An Open Label, Dose Escalation Study to Evaluate the Safety and Efficacy of Intralesional Injection of STP705 in Adult Patients With Cutaneous Squamous Cell Carcinoma in Situ (isSCC)
试验速览
- 阶段
- 1 期
- 状态
- 已完成
- 发起方
- 入组人数
- 25
- 试验地点
- 1
- 主要终点
- Proportion of participants with histological clearance of treated isSCC lesion at the End of Treatment (EOT).
研究概览
简要总结
This is an open label, dose escalation study to evaluate the safety and efficacy of intralesional injection of STP705 in adult patients with Cutaneous Squamous Cell Carcinoma in situ (isSCC, Bowen's disease). The purpose of this trial is to evaluate the safety, tolerability and efficacy of various doses of STP705 administered as Intralesional injection in subjects with isSCC.
Goals:
- To determine the safe and effective recommended dose of STP705 for the treatment of isSCC.
- Analysis of biomarkers common to isSCC formation pathway including TGF-β1 and COX-2.
详细描述
This open label, dose escalation study is designed to evaluate the safety and efficacy of various doses of STP705 administered as an intralesional injection in subjects with cutaneous in situ squamous cell carcinoma (isSCC).
The primary objective of this study is to evaluate the safety, tolerability, and efficacy of various doses of STP705 administered as an Intralesional injection in subjects with cutaneous squamous cell carcinoma in situ skin cancer (isSCC). This study seeks to establish a safe and effective recommended dose of STP705 for the treatment of isSCC. Expression of biomarkers common to the isSCC formation pathway, including TGF-β1 and COX-2, will be evaluated.
The primary endpoint will be the proportion of participants with histological clearance of treated isSCC lesion at the End of Treatment (EOT). Histological clearance (HC) will be defined as the absence of detectable evidence of isSCC tumor cell nests as determined by central pathology review.
Secondary endpoints will include i) time to histological clearance of treated isSCC lesion over the 6 week treatment period, ii) proportion of participants with complete clinical clearance of treated isSCC lesion based on investigator assessment at the End of Treatment (EOT), iii) time to complete clinical clearance of treated isSCC lesion based on investigator assessment over the 6 week treatment period, and iv) the change in size of the treated isSCC lesion over the 6 week treatment period.
Safety and tolerability will be assessed by the number of incidence of adverse events (AEs) and serious adverse events (SAEs); the incidence of AEs and SAEs leading to discontinuation of trial medication; the incidence and severity of Local Skin Response (LSR); hypopigmentation and hyperpigmentation following treatment; and the tolerability of repeated Intralesional administration of STP705 as assessed by investigator-evaluation of injection site reactions for all patients and within each cohort.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Sequential
- 主要目的
- Treatment
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Male or female adult ≥ 18 years of age.
- •Primary, histologically confirmed trunk or extremity (non-peri-orbital/-anogenital/-facial/-scalp) isSCC lesion suitable for excision with a minimum diameter of 0.5cm and with a maximum diameter of 2.0cm.
- •Histological diagnosis made no more than 6 months prior to the screening visit.
- •Histological biopsy removed ≤25% of the original area of the target lesion.
- •No other dermatological disease in the isSCC target site or surrounding area, which in the opinion of the investigator, could interfere with the study.
- •Willing to refrain from using non-approved lotions or creams on the target site and surrounding area during the treatment period.
- •Willing to refrain from exposure to excessive direct sunlight or ultraviolet light and to avoid the use of tanning parlors for the duration of the study.
- •Laboratory values for the tests (listed in the Study Schedule) within the reference ranges as defined by the central laboratory, or "out of range" test results that is clinically acceptable to the investigator. Acceptable "out of range" values are generally those within 2 standard deviations of the mean or explainable due to concurrent medications or disease processes.
- •Ability to follow study instructions and likely to complete all study requirements.
- •Written informed consent obtained, including consent for tissue to be examined and stored by the Central Histology Lab.
- •Written consent to allow photographs of the target isSCC lesion to be used as part of the study data and documentation.
- •For females of childbearing potential, a negative pregnancy test at screening and using an acceptable form of birth control (oral / implant/ injectable/ transdermal contraceptives, intrauterine device, condom, diaphragm, abstinence, or a monogamous relationship with a partner who has had a vasectomy).
