NCT01053897已完成2 期
A Phase 2, Multicenter, Double-Blind, Placebo-Controlled Study of GBT009 for Treatment of Incisional Wounds Following Breast Reconstruction Surgery
适应症
试验速览
- 阶段
- 2 期
- 状态
- 已完成
- 入组人数
- 5
- 试验地点
- 2
- 主要终点
- Photography- Independent Scar Assessment Panel
研究概览
简要总结
The primary objective of this study is to assess whether intradermal injections of GBT009 along full thickness incisions following surgery results in an improvement in scar appearance.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Single Group
- 主要目的
- Treatment
- 盲法
- Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
入排标准
- 年龄范围
- 18 Years 至 70 Years（Adult, Older Adult）
- 性别
- Female
- 接受健康志愿者
- 否
入选标准
- •Subjects must meet all of the following criteria to be considered eligible to participate in the study:
- •be a female between 18 and 70 years of age, inclusive
- •have a body mass index ≤ 32 kg/m2 and a body weight between 50 and 95 kg, inclusive
- •be scheduled for a mastectomy with breast reconstruction surgery using an abdominal flap technique
- •for women diagnosed with breast cancer, has standard of care treatment for breast cancer prior to surgery and will have standard of care treatment for breast cancer after surgery
- •for subjects of childbearing potential, be surgically sterile or using an insertable, injectable, transdermal, or combination oral contraceptive approved by the FDA through completion of the study and have negative results on a serum pregnancy test done before administration of study medication (women who are postmenopausal [no menses for at least 2 years] are also eligible to participate)
- •be able to understand the study procedures, agree to participate in the study program, and voluntarily provide written informed consent
排除标准
- •Subjects who meet any of the following criteria will be excluded from participating in the study:
- •have clinically significant laboratory abnormalities at screening
- •have, as determined by the investigator or the sponsor's medical monitor, a history or clinical manifestations of significant renal, hepatic, cardiovascular, metabolic, neurologic, psychiatric, coagulopathic disorder or other condition that would preclude participation in the study
- •have received treatment for a severe, uncontrolled inflammatory disease or allergic condition within three months of screening
- •have a life expectancy ≤ 2 years
- •have a history of alcoholism or drug addiction or abuse within 5 years
- •have evidence of a clinically significant abnormality upon evaluation of 12 lead ECG
- •have evidence of any past or present clinically significant medical condition, including skin disease, that would impair wound healing
- •have a history of keloid scar formation
- •have existing scarring in the abdominal area of study that would interfere with the efficacy assessments
- •have a history of (within the past 5 years) or an active malignancy, other than breast cancer
- •have a breast cancer that has been staged at Stage IIIB, IIIC or IV
- •have received a cytotoxic agent or have been treated with radiation within 90 days of screening and/or, in the opinion of the investigator, will likely require treatment in the 30 day period following the administration of study medication
- •have received anticoagulation medication within 5 days of dosing with study medication
- •have participated in any study involving an investigational product within 30 days before dosing with study medication
- •have routinely used tobacco products within 6 months preceding the study period
结局指标
主要结局
Photography- Independent Scar Assessment Panel
时间窗: 0.5, 1, 2, 3, 6, 9 and 12 Months
An independent panel was planned to review scar photography to determine more preferable outcomes. Panel was not performed.
次要结局
- Patient Observer Scar Assessment Scale (POSAS)(12 Month (End of Study))
- Manchester Scar Scale (MSS)(12 Month (End of Study))
- Overall Scar Preference(12 Month (End of Study))
研究者
研究点 (2)
Loading locations...
相似试验
终止
2 期
BG9924 in Combination With Methotrexate for Participants With Active Rheumatoid ArthritisRheumatoid ArthritisNCT00458861Biogen115
已完成
2 期
Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) Neutralizing Antibody BGB-DXP593 in Participants With Mild-to-Moderate Coronavirus Disease 2019 (COVID-19)Covid19NCT04551898BeiGene181
已完成
2 期
BTRX-246040 Study in Participants With Parkinson's Disease With Motor FluctuationsMotor DisorderParkinson DiseaseNCT03608371BlackThorn Therapeutics, Inc.24
已完成
3 期
A Study of the Efficacy and Safety of GB-0998 in Patients With Unexplained Recurrent MiscarriageRecurrent MiscarriageNCT02184741Japan Blood Products Organization99
已完成
3 期
Assessment of Efficacy and Safety of Topical Administration of 1% Glycopyrronium Bromide (GPB) in Patients With Primary Axillary Hyperhidrosis and the Assessment of Long-term Efficacy and Safety of Topical Administration of 1% GPB Cream in Patients With Primary Axillary Hyperhidrosis.Primary Axillary HyperhidrosisNCT03658616Dr. August Wolff GmbH & Co. KG Arzneimittel518