Cisplatin-Induced Hearing Loss in Children Who Had Standard-risk Hepatoblastoma Clinical Trial
Official title:
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
| NCT number | NCT04132882 |
| Other study ID # | TRP-STS-001 |
| Secondary ID | |
| Status | Available |
| Phase | |
| First received | |
| Last updated |
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.
| Status | Available |
| Enrollment | 0 |
| Est. completion date | |
| Est. primary completion date | |
| Accepts healthy volunteers | |
| Gender | All |
| Age group | 1 Month to 18 Years |
| Eligibility | Inclusion Criteria: I-1. 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. I-2. A written informed consent was provided from all the patients and/or parents or legal guardians of children. Exclusion Criteria: E-1. Any previous participation in an STS clinical trial. E-2. Participation in another clinical study with an investigational product during the most recent chemotherapy course. E-3. Patients with a known hypersensitivity to STS or any of the excipients of the product. E-4. Patients receiving any systemic chemotherapy or radiotherapy (except for palliative reasons) or major surgery within 3 weeks prior to STS treatment. E-5. Persistent toxicities (>Common Terminology Criteria for Adverse Event (CTCAE) CTCAE grade 2) caused by previous cancer therapy, excluding alopecia. E-6. Breast feeding or pregnant women. |
| Country | Name | City | State |
|---|---|---|---|
| Turkey | Ankara University School of Medicine | Ankara |
| Lead Sponsor | Collaborator |
|---|---|
| TRPHARM | Fennec Pharma |
Turkey,