Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
| Name | Class |
|---|---|
| Big Leap Research | OTHER |
Not provided
Not provided
Not provided
Preclinical trials in animal models have suggested that the estimated dose of TD0015 in clinical presents no safety concerns.The investigational product is TD0015 pilulae, which is based on the traditional prescription named "Độc hoạt tang ký sinh thang" (Thien Kim Phuong).
The traditional prescription has the effect of circulating blood in the tendons and bones to bring out evil spirits, blood tonic, kidney tonic to prevent recurrence of diseases and against joint degeneration, joint deformation, muscle atrophy, stiffness to recover normal joint function.
The study objective is to evaluate the safety and efficacy of TD0015 pilulae to determine the optimal dose for investigational product. Phase II analyzes is performed on 90 patients and based on the results of phase II to adjust sample size and study design (if applicable) for phase III.
The trial lasts for ~ 30 months with 6 subject visits (from T0 to T5) and is conducted in National Hospital of Traditional Medicine (Hanoi, Vietnam).
Screening procedure occurs at T0 visit, followed by T1 (15+/-3 days), T2 (30+/-3 days), T3 (45+/-3 days), T4 (60+/-3 days) and T5 (90+/-3 days). The telephone contact visits are performed every 2 weeks by Investigators There are 2 levels of dosages: estimated dose - 5g (arm 1) and 1.5 times (arm 2) of estimated dose - 7.5g. There is also another arm using placebo, thus the trial have 3 arms in total.
As for 3 arms, patients is allowed to use oral NSAIDs (meloxicam 7,5mg x 1-2 tablets/day) when pain is severe.
Treatment time is 60 days. IP is used after a meal, 1 pack/time x 2 times/day.
Not provided
Not provided
Not provided
Not provided
Not provided
| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Placebo | Placebo Comparator | Placebo pilulae weighing 5g/pack, after a meal, 1pack/time x 2 times/day |
|
| Investigational product 1 | Experimental | estimated dose:TD0015 pilulae weighing 5g/pack , after a meal, 1pack/time x 2 times/day |
|
| Investigational product 2 | Experimental | 1.5 times of estimated dose: TD0015 pilulae weighing 7.5g/pack , after a meal, 1pack/time x 2 times/day |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| TD0015 | Drug | TD0015 is black, dark brown inside pilulae and has special smell of herbal, slightly sour then bitter taste. |
|
| Measure | Description | Time Frame |
|---|---|---|
| Change from baseline on the Western Ontario and McMaster Universities Osteoarthrities Index) WOMAC to evaluate the level of symptoms | WOMAC was scored by investigator in visits (T1, T2, T3, T4, T5) and compared with T0 | Day 15th, day 30th, day 45th, day 60th and day 30th after end of study |
| Change from baseline in Pain Scores on the Visual Analog Scale | VAS scale: 0 = no pain | 0-->2: mild | 2-->4: moderate | 4--> 6: severe | 6->8: extreme | 8-->10: untolerable Evaluate outcome of treatment according to VAS scale:
| day 15th, day 30th, day 45th, day 60th and day 30th after end of study |
| Change in symptoms severity was reported by patient on the Lequesne Index | Lequesne Index at prior and after treatment (day 15th, day 30th, day 45th, day 60th and day 30th after end of study). | day 15th, day 30th, day 45th, day 60th and day 30th after end of study |
| Percentage of patients taking rescue medication | 3 Arms were allowed to use oral NSAIDs (meloxicam 7,5 mg x 1-2 tablets/day) when pain was severe. All NSAIDs in the study need to be documented in detail | 90 days |
| The average dose of rescue medication was used | 90 days | |
| Frequency of AE, SAE | Reference CTCAE 4.03 | 90 days |
Not provided
Not provided
Inclusion Criteria:
Male or female patients ≥ 18 years old must meet ALL or the following criteria clusters 1,2,6 or 1,3,5,6 or 1,4,5,6 to be enrolled:
According to traditional medicine: The disease type is Wind-Cold-Damp Bi with Kidney and Liver Deficiency. Symptoms are knee joint is pain, cold and heavy. Pain is usually fixed, little movement, mild during the day, severe at night, increased in cold and wet weather. Warm compresses to relieve pain, knee joint may be swollen, limited movement, may have morning stiffness, joint deformity associated with muscle atrophy, back pain, not warm limbs.The tongue is pale, the tongue is white and greasy, and deep-thready-weak pulse.
Exclusion Criteria:
Not provided
Not provided
Not provided
Not provided
Not provided
| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Hong Van Thi Nguyen, MSC | Contact | (+84)916451269 | vannh@thaiduong.com.vn |
Not provided
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| National Hospital of Traditional Medicine | Recruiting | Hanoi | 100000 | Vietnam |
| PubMed Identifier | Type | Citation | Retractions |
|---|---|---|---|
| 40290409 | Derived | Ha NTT, Nghia DT, Nga HTV, Lua TT, Hong NTB, Hanh NT, Ngoc NK, Vuong NL. Traditional Vietnamese herbal medicine TD0015 in Knee Osteoarthritis: A Phase-II randomized controlled trial. Integr Med Res. 2025 Jun;14(2):101143. doi: 10.1016/j.imr.2025.101143. Epub 2025 Mar 31. |
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
| ID | Term |
|---|---|
| D020370 | Osteoarthritis, Knee |
| ID | Term |
|---|---|
| D010003 | Osteoarthritis |
| D001168 | Arthritis |
| D007592 | Joint Diseases |
| D009140 | Musculoskeletal Diseases |
Not provided
Not provided
Three arms: basic dose, 1.5 basic dose and placebo
Not provided
Not provided
Not provided
| TD0015 Placebo | Drug | Placebo was packed in pack 5g |
|
| D012216 |
| Rheumatic Diseases |