A Compassionate Use Program to Provide Access to Sodium Thiosulfate for the Protection From Cisplatin-Induced Hearing Loss in Children Who Had Standard-risk Hepatoblastoma
试验速览
- 阶段
- 不适用
- 状态
- Available
- 发起方
- TRPHARM
- 试验地点
- 1
研究概览
简要总结
This is a CUP which is designed to provide treatment access of STS to pediatric patients for the protection from Cisplatin-Induced Hearing Loss in children who had standard-risk hepatoblastoma.
Approximately 10 patients will be treated as part of this program as specified below:
Sodium Thiosulfate vials i.v. 80 mg/mL.
This Compassionate Use Program for STS will consist of 2 phases:
Screening:
Patients will only be able to participate in this CUP if they meet the eligibility criteria.
Treatment:
Any clinical assessments, physical examinations, and dosage changes will be determined by the treating physician as per local standard medical practice.
All serious adverse events (SAEs) will be reported. All related non-serious adverse events (AEs) will be reported where "related" means any event where a causal relationship between STS and the event is at least, a reasonable possibility. All non-serious AEs leading to dose modification or discontinuation will be reported. Pregnancies, outcomes of pregnancies, and exposure through breastfeeding will also be reported.
研究设计
- 研究类型
- Expanded Access
入排标准
- 年龄范围
- 1 Month 至 18 Years（Child, Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Children older than 1 month and younger than 18 years of age who had standard-risk hepatoblastoma that had not been treated previously with STS and receive cisplatin.
- •A written informed consent was provided from all the patients and/or parents or legal guardians of children.
排除标准
- •Any previous participation in an STS clinical trial. E-
- •Participation in another clinical study with an investigational product during the most recent chemotherapy course.
- •Patients with a known hypersensitivity to STS or any of the excipients of the product.
- •Patients receiving any systemic chemotherapy or radiotherapy (except for palliative reasons) or major surgery within 3 weeks prior to STS treatment.
- •Persistent toxicities (>Common Terminology Criteria for Adverse Event (CTCAE) CTCAE grade 2) caused by previous cancer therapy, excluding alopecia.
- •Breast feeding or pregnant women.