/ CompletedNot Applicable [Translation] Bioequivalence study of tetracaine hydrochloride gel in humans
主要目的:
比较空腹条件下德全药品(江苏)股份有限公司提供的受试制剂盐酸丁卡因凝胶(规格:4%(以丁卡因计))与 Alliance Pharmaceuticals Limited 持证的参比制剂盐酸丁卡因凝胶(商品名:Ametop®;规格:4%(以丁卡因计))在健康参与者中吸收程度和吸收速度的差异,评价两制剂的生物等效性。
次要目的:
1)评价受试制剂与参比制剂在健康参与者中的安全性;
2)评价受试制剂与参比制剂对健康参与者的皮肤刺激性。
[Translation] Primary Objective: To compare the absorption extent and rate of absorption of the test formulation (tetracaine hydrochloride gel, 4% (based on tetracaine)) provided by Dequan Pharmaceuticals (Jiangsu) Co., Ltd., and the reference formulation (tetracaine hydrochloride gel, trade name: Ametop®; 4% (based on tetracaine)) certified by Alliance Pharmaceuticals Limited, in healthy participants under fasting conditions, and to evaluate the bioequivalence of the two formulations.
Secondary Objectives:
1) To evaluate the safety of the test formulation and the reference formulation in healthy participants;
2) To evaluate the skin irritation of the test formulation and the reference formulation in healthy participants.
/ CompletedNot Applicable [Translation] Bioequivalence study of minocycline hydrochloride capsules
主要研究目的
评价中国健康成年受试者空腹及餐后条件下单次单剂量口服盐酸米诺环素胶囊受试制剂[规格:100mg(按C23H27N3O7计),申办者:德全药品(江苏)股份有限公司]和参比制剂[商品名:ミノマイシン®(MINOMYCIN®),规格:100mg(按C23H27N3O7计),持证商:Pfizer Japan Inc.]后的药代动力学特点和生物等效性。
次要研究目的
研究盐酸米诺环素胶囊受试制剂[规格:100mg(按C23H27N3O7计)]和参比制剂[商品名:ミノマイシン®(MINOMYCIN®),规格:100mg(按C23H27N3O7计)]在中国健康成年受试者中的安全性。
[Translation] Main study objectives
To evaluate the pharmacokinetic characteristics and bioequivalence of the test formulation of minocycline hydrochloride capsules [Specification: 100 mg (calculated in C23H27N3O7), applicant: Dequan Pharmaceutical (Jiangsu) Co., Ltd.] and the reference formulation [trade name: MINOMYCIN®, specification: 100 mg (calculated in C23H27N3O7), licensee: Pfizer Japan Inc.] after a single oral dose in healthy Chinese adult subjects under fasting and postprandial conditions.
Secondary study objectives
To study the safety of the test formulation of minocycline hydrochloride capsules [Specification: 100 mg (calculated in C23H27N3O7)] and the reference formulation [trade name: MINOMYCIN®, specification: 100 mg (calculated in C23H27N3O7)] in healthy Chinese adult subjects.
/ Not yet recruitingNot ApplicableIIT Quantified Evaluation of Whole Face 8-points Supra-periosteum High Molecular Weight Hyaluronic Acid Injection in Asian
Facial aging is a complex process characterized by skin atrophy, subcutaneous fat loss, and alterations in bone structure. The loss of volume, primarily due to bone resorption and loss of adjacent fat volume from different facial regions, leads to soft tissue flattening. Hyaluronic acid (HA) is a widely used biomaterial in clinical practice, known for its excellent tissue compatibility, low risk, and safety. Previous research and clinical practice have demonstrated that HA for facial lifting can help restore facial fullness, elasticity, and promote a more youthful appearance. Dermatologist previously utilized the supra-periosteum lift technique in high molecular weight hyaluronic acid injection. It was found that the material properties of high molecular weight hyaluronic acid not only made it suitable for filling but also provided lifting support, resulting in improvements in cheek fullness and facial aging. However, there has been no detailed quantitative study on the efficacy of high molecular weight hyaluronic acid for facial lifting.
To further investigate this effect, the investigators plan to conduct a prospective, open-label clinical trial. The investigators will recruit 25 adult and use an 8-point supra-periosteum facial lifting technique to inject high molecular weight hyaluronic acid. Assessments will be conducted preoperatively, postoperatively, and 4 weeks, 12 weeks and 24 weeks postoperatively to analyze the treatment efficacy. The eight injection points will be located at the brow peak, brow tail, pterion, lateral canthus, zygomatic ligament, mid-cheek, nasolabial fold, and mentalis. The investigators will use evaluation forms with four angles and six lengths, as well as the Global Aesthetic Improvement Scale, to quantify the degree of improvement in facial aging. Additionally, The investigators will use a satisfaction survey to understand subjects' perceptions of postoperative lifting effects and overall improvement satisfaction. The investigators hypothesized this study to improve facial aging in Asian patients and provide long-lasting effects.
100 Clinical Results associated with Yung Shin Pharm Ind Kunshan Co. Ltd.
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