排除标准
- •Pregnant or lactating.
- •Presence of known or suspected systemic cancer.
- •Histological evidence of nBCC, sBCC, invasive SCC, or any other non-isSCC tumor in the biopsy specimen.
- •Histological evidence of severe squamous metaplasia, infiltrative, desomoplastic or micronodular growth patterns in the biopsy specimen.
- •History of recurrence of the target isSCC lesion.
- •Prior exposure to STP
- •Evidence of dermatological disease or confounding skin condition in the treatment area, e.g., BCC, actinic keratosis, rosacea, psoriasis, atopic dermatitis, eczema, xeroderma pigmentosa.
- •Concurrent disease or treatment that suppresses the immune system;
- •Patients with baseline QTC > 480 msec using Frederica's formula
- •Chronic medical condition that in the judgment of the investigator(s) would interfere with the performance of the study or would place the patient at undue risk.
- •Known sensitivity to any of the ingredients in the study medication.
- •Use of a tanning beds or other excessive or prolonged exposure to ultraviolet light or direct sunlight during the study.
- •Treatment with systemic chemotherapeutic agents within the 6 months prior to the screening visit.
- •Use of systemic retinoids within the 6 months prior to the screening period.
- •Treatment with systemic immunomodulators or immunosuppressants within the 6 months prior to the screening period.
- •Use of topical immunomodulators within 2cm of the target isSCC lesion within the 4 weeks prior to the screening period.
- •Treatment with the following topical agents within 2cm of the target isSCC lesion within the 4 weeks prior to the screening visit: amino-levulanic acid, 5-fluorouracil, corticosteroids, retinoids, diclofenac, ingenol mebutate, or imiquimod.
- •Treatment with liquid nitrogen, surgical excision (excluding diagnostic incisional biopsy) or curettage within 2cm of the target isSCC lesion during the 4 weeks prior to the screening visit.
- •Elective surgery within 4 weeks prior to the screening visit, during the study, or 4 weeks after the study period.
- •Evidence of current chronic alcohol or drug abuse.
- •Current enrollment in an investigational drug or device study or participation in such a study within 4 weeks of the screening visit.
- •In the investigator's opinion, evidence of unwillingness, or inability to follow the restrictions and requirements of the protocol and complete the study.
- •Taking any investigational product within 1 month of first dose of STP705.
研究组 & 干预措施
Cohort A: STP705 10 μg dose
Cohort A: STP705 10 μg dose, intradermal injection, given once a week for up to 6 weeks
干预措施: STP705 (Drug)
Cohort B: STP705 20 μg dose
Cohort B: STP705 20 μg dose, intradermal injection, given once a week for up to 6 weeks
干预措施: STP705 (Drug)
Cohort C: STP705 30 μg dose
Cohort C: STP705 30 μg dose, intradermal injection, given once a week for up to 6 weeks
干预措施: STP705 (Drug)
Cohort D: STP705 60 μg dose
Cohort D: STP705 60 μg dose, intradermal injection, given once a week for up to 6 weeks
干预措施: STP705 (Drug)
Cohort E: STP705 120 μg dose
Cohort E: STP705 120 μg dose, intradermal injection, given once a week for up to 6 weeks
干预措施: STP705 (Drug)
结局指标
主要结局
Proportion of participants with histological clearance of treated isSCC lesion at the End of Treatment (EOT).
时间窗: 6 weeks
Proportion of participants with histological clearance of treated isSCC lesion at the End of Treatment (EOT). Histological clearance (HC) will be defined as the absence of detectable evidence of isSCC tumor cell nests as determined by central pathology review.
次要结局
- Time to histological clearance of treated isSCC lesion over the 6 week treatment period.(over the 6 week treatment period)
- Proportion of participants with complete clinical clearance of treated isSCC lesion based on investigator assessment at the End of Treatment (EOT).(6 weeks)
- Time to complete clinical clearance of treated isSCC lesion based on investigator assessment over the 6 week treatment period.(over the 6 week treatment period)
- Change in size of the treated isSCC lesion over the 6 week treatment period.(over the 6 week treatment period)