AST/SGOT)21.48 U/LStandard Deviation 6.43
Primary

Serum Glutamic Pyruvate Transaminase (ALT/SGPT)

Time frame: 90 days

ArmMeasureValue (MEAN)Dispersion
GD Antrodia CamphorataSerum Glutamic Pyruvate Transaminase (ALT/SGPT)21.94 U/LStandard Deviation 10.1
Primary

Total Bilirubin

Bilirubin is released into the blood when red blood cells break down. The liver uses bilirubin to make bile. Normally there is only a small amount of bilirubin in the blood. High levels may be caused by liver or blood problems.

Time frame: 90 days

ArmMeasureValue (MEAN)Dispersion
GD Antrodia CamphorataTotal Bilirubin0.73 mg/dLStandard Deviation 0.32
Primary

Total Protein

The total protein test measures the total amount of two classes of proteins in the blood, albumin and globulin.

Time frame: 90 days

ArmMeasureValue (MEAN)Dispersion
GD Antrodia CamphorataTotal Protein7.25 g/dLStandard Deviation 0.34
Primary

Triglycerides (TG)

Time frame: 90 days

ArmMeasureValue (MEAN)Dispersion
GD Antrodia CamphorataTriglycerides (TG)56.39 mg/dLStandard Deviation 23.17
Primary

Uric Acid

Time frame: 90 days

ArmMeasureValue (MEAN)Dispersion
GD Antrodia CamphorataUric Acid5.47 mg/dLStandard Deviation 1.25

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